Fernando Rivadeneira

Professor Dr. M.D PhD.

I am a medical doctor and genetic epidemiologist by training, Professor of Translational Genomics with emphasis on the skeletal system. In Erasmus MC I hold appointments in the Department of Internal Medicine and the Department of Oral and Maxillofacial Surgery. My passion is my research; focusing on seeking the translation of genomic discoveries to clinical settings, holding particular emphasis on musculoskeletal health and disease outcomes. This research employs a life-course approach integrating epidemiological, imaging and genomic data within the setting of large population-based epidemiological cohorts, including the Generation R (in children) and the Rotterdam Study (in the elderly) cohorts.

My team has played pivotal roles in the identification of genetic determinants of musculoskeletal traits applying high throughput technology, (i.e., GWAS and NGS), making part of large-scale collaborations in the setting of large international GWAS consortia and making use of large scale resources, like the UK Biobank.

Favorite

“My favorite thing to do is play sports, especially football”

I am co-leading the European Commission (EC-FP7)-funded “Genetics Factors of Osteoporosis” (GEFOS) consortium and since then have been partner in multiple EC- Horizon projects. Until recently, I was chair of the “GEnomics of MusculoSkeletal traits TranslatiOnal Network” (GEMSTONE) Cost Action of the EC; and have been awarded an – European Research Council – ERC Advanced Grant for the program “LEveraging GENomic Discoveries and skeletal phenotyping to improve osteoporosis patient cARE” (LEGENDARE).

2024

Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

Bradfield, J. P., Kember, R. L., Early Growth Genetics (EGG) consortium, Ulrich, A., Balkiyarova, Z., Alyass, A., Aris, I. M., Bell, J. A., Broadaway, K. A., Chen, Z., Chai, J. F., Davies, N. M., Fernandez-Orth, D., Bustamante, M., Fore, R., Ganguli, A., Heiskala, A., Hottenga, J. J., Íñiguez, C. & Kobes, S. & 31 others, , Dec 2024In: Genome Biology. 251p. 22 1 p., 22.

 
 

Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses

Demidov, G., Yaldiz, B., Garcia-Pelaez, J., Solve-RD Consortium, de Boer, E., Schuermans, N., Van de Vondel, L., Paramonov, I., Johansson, L. F., Musacchia, F., Benetti, E., Bullich, G., Sablauskas, K., Beltran, S., Gilissen, C., Hoischen, A., Ossowski, S., de Voer, R., Lohmann, K. & Oliveira, C. & 4 others, , 26 Oct 2024In: npj Genomic Medicine. 91, 49.

 
 

LINE-1 RNA triggers matrix formation in bone cells via a PKR-mediated inflammatory response

Mangiavacchi, A., Morelli, G., Reppe, S., Saera-Vila, A., Liu, P., Eggerschwiler, B., Zhang, H., Bensaddek, D., Casanova, E. A., Medina Gomez, C.Prijatelj, V., Della Valle, F., Atinbayeva, N., Izpisua Belmonte, J. C., Rivadeneira, F., Cinelli, P., Gautvik, K. M. & Orlando, V., Sept 2024In: EMBO Journal. 4317p. 3587-3603 17 p.

 

Lifestyle factors and metabolomic aging biomarkers: Meta-analysis of cross-sectional and longitudinal associations in three prospective cohorts

Kuiper, L. M., Smit, A. P., Bizzarri, D., van den Akker, E. B., Reinders, M. J. T., Ghanbari, M.van Rooij, J. G. J.Voortman, T.Rivadeneira, F., Dollé, M. E. T., Herber, G. C. M., Rietman, M. L., Picavet, H. S. J., van Meurs, J. B. J. & Verschuren, W. M. M., Aug 2024In: Mechanisms of Ageing and Development. 220, 111958.

Identification of Transcripts with Shared Roles in the Pathogenesis of Postmenopausal Osteoporosis and Cardiovascular Disease

Reppe, S., Gundersen, S., Sandve, G. K., Wang, Y., Andreassen, O. A., Medina-Gomez, C.Rivadeneira, F., Utheim, T. P., Hovig, E. & Gautvik, K. M., 20 May 2024In: International Journal of Molecular Sciences. 2510, 5554.

 
 
 
 

Sarcopenia and Sarcopenic Obesity and Mortality Among Older People

Benz, E., Pinel, A., Guillet, C., Capel, F., Pereira, B., De Antonio, M., Pouget, M., Cruz-Jentoft, A. J., Eglseer, D., Topinkova, E., Barazzoni, R., Rivadeneira, F.Ikram, M. A.Steur, M.Voortman, T., Schoufour, J. D., Weijs, P. J. M. & Boirie, Y., 25 Mar 2024In: JAMA network open. 73, e243604.

 

A meta-analysis of previous falls and subsequent fracture risk in cohort studies

Vandenput, L., Johansson, H., McCloskey, E. V., Liu, E., Schini, M., Åkesson, K. E., Anderson, F. A., Azagra, R., Bager, C. L., Beaudart, C., Bischoff-Ferrari, H. A., Biver, E., Bruyère, O., Cauley, J. A., Center, J. R., Chapurlat, R., Christiansen, C., Cooper, C., Crandall, C. J. & Cummings, S. R. & 67 others, , Mar 2024In: Osteoporosis International. 353p. 469-494 26 p.

 
 

Bone mineral density and the risk of incident dementia: A meta-analysis

Lary, C. W., Ghatan, S., Gerety, M., Hinton, A., Nagarajan, A., Rosen, C., Ross, R. D., Bennett, D. A., DeStefano, A. L., Ikram, M. A.Rivadeneira, F., Kiel, D. P., Seshadri, S. & Beiser, A., Jan 2024In: Journal of the American Geriatrics Society. 721p. 194-200 7 p.

 
2023

Previous fracture and subsequent fracture risk: a meta-analysis to update FRAX

Kanis, J. A., Johansson, H., McCloskey, E. V., Liu, E., Åkesson, K. E., Anderson, F. A., Azagra, R., Bager, C. L., Beaudart, C., Bischoff-Ferrari, H. A., Biver, E., Bruyère, O., Cauley, J. A., Center, J. R., Chapurlat, R., Christiansen, C., Cooper, C., Crandall, C. J., Cummings, S. R. & da Silva, J. A. P. & 64 others, , Dec 2023In: Osteoporosis International. 3412p. 2027-2045 19 p.

 

Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth

Beaumont, R. N., Flatley, C., Vaudel, M., Wu, X., Chen, J., Moen, G. H., Skotte, L., Helgeland, Ø., Solé-Navais, P., Banasik, K., Albiñana, C., Ronkainen, J., Fadista, J., Stinson, S. E., Trajanoska, K., Wang, C. A., Westergaard, D., Srinivasan, S., Sánchez-Soriano, C. & Bilbao, J. R. & 68 others, , Nov 2023In: Nature Genetics. 5511p. 1807-1819 13 p.

 

Generic Platform for the Multiplexed Targeted Electrochemical Detection of Osteoporosis-Associated Single Nucleotide Polymorphisms Using Recombinase Polymerase Solid-Phase Primer Elongation and Ferrocene-Modified Nucleoside Triphosphates

Ortiz, M., Jauset-Rubio, M., Trummer, O., Foessl, I., Kodr, D., Acero, J. L., Botero, M. L., Biggs, P., Lenartowicz, D., Trajanoska, K.Rivadeneira, F., Hocek, M., Obermayer-Pietsch, B. & O’Sullivan, C. K., 23 Aug 2023In: ACS Central Science. 98p. 1591-1602 12 p.

 
 

Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis

Medina-Gomez, C., Mullin, B. H., Chesi, A., Prijatelj, V., Kemp, J. P., Shochat-Carvalho, C., Trajanoska, K., Wang, C., Joro, R., Evans, T. E., Schraut, K. E., Li-Gao, R., Ahluwalia, T. S., Zillikens, M. C., Zhu, K., Mook-Kanamori, D. O., Evans, D. S., Nethander, M., Knol, M. J. & Thorleifsson, G. & 38 others, , 4 Jul 2023In: Communications Biology. 61, 691.

 
 
 
 

Novel Genetic Determinants of Dental Maturation in Children

Grgic, O., Prijatelj, V., Dudakovic, A., Vucic, S., Dhamo, B., Trajanoska, K., Monnereau, C., Zrimsek, M., Gautvik, K. M., Reppe, S., Shimizu, E., Timpson, N. J., Jaddoe, V. W. V., Jarvelin, M. R., Evans, D., Uitterlinden, A. G., Ongkosuwito, E. M., van Wijnen, A. J., Medina-Gomez, C. & Rivadeneira, F. & 1 others, , Mar 2023In: Journal of Dental Research. 1023p. 349-356 8 p.

 
 

Embracing Monogenic Parkinson’s Disease: The MJFF Global Genetic PD Cohort

the MJFF Global Genetic Parkinson’s Disease Study Group, Vollstedt, E. J., Schaake, S., Lohmann, K., Padmanabhan, S., Brice, A., Lesage, S., Tesson, C., Vidailhet, M., Wurster, I., Hentati, F., Mirelman, A., Giladi, N., Marder, K., Waters, C., Fahn, S., Kasten, M., Brüggemann, N., Borsche, M. & Foroud, T. & 31 others, , 1 Feb 2023In: Movement Disorders. 382p. 286-303 18 p.

 
 

High Bone Mass Disorders: New Insights From Connecting the Clinic and the Bench

Bergen, D. J. M., Maurizi, A., Formosa, M. M., McDonald, G. L. K., El-Gazzar, A., Hassan, N., Brandi, M. L., Riancho, J. A., Rivadeneira, F., Ntzani, E., Duncan, E. L., Gregson, C. L., Kiel, D. P., Zillikens, M. C., Sangiorgi, L., Högler, W., Duran, I., Mäkitie, O., Van Hul, W. & Hendrickx, G., Feb 2023In: Journal of Bone and Mineral Research. 382p. 229-247 19 p.

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

Young, K. L., Fisher, V., Deng, X., Brody, J. A., Graff, M., Lim, E., Lin, B. M., Xu, H., Amin, N., An, P., Aslibekyan, S., Fohner, A. E., Hidalgo, B., Lenzini, P., Kraaij, R.Medina-Gomez, C., Prokić, I., Rivadeneira, F., Sitlani, C. & Tao, R. & 42 others, , 12 Jan 2023In: Human Genetics and Genomics Advances. 41, 100163.

 
2022
 

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

Longchamps, R. J., Yang, S. Y., Castellani, C. A., Shi, W., Lane, J., Grove, M. L., Bartz, T. M., Sarnowski, C., Liu, C., Burrows, K., Guyatt, A. L., Gaunt, T. R., Kacprowski, T., Yang, J., De Jager, P. L., Yu, L., Bergman, A., Xia, R., Fornage, M. & Feitosa, M. F. & 32 others, , 2 Dec 2022In: Human Genetics. 1411p. 127-146 20 p.

 

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Winkler, T. W., Rasheed, H., The LifeLines Cohort StudyDiscovEHR and MyCode Community Health InitiativeVA Million Veteran Program, Teumer, A., Gorski, M., Rowan, B. X., Stanzick, K. J., Thomas, L. F., Tin, A., Hoppmann, A., Chu, A. Y., Tayo, B., Thio, C. H. L., Cusi, D., Chai, J. F., Sieber, K. B., Horn, K. & Li, M. & 33 others, , 1 Dec 2022In: Communications Biology. 51, 580.

 
 

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

Holstege, H., Hulsman, M., Charbonnier, C., Grenier-Boley, B., Quenez, O., Grozeva, D., van Rooij, J. G. J., Sims, R., Ahmad, S., Amin, N., Norsworthy, P. J., Dols-Icardo, O., Hummerich, H., Kawalia, A., Amouyel, P., Beecham, G. W., Berr, C., Bis, J. C., Boland, A. & Bossù, P. & 87 others, , Dec 2022In: Nature Genetics. 5412p. 1786-1794 9 p.

 

Gender and Geographic Origin as Determinants of Manuscript Publication Outcomes: JBMR® Bibliometric Analysis from 2017 to 2019

Rivadeneira, F., Loder, R. T., McGuire, A. C., Chitwood, J. R., Duffy, K., Civitelli, R., Kacena, M. A. & Westendorf, J. J., Dec 2022In: Journal of Bone and Mineral Research. 3712p. 2420-2434 15 p.

 

A saturated map of common genetic variants associated with human height

Yengo, L., Vedantam, S., 23andMe Inc.VA Million Veteran ProgramDiscovEHR and MyCode Community Health InitiativeeMERGE (Electronic Medical Records and Genomics Network) ConsortiumThe LifeLines Cohort StudyThe PRACTICAL ConsortiumUnderstanding Society Scientific Group, Marouli, E., Sidorenko, J., Bartell, E., Sakaue, S., Graff, M., Eliasen, A. U., Jiang, Y., Raghavan, S., Miao, J., Arias, J. D. & Graham, S. E. & 37 others, , 27 Oct 2022In: Nature. 6107933p. 704-712 9 p.

 
 

Update of the fracture risk prediction tool FRAX: a systematic review of potential cohorts and analysis plan

Vandenput, L., Johansson, H., McCloskey, E. V., Liu, E., Åkesson, K. E., Anderson, F. A., Azagra, R., Bager, C. L., Beaudart, C., Bischoff-Ferrari, H. A., Biver, E., Bruyère, O., Cauley, J. A., Center, J. R., Chapurlat, R., Christiansen, C., Cooper, C., Crandall, C. J., Cummings, S. R. & da Silva, J. A. P. & 65 others, , Oct 2022In: Osteoporosis International. 3310p. 2103-2136 34 p.

 
 
 

Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms

Jami, E. S., Hammerschlag, A. R., Ip, H. F., Allegrini, A. G., Benyamin, B., Border, R., Diemer, E. W., Jiang, C., Karhunen, V., Lu, Y., Lu, Q., Mallard, T. T., Mishra, P. P., Nolte, I. M., Palviainen, T., Peterson, R. E., Sallis, H. M., Shabalin, A. A., Tate, A. E. & Thiering, E. & 74 others, , 1 Jul 2022In: Journal of the American Academy of Child and Adolescent Psychiatry. 617p. 934-945 12 p.

 
 
 

Candidate genetic variants and antidepressant-related fall risk in middle-aged and older adults

Pronk, A. C., Seppala, L. J., Trajanoska, K., Stringa, N., van de Loo, B., de Groot, L. C. P. G. M., van Schoor, N. M., Koskeridis, F., Markozannes, G., Ntzani, E., Uitterlinden, A. G.Rivadeneira, F.Stricker, B. H. & van der Velde, N., 14 Apr 2022In: PLoS ONE. 174 April, e0266590.

 

Bone fragility in diabetes: novel concepts and clinical implications

Hofbauer, L. C., Busse, B., Eastell, R., Ferrari, S., Frost, M., Müller, R., Burden, A. M., Rivadeneira, F., Napoli, N. & Rauner, M., Mar 2022In: The Lancet Diabetes and Endocrinology. 103p. 207-220 14 p.

 

Skin Autofluorescence, a Noninvasive Biomarker for Advanced Glycation End-products, Is Associated With Sarcopenia

Waqas, K.Chen, J.Trajanoska, K.Ikram, M. A.Uitterlinden, A. G.Rivadeneira, F. & Zillikens, M. C., 1 Feb 2022In: The Journal of clinical endocrinology and metabolism. 1072p. e793-e803.

The health effects of vitamin D supplementation: evidence from human studies

Bouillon, R., Manousaki, D., Rosen, C., Trajanoska, K.Rivadeneira, F. & Richards, J. B., Feb 2022, In: Nature Reviews Endocrinology. 18, 2, p. 96-110 15 p.

2021

Bone Phenotyping Approaches in Human, Mice and Zebrafish – Expert Overview of the EU Cost Action GEMSTONE (“GEnomics of MusculoSkeletal traits TranslatiOnal NEtwork”)

Foessl, I., Bassett, J. H. D., Bjørnerem, Å., Busse, B., Calado, Â., Chavassieux, P., Christou, M., Douni, E., Fiedler, I. A. K., Fonseca, J. E., Hassler, E., Högler, W., Kague, E., Karasik, D., Khashayar, P., Langdahl, B. L., Leitch, V. D., Lopes, P., Markozannes, G. & McGuigan, F. E. A. & 14 others, , 1 Dec 2021, In: Frontiers in Endocrinology. 12, 720728.

Exome sequencing identifies rare damaging variants in the ATB8B4 and ABCA1 genes as novel risk factors for Alzheimer’s disease

Holstege, H., Hulsman, M., Charbonnier, C., Grenier-Boley, B., Quenez, O., Grozeva, D., van Rooij, J. G. J., Sims, R., Ahmad, S., Amin, N., Norsworthy, P., Dols-Icardo, O., Hummerich, H., Kawalia, A., Amouyel, P., Beecham, G. W., Berr, C., Bis, J. C., Boland, A. & Bossù, P. & 84 others, , 1 Dec 2021, In: Alzheimer’s & dementia : the journal of the Alzheimer’s Association. 17, p. e055982

Perspective of the GEMSTONE Consortium on Current and Future Approaches to Functional Validation for Skeletal Genetic Disease Using Cellular, Molecular and Animal-Modeling Techniques

Rauner, M., Foessl, I., Formosa, M. M., Kague, E., Prijatelj, V., Lopez, N. A., Banerjee, B., Bergen, D., Busse, B., Calado, Â., Douni, E., Gabet, Y., Giralt, N. G., Grinberg, D., Lovsin, N. M., Solan, X. N., Ostanek, B., Pavlos, N. J., Rivadeneira, F. & Soldatovic, I. & 8 others, , 30 Nov 2021, In: Frontiers in Endocrinology. 12, 731217.

CYP11B1 variants influence skeletal maturation via alternative splicing

Grgic, O., Gazzara, M. R., Chesi, A., Medina-Gomez, C., Cousminer, D. L., Mitchell, J. A., Prijatelj, V.de Vries, J., Shevroja, E., McCormack, S. E., Kalkwarf, H. J., Lappe, J. M., Gilsanz, V., Oberfield, S. E., Shepherd, J. A., Kelly, A., Mahboubi, S., Faucz, F. R., Feelders, R. A. & de Jong, F. H. & 10 others, , 9 Nov 2021, In: Communications Biology. 4, 1, 1274.

A comparison of genotyping arrays

Verlouw, J. A. M., Clemens, E., de Vries, J. H., Zolk, O., Verkerk, A. J. M. H., am Zehnhoff-Dinnesen, A., Medina-Gomez, C., Lanvers-Kaminsky, C., Rivadeneira, F., Langer, T., van Meurs, J. B. J.van den Heuvel-Eibrink, M. M.Uitterlinden, A. G. & Broer, L., Nov 2021, In: European Journal of Human Genetics. 29, 11, p. 1611-1624 14 p.

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

Min, J. L., Hemani, G., the Biobank-based Integrative Omics Study (BIOS) Consortium, Hannon, E., Dekkers, K. F., Castillo-Fernandez, J., Luijk, R., Carnero-Montoro, E., Lawson, D. J., Burrows, K., Suderman, M., Bretherick, A. D., Richardson, T. G., Klughammer, J., Iotchkova, V., Sharp, G., Al Khleifat, A., Shatunov, A., Iacoangeli, A. & McArdle, W. L. & 35 others, , 6 Sept 2021, In: Nature Genetics. 53, 9, p. 1311-1321 11 p.

The “GEnomics of Musculo Skeletal Traits TranslatiOnal NEtwork”: Origins, Rationale, Organization, and Prospects

Koromani, F., Alonso, N., Alves, I., Brandi, M. L., Foessl, I., Formosa, M. M., Morgenstern, M. F., Karasik, D., Kolev, M., Makitie, O., Ntzani, E., Pietsch, B. O., Ohlsson, C., Rauner, M., Soe, K., Soldatovic, I., Teti, A., Valjevac, A. & Rivadeneira, F., 16 Aug 2021, In: Frontiers in Endocrinology. 12, 709815.

Pharmacogenomic Effects of β-Blocker Use on Femoral Neck Bone Mineral Density

Nevola, K. T., Nagarajan, A., Hinton, A. C., Trajanoska, K., Formosa, M. M., Xuereb-Anastasi, A., Van Der Velde, N., Stricker, B. H.Rivadeneira, F., Fuggle, N. R., Westbury, L. D., Dennison, E. M., Cooper, C., Kiel, D. P., Motyl, K. J. & Lary, C. W., 1 Aug 2021, In: Journal of the Endocrine Society. 5, 8, bvab092.

Associations between Prenatal, Perinatal, and Early Childhood Vitamin D Status and Risk of Dental Caries at 6 Years

Navarro, C. L. A., Grgic, O., Trajanoska, K.Van Der Tas, J. T.Rivadeneira, F.Wolvius, E. B.Voortman, T. & Kragt, L., 1 Jul 2021, In: Journal of Nutrition. 151, 7, p. 1993-2000 8 p.

The trans-ancestral genomic architecture of glycemic traits

Chen, J., Spracklen, C. N., Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)The LifeLines Cohort Study, Marenne, G., Varshney, A., Corbin, L. J., Luan, J., Willems, S. M., Wu, Y., Zhang, X., Horikoshi, M., Boutin, T. S., Mägi, R., Waage, J., Li-Gao, R., Chan, K. H. K., Yao, J., Anasanti, M. D. & Chu, A. Y. & 36 others, , 1 Jun 2021, In: Nature Genetics. 53, 6, p. 840-860 21 p.

Caries experience among children born after a complicated pregnancy

van der Tas, J. T.Wolvius, E. B.Kragt, L.Rivadeneira, F.Moll, H. A.Steegers, E. A. P. & Schalekamp-Timmermans, S., Jun 2021, In: Community Dentistry and Oral Epidemiology. 49, 3, p. 225-231 7 p.

An ARHGAP25 variant links aberrant Rac1 function to early-onset skeletal fragility

Mäkitie, R. E., Henning, P., Jiu, Y., Kämpe, A., Kogan, K., Costantini, A., Välimäki, V. V., Medina-Gomez, C., Pekkinen, M., Salusky, I. B., Schalin-Jäntti, C., Haanpää, M. K., Rivadeneira, F., Bassett, J. H. D., Williams, G. R., Lerner, U. H., Pereira, R. C., Lappalainen, P. & Mäkitie, O., 6 May 2021, In: JBMR Plus. 5, 7, e10509.

Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease

Youlten, S. E., Kemp, J. P., Logan, J. G., Ghirardello, E. J., Sergio, C. M., Dack, M. R. G., Guilfoyle, S. E., Leitch, V. D., Butterfield, N. C., Komla-Ebri, D., Chai, R. C., Corr, A. P., Smith, J. T., Mohanty, S. T., Morris, J. A., McDonald, M. M., Quinn, J. M. W., McGlade, A. R., Bartonicek, N. & Jansson, M. & 17 others, , 5 May 2021, In: Nature Communications. 12, 1, 2444.

A population-based study on associations of stool microbiota with atopic diseases in school-age children

Hu, C.van Meel, E. R.Medina-Gomez, C.Kraaij, R., Barroso, M., Kiefte-de Jong, J., Radjabzadeh, D.Pasmans, S. G. M. A., de Jong, N. W., de Jongste, J. C., Moll, H. A.Nijsten, T.Rivadeneira, F.Pardo, L. M. & Duijts, L., 13 Apr 2021, In: Journal of Allergy and Clinical Immunology. 148, 2, p. 612-620 9 p.

Common and Rare Variants Genetic Association Analysis of Circulating Neutrophil Extracellular Traps

Donkel, S., Portilla Fernández, E., Ahmad, S., Rivadeneira, F.van Rooij, F.Ikram, A.Leebeek, F.de Maat, M. & Ghanbari, M., 24 Feb 2021, In: Frontiers in Immunology. 12, 615527.

Opportunities and Challenges in Functional Genomics Research in Osteoporosis: Report From a Workshop Held by the Causes Working Group of the Osteoporosis and Bone Research Academy of the Royal Osteoporosis Society on October 5th 2020

Tobias, J., Duncan, E., Kague, E., Hammond, C., Gregson, C., Bassett, D., Williams, G., Min, J., Gaunt, T., Karasik, D., Ohlsson, C., Rivadeneira, F., Edwards, J., Hannan, F., Kemp, J., Gilbert, S., Alonso, N., Hassan, N., Compston, J. & Ralston, S., 15 Feb 2021, In: Frontiers in Endocrinology (Lausanne) (online). 11, 630875.

Large-scale association analyses identify host factors influencing human gut microbiome composition

Kurilshikov, A., Medina Gomez, M., Bacigalupe, R., Radjabzadeh, D., Wang, J., Demirkan, A., Le Roy, C., Garay, J., Finnicum, C., Liu, X., Zhernakova, D., Bonder, M., Hansen, T., Frost, F., Ruhlemann, M., Turpin, W., Moon, J., Kim, H., Lull, K. & Barkan, E. & 84 others, , Feb 2021, In: Nature Genetics. 53, 2, p. 156-165 10 p.

Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women

Jones, G., Trajanoska, K., Santanasto, A., Stringa, N., Kuo, C., Atkins, J., Lewis, J., Duong, T., Hong, S., Biggs, M., Luan, J., Sarnowski, C., Lunetta, K., Tanaka, T., Wojczynski, M., Cvejkus, R., Nethander, M., Ghasemi, S., Yang, J. & Zillikens, M. C. & 46 others, , 28 Jan 2021, In: Nature Communications. 12, 1, 654.

Type 2 Diabetes Mellitus and Vertebral Fracture Risk

Koromani, F.Ghatan, S.van Hoek, M., Zillikens, M. C., Oei, E.Rivadeneira, F. & Oei – Oei, L., 12 Jan 2021, In: Current Osteoporosis Reports. 19, 1, p. 50-57 8 p.

The association of BMI and physical activity on acetabular dysplasia in children

Chung, K.de Vos – Jakobs, S.Rivadeneira, F.Bierma – Zeinstra, S. & Waarsing, J., 1 Jan 2021, In: Osteoarthritis and Cartilage. 29, 1, p. 50-58 9 p.

Genome-wide association study identifies 48 common genetic variants associated with handedness

Cuellar-Partida, G., Tung, J., Eriksson, N., Albrecht, E., Aliev, F., Andreassen, O., Barroso, I., Beckmann, J., Boks, M. P., Boomsma, D., Boyd, H., Breteler, M., Campbell, H., Chasman, D., Cherkas, L., Davies, G., de Geus, E., Deary, I., Deloukas, P. & Dick, D. & 98 others, , Jan 2021, In: Nature Human Behaviour. 5, 1, p. 59-70 12 p.

 

2020

Bringing Genomic Discoveries to the Clinic: Integrating Omic Data Into the Musculoskeletal Field Through International Teamwork and Collaboration

Rivadeneira, F. & Westendorf, J., 2020, In: Journal of Bone and Mineral Research. 35, 9, p. 1623-1625 3 p.

Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

Forgetta, V., Keller-Baruch, J., Forest, M., Durand, A., Bhatnagar, S., Kemp, J., Nethander, M., Evans, D., Morris, J., Kiel, D., Rivadeneira, F., Johansson, H., Harvey, N., Mellstrom, D., Karlsson, M., Cooper, C., Evans, D., Clarke, R., Kanis, J. & Orwoll, E. & 6 others, , 2020, In: PLoS Medicine (print). 17, 7, e1003152.

 

Diet quality in early and mid-childhood in relation to trajectories of growth and body composition

Nguyen, A. N., Jen, V., Jaddoe, V.Rivadeneira, F.Jansen, P.Ikram, A. & Voortman, T., 2020, In: Clinical Nutrition. 39, 3, p. 845-852 8 p.

Distinct Subsets of Noncoding RNAs Are Strongly Associated With BMD and Fracture, Studied in Weight-Bearing and Non–Weight-Bearing Human Bone

Gautvik, K., Günther, C., Prijatelj, V.Medina Gomez, M., Shevroja, E., Rad, L., Yazdani, M., Lindalen, E., Valland, H., Gautvik, V., Olstad, O., Holden, M., Rivadeneira, F., Utheim, T. & Reppe, S., 2020, In: Journal of Bone and Mineral Research. 35, 6, p. 1065-1076 12 p.

 

Diversity, compositional and functional differences between gut microbiota of children and adults

Radjabzadeh, D.Boer, C., Beth, S., van der Wal, P., Jong, J., Jansen, M., Konstantinov, S., Peppelenbosch, M.Hays, J.Jaddoe, V.Ikram, A.Rivadeneira, F.van Meurs, J.Uitterlinden, A.Medina Gomez, M.Moll, H. & Kraaij, R., 2020, In: Scientific Reports. 10

Do Vitamin D Level and Dietary Calcium Intake Modify the Association Between Loop Diuretics and Bone Health?

Oliai Araghi, S., Jong, J., Trajanoska, K.Koromani, F.Rivadeneira, F., Zillikens, M. C., Schoor, N., de Groot, L., Ikram, A.Uitterlinden, A.Stricker, B. & van der Velde, N., 2020, In: Calcified Tissue International. 106, p. 104-114 11 p.

Fetal exposure to bisphenols and phthalates and childhood bone mass: a population-based prospective cohort study

van Zwol – Janssens, C., Trasande, L., Asimakopoulos, A., Martinez-Moral, M., Kannan, K., Philips, E., Rivadeneira, F.Jaddoe, V. & Moreira da Silva Santos, S., 2020, In: Environmental Research. 186, 109602.

Genetic Associations Between Childhood Psychopathology and Adult Depression and Associated Traits in 42998 Individuals A Meta-analysis

Akingbuwa, W., Hammerschlag, A., Jami, E., Allegrini, A., Karhunen, V., Sallis, H., Ask, H., Askeland, R., Baselmans, B., Diemer, E., Hagenbeek, F., Havdahl, A., Hottenga, J., Mbarek, H., Rivadeneira, F., Tesli, M., van Beijsterveldt, C., Breen, G., Lewis, C. & Thapar, A. & 17 others, , 2020, In: JAMA Psychiatry. 77, 7, p. 715-728 14 p.

 

Genetic basis of falling risk susceptibility in the UK Biobank Study

Trajanoska, K., Seppala, L., Medina Gomez, M., Hsu, Y., Zhou, S., Schoor, N., de Groot, L., Karasik, D., Richards, J., Kiel, D., Uitterlinden, A., Perry, J., van de Velde, N., Day, F. & Rivadeneira, F., 2020, In: Communications Biology. 3, 1, 543.

 

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

Hahn, J., Fu, Y. P., Brown, M., Bis, J., Vries, P., Feitosa, M., Yanek, L., Weiss, S., Giulianini, F., Smith, A., Guo, X., Bartz, T., Becker, D., Becker, L., Boerwinkle, E., Brody, J., Chen, Y., Franco Duran, O., Grove, M. & Harris, T. & 25 others, , 2020, In: PLoS One (print). 15, 11 November, e0230035.

 

Genomic Medicine: Lessons Learned From Monogenic and Complex Bone Disorders

Trajanoska, K. & Rivadeneira, F., 2020, In: Frontiers in Endocrinology (Lausanne) (online). 11, 556610.

 

Identifying potential causal effects of age at menarche: a Mendelian randomization phenome-wide association study

Magnus, M., Guyatt, A., Lawn, R., Wyss, A., Trajanoska, K., Kupers, L., Rivadeneira, F., Tobin, M., London, S., Lawlor, D., Millard, L. & Fraser, A., 2020, In: BMC Medicine. 18, 1, 71.

 

Macronutrient intake and frailty: the Rotterdam Study

Verspoor, E., Voortman, T.van Rooij, F.Rivadeneira, F., Franco Duran, O., Jong, J. & Schoufour, J., 2020, In: European Journal of Nutrition. 59, 7, p. 2919-2928 10 p.

Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood

Zheng, Y., Huang, T., Wang, T., Mei, Z., Sun, Z., Zhang, T., Voortman, T.van Rooij, F.Hofman, B.Felix, J.Jaddoe, V. & Rivadeneira, F., 2020, In: European Journal of Epidemiology. 35, 7, p. 685-697 13 p.

 

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

Vogelezang, S., Bradfield, J., Ahluwalia, T., Curtin, J., Lakka, T., Grarup, N., Monnereau, C., Medina Gomez, M.Rivadeneira, F.Uitterlinden, A., Grant, S., Jaddoe, V. & Felix, J., 2020, In: PLoS Genetics (online). 16, 10, e1008718.

 

Response to Comment on Koromani et al. Vertebral Fractures in Individuals With Type 2 Diabetes: More Than Skeletal Complications Alone. Diabetes Care 2020;43:137-144

Koromani, F. & Rivadeneira, F., 2020, In: Diabetes Care. 43, 6, p. E69-E69

Research output: Contribution to journal › Article › Academic › peer-review

1Citation (Scopus)

Hofbauer, L., Rivadeneira, F., Westendorf, J. & Civitelli, R., 2020, In: Journal of Bone and Mineral Research. 35, 6, p. 1005-1008 4 p.

 

Skeletal maturation in relation to ethnic background in children of school age: The Generation R Study

Grgic, O., Shevroja, E., Dhamo, B.Uitterlinden, A.Wolvius, E.Rivadeneira, F. & Medina Gomez, M., 2020, In: Bone. 132, Unsp 115180.

 

Skin Autofluorescence, a Noninvasive Biomarker for Advanced Glycation End-Products, Is Associated With Prevalent Vertebral and Major Osteoporotic Fractures: The Rotterdam Study

Waqas, K.Chen, J.Koromani, F.Trajanoska, K.van der Eerden, B.Uitterlinden, A.Rivadeneira, F. & Zillikens, M. C., 2020, In: Journal of Bone and Mineral Research. 35, 10, p. 1904-1913 10 p.

The impact of thiazide diuretics on bone mineral density and the trabecular bone score: the Rotterdam Study

van der Burgh, L., Oliai Araghi, S., Zillikens, M. C., Koromani, F.Rivadeneira, F.van der Velde, N.Hoorn, E.Uitterlinden, A.Ikram, A. & Stricker, B., 2020, In: Bone. 138, 115475.

 

The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community

Kiel, D., Kemp, J., Rivadeneira, F., Westendorf, J., Karasik, D., Duncan, E., Imai, Y., M?ller, R., Flannick, J., Bonewald, L. & Burtt, N., 2020, In: Journal of Bone and Mineral Research. 35, 9, p. 1626-1633 8 p.

 

Total Dietary Antioxidant Capacity and Longitudinal Trajectories of Body Composition

Schaft, N., Trajanoska, K.Rivadeneira, F.Ikram, A., Schoufour, J. & Voortman, T., 2020, In: Antioxidants. 9, 8, 728.

 

Vertebral Fractures in Individuals With Type 2 Diabetes: More Than Skeletal Complications Alone

Koromani, F., Oei – Oei, L., Shevroja, E., Trajanoska, K., Schoufour, J., Muka, T., Franco Duran, O., Ikram, A., Zillikens, M. C., Uitterlinden, A.Krestin, G., Anastassiades, T., Josse, R., Kaiser, S., Goltzman, D., Lentle, B., Prior, J., Leslie, W., McCloskey, E. & Lamy, O. & 3 others, , 2020, In: Diabetes Care. 43, 1, p. 137-144 8 p.

 

2019

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

CHD Exome+ ConsortiumCohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumEPIC-CVD ConsortiumExomeBP ConsortiumGlobal Lipids Genetics ConsortiumGoT2D Genes ConsortiumThe InterAct consortiumReproGen ConsortiumT2D-Genes ConsortiumThe MAGIC Investigators, Justice, A. E., Karaderi, T., Highland, H. M., Young, K. L., Graff, M., Lu, Y., Turcot, V., Auer, P. L., Fine, R. S. & Guo, X. & 42 others, , Mar 2019, In: Nature Genetics. 51, 3, p. 452-469 18 p.

A catalog of genetic loci associated with kidney function from analyses of a million individuals

Wuttke, M., Li, Y., Li, M., Sieber, K., Feitosa, M., Gorski, M., Uitterlinden, A.Rivadeneira, F., Miliku, K., Felix, J.Jaddoe, V., Sedaghat, S., Amin, N., Demirkan, A., Franco Duran, O., Ikram, A., Liu, J., Kottgen, A. & Pattaro, C., 2019, In: Nature Genetics. 51, 6, p. 957-+

A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

Vries, P., Sabater-Lleal, M., Huffman, J., Marten, J., Song, C., Pankratz, N., de Maat, M.Rivadeneira, F.Uitterlinden, A.Ikram, K., Dehghan, A., O’Donnel, C. & Smith, N., 2019, In: Blood. 133, 9, p. 967-977 11 p.

 

Are Bone Mineral Density and Fractures Related to the Incidence and Progression of Radiographic Osteoarthritis of the Knee, Hip, and Hand in Elderly Men and Women? The Rotterdam Study

Bergink, A., Rivadeneira, F.Bierma – Zeinstra, S., Zillikens, M. C., Ikram, A.Uitterlinden, A. & van Meurs, J., 2019, In: ARTHRITIS & RHEUMATOLOGY. 71, 3, p. 361-369 9 p.

 

Association of Birth Weight With Type 2 Diabetes and Glycemic Traits A Mendelian Randomization Study

Huang, T., Wang, T., Zheng, Y., Ellervik, C., Li, X., Gao, M., Voortman, T.van Rooij, F., Franco Duran, O., Felix, J.Rivadeneira, F.Jaddoe, V., Chasman, D. & Qi, L., 2019, In: JAMA network open. 2, 9, e1910915.

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

Kraja, A., Liu, C., Fetterman, J., Graff, M., Have, C., Gu, C., Yanek, L., Feitosa, M., Arking, D., Chasman, D., Young, K., Ligthart, S., Hill, W., Weiss, S., Luan, J., Giulianini, F., Li-Gao, R., Hartwig, F., Lin, S. & Wang, L. & 132 others, , 2019, In: American Journal of Human Genetics. 104, 1, p. 112-138 27 p.

A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity

Bradfield, J., Vogelezang, S., Felix, J., Chesi, A., Helgeland, O., Horikoshi, M., Vilor Tejedor, N., Monnereau, C., Rivadeneira, F.Uitterlinden, A., Hakonarson, H. & Jaddoe, V., 2019, In: Human Molecular Genetics. 28, 19, p. 3327-3338 12 p.

 

Body Composition Is Not Related to Structural or Vascular Brain Changes

Croll, P.Bos, D.Ikram, A.Rivadeneira, F.Voortman, T. & Vernooij, M., 2019, In: Frontiers in Neurology. 10, 559.

Cohort Profile: The OsteoLaus study

Shevroja, E., Marques-Vidal, P., Aubry-Rozier, B., Hans, G., Rivadeneira, F., Lamy, O. & Hans, D., 2019, In: International Journal of Epidemiology. 48, 4, p. 1046-+

 

Disentangling the genetics of lean mass

Karasik, D., Zillikens, M. C., Hsu, Y., Aghdassi, A., Akesson, K., Amin, N.Broer, L.Campos Obando, N., Enneman, A., Estrada Gil, K., Hofman, B., Kloth, J., Medina Gomez, M., Oostra, B., Rivadeneira, F., Stolk, L., Uitterlinden, A., Duijn, C., Kiel, D. & Ohlsson, C., 2019, In: American Journal of Clinical Nutrition. 109, 2, p. 276-287 12 p.

Femoral stress is prominently associated with fracture risk in children: The Generation R Study

Grgic, O., Rivadeneira, F., Shevroja, E., Trajanoska, K.Jaddoe, V.Uitterlinden, A., Beck, T., Wolvius, E. & Medina Gomez, M., 2019, In: Bone. 122, p. 150-155 6 p.

 

Fractures in school age children in relation to sex and ethnic background: The Generation R Study

Grgic, O., Chung, K., Shevroja, E., Trajanoska, K.Uitterlinden, A.Wolvius, E.Rivadeneira, F. & Medina Gomez, M., 2019, In: Bone. 121, p. 227-231 5 p.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates A beta, tau, immunity and lipid processing

Kunkle, B., Grenier-Boley, B., Sims, R., Bis, J., Damotte, V., Naj, A., van der Lee, S., Ahmad, S., Adams, H., Vojinovic, D., Comic, H.Roshchupkin, G.Rivadeneira, F.Uitterlinden, A.Amin, N.Ikram, A., Duijn, C., Lambert, J. & Pericak-Vance, M., 2019, In: Nature Genetics. 51, 3, p. 414-+

 

Genetic predisposition to increased serum calcium, bone mineral density, and fracture risk in individuals with normal calcium levels: mendelian randomisation study

Cerani, A., Zhou, S., Forgetta, V., Morris, J., Trajanoska, K.Rivadeneira, F., Larsson, S., Michaelsson, K. & Richards, J., 2019, In: BMJ-British medical journal. 366, l4410.

 

Genetics of Bone and Muscle Interactions in Humans

Trajanoska, K.Rivadeneira, F., Kiel, D. & Karasik, D., 2019, In: Current Osteoporosis Reports. 17, 2, p. 86-95 10 p.

 

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

Teumer, A., Li, Y., Ghasemi, S., Prins, B., Wuttke, M., Hermle, T., Sedaghat, S., Felix, J., Franco Duran, O., Ikram, A.Jaddoe, V., Miliku, K., Rivadeneira, F.Uitterlinden, A., Vogelezang, S., Pattaro, C. & Kottgen, A., 2019, In: Nature Communications. 10, 4130.

 

Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

Sabater-Lleal, M., Huffman, J., Vries, P., Marten, J., Mastrangelo, M., Song, C., de Maat, M.Rivadeneira, F.Uitterlinden, A.Hofman, B., Franco Duran, O., Dehghan, A., Lowenstein, C. & Smith, N., 2019, In: Circulation. 139, 5, p. 620-635 16 p.

 

GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

Styrkarsdottir, U., Stefansson, O. A., Gunnarsdottir, K., Thorleifsson, G., Lund, S., Stefansdottir, L., Juliusson, K., Agustsdottir, A., Zink, F., Halldorsson, G., Ivarsdottir, E., Benonisdottir, S., Jonsson, H., Gylfason, A., Norland, K., Trajanoska, K.Boer, C., Southam, L., Leung, J. & Tang, N. & 31 others, , 2019, In: Nature Communications. 10, Unsp 2054.

 

GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

Alves, A., De Silva, N., Karhunen, V., Sovio, U., Das, S., Taal, R., Warrington, N., Lewin, A., Kaakinen, M., Cousminer, D., Thiering, E., Timpson, N., Bond, T., Lowry, E., Brown, C., Estivill, X., Lindi, V., Bradfield, J., Geller, F. & Speed, D. & 71 others, , 2019, In: Science advances. 5, 9, eaaw3095.

 

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

Haworth, S., Shapland, C., Hayward, C., Prins, B., Felix, J.Medina Gomez, M.Rivadeneira, F., Wang, C., Ahluwalia, T., Vrijheid, M., Guxens Junyent, M., Sunyer, J., Tachmazidou, I., Walter, K., Iotchkova, V., Jackson, A., Cleal, L., Huffmann, J., Min, J. & Sass, L. & 221 others, , 2019, In: Nature Communications. 10, 357.

 

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Warrington, N., Beaumont, R., Horikoshi, M., Day, F., Helgeland, O., Laurin, C., Medina Gomez, M., Kooijman, M., Rivadeneira, F.Hofman, B.Felix, J.Jaddoe, V. & Uitterlinden, A., 2019, In: Nature Genetics. 51, 5, p. 804-+

 

Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry

Hsu, Y., Estrada Gil, K., Evangelou, E., Ackert-Bicknell, C., Akesson, K., Beck, T., Medina Gomez, M.Trajanoska, K.Uitterlinden, A., Zillikens, M. C., Rivadeneira, F., Kiel, D. & Karasik, D., 2019, In: Journal of Bone and Mineral Research. 34, 7, p. 1284-1296 13 p., UNSP e3698.

 

New Guidelines for Data Reporting and Statistical Analysis: Helping Authors With Transparency and Rigor in Research

Nguyen, T., Rivadeneira, F. & Civitelli, R., 2019, In: Journal of Bone and Mineral Research. 34, 11, p. 1981-1984 4 p.

 

Nonalcoholic Fatty Liver Disease in The Rotterdam Study: About Muscle Mass, Sarcopenia, Fat Mass, and Fat Distribution

Alferink, L.Trajanoska, K.Erler, N., Schoufour, J., de Knegt, R.Ikram, A.Janssen, H., Franco Duran, O., Metselaar, H., Rivadeneira, F. & Darwish Murad, S., 2019, In: Journal of Bone and Mineral Research. 34, 7, p. 1254-1263 10 p.

 

 

Novel metabolic indices and incident type 2 diabetes among women and men: the Rotterdam Study

Brahimaj, A., Rivadeneira, F., Muka, T., Sijbrands, E. J. G., Franco Duran, O., Dehghan, A. & Kavousi, M., 2019, In: Diabetologia. 62, 9, p. 1581-1590 10 p.

Osteoblast-derived NOTUM reduces cortical bone mass in mice and the NOTUM locus is associated with bone mineral density in humans

Moverare-Skrtic, S., Nilsson, K., Henning, P., Funck-Brentano, T., Nethander, M., Rivadeneira, F., Nunes, G., Koskela, A., Tuukkanen, J., Tuckermann, J., Perret, C., Souza, P., Lerner, U. & Ohlsson, C., 2019, In: FASEB Journal. 33, 10, p. 11163-11179 17 p.

 

Plant-based Diet and Adiposity Over Time in a Middle-aged and Elderly Population The Rotterdam Study

Chen, Z., Schoufour, J., Rivadeneira, F.Lamballais Tessensohn, S.Ikram, A., Franco Duran, O. & Voortman, T., 2019, In: Epidemiology. 30, 2, p. 303-310 8 p.

 

Potential Interplay between Dietary Saturated Fats and Genetic Variants of the NLRP3 Inflammasome to Modulate Insulin Resistance and Diabetes Risk: Insights from a Meta-Analysis of 19 005 Individuals

Murphy, A., Smith, C., Murphy, L., Follis, J., Tanaka, T., Richardson, K., Noordam, R., Lemaitre, R., Kahonen, M., Dupuis, J., Voortman, T., Marouli, E., Mook-Kanamori, D., Raitakari, O., Hong, J., Dehghan, A., Dedoussis, G., de Mutsert, R., Lehtimaki, T. & Liu, C.-T. & 11 others, , 2019, In: Molecular Nutrition & Food Research. 63, 22, p. e1900226

 

Recent Advances in the Genetics of Fractures in Osteoporosis

Koromani, F.Trajanoska, K.Rivadeneira, F. & Oei – Oei, L., 2019, In: Frontiers in Endocrinology (Lausanne) (online). 10, 337.

 

Sarcopenia in COPD: a systematic review and meta-analysis

Benz Inalaf, G.Trajanoska, K.Lahousse, L., Schoufour, J., Terzikhan, N.de Roos, E., de Jonge, G., Williams, R., Franco Duran, O., Brusselle, G. & Rivadeneira, F., 2019, In: European Respiratory Review. 28, 154, 190049.

 

Skewed X-inactivation is common in the general female population

Shvetsova, E., Sofronova, A., Monajemi, R., Gagalova, K., Draisma, H., White, S., van Meurs, J., Duijn, C., Hofman, B.Uitterlinden, A.Jhamai, M.Verbiest, M., Verkerk, M., van Rooij, J., Isaacs, A., Leeuwen, E., Oven, M., Karssen, L., Koval, S. & Rivadeneira, F. & 6 others, , 2019, In: European Journal of Human Genetics. 27, 3, p. 455-465 11 p.

The association between dietary protein intake, energy intake and physical frailty: results from the Rotterdam Study

Schoufour, J., Franco Duran, O., Jong, J., Trajanoska, K.Stricker, B.Brusselle, G.Rivadeneira, F.Lahousse, L. & Voortman, T., 2019, In: British Journal of Nutrition. 121, 4, p. 393-401 9 p.

The association between obesity, diet quality and hearing loss in older adults

Croll, P.Voortman, T.Vernooij, M., Baatenburg de Jong, R. J., Lin, F., Rivadeneira, F.Ikram, A. & Goedegebure, A., 2019, In: Aging-Us. 11, 1, p. 48-62 15 p.

 

The genetic architecture of osteoporosis and fracture risk

Trajanoska, K. & Rivadeneira, F., 2019, In: Bone. 126, p. 2-10 9 p.

 

The Radiology of Osteoporotic Vertebral Fractures Revisited

Lentle, B., Koromani, F., Brown, J., Oei, L., Ward, L., Goltzman, D., Rivadeneira, F., Leslie, W., Probyn, L., Prior, J., Hammond, I., Cheung, A. & Oei, E., 2019, In: Journal of Bone and Mineral Research. 34, 3, p. 409-418 10 p.

 

Trabecular Bone Score and Hip Structural Analysis in Patients With Atypical Femur Fractures

Buitendijk, S., van de Laarschot, D., Smits, S., Koromani, F.Rivadeneira, F., Beck, T. & Zillikens, M. C., 2019, In: Journal of Clinical Densitometry. 22, 2, p. 257-265 9 p.

 

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

Liu, X., Helenius, D., Skotte, L., Beaumont, R., Vogelezang, S., Rivadeneira, F.Jaddoe, V.Felix, J., Wielscher, M. & Geller, F., 2019, In: Nature Communications. 10, 3927.

 

Vitamin D status and bone health: a possible inverse association Authors’ reply

Rivadeneira, F.Trajanoska, K., Morris, J. & Richards, J., 2019, In: BMJ-British medical journal. 364, l115.

 

WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene

Nersisyan, L., Nikoghosyan, M., Francioli, L., Menelaou, A., Pulit, S., Elbers, C., Leeuwen, E., Karssen, L., Amin, N.Rivadeneira, F., Isaacs, A., Hofman, B.Uitterlinden, A., Duijn, C., Oven, M., Kayser, M., Estrada Gil, K., Koval, S., Medina Gomez, M. & Oostra, B. & 2 others, , 2019, In: Scientific Reports. 9, 18758.

 

2018

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

CHD Exome+ ConsortiumEPIC-CVD ConsortiumExomeBP ConsortiumGlobal Lipids Genetics ConsortiumGoT2D Genes ConsortiumEPIC-InterAct ConsortiumINTERVAL StudyReproGen ConsortiumT2D-Genes ConsortiumThe MAGIC InvestigatorsUnderstanding Society Scientific Group, Turcot, V., Lu, Y., Highland, H. M., Schurmann, C., Justice, A. E., Fine, R. S., Bradfield, J. P., Esko, T. & Giri, A. & 48 others, , Jan 2018, In: Nature Genetics. 50, 1, p. 26-41 16 p.

[Erratum:] Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

Manousaki, D., Dudding, T., Haworth, S., Hsu, Y., Liu, C., Medina Gomez, M.Voortman, T.van der Velde, N., Melhus, H., Robinson-Cohen, C., Cousminer, D., Nethander, M., Vandenput, L., Noordam, R., Forgetta, V., Greenwood, C., Biggs, M., Psaty, B., Rotter, J. & Zemel, B. & 33 others, , 2018, In: American Journal of Human Genetics. 103, 6, p. 1053

 

A genome-wide association study of corneal astigmatism: The CREAM Consortium

Shah, R., Li, Q., Zhao, W., Tedja, M.Tideman, W., Khawaja, A., Fan, Q., Yazar, S., Williams, K., Verhoeven, V., Xie, J., Wang, Y., Hess, M., Nickels, S., Lackner, K., Parssinen, O., Wedenoja, J., Biino, G., Concas, M. & Uitterlinden, A. & 23 others, , 2018, In: Molecular Vision. 24, p. 127-142 16 p.

 

Ancestry and dental development: A geographic and genetic perspective

Dhamo, B.Kragt, L., Grgic, O., Vucic, S., Medina Gomez, M.Rivadeneira, F.Jaddoe, V.Wolvius, E. & Ongkosuwito, E., 2018, In: American Journal of Physical Anthropology. 165, 2, p. 299-308 10 p.

Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study

Trajanoska, K., Morris, J., Oei – Oei, L., Zheng, H., Evans, D., Kiel, D., Ohlsson, C., Richards, J. & Rivadeneira, F., 2018, In: BMJ-British medical journal. 362, k3225.

 

Association between subclinical thyroid dysfunction and change in bone mineral density in prospective cohorts

Segna, D., Bauer, D., Feller, M., Schneider, C., Fink, H., Aubert, C., Collet, T., da Costa, B., Fischer, K., Peeters, R., Cappola, A., Blum, M., van Dorland, H., Robbins, J., Naylor, K., Eastell, R., Uitterlinden, A.Rivadeneira, F., Gogakos, A. & Gussekloo, J. & 6 others, , 2018, In: Journal of Internal Medicine. 283, 1, p. 56-72 17 p.

 

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Lin, H., van Setten, J., Smith, A., Bihlmeyer, N., Warren, H., Brody, J., Radmanesh, F., Hall, L., Grarup, N., Muller-Nurasyid, M., Boutin, T., Verweij, N., Lin, H. J., Li-Gao, R., van den Berg, M., Marten, J., Weiss, S., Prins, B., Haessler, J. & Lyytikainen, L. & 78 others, , 2018, In: Circulation-Genomic and Precision Medicine. 11, 5, UNSP e002037.

 

Consortium-based genome-wide meta-analysis for childhood dental caries traits

Haworth, S., Shungin, D., van der Tas, J., Vucic, S., Medina Gomez, M., Yakimov, V., Feenstra, B., Shaffer, J., Lee, M., Standl, M., Thiering, E., Wang, C., Bonnelykke, K., Waage, J., Jessen, L., Norrisgaard, P., Joro, R., Seppala, I., Raitakari, O. & Dudding, T. & 23 others, , 2018, In: Human Molecular Genetics. 27, 17, p. 3113-3127 15 p.

 

Dietary patterns and changes in frailty status: the Rotterdam study

Haas, S., Jonge, E., Voortman, T., Graaff, J., Franco Duran, O., Ikram, A.Rivadeneira, F., Jong, J. & Schoufour, J., 2018, In: European Journal of Nutrition. 57, 7, p. 2365-2375 11 p.

Dietary patterns in an elderly population and their relation with bone mineral density: the Rotterdam Study

Jonge, E., Rivadeneira, F.Erler, N.Hofman, B.Uitterlinden, A., Franco Duran, O. & Jong, J., 2018, In: European Journal of Nutrition. 57, 1, p. 61-73 13 p.

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Bihlmeyer, N., Brody, J., Smith, A., Warren, H., Lin, H., Isaacs, A., Liu, C., Marten, J., Radmanesh, F., Hall, L., Grarup, N., Mei, H., Muller-Nurasyid, M., Huffman, J., Verweij, N., Guo, X., Yao, J., Li-Gao, R., van den Berg, M. & Weiss, S. & 80 others, , 2018, In: Circulation-cardiovascular genetics. 11, 1, UNSP e001758.

Focusing on the Science: JBMR Manuscript Types

Civitelli, R., Westendorf, J., Hofbauer, L. & Rivadeneira, F., 2018, In: Journal of Bone and Mineral Research. 33, 9, p. 1556-1557 2 p.

Foetal, neonatal and child vitamin D status and enamel hypomineralization

van der Tas, J., Elfrink, M., Heijboer, A., Rivadeneira, F.Jaddoe, V., Tiemeier, H., Schoufour, J., Moll, H., Ongkosuwito, E., Wolvius, E. & Voortman, T., 2018, In: Community Dentistry and Oral Epidemiology. 46, 4, p. 343-351 9 p.

 

Fracture incidence and secular trends between 1989 and 2013 in a population based cohort: The Rotterdam Study

Trajanoska, K., Schoufour, J., Jonge, E., Leening – Kieboom, B., Mulder, M., Stricker, B.Voortman, T.Uitterlinden, A.Oei, E.Ikram, A., Zillikens, M. C., Rivadeneira, F. & Oei – Oei, L., 2018, In: Bone. 114, p. 116-124 9 p.

 

Genetic Determinants of Circulating Estrogen Levels and Evidence of a Causal Effect of Estradiol on Bone Density in Men

Eriksson, A., Perry, J., Coviello, A., Delgado, G., Ferrucci, L., Hoffman, A., Huhtaniemi, I., Ikram, A., Karlsson, M., Kleber, M., Laughlin, G., Liu, Y., Lorentzon, M., Lunetta, K., Mellstrom, D., Murabito, J., Murray, A., Nethander, M., Nielson, C. & Prokopenko, I. & 20 others, , 2018, In: Journal of Clinical Endocrinology and Metabolism. 103, 3, p. 991-1004 14 p.

 

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

Ligthart, S., Vaez, A., Vosa, U., Stathopoulou, M., Vries, P., Prins, B., van der Most, P., Tanaka, T., Naderi, E., Rose, L., Wu, Y., Karlsson, R., Barbalic, M., Lin, H., Pool, R., Zhu, G., Mace, A., Sidore, C., Trompet, S. & Mangino, M. & 266 others, , 2018, In: American Journal of Human Genetics. 103, 5, p. 691-706 16 p.

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

Teumer, A., Chaker, L.Groeneweg, S., Li, Y., Di Munno, C., Barbieri, C., Schultheiss, U., Traglia, M., Ahluwalia, T., Akiyama, M., Appel, E., Arking, D., Arnold, A., Astrup, A., Beekman, M., Beilby, J., Bekaert, S., Boerwinkle, E., Brown, S. & de Buyzere, M. & 108 others, , 2018, In: Nature Communications. 9, 4455.

 

Genome-wide Analysis of Large-scale Longitudinal Outcomes using Penalization – GALLOP algorithm

Sikorska, K., Lesaffre, E., Groenen, P., Rivadeneira, F. & Eilers, P., 2018, In: Scientific Reports. 8, 6815.

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Tedja, M., Wojciechowski, R., Hysi, P., Eriksson, N., Furlotte, N., Verhoeven, V.Iglesias Gonzalez, A.Meester – Smoor, M., Tompson, S., Fan, Q., Khawaja, A., Cheng, C., Hohn, R., Yamashiro, K., Wenocur, A., Grazal, C., Haller, T., Metspalu, A., Wedenoja, J. & Jonas, J. & 78 others, , 2018, In: Nature Genetics. 50, 6, p. 834-848 15 p.

 

Genome-wide association study identifies nine novel loci for 2D: 4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

Warrington, N., Shevroja, E., Hemani, G., Hysi, P., Jiang, Y., Auton, A., Boer, C., Mangino, M., Wang, C., Kemp, J., McMahon, G., Medina Gomez, M., Hickey, M., Trajanoska, K., Wolke, D., Ikram, A., Montgomery, G., Felix, J., Wright, M. & Mackey, D. & 10 others, , 2018, In: Human Molecular Genetics. 27, 11, p. 2025-2038 14 p.

Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels

Jiang, X., O’Reilly, P., Aschard, H., Hsu, Y., Richards, J., Dupuis, J., Ingelsson, E., Karasik, D., Pilz, S., Berry, D., Kestenbaum, B., Zheng, J., Luan, J., Sofianopoulou, E., Streeten, E., Albanes, D., Lutsey, P., Yao, L., Tang, W. & Econs, M. & 84 others, , 2018, In: Nature Communications. 9, 260.

Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent

Smith, C., Follis, J., Dashti, H., Tanaka, T., Graff, M., Fretts, A., Kilpelainen, T., Wojczynski, M., Richardson, K., Nalls, M., Schulz, C. A., Liu, Y., Frazier-Wood, A., van Eekelen, E., Wang, C., Vries, P., Mikkila, V., Rohde, R., Psaty, B. & Hansen, T. & 43 others, , 2018, In: Molecular Nutrition & Food Research. 62, 3, 1700347.

 

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

Franceschini, N., Giambartolomei, C., de Vries, P., Finan, C., Bis, J., Huntley, R., Lovering, R., Tajuddin, S. M., Winkler, T., Graff, M., Kavousi, M., Dale, C., Smith, A., Hofer, E., Leeuwen, E., Nolte, I., Lu, L., Scholz, M., Sargurupremraj, M. & Pitkanen, N. & 138 others, , 2018, In: Nature Communications. 9, 5141.

 

Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density

Alonso, N., Estrada Gil, K., Albagha, O., Herrera Duran, L., Reppe, S., Olstad, O., Gautvik, K., Ryan, N., Evans, K., Nielson, C., Hsu, Y., Kiel, D., Markozannes, G., Ntzani, E., Evangelou, E., Feenstra, B., Liu, X., Melbye, M., Masi, L. & Brandi, M. & 41 others, , 2018, In: Annals of the Rheumatic Diseases. 77, 3

 

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

Medina Gomez, M., Kemp, J., Trajanoska, K., Luan, J., Chesi, A., Ahluwalia, T., Mook, D., Ham, A., Hartwig, F., Evans, D., Joro, R., Prokic, I., Zheng, H., Zhu, K., Atalay, M., Liu, C., Nethander, M., Broer, L., Porleifsson, G. & Mullin, B. & 69 others, , 2018, In: American Journal of Human Genetics. 102, 1, p. 88-102 15 p.

 

Maternal and fetal genetic contribution to gestational weight gain

Warrington, N., Richmond, R., Fenstra, B., Myhre, R., Gaillard, R., Paternoster, L., Wang, C., Beaumont, R., Das, S., Murcia, M., Barton, S., Espinosa, A., Thiering, E., Atalay, M., Pitkanen, N., Ntalla, I., Jonsson, A., Freathy, R., Karhunen, V. & Tiesler, C. & 44 others, , 2018, In: International Journal of Obesity. 42, 4, p. 775-784 10 p.

Osteoporosis Genes Identified by Genome-Wide Association Studies

Rivadeneira, F. & Uitterlinden, A. G., 2018, Genetics of Bone Biology and Skeletal Disease: Second Edition. Elsevier Inc., p. 377-395 19 p.

Osteoporotic Vertebral Fracture Prevalence Varies Widely Between Qualitative and Quantitative Radiological Assessment Methods: The Rotterdam Study

Oei – Oei, L., Koromani, F., Breda, S., Schousboe, J., Clark, E., van Meurs, J.Ikram, A., Waarsing, J., van Rooij, F., Zillikens, M. C., Krestin, G.Oei, E. & Rivadeneira, F., 2018, In: Journal of Bone and Mineral Research. 33, 4, p. 560-568 9 p.

 

Rare and Common Variants Conferring Risk of Tooth Agenesis

Jonsson, L., Magnusson, T., Thordarson, A., Jonsson, T., Geller, F., Feenstra, B., Melbye, M., Nohr, E., Vucic, S., Dhamo, B.Rivadeneira, F., Ongkosuwito, E., Wolvius, E., Leslie, E., Marazita, M., Howe, B., Uribe, L., Alonso, I., Santos, M. & Pinho, T. & 16 others, , 2018, In: Journal of Dental Research. 97, 5, p. 515-522 8 p.

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

Mahajan, A., Wessel, J., Willems, S., Zhao, W., Robertson, N., Chu, A., Gan, W., Kitajima, H., Taliun, D., Rayner, N., Guo, X., Lu, Y., Li, M., Jensen, R., Hu, Y., Huo, S., Lohman, K., Zhang, W., Cook, J. P. & Prins, B. & 220 others, , 2018, In: Nature Genetics. 50, 4, p. 559-+

Response to Osteoporotic Vertebral Fracture Prevalence Varies Widely

Oei, E.Koromani, F.Rivadeneira, F. & Oei – Oei, L., 2018, In: Journal of Bone and Mineral Research. 33, 8, p. 1550-1550 1 p.

Sarcopenia and Its Clinical Correlates in the General Population: The Rotterdam Study

Trajanoska, K., Schoufour, J., Darweesh, S., Benz Inalaf, G.Medina Gomez, M.Alferink, L.Lahousse, L.Brusselle, G.Stricker, B.Darwish Murad, S., Zillikens, M. C., Uitterlinden, A.Ikram, A., Franco Duran, O. & Rivadeneira, F., 2018, In: Journal of Bone and Mineral Research. 33, 7, p. 1209-1218 10 p.

 

The association between lifestyle and overall health, using the frailty index

Brinkman, S., Voortman, T., Jong, J., van Rooij, F.Ikram, A.Rivadeneira, F., Franco Duran, O. & Schoufour, J., 2018, In: Archives of Gerontology and Geriatrics. 76, p. 85-91 7 p.

 

The Association of Thyroid Function With Bone Density During Childhood

Veldscholte, K., Barjaktarovic, M., Trajanoska, K.Jaddoe, V., Visser, T., de Rijke, Y., Peeters, R.Rivadeneira, F. & Korevaar, T., 2018, In: Journal of clinical endocrinology and metabolism (online). 103, 11, p. 4125-4134 10 p.

 

Using Mendelian Randomization to Decipher Mechanisms of Bone Disease

Trajanoska, K. & Rivadeneira, F., 2018, In: Current Osteoporosis Reports. 16, 5, p. 531-540 10 p.

 

Vertebral Fractures and Morphometric Deformities

Lentle, B., Oei, E., Goltzman, D., Rivadeneira, F., Hammond, I., Oei – Oei, L., Kovacs, C., Hanley, D., Prior, J., Leslie, W., Kaiser, S., Adachi, J., Probyn, L., Brown, J., Cheung, A. & Towheed, T., 2018, In: Journal of Bone and Mineral Research. 33, 8, p. 1544-1545 2 p.

Vitamin D and risk of pregnancy related hypertensive disorders: mendelian randomisation study

Magnus, M., Miliku, K., Bauer, A., Engel, S., Felix, J.Jaddoe, V., Lawlor, D., London, S., Magnus, P., McGinnis, R., Nystad, W., Page, C., Rivadeneira, F., Stene, L., Tapia, G., Williams, N., Bonilla, C. & Fraser, A., 2018, In: BMJ-British medical journal. 361, k2167.

Vitamin D and Risk of Pregnancy-Related Hypertensive Disorders: Mendelian Randomization Study

Magnus, M., Miliku, K., Bauer, A., Engel, S., Felix, J.Jaddoe, V., Lawlor, D., London, S., Magnus, P., McGinnis, R., Nystad, W., Page, C., Rivadeneira, F., Stene, L., Tapia, G., Williams, N., Bonilla, C. & Fraser, A., 2018, In: Obstetrical and Gynecological Survey. 73, 11, p. 617-619 3 p.

2017

Population-specific genetic variation in large sequencing data sets: why more data is still better

van Rooij, J. G. J.Jhamai, M., Arp, P. P., Nouwens, S. C. A., Verkerk, M., Hofman, A.Ikram, M. A.Verkerk, A. J.van Meurs, J. B. J.Rivadeneira, F.Uitterlinden, A. G. & Kraaij, R., Oct 2017, In: European Journal of Human Genetics. 25, 10, p. 1173-1175 3 p.

 

Correction: Genome-wide physical activity interactions in adiposity – A meta-analysis of 200,452 adults

CHARGE ConsortiumEPIC-InterAct Consortium & The PAGE Consortium, 23 Aug 2017, In: PLoS Genetics. 13, 8, p. e1006972

 

 NFAT5 and SLC4A10 loci associate with plasma osmolality

groep, Aug 2017, In: Journal of the American Society of Nephrology. 28, 8, p. 2311-2321 11 p.

 

Genome-wide pleiotropy between Parkinson disease and autoimmune diseases

Witoelar, A., Jansen, I. E., the IPDGC, UKBEC Investigators, NABEC, Wang, Y., Desikan, R. S., Gibbs, J. R., Blauwendraat, C., Thompson, W. K., Hernandez, D. G., Djurovic, S., Schork, A. J., Bettella, F., Ellinghaus, D., Franke, A., Lie, B. A., McEvoy, L. K., Karlsen, T. H., Lesage, S., Morris, H. R. & Brice, A. & 8 others, , Jul 2017, In: JAMA Neurology. 74, 7, p. 780-792 13 p.

Use of Trabecular Bone Score (TBS) as a Complementary Approach to Dual-energy X-ray Absorptiometry (DXA) for Fracture Risk Assessment in Clinical Practice

Shevroja, E., Lamy, O., Kohlmeier, L., Koromani, F.Rivadeneira, F. & Hans, D., Jul 2017, In: Journal of Clinical Densitometry. 20, 3, p. 334-345 12 p.

 

Causal effect of plasminogen activator inhibitor type 1 on coronary heart disease

Song, C., Burgess, S., Eicher, J. D., CHARGE Consortium Hemostatic Factor Working GroupICBP ConsortiumCohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Subclinical Working Group, O’Donnell, C. J. & Johnson, A. D., 1 Jun 2017, In: Journal of the American Heart Association. 6, 6, e004918.

No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs

International Parkinson Disease Genomics Consortium membersHofman, A.Rivadeneira, F.Rivadeneira, F.Uitterlinden, A. G. & Heutink, P., 1 Jun 2017, In: ADHD Attention Deficit and Hyperactivity Disorders. 9, 2, p. 121-127 7 p.

 

Genome-wide physical activity interactions in adiposity: A meta-analysis of 200,452 adults

CHARGE ConsortiumEPIC-InterAct Consortium & The PAGE Consortium, 27 Apr 2017, In: PLoS Genetics (online). 13, 4, e1006528.

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

groep, McLaughlin, R. L., Schijven, D., Van Rheenen, W., Van Eijk, K. R., O’Brien, M., Kahn, R. S., Ophoff, R. A., Goris, A., Bradley, D. G., Al-Chalabi, A., Van Den Berg, L. H., Luykx, J. J., Hardiman, O., Veldink, J. H., Shatunov, A., Uitterlinden, A. G.Rivadeneira, F.Hofman, A. & Georgieva, L. & 2 others, , 21 Mar 2017, In: Nature Communications. 8, 14774.

Rare and low-frequency coding variants alter human adult height

EPIC-InterAct ConsortiumReproGen ConsortiumCHD Exome+ ConsortiumExomeBP ConsortiumT2D-Genes ConsortiumGoT2D Genes ConsortiumGlobal Lipids Genetics ConsortiumThe MAGIC Investigators, Marouli, E., Graff, M., Medina-Gomez, C., Lo, K. S., Wood, A. R., Kjaer, T. R., Fine, R. S., Lu, Y., Schurmann, C., Highland, H. M., Rüeger, S. & Thorleifsson, G. & 43 others, , 1 Feb 2017, In: Nature. 542, 7640, p. 186-190 5 p.

Dietary patterns explaining differences in bone mineral density and hip structure in the elderly: The Rotterdam study

De Jonge, E. A. L., Kiefte-De Jong, J. C., Hofman, A.Uitterlinden, A. G., Kieboom, B. C. T., Voortman, T., Franco, O. H. & Rivadeneira, F., 1 Jan 2017, In: American Journal of Clinical Nutrition. 105, 1, p. 203-211 9 p.

1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

Gorski, M., van der Most, P., Teumer, A., Chu, A., Li, M., Mijatovic, V., Nolte, I., Cocca, M., Taliun, D., Gomez, F., Li, Y., Tayo, B., Tin, A., Feitosa, M., Aspelund, T., Attia, J., Biffar, R., Bochud, M., Boerwinkle, E. & Borecki, I. & 106 others, , 2017, In: Scientific Reports. 7, 45040.

 

25-hydroxyvitamin D concentrations during fetal life and bone health in children aged 6 years: a population-based prospective cohort study

Garcia Gutierrez, A., Erler, N.Jaddoe, V., Tiemeier, H., Hooven, E., Franco Duran, O., Rivadeneira, F. & Voortman, T., 2017, In: The Lancet Diabetes & Endocrinology. 5, 5, p. 367-376 10 p.

Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus

Medina-Gomez, C., Kemp, J., Dimou, N., Kreiner, E., Chesi, A., Zemel, B., Bonnelykke, K., Boer, C., Ahluwalia, T., Bisgaard, H., Evangelou, E., Heppe, D., Bonewald, L., Gorski, J., Ghanbari, M., Demissie, S., Duque, G., Maurano, M., Kiel, D. & Hsu, Y.-H. & 14 others, , 2017, In: Nature Communications. 8, 1, 121.

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

Vries, P., Sabater-Lleal, M., Chasman, D., Trompet, S., Ahluwalia, T., Teumer, A., Kleber, M., Chen, M., Wang, J., Attia, J., Marioni, R., Steri, M., Weng, L., Pool, R., Grossmann, V., Brody, J., Venturini, C., Tanaka, T., Rose, L. & Oldmeadow, C. & 66 others, , 2017, In: PLoS One (print). 12, 1, e0167742.

 

Design of a frailty index among community living middle-aged and older people: The Rotterdam study

Schoufour, J., Erler, N., Jaspers, L., Jong, J., Voortman, T.Ziere, B., Lindemans, J., Klaver, C., Tiemeier, H., Stricker, B.Ikram, A.Laven, J.Brusselle, G.Rivadeneira, F. & Franco Duran,

Discovery of novel heart rate-associated loci using the Exome Chip

van den Berg, M., Warren, H., Cabrera, C. P., Verweij, N., Mifsud, B., Haessler, J., Bihlmeyer, N., Fu, Y. P., Weiss, S., Lin, H. J., Grarup, N., Li-Gao, R., Pistis, G., Shah, N., Brody, J., Muller-Nurasyid, M., Lin, H., Mei, H., Smith, A. & Lyytikainen, L. & 101 others, , 2017, In: Human Molecular Genetics. 26, 12, p. 2346-2363 18 p.

 

Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus

Hackinger, S., Trajanoska, K., Styrkarsdottir, U., Zengini, E., Steinberg, J., Ritchie, G., Hatzikotoulas, K., Gilly, A., Evangelou, E., Kemp, J., Evans, D., Ingvarsson, T., Jonsson, H., Thorsteinsdottir, U., Stefansson, K., McCaskie, A., Brooks, R., Wilkinson, J., Rivadeneira, F. & Zeggini, E., 2017, In: Human Molecular Genetics. 26, 19, p. 3850-3858 9 p.

Genetic Polymorphism of miR-196a-2 is Associated with Bone Mineral Density (BMD)

Karabegovic, I., Maas, S., Medina-Gomez, C., Zrimsek, M., Reppe, S., Gautvik, K., Uitterlinden, A.Rivadeneira, F. & Ghanbari, M., 2017, In: International Journal of Molecular Sciences. 18, 12, 2529.

 

Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysms

van ‘t Hof, F., Vaucher, J., Holmes, M., Wilde, A., Baas, A., Blankensteijn, J., Hofman, B., Kiemeney, L., Rivadeneira, F.Uitterlinden, A., Vermeulen, S., Rinkel, G., de Bakker, P. & Ruigrok, Y., 2017, In: European Journal of Human Genetics. 25, 6, p. 758-762 5 p.

 

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

Zillikens, M. C., Demissie, S., Hsu, Y., Yerges-Armstrong, L., Chou, W., Stolk, L., Livshits, G., Broer, L., Johnson, T., Koller, D., Kutalik, Z., Luan, J., Malkin, I., Ried, J., Smith, A., Thorleifsson, G., Vandenput, L., Zhao, J., Zhang, W. & Aghdassi, A. & 173 others, , 2017, In: Nature Communications. 8, 80.

 

Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

Wild, P., Felix, J., Schillert, A., Teumer, A., Chen, M., Leening, M., Volker, U., Grossmann, V., Brody, J., Irvin, M. R., Shah, S., Pramana, S., Lieb, W., Schmidt, R., Stanton, A., Malzahn, D., Smith, A., Sundstrom, J., Minelli, C. & Ruggiero, D. & 103 others, , 2017, In: Journal of Clinical Investigation. 127, 5, p. 1798-1812 15 p.

 

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness

Willems, S., Wright, D., Day, F., Trajanoska, K., Joshi, P., Morris, J., Matteini, A. M., Garton, F., Grarup, N., Oskolkov, N., Thalamuthu, A., Mangino, M., Liu, J., Demirkan, A., Lek, M., Xu, L., Wang, G., Oldmeadow, C., Gaulton, K. & Lotta, L. & 56 others, , 2017, In: Nature Communications. 8, 16015.

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

Manousaki, D., Dudding, T., Haworth, S., Hsu, Y., Liu, C., Medina Gomez, M.Voortman, T.van der Velde, N., Melhus, H., Robinson-Cohen, C., Cousminer, D., Nethander, M., Vandenput, L., Noordam, R., Forgetta, V., Greenwood, C., Biggs, M., Psaty, B., Rotter, J. & Zemel, B. & 33 others, , 2017, In: American Journal of Human Genetics. 101, 2, p. 227-238 12 p.

 

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics

Springelkamp, H., Iglesias Gonzalez, A., Mishra, A., Hohn, R., Wojciechowski, R., Khawaja, A., Nag, A., Wang, Y., Wang, J., Cuellar-Partida, G., Gibson, J., Bailey, J., Vithana, E., Gharahkhani, P., Boutin, T., Ramdas, W., Zeller, T., Luben, R., Yonova-Doing, E. & Viswanathan, A. & 63 others, , 2017, In: Human Molecular Genetics. 26, 2, p. 438-453 16 p.

 

Protein intake during pregnancy and offspring body composition at 6 years: the Generation R Study

Tielemans, M., Steegers, E.Voortman, T.Jaddoe, V.Rivadeneira, F., Franco Duran, O. & Jong, J., 2017, In: European Journal of Nutrition. 56, 6, p. 2151-2160 10 p.

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer’s disease

Sims, R., van der Lee, S., Naj, A., Bellenguez, C., Badarinarayan, N., Jakobsdottir, J., Kunkle, B., Boland, A., Raybould, R., Bis, J., Martin, E., Grenier-Boley, B., Heilmann-Heimbach, S., Chouraki, V., Kuzma, A., Sleegers, K., Vronskaya, M., Ruiz, A., Graham, R. & Olaso, R. & 428 others, , 2017, In: Nature Genetics. 49, 9, p. 1373-+

 

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

Li, M., Li, Y., Weeks, O., Mijatovic, V., Teumer, A., Huffman, J., Tromp, G., Fuchsberger, C., Gorski, M., Lyytikainen, L., Nutile, T., Sedaghat, S., Sorice, R., Tin, A., Yang, Q., Ahluwalia, T., Arking, D., Bihlmeyer, N., Boger, C. & Carroll, R. J. & 136 others, , 2017, In: Journal of the American Society of Nephrology. 28, 3, p. 981-994 14 p.

Franck, S., Broer, L.Lelij, A. J., Kamenicky, P., Bernabeu, I., Malchiodi, E., Delhanty, P.Rivadeneira, F. & Neggers, S. J. C. M. M., 2017, In: Neuroendocrinology. 105, 2, p. 131-140 10 p.

Thyroid Function Tests in the Reference Range and Fracture: Individual Participant Analysis of Prospective Cohorts

Aubert, C., Floriani, C., Bauer, D., da Costa, B., Segna, D., Blum, M., Collet, T., Fink, H., Cappola, A., Syrogiannouli, L., Peeters, R., Asvold, B., den Elzen, W., Luben, R., Bremner, A., Gogakos, A., Eastell, R., Kearney, P., van t Hoff, M. & Le Blanc, E. & 13 others, , 2017, In: Journal of Clinical Endocrinology and Metabolism. 102, 8, p. 2719-2728 10 p.

 

Use of Selective Serotonin Reuptake Inhibitors and Bone Mineral Density Change A Population-Based Longitudinal Study in Middle-Aged and Elderly Individuals

van der Ham, A., Aarts, N., Noordam, R., Rivadeneira, F.Ziere, B., Zillikens, M. C., Tiemeier, H., van der Velde, N.Hofman, B.Uitterlinden, A.Visser, L. & Stricker, B., 2017, In: Journal of Clinical Psychopharmacology. 37, 5, p. 524-530 7 p.

 

Vitamin D and body composition in the elderly

Vitezova, Muka, T., Zillikens, M. C., Voortman, T.Uitterlinden, A.Hofman, B.Rivadeneira, F., Jong, J. & Franco Duran, O., 2017, In: Clinical Nutrition. 36, 2, p. 585-592 8 p.

 

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

Tachmazidou, I., Suveges, D., Min, J., Ritchie, G., Steinberg, J., Walter, K., Iotchkova, V., Schwartzentruber, J., Huang, J., Memari, Y., McCarthy, S., Crawford, A., Bombieri, C., Cocca, M., Farmaki, A., Gaunt, T., Jousilahti, P., Kooijman, M., Lehne, B. & Malerba, G. & 83 others, , 2017, In: American Journal of Human Genetics. 100, 6, p. 865-884 20 p.

 

2016

Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: The Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study

Hsu, Y. H., Li, G., Liu, C. T., Brody, J. A., Karasik, D., Chou, W. C., Demissie, S., Nandakumar, K., Zhou, Y., Cheng, C. H., Gill, R., Gibbs, R. A., Muzny, D., Santibanez, J., Estrada, K., Rivadeneira, F., Harris, T., Gudnason, V., Uitterlinden, A. & Psaty, B. M. & 3 others, , 1 Dec 2016, In: Human Molecular Genetics. 25, 23, p. 5234-5243 10 p.

 

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

Ried, J., Jeff, J., Chu, A., Bragg-Gresham, J., Dongen, J., Huffman, J., Ahluwalia, T., Cadby, G., Eklund, N., Eriksson, J., Esko, T., Feitosa, M., Goel, A., Gorski, M., Hayward, C., Heard-Costa, N., Jackson, A., Jokinen, E., Kanoni, S. & Kristiansson, K. & 256 others, , 23 Nov 2016, In: Nature Communications. 7, 13357.

 

A Genome-Wide Approach to Children’s Aggressive Behavior: The EAGLE consortium

Pappa, I., St Pourcain, B., Benke, K., Cavadino, A., Hakulinen, C., Nivard, M., Nolte, I., Tiesler, C., Bakermans-Kranenburg, M., Davies, G., Evans, D., Geoffroy, M. C., Grallert, H., Groen-Blokhuis, M., Hudziak, J. J., Kemp, J., Keltikangas-Jarvinen, L., McMahon, G., Mileva – Seitz, V. & Motazedi, E. & 23 others, , 2016, In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics. 171, 5, p. 562-572 11 p.

 

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways

Bustamante, M., Standl, M., Bassat, Q., Vilor-Tejedor, N., Medina Gomez, M., Bonilla, C., Ahluwalia, T., Bacelis, J., Bradfield, J., Tiesler, C., Rivadeneira, F., Ring, S., Vissing, N., Jugessur, A., Mentch, F., Ballester, F., Kriebel, J., Jong, J., Wolsk, H. & Llop, S. & 18 others, , 2016, In: Human Molecular Genetics. 25, 18, p. 4142 4127.

Research output: Contribution to journal › Article › Academic › peer-review

36Citations (Scopus)

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

Vries, P., Chasman, D., Sabater-Lleal, M., Chen, M., Huffman, J., Steri, M., Tang, W., Teumer, A., Marioni, R., Grossmann, V., Hottenga, J., Trompet, S., Muller-Nurasyid, M., Zhao, J., Brody, J., Kleber, M., Guo, X., Wang, J., Auer, P. & Attia, J. & 111 others, , 2016, In: Human Molecular Genetics. 25, 2, p. 358-370 13 p.

 

A Meta-Analysis of Trabecular Bone Score in Fracture Risk Prediction and Its Relationship to FRAX

McCloskey, E., Oden, A., Harvey, N., Leslie, W., Hans, D., Johansson, H., Barkmann, R., Boutroy, S., Brown, J., Chapurlat, R., Elders, P., Fujita, Y., Gluer, C., Goltzman, D., Iki, M., Karlsson, M., Kindmark, A., Kotowicz, M., Kurumatani, N. & Kwok, T. & 16 others, , 2016, In: Journal of Bone and Mineral Research. 31, 5, p. 940-948 9 p.

 

Association between Bone Mass and Dental Hypomineralization

van der Tas, J., Elfrink, M., Vucic, S., Heppe, D., Veerkamp, J., Jaddoe, V.Rivadeneira, F.Hofman, B.Moll, H. & Wolvius, E., 2016, In: Journal of Dental Research. 95, 4, p. 395-401 7 p.

 

Association of anthropometric measures with fat and fat-free mass in the elderly: The Rotterdam study

Dhana, K., Koolhaas, C., Schoufour, J., Rivadeneira, F.Hofman, B.Kavousi, M. & Franco Duran, O., 2016, In: Maturitas. 88, p. 96-100 5 p.

 

Associations of breast-feeding patterns and introduction of solid foods with childhood bone mass: The Generation R Study

Hooven, E., Gharsalli, M., Heppe, D., Raat, H.Hofman, B., Franco Duran, O., Rivadeneira, F. & Jaddoe, V., 2016, In: British Journal of Nutrition. 115, 6, p. 1024-1032 9 p.

 

Bone Mass and Strength in School-Age Children Exhibit Sexual Dimorphism Related to Differences in Lean Mass: The Generation R Study

Medina Gomez, M., Heppe, D., Yin, J.-L., Trajanoska, K.Uitterlinden, A., Beck, T., Jaddoe, V. & Rivadeneira, F., 2016, In: Journal of Bone and Mineral Research. 31, 5, p. 1099-1106 8 p.

 

Counter-regulation of rejection activity against human liver grafts by donor PD-L1 and recipient PD-1 interaction

Shi, X., Mancham, S.Hansen, B.de Knegt, R.de Jonge, J.van der Laan, L.Rivadeneira, F., Metselaar, H. & Kwekkeboom, J., 2016, In: Journal of Hepatology. 64, 6, p. 1274-1282 9 p.

 

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

Iotchkova, V., Huang, J., Morris, J., Jain, D., Barbieri, C., Walter, K., Min, J., Chen, L., Astle, W., Cocca, M., Deelen, P., Elding, H., Farmaki, A., Franklin, C., Franberg, M., Gaunt, T., Hofman, B., Jiang, T., Kleber, M. & Lachance, G. & 47 others, , 2016, In: Nature Genetics. 48, 11, p. 1303-1312 10 p.

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

Chami, N., Chen, M., Slater, A. J., Eicher, J., Evangelou, E., Tajuddin, S. M., Love-Gregory, L., Kacprowski, T., Schick, U., Nomura, A., Giri, A., Lessard, S., Brody, J., Schurmann, C., Pankratz, N., Yanek, L., Manichaikul, A., Pazoki, R., Mihailov, E. & Hill, W. & 93 others, , 2016, In: American Journal of Human Genetics. 99, 1, p. 8-21 14 p.

 

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Pattaro, C., Teumer, A., Gorski, M., Chu, A., Li, M., Mijatovic, V., Garnaas, M., Tin, A., Sorice, R., Li, Y., Taliun, D., Olden, M., Foster, M., Yang, Q., Chen, M., Pers, T., Johnson, A., Ko, Y. A., Fuchsberger, C. & Tayo, B. & 232 others, , 2016, In: Nature Communications. 7, 10023.

Genetics of Osteoporotic Vertebral Fractures

Oei – Oei, L., Zillikens, M. C., Rivadeneira, F. & Oei, E., 2016, In: Journal of Clinical Densitometry. 19, 1, p. 23-28 6 p.

 

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

van Rheenen, W., Shatunov, A., Dekker, A., McLaughlin, R., Diekstra, F., Pulit, S., van der Spek, R. A. A., Vosa, U., de Jong, S., Robinson, M., Yang, J., Fogh, I., van Doormaal, P., Tazelaar, G. H. P., Koppers, M., Blokhuis, A., Sproviero, W., Jones, A. R., Kenna, K. P. & van Eijk, K. & 157 others, , 2016, In: Nature Genetics. 48, 9, p. 1043-1048 6 p.

 

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

Felix, J., Bradfield, J., Monnereau, C., Valk, R., Stergiakouli, E., Chesi, A., Gaillard, R., Feenstra, B., Thiering, E., Kreiner-Moller, E., Mahajan, A., Pitkanen, N., Joro, R., Cavadino, A., Huikari, V., Franks, S., Groen-Blokhuis, M., Cousminer, D., Marsh, J. & Lehtimaki, T. & 91 others, , 2016, In: Human Molecular Genetics. 25, 2, p. 389-403 15 p.

 

Genome-wide associations for birth weight and correlations with adult disease

Horikoshi, M., Beaumont, R., Day, F., Warrington, N., Kooijman, M., Fernandez-Tajes, J., Feenstra, B., van Zuydam, N., Gaulton, K., Grarup, N., Bradfield, J., Strachan, D., Li-Gao, R., Ahluwalia, T., Kreiner, E., Rueedi, R., Lyytikainen, L., Cousminer, D., Wu, F. & Thiering, E. & 143 others, , 2016, In: Nature. 538, 7624, p. 248-252 5 p.

 

Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

van Ingen, G., Li, J., Goedegebure, A., Pandey, R., Li, Y., March, M., Jaddoe, V., Bakay, M., Mentch, F., Thomas, K., Wei, Z., Chang, X., Hain, H., Uitterlinden, A.Moll, H., Duijn, C., Rivadeneira, F.Raat, H., Baatenburg de Jong, R. J. & Sleiman, P. & 2 others, , 2016, In: Nature Communications. 7

Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium

Dehghan, A., Bis, J., White, C., Smith, A., Morrison, A., Cupples, L., Trompet, S., Chasman, D., Lumley, T., Volker, U., Buckley, B., Ding, J., Jensen, M., Folsom, A., Kritchevsky, S., Girman, C. J., Ford, I., Dorr, M., Salomaa, V. & Uitterlinden, A. & 47 others, , 2016, In: PLoS One (print). 11, 3, e0144997.

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

Kilpelainen, T., Carli, J. F. M., Skowronski, A. A., Sun, Q., Kriebel, J., Feitosa, M., Hedman, A., Drong, A., Hayes, J. E., Zhao, J., Pers, T., Schick, U., Grarup, N., Kutalik, Z., Trompet, S., Mangino, M., Kristiansson, K., Beekman, M., Lyytikainen, L. & Eriksson, J. & 157 others, , 2016, In: Nature Communications. 7, 10494.

 

GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium

Matteini, A. M., Tanaka, T., Karasik, D., Atzmon, G., Chou, W., Eicher, J., Johnson, A., Arnold, A., Callisaya, M., Davies, G., Evans, D., Holtfreter, B., Lohman, K., Lunetta, K., Mangino, M., Smith, A., Smith, J., Teumer, A., Yu, L. & Arking, D. & 47 others, , 2016, In: Aging Cell. 15, 5, p. 792-800 9 p.

 

Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium

Marinelli, M., Pappa, I., Bustamante, M., Bonilla, C., Suarez, A., Tiesler, C., Vilor-Tejedor, N., Zafarmand, M., Alvarez-Pedrerol, M., Andersson, S., Bakermans-Kranenburg, M., Estivill, X., Evans, D., Flexeder, C., Forns, J., Gonzalez, J., Guxens Junyent, M., Huss, A., van IJzendoorn, M. & Jaddoe, V. & 24 others, , 2016, In: Sleep. 39, 10, p. 1859-1869 11 p.

 

International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents

Parmar, P., Taal, R., Timpson, N., Thiering, E., Lehtimaki, T., Marinelli, M., Lind, P., Howe, L., Verwoert, G., Aalto, V., Uitterlinden, A., Briollais, L., Evans, D., Wright, M., Newnham, J., Whitfield, J., Lyytikainen, L., Rivadeneira, F., Boomsma, D. & Viikari, J. & 18 others, , 2016, In: Circulation-cardiovascular genetics. 9, 3, p. 266-+

 

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Leeuwen, E., Sabo, A., Bis, J., Huffman, J., Manichaikul, A., Smith, A., Feitosa, M., Demissie, S., Joshi, P., Duan, Q., Marten, J., van Klinken, J., Surakka, I., Nolte, I., Zhang, W., Mbarek, H., Li-Gao, R., Trompet, S., Verweij, N. & Evangelou, E. & 78 others, , 2016, In: Journal of Medical Genetics. 53, 7, p. 441-449 9 p.

 

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

Fan, Q., Verhoeven, V., Wojciechowski, R., Barathi, V., Hysi, P., Guggenheim, J., Hohn, R., Vitart, V., Khawaja, A., Yamashiro, K., Hosseini, S., Lehtimaki, T., Lu, Y., Haller, T., Xie, J., Delcourt, C., Pirastu, M., Wedenoja, J., Gharahkhani, P. & Venturini, C. & 134 others, , 2016, In: Nature Communications. 7

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

Postmus, I., Warren, H., Trompet, S., Arsenault, B., Avery, C., Bis, J., Chasman, D., de Keyser, T., Deshmukh, H., Evans, D., Feng, Q., Li, X., Smit, R., Smith, A., Sun, F., Taylor, K., Arnold, A., Barnes, M., Barratt, B. & Betteridge, J. & 68 others, , 2016, In: Journal of Medical Genetics. 53, 12, p. 835-845 11 p.

 

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

Pankratz, N., Schick, U., Zhou, Y., Zhou, W., Ahluwalia, T., Allende, M. L., Auer, P., Bork-Jensen, J., Brody, J., Chen, M., Clavo, V., Eicher, J., Grarup, N., Hagedorn, E. J., Hu, B., Hunker, K., Johnson, A., Leusink, M., Lu, Y. & Lyytikainen, L. & 61 others, , 2016, In: Nature Genetics. 48, 8, p. 867-876 10 p.

 

Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis

Natarajan, P., Bis, J., Bielak, L., Cox, A. J., Dorr, M., Feitosa, M., Franceschini, N., Guo, X., Hwang, S.-J., Isaacs, A., Jhun, M., Kavousi, M., Li-Gao, R., Lyytikainen, L.-P., Marioni, R., Schminke, U., Stitziel, N., Tada, H., van Setten, J. & Smith, A. & 80 others, , 2016, In: Circulation-cardiovascular genetics. 9, 6, p. 511-520 10 p.

 

Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2

Nielson, C., Liu, C., Smith, A., Ackert-Bicknell, C., Reppe, S., Jakobsdottir, J., Wassel, C., Register, T. C., Oei – Oei, L., Alonso, N., Oei, E., Parimi, N., Samelson, E. J., Nalls, M., Zmuda, J., Lang, T., Bouxsein, M., Latourelle, J., Claussnitzer, M. & Siggeirsdottir, K. & 31 others, , 2016, In: Journal of Bone and Mineral Research. 31, 12, p. 2085-2097 13 p.

 

Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis

Castano Betancourt, M., Evans, D., Ramos, Y., Boer, C., Metrustry, S., Liu, Y., den Hollander, W., van Rooij, J., Kraus, V. B., Yau, M., Mitchell, B., Muir, K., Hofman, B., Doherty, M., Doherty, S., Zhang, W., Kraaij, R.Rivadeneira, F., Barrett-Connor, E. & Maciewicz, R. & 17 others, , 2016, In: PLoS Genetics (online). 12, 10, e1006260.

 

Osteoporosis and Bone Mass Disorders: From Gene Pathways to Treatments

Rivadeneira, F. & Makitie, O., 2016, In: Trends in Endocrinology and Metabolism. 27, 5, p. 262-281 20 p.

 

Osteoporotic Vertebral Fractures as Part of Systemic Disease

Oei – Oei, L., Zillikens, M. C., Rivadeneira, F. & Oei, E., 2016, In: Journal of Clinical Densitometry. 19, 1, p. 70-80 11 p.

Research output: Contribution to journal › Article › Academic › peer-review

8Citations (Scopus)

Quantitative imaging methods in osteoporosis

Oei – Oei, L., Koromani, F.Rivadeneira, F., Zillikens, M. C. & Oei, E., 2016, In: Quantitative Imaging in Medicine and Surgery. 6, 6, p. 680-698 19 p.

Research output: Contribution to journal › Article › Academic › peer-review

82Citations (Scopus)

Risk of Frailty in Elderly With COPD: A Population-Based Study

Lahousse, L.Ziere, B., Verlinden, V., Zillikens, M. C., Uitterlinden, A.Rivadeneira, F., Tiemeier, H., Joos, G., Hofman, B.Ikram, A., Franco Duran, O., Brusselle, G. & Stricker, B., 2016, In: Journals of Gerontology Series A-Biological Sciences and Medical Sciences. 71, 5, p. 689-695 7 p.

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

van ‘t Hof, F., Ruigrok, Y., Lee, C., Ripke, S., Anderson, G., de Andrade, M., Baas, A., Blankensteijn, J., Bottinger, E., Bown, M., Broderick, J., Bijlenga, P., Carrell, D., Crawford, D., Crosslin, D., Ebeling, C., Eriksson, J., Fornage, M., Foroud, T. & von und zu Fraunberg, M. & 50 others, , 2016, In: Journal of the American Heart Association. 5, 7, e002603.

 

Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies

Demirkan, A., Lahti, J., Direk, N., Viktorin, A., Lunetta, K., Terracciano, A., Nalls, M., Tanaka, T., Hek, K., Fornage, M., Wellmann, J., Cornelis, M., Ollila, H., Yu, L., Smith, J., Pilling, L., Isaacs, A., Palotie, A., Zhuang, W. & Zonderman, A. & 37 others, , 2016, In: Psychological Medicine. 46, 8, p. 1613-1623 11 p.

 

The case for genome-wide association studies of bone acquisition in paediatric and adolescent populations

Kemp, J., Medina Gomez, M., Tobias, J., Rivadeneira, F. & Evans, D., 2016, In: Bonekey Reports. 5, 796.

 

The Generation R Study: design and cohort update 2017

Kooijman, M., Kruithof, C., Duijn, C., Duijts, L., Franco Duran, O., van IJzendoorn, M., Jongste, J., Klaver, C.van der Lugt, A.Mackenbach, J.Moll, H.Peeters, R.Raat, H.Rings, E.Rivadeneira, F.van der Schroeff, M. P.Steegers, E., Tiemeier, H., Uitterlinden, A. & Verhulst, F. & 3 others, , 2016, In: European Journal of Epidemiology. 31, 12, p. 1243-1264 22 p.

The genetics of bone mass and susceptibility to bone diseases

Karasik, D., Rivadeneira, F. & Johnson, M. L., 2016, In: Nature Reviews Rheumatology. 12, 6, p. 323-334 12 p.

 

The Influence of Serum Uric Acid on Bone Mineral Density, Hip Geometry, and Fracture Risk: The Rotterdam Study

Muka, T., Jonge, E., Jong, J., Uitterlinden, A.Hofman, B., Dehghan, A., Zillikens, M. C., Franco Duran, O. & Rivadeneira, F., 2016, In: Journal of Clinical Endocrinology and Metabolism. 101, 3, p. 1113-1122 10 p.

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

Polfus, L. M., Khajuria, R. K., Schick, U., Pankratz, N., Pazoki, R., Brody, J., Chen, M., Auer, P., Floyd, J. S., Huang, J., Lange, L., van Rooij, F., Gibbs, R., Metcalf, G., Muzny, D., Veeraraghavan, N., Walter, K., Chen, L., Yanek, L. & Becker, L. & 36 others, , 2016, In: American Journal of Human Genetics. 99, 2, p. 481-488 8 p.

 

y New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk

Lu, Y., Day, F., Gustafsson, S., Buchkovich, M., Na, J., Bataille, V., Cousminer, D., Dastani, Z., Drong, A., Esko, T., Evans, D., Falchi, M., Feitosa, M., Ferreira, T., Hedman, A., Haring, R., Hysi, P., Iles, M., Justice, A. & Kanoni, S. & 239 others, , 2016, In: Nature Communications. 7

 

2015

Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci

Reppe, S., Wang, Y., GEFOS Consortium, Thompson, W. K., McEvoy, L. K., Schork, A. J., Zuber, V., LeBlanc, M., Bettella, F., Mills, I. G., Desikan, R. S., Djurovic, S., Gautvik, K. M., Dale, A. M., Andreassen, O. A., Oei, L., Amin, N., Li, G., Aulchenko, Y. S. & Castano-Betancourt, M. & 13 others, , 1 Dec 2015, In: PLoS ONE. 10, 12, e0144531.

Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C

van Leeuwen, E. M., Huffman, J. E., Generation Scotland, Bis, J. C., Isaacs, A., Mulder, M., Sabo, A., Smith, A. V., Demissie, S., Manichaikul, A., Brody, J. A., Feitosa, M. F., Duan, Q., Schraut, K. E., Navarro, P., van Vliet-Ostaptchouk, J. V., Zhu, G., Mbarek, H., Trompet, S. & Verweij, N. & 31 others, , 12 Nov 2015, In: npj Aging and Mechanisms of Disease. 1, 15011.

An atlas of genetic correlations across human diseases and traits

Bulik-Sullivan, B., Finucane, H. K., Anttila, V., Gusev, A., Day, F. R., Loh, P.-R., ReproGen ConsortiumPsychiatric Genomics ConsortiumGenetic Consortium for Anorexia Nervosa (GCAN)Wellcome Trust Case Control Consortium 3 (WTCCC3), Duncan, L., Perry, J. R. B., Patterson, N., Robinson, E. B., Daly, M. J., Price, A. L. & Neale, B. M., Nov 2015, In: Nature Genetics. 47, 11, p. 1236-1241 6 p.

 

Partitioning heritability by functional annotation using genome-wide association summary statistics

Finucane, H. K., Bulik-Sullivan, B., Gusev, A., Trynka, G., Reshef, Y., Loh, P.-R., Anttila, V., Xu, H., Zang, C., Farh, K., Ripke, S., Day, F. R., ReproGen ConsortiumSchizophrenia Working Group of the Psychiatric Genomics ConsortiumThe RACI Consortium, Purcell, S., Stahl, E., Lindstrom, S., Perry, J. R. B. & Okada, Y. & 5 others, , Nov 2015, In: Nature Genetics. 47, 11, p. 1228-1235 8 p.

Genetic studies of body mass index yield new insights for obesity biology

ADIPOGen ConsortiumThe AGEN-BMI Working GroupThe CARDIOGRAMplusC4D ConsortiumThe CKDGen ConsortiumThe GLGCICBP ConsortiumThe MAGIC InvestigatorsThe MuTHER ConsortiumThe MIGen ConsortiumThe PAGE ConsortiumThe GENIE ConsortiumThe International Endogene Consortium, Locke, A. E., Kahali, B., The LifeLines Cohort StudyReproGen Consortium, Berndt, S. I., Justice, A. E., Pers, T. H. & Day, F. R. & 50 others, , 11 Feb 2015, In: Nature. 518, 7538, p. 197-206 10 p.

 

New genetic loci link adipose and insulin biology to body fat distribution

ADIPOGen ConsortiumReproGen ConsortiumThe CARDIOGRAMplusC4D ConsortiumCDKGen ConsortiumThe GEFOS ConsortiumThe GENIE ConsortiumThe GLGCICBP ConsortiumThe International Endogene ConsortiumThe LifeLines Cohort StudyThe MAGIC InvestigatorsThe MuTHER ConsortiumThe PAGE Consortium, Shungin, D., Winkler, T. W., Croteau-Chonka, D. C., Ferreira, T., Locke, A. E., Mägi, R. & Strawbridge, R. J. & 63 others, , 11 Feb 2015, In: Nature. 518, 7538, p. 187-196 10 p.

 

A Genome Wide Association Study Links Glutamate Receptor Pathway to Sporadic Creutzfeldt-Jakob Disease Risk

Sanchez-Juan, P., Bishop, M., Kovacs, G., Calero, M., Aulchenko, Y., Ladogana, A., Boyd, A., Lewis, V., Ponto, C., Calero, O., Poleggi, A., Carracedo, A., van der Lee, S., Strobel, T., Rivadeneira, F.Hofman, B., Haik, S., Combarros, O., Berciano, J. & Uitterlinden, A. & 9 others, , 2015, In: PLoS One (print). 10, 4

 

A novel common variant in DCST2 is associated with length in early life and height in adulthood

Valk, R., Kreiner-Moller, E., Kooijman, M., Guxens Junyent, M., Stergiakouli, E., Saaf, A., Bradfield, J., Geller, F., Hayes, M., Cousminer, D., Korner, A., Thiering, E., Curtin, J., Myhre, R., Huikari, V., Joro, R., Kerkhof, M., Warrington, N., Pitkanen, N. & Ntalla, I. & 97 others, , 2015, In: Human Molecular Genetics. 24, 4, p. 1155-1168 14 p.

Research output: Contribution to journal › Article › Academic › peer-review

82Citations (Scopus)

ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure

Springelkamp, H., Iglesias Gonzalez, A., Cuellar-Partida, G., Amin, N., Burdon, K., Leeuwen, E., Gharahkhani, P., Mishra, A., van der Lee, S., Hewitt, A., Rivadeneira, F., Viswanathan, A., Wolfs, R. C. W., Martin, N., Ramdas, W., van Koolwijk, L., Pennell, C., Vingerling, H., Mountain, J. & Uitterlinden, A. & 9 others, , 2015, In: Human Molecular Genetics. 24, 9, p. 2689-2699 11 p.

 

Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral density

Veldhuis-Vlug, A., Oei – Oei, L., Souverein, P., Tanck, M., Rivadeneira, F., Zillikens, M. C., Kamphuisen, P., Zee, A., de Groot, M., Hofman, B.Uitterlinden, A., Fliers, E., Boer, A. & Bisschop, P., 2015, In: Osteoporosis International. 26, 7, p. 2019-2027 9 p.

 

BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection Pressures

Medina Gomez, M., Chesi, A., Heppe, D., Zemel, B., Yin, J.-L., Kalkwarf, H., Hofman, B., Lappe, J., Kelly, A., Kayser, M., Oberfield, S., Gilsanz, V., Uitterlinden, A., Shepherd, J., Jaddoe, V., Grant, S., Lao Grueso, O. & Rivadeneira, F., 2015, In: Molecular Biology and Evolution. 32, 11, p. 2961-2972 12 p.

 

Bone health and coronary artery calcification: The Rotterdam Study

Campos-Obando, N., Kavousi, M.Roeters van Lennep, J.Rivadeneira, F.Hofman, B.Uitterlinden, A., Franco Duran, O. & Zillikens, M. C., 2015, In: Atherosclerosis. 241, 1, p. 278-283 6 p.

 

Cell Specific eQTL Analysis without Sorting Cells

Westra, H., Arends, D., Esko, T., Peters, M., Schurmann, C., Schramm, K., Kettunen, J., Yaghootkar, H., Fairfax, B., Andiappan, A., Li, Y., Fu, J., Karjalainen, J., Platteel, M., Visschedijk, M., Weersma, R., Kasela, S., Milani, L., Tserel, L. & Peterson, P. & 38 others, , 2015, In: PLoS Genetics (print). 11, 5

 

Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study

Medina Gomez, M.Felix, J., Estrada Gil, K., Peters, M., Herrera Duran, L., Kruithof, C.Duijts, L.Hofman, B., Duijn, C., Uitterlinden, A.Jaddoe, V. & Rivadeneira, F., 2015, In: European Journal of Epidemiology. 30, 4, p. 317-330 14 p.

 

\Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014)

Rietveld, C., Esko, T., Davies, G., Pers, T., Turley, P., Benyamin, B., Chabris, C., Emilsson, V., Johnson, A., Lee, J., de Leeuw, C., Marioni, R., Medland, S., Miller, M., Rostapshova, O., van der Lee, S., Vinkhuyzen, A., Amin, N., Conley, D. & Derringer, J. & 39 others, , 2015, In: Proceedings of the National Academy of Sciences of the U.S.A.. 112, 4, p. E380-E380

Development of a Food Group-Based Diet Score and Its Association with Bone Mineral Density in the Elderly: The Rotterdam Study

Jonge, E., Jong, J., de Groot, L., Voortman, T., Schoufour, J., Zillikens, M. C., Hofman, B.Uitterlinden, A., Franco Duran, O. & Rivadeneira, F., 2015, In: Nutrients. 7, 8, p. 6974-6990 17 p.

 

Diabetes, Diabetic Complications, and Fracture Risk

Oei – Oei, L., Rivadeneira, F., Zillikens, M. C. & Oei, E., 2015, In: Current Osteoporosis Reports. 13, 2, p. 106-115 10 p.

 

Dietary acid load in early life and bone health in childhood: the Generation R Study

Garcia Gutierrez, A., Franco Duran, O., Voortman, T., Jonge, E., Gordillo, N., Jaddoe, V.Rivadeneira, F. & Hooven, E., 2015, In: American Journal of Clinical Nutrition. 102, 6, p. 1595-1603 9 p.

 

Dietary vitamin A intake and bone health in the elderly: the Rotterdam Study

Jonge, E., Jong, J., Campos-Obando, N., Booij, L., Franco Duran, O., Hofman, B.Uitterlinden, A.Rivadeneira, F. & Zillikens, M. C., 2015, In: European Journal of Clinical Nutrition. 69, 12, p. 1360-1368 9 p.

 

Dietary vitamin A intake and bone health in the elderly: the Rotterdam Study (vol 69, pg 1360, 2015)

Jonge, E., Jong, J., Campos-Obando, N., Booij, L., Franco Duran, O., Hofman, B.Uitterlinden, A.Rivadeneira, F. & Zillikens, M. C., 2015, In: European Journal of Clinical Nutrition. 69, 12, p. 1375-1375 1 p.

 

Does fetal smoke exposure affect childhood bone mass? The Generation R Study

Heppe, D., Medina Gomez, M.Hofman, B.Rivadeneira, F. & Jaddoe, V., 2015, In: Osteoporosis International. 26, 4, p. 1319-1329 11 p.

 

Estimation of Genetic Relationships Between Individuals Across Cohorts and Platforms: Application to Childhood Height

Fedko, I., Hottenga, J., Medina Gomez, M., Pappa, I., Beijsterveld, C., Ehli, E., Davies, G., Rivadeneira, F., Tiemeier, H., Swertz, M., Middeldorp, C., Bartels, M. & Boomsma, D., 2015, In: Behavior Genetics. 45, 5, p. 514-528 15 p.

Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up

Liu, F., Visser, M., Duffy, D., Hysi, P., Jacobs, L., Lao Grueso, O., Zhong, K., Walsh, S., Chaitanya, L., Wollstein, A., Zhu, G., Montgomery, G., Henders, A., Mangino, M., Glass, D., Bataille, V., Sturm, R., Rivadeneira, F.Hofman, B. & van Ijcken, W. & 6 others, , 2015, In: Human Genetics. 134, 8, p. 823-835 13 p.

Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity

Vries, P., Boender, J., Sonneveld, M., Rivadeneira, F.Ikram, A., Rottensteiner, H., Hofman, B.Uitterlinden, A.Leebeek, F., Franco Duran, O., Dehghan, A. & de Maat, M., 2015, In: Blood. 125, 25, p. 3949-3955 7 p.

Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

Leeuwen, E., Karssen, L., Deelen, J., Isaacs, A., Medina-Gomez, C., Mbarek, H., Kanterakis, A., Trompet, S., Postmus, I., Verweij, N., van Enckevort, D., Huffman, J., White, C., Feitosa, M., Bartz, T., Manichaikul, A., Joshi, P., Peloso, G., Deelen, P. & Dijk, F. & 52 others, , 2015, In: Nature Communications. 6

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Li, Q., Wojciechowski, R., Simpson, C., Hysi, P., Verhoeven, V., Ikram, M., Hohn, R., Vitart, V., Hewitt, A., Oexle, K., Makela, K., Macgregor, S., Pirastu, M., Fan, Q., Cheng, C., St Pourcain, B., McMahon, G., Kemp, J., Northstone, K. & Rahi, J. & 69 others, , 2015, In: Human Genetics. 134, 2, p. 131-146 16 p.

 

Genome-Wide Association Study in an Admixed Case Series Reveals IL12A as a New Candidate in Behcet Disease

Kappen, J., Medina Gomez, M.van Hagen, P. M., Stolk, L., Estrada Gil, K., Rivadeneira, F.Uitterlinden, A., Stanford, M., Ben-Chetrit, E., Wallace, G., Soylu, M. & van Laar, J., 2015, In: PLoS One (print). 10, 3

Genome-wide association study of kidney function decline in individuals of European descent

Gorski, M., Tin, A., Garnaas, M., McMahon, G., Chu, A., Tayo, B., Pattaro, C., Teumer, A., Chasman, D., Chalmers, J., Hamet, P., Tremblay, J., Woodward, M., Aspelund, T., Eiriksdottir, G., Gudnason, V., Harris, T., Launer, L., Smith, A. & Mitchell, B. & 84 others, , 2015, In: Kidney International. 87, 5, p. 1017-1029 13 p.

GWAS of Longevity in CHARGE Consortium Confirms APOE and FOXO3 Candidacy

Broer, L., Buchman, A., Deelen, J., Evans, D., Faul, J., Lunetta, K., Sebastiani, P., Smith, J., Smith, A., Tanaka, T., Yu, L., Arnold, A., Aspelund, T., Benjamin, E., De Jager, P., Eirkisdottir, G., Evans, D., Garcia, M., Hofman, B. & Kaplan, R. & 27 others, , 2015, In: Journals of Gerontology Series A-Biological Sciences and Medical Sciences. 70, 1, p. 110-118 9 p.

GWAS with longitudinal phenotypes: performance of approximate procedures

Sikorska, K., Montazeri, N., Uitterlinden, A.Rivadeneira, F.Eilers, P. & Lesaffre, E., 2015, In: European Journal of Human Genetics. 23, 10, p. 1384-1391 8 p.

Improving accuracy of rare variant imputation with a two-step imputation approach

Moller, G., Medina Gomez, M.Uitterlinden, A.Rivadeneira, F. & Estrada Gil, K., 2015, In: European Journal of Human Genetics. 23, 3, p. 395-400 6 p.

Infant dietary patterns and bone mass in childhood: the Generation R Study

Hooven, E., Heppe, D., Jong, J., Medina Gomez, M.Moll, H.Hofman, B.Jaddoe, V.Rivadeneira, F. & Franco Duran, O., 2015, In: Osteoporosis International. 26, 5, p. 1595-1604 10 p.

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair EDITORIAL COMMENT

Day, F., Ruth, K., Thompson, D., Lunetta, K., Pervjakova, N., Chasman, D., Stolk, L., Finucane, H., Sulem, P., Bulik-Sullivan, B., Esko, T., Johnson, A., Elks, C., Franceschini, N., He, C., Altmaier, E., Brody, J., Franke, L., Huffman, J. & Keller, M. & 221 others, , 2015, In: Obstetrical and Gynecological Survey. 70, 12, p. 758-762 5 p.

 

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

Day, F., Ruth, K., Thompson, D., Lunetta, K., Pervjakova, N., Chasman, D., Stolk, L., Finucane, H., Sulem, P., Bulik-Sullivan, B., Esko, T., Johnson, A., Elks, C., Franceschini, N., He, C., Altmaier, E., Brody, J., Franke, L., Huffman, J. & Keller, M. & 221 others, , 2015, In: Nature Genetics. 47, 11, p. 1294-+

 

Maternal dietary patterns during pregnancy and body composition of the child at age 6 y: the Generation R Study

van den Broek, M., Leermakers, L., Jaddoe, V.Steegers, E.Rivadeneira, F.Raat, H.Hofman, B., Franco Duran, O. & Jong, J., 2015, In: American Journal of Clinical Nutrition. 102, 4, p. 873-880 8 p.

 

Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

Springelkamp, H., Mishra, A., Hysi, P., Gharahkhani, P., Hohn, R., Khor, C., Bailey, J., Luo, X., Ramdas, W., Vithana, E., Koh, V., Yazar, S., Xu, L., Forward, H., Kearns, L., Amin, N.Iglesias Gonzalez, A., Sim, K., Leeuwen, E. & Demirkan, A. & 36 others, , 2015, In: Genetic Epidemiology. 39, 3, p. 207-216 10 p.

Methylation of Bone SOST, Its mRNA, and Serum Sclerostin Levels Correlate Strongly With Fracture Risk in Postmenopausal Women

Reppe, S., Noer, A., Grimholt, R., Halldorsson, B., Medina Gomez, M., Gautvik, V., Olstad, O., Berg, J., Datta, H., Estrada Gil, K., Hofman, B.Uitterlinden, A.Rivadeneira, F., Lyle, R., Collas, P. & Gautvik, K., 2015, In: Journal of Bone and Mineral Research. 30, 2, p. 249-256 8 p.

 

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

Paternoster, L., Standl, M., Waage, J., Baurecht, H., Hotze, M., Strachan, D., Curtin, J., Bonnelykke, K., Tian, C., Takahashi, A., Esparza-Gordillo, J., Alves, A., Thyssen, J., den Dekker, M., Ferreira, M., Altmaier, E., Sleiman, P., Xiao, F., Gonzalez, J. & Marenholz, I. & 130 others, , 2015, In: Nature Genetics. 47, 12, p. 1449-+

Polyunsaturated Fatty Acids and Serum C-Reactive Protein The Rotterdam Study

Muka, T., Jong, J., Hofman, B., Dehghan, A., Rivadeneira, F. & Franco Duran, O., 2015, In: American Journal of Epidemiology. 181, 11, p. 846-856 11 p.

 

Population genetic differentiation of height and body mass index across Europe

Robinson, M., Hemani, G., Medina-Gomez, C., Mezzavilla, M., Esko-, T., Shakhbazov, K., Powell, J., Vinkhuyzen, A., Berndt, S., Gustafsson, S., Justice, A., Kahali, B., Locke, A., Pers, T., Vedantam, S., Wood, A., van Rheenen, W., Andreassen, O., Gasparini, P. & Metspalu, A. & 23 others, , 2015, In: Nature Genetics. 47, 11, p. 1357-+

 

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

Huffman, J., Vries, P., Morrison, A., Sabater-Lleal, M., Kacprowski, T., Auer, P., Brody, J., Chasman, D., Chen, M., Guo, X., Lin, L., Marioni, R., Muller-Nurasyid, M., Yanek, L., Pankratz, N., Grove, M., de Maat, M., Cushman, M., Wiggins, K. & Qi, L. & 47 others, , 2015, In: Blood. 126, 11, p. E19-E29

Rare coding variants and X-linked loci associated with age at menarche

Lunetta, K., Day, F., Sulem, P., Ruth, K., Tung, J., Hinds, D., Esko, T., Elks, C., Altmaier, E., He, C., Huffman, J., Mihailov, E., Porcu, E., Robino, A., Rose, L., Schick, U., Stolk, L., Teumer, A., Thompson, D. & Traglia, M. & 101 others, , 2015, In: Nature Communications. 6

Single Nucleotide Polymorphism Heritability of Behavior Problems in Childhood: Genome-Wide Complex Trait Analysis

Pappa, I., Fedko, I., Mileva – Seitz, V., Hottenga, J., Bakermans-Kranenburg, M., Bartels, M., van Beijsterveldt, C., Jaddoe, V., Middeldorp, C., Rippe, R., Rivadeneira, F., Tiemeier, H., Verhulst, F., van IJzendoorn, M. & Boomsma, D., 2015, In: Journal of the American Academy of Child and Adolescent Psychiatry. 54, 11, p. 737-744 8 p.

Research output: Contribution to journal › Article › Academic › peer-review

1Citation (Scopus)

Subclinical Thyroid Dysfunction and Fracture Risk A Meta-analysis

Blum, M., Bauer, D., Collet, T., Fink, H., Cappola, A., da Costa, B., Wirth, C., Peeters, R., Asvold, B., den Elzen, W., Luben, R., Imaizumi, M., Bremner, A., Gogakos, A., Eastell, R., Kearney, P., Strotmeyer, E., Wallace, E., van ‘t Hoff, M. & Ceresini, G. & 13 others, , 2015, In: JAMA – Journal of the American Medical Association. 313, 20, p. 2055-2065 11 p.

Sugar-containing beverage intake in toddlers and body composition up to age 6 years: The Generation R Study

Leermakers, L., Felix, J.Erler, N., Cerimagic, A., Wijtzes, A., Hofman, B.Raat, H.Moll, H.Rivadeneira, F.Jaddoe, V., Franco Duran, O. & Jong, J., 2015, In: European Journal of Clinical Nutrition. 69, 3, p. 314-321 8 p.

 

The Association between Metabolic Syndrome, Bone Mineral Density, Hip Bone Geometry and Fracture Risk: The Rotterdam Study

Muka, T., Trajanoska, K., Jong, J., Oei – Oei, L., Uitterlinden, A.Hofman, B., Dehghan, A., Zillikens, M. C., Franco Duran, O. & Rivadeneira, F., 2015, In: PLoS One (print). 10, 6

 

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Winkler, T., Justice, A., Graff, M., Barata, L., Feitosa, M., Chu, S., Czajkowski, J., Esko, T., Fall, T., Kilpelainen, T., Lu, Y., Magi, R., Mihailov, E., Pers, T., Rueger, S., Teumer, A., Ehret, G., Ferreira, T., Heard-Costa, N. & Karjalainen, J. & 419 others, , 2015, In: PLoS Genetics (online). 11, 10

 

The transcriptional landscape of age in human peripheral blood

Peters, M., Joehanes, R., Pilling, L., Schurmann, C., Conneely, K., Powell, J., Reinmaa, E., Sutphin, G., Zhernakova, A., Schramm, K., Wilson, Y., Kobes, S., Tukiainen, T., Ramos, Y., Goring, H., Fornage, M., Liu, Y., Gharib, S., Stranger, B. & De Jager, P. & 95 others, , 2015, In: Nature Communications. 6

 

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

Zheng, H., Forgetta, V., Hsu, Y., Estrada Gil, K., Rosello-Diez, A., Leo, P., Dahia, C., Park-Min, K., Tobias, J., Kooperberg, C., Kleinman, A., Styrkarsdottir, U., Liu, C., Uggla, C., Evans, D., Nielson, C., Walter, K., Pettersson-Kymmer, U., McCarthy, S. & Eriksson, J. & 136 others, , 2015, In: Nature. 526, 7571, p. 112-+

 

2014

No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index: Results from Meta-Analyses of 80,607 Subjects

Baumert, J., Huang, J., McKnight, B., Sabater-Lleal, M., Steri, M., Chu, A. Y., Trompet, S., Lopez, L. M., Fornage, M., Teumer, A., Tang, W., Rudnicka, A., Malarstig, A., Hottenga, J., Kavousi, M., Lahti, J., Tanaka, T., Hayward, C., Huffman, J. & Morange, P. & 83 others, , 31 Dec 2014, In: PLoS One (print). 9, 12

 

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

Rietveld, C. A., Esko, T., Davies, G., Pers, T. H., Turley, P., Benyamin, B., Chabris, C. F., Emilsson, V., Johnson, A. D., Lee, J. J., De Leeuw, C., Marioni, R. E., Medland, S. E., Miller, M. B., Rostapshova, O., Van Der Lee, S. J., Vinkhuyzen, A. A. E., Amin, N., Conley, D. & Derringer, J. & 39 others, , 23 Sept 2014, In: Proceedings of the National Academy of Sciences of the U.S.A.. 111, 38, p. 13790-13794 5 p.

Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty

Cousminer, D. L., Stergiakouli, E., Berry, D. J., Ang, W., Groen-Blokhuis, M. M., Körner, A., Siitonen, N., Ntalla, I., Marinelli, M., Perry, J. R. B., Kettunen, J., Jansen, R., Surakka, I., Timpson, N. J., Ring, S., Mcmahon, G., Power, C., Wang, C., Kähönen, M. & Viikari, J. & 25 others, , 15 Aug 2014, In: Human Molecular Genetics. 23, 16, p. 4452-4464 13 p.

 DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

Perry, J. R. B., Hsu, Y.-H., Chasman, D. I., Johnson, A. D., Elks, C., Albrecht, E., Andrulis, I. L., Beesley, J., Berenson, G. S., Bergmann, S., Bojesen, S. E., Bolla, M. K., Brown, J., Buring, J. E., Campbell, H., Chang-Claude, J., Chenevix-Trench, G., Corre, T., Couch, F. J. & Cox, A. & 32 others, , 1 May 2014, In: Human Molecular Genetics. 23, 9, p. 2490-2497 8 p.

Adverse outcomes of frailty in the elderly: the Rotterdam Study

Lahousse, L., Maes, B., Ziere, B., Loth, D., Verlinden, V., Zillikens, M. C., Uitterlinden, A.Rivadeneira, F., Tiemeier, H., Franco Duran, O., Ikram, A.Hofman, B.Brusselle, G. & Stricker, B., 2014, In: European Journal of Epidemiology. 29, 6, p. 419-427 9 p.

A Genome-wide Association Meta-analysis of Preschool Internalizing Problems

Benke, K., Nivard, M., Velders, F., Walters, R., Pappa, I., Scheet, P., Xiao, X., Ehli, E., Palmer, L., Whitehouse, A., Verhulst, F., Jaddoe, V.Rivadeneira, F., Groen-Blokhuis, M., van Beijsterveldt, C., Davies, G., Hudziak, J. J., Lubke, G., Boomsma, D. & Pennell, C. & 2 others, , 2014, In: Journal of the American Academy of Child and Adolescent Psychiatry. 53, 6, p. 667-676 10 p.

A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age

Ahsan, H., Halpern, J., Kibriya, M., Pierce, B., Tong, L., Gamazon, E., McGuire, V., Felberg, A., Shi, J., Jasmine, F., Roy, S., Brutus, R., Argos, M., Melkonian, S., Chang-Claude, J., Andrulis, I., Hopper, J., John, E., Malone, K. & Ursin, G. & 56 others, , 2014, In: Cancer Epidemiology Biomarkers & Prevention. 23, 4, p. 658-669 12 p.

A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus

Oei – Oei, L., Hsu, Y., Styrkarsdottir, U., Eussen, B., de Klein, A., Peters, M., Halldorsson, B., Liu, C., Alonso, N., Kaptoge, S., Thorleifsson, G., Hallmans, G., Hocking, L., Husted, L., Jameson, K., van der Kruk, M., Lewis, J., Patel, M., Scollen, S. & Svensson, O. & 48 others, , 2014, In: Journal of Medical Genetics. 51, 2, p. 122-131 10 p.

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

Evangelou, E., Kerkhof, H., Styrkarsdottir, U., Ntzani, E., Bos, S., Esko, T., Evans, D., Metrustry, S., Panoutsopoulou, K., Ramos, Y., Thorleifsson, G., Tsilidis, K., Arden, N., Aslam, N., Bellamy, N., Birrell, F., Blanco, F., Carr, A., Chapman, K. & Day-Williams, A. & 46 others, , 2014, In: Annals of the Rheumatic Diseases. 73, 12, p. 2130-2136 7 p.

A Meta-Analysis of the Association of Fracture Risk and Body Mass Index in Women

Johansson, H., Kanis, J., Oden, A., McCloskey, E., Chapurlat, R., Christiansen, C., Cummings, S., Diez-Perez, A., Eisman, J., Fujiwara, S., Gluer, C., Goltzman, D., Hans, D., Khaw, K., Krieg, M., Kroger, H., Lacroix, A., Lau, E., Leslie, W. & Mellstrom, D. & 9 others, , 2014, In: Journal of Bone and Mineral Research. 29, 1, p. 223-233 11 p.

 

Assessment of Osteoarthritis Candidate Genes in a Meta-Analysis of Nine Genome-Wide Association Studies

Rodriguez-Fontenla, C., Calaza, M., Evangelou, E., Valdes, A., Arden, N., Blanco, F., Carr, A., Chapman, K., Deloukas, P., Doherty, M., Esko, T., Aleta, C., Carnota, J., Helgadottir, H., Hofman, B., Jonsdottir, I., Kerkhof, H., Kloppenburg, M., McCaskie, A. & Ntzani, E. & 27 others, , 2014, In: ARTHRITIS & RHEUMATOLOGY. 66, 4, p. 940-949 10 p.

Bone Mineral Density and Chronic Lung Disease Mortality: The Rotterdam Study

Campos Obando, N., Castano Betancourt, M., Oei – Oei, L., Franco Duran, O., Stricker, B.Brusselle, G.Lahousse, L.Hofman, B., Tiemeier, H., Rivadeneira, F.Uitterlinden, A. & Zillikens, M. C., 2014, In: Journal of Clinical Endocrinology and Metabolism. 99, 5, p. 1834-1842 9 p.

C9orf72 and UNC13A Are Shared Risk Loci for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia: A Genome-Wide Meta-Analysis

Diekstra, F., Van Deerlin, V., van Swieten, J. C., Al-Chalabi, A., Ludolph, A., Weishaupt, J., Hardiman, O., Landers, J., Brown, R., van Es, M., Pasterkamp, R., Koppers, M., Andersen, P., Estrada Gil, K., Rivadeneira, F.Hofman, B.Uitterlinden, A., van Damme, P., Melki, J. & Meininger, V. & 16 others, , 2014, In: Annals of Neurology. 76, 1, p. 120-133 14 p.

 

Common DNA variants predict tall stature in Europeans

Liu, F., Hendriks, E., Ralf, A., Boot, A., Benyi, E., Savendahl, L., Oostra, B., Duijn, C., Hofman, B.Rivadeneira, F.Uitterlinden, A.Drop, S. & Kayser, M., 2014, In: Human Genetics. 133, 5, p. 587-597 11 p.

Common variation near ROBO2 is associated with expressive vocabulary in infancy

St Pourcain, B., Cents, R., Whitehouse, A., Haworth, C., Davis, O., O’Reilly, P., Roulstone, S., Wren, Y., Ang, Q., Velders, F., Evans, D., Kemp, J., Warrington, N., Miller, L., Timpson, N., Ring, S., Verhulst, F., Hofman, B.Rivadeneira, F. & Meaburn, E. & 12 others, , 2014, In: Nature Communications. 5

Defining the role of common variation in the genomic and biological architecture of adult human height

Wood, A., Esko, T., Yang, J., Vedantam, S., Pers, T., Gustafsson, S., Chun, A., Estrada Gil, K., Luan, J., Kutalik, Z., Amin, N., Buchkovich, M., Croteau-Chonka, D., Day, F., Duan, Y., Fall, T., Fehrmann, R., Ferreira, T., Jackson, A. & Karjalainen, J. & 425 others, , 2014, In: Nature Genetics. 46, 11, p. 1173-1186 14 p.

Dissecting the relationship between high-sensitivity serum C-reactive protein and increased fracture risk: the Rotterdam Study

Oei – Oei, L., Campos Obando, N., Dehghan, A., Oei, E., Stolk, L., van Meurs, J.Hofman, B.Uitterlinden, A., Franco Duran, O., Zillikens, M. C. & Rivadeneira, F., 2014, In: Osteoporosis International. 25, 4, p. 1247-1254 8 p.

Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations

Ganesh, S., Chasman, D., Larson, M., Guo, X., Verwoert, G., Bis, J., Gu, X., Smith, A., Yang, M., Zhang, Y., Ehret, G., Rose, L., Hwang, S., Papanicolau, G., Sijbrands, E. J. G., Rice, K., Eiriksdottir, G., Pihur, V., Ridker, P. & Vasan, R. & 34 others, , 2014, In: American Journal of Human Genetics. 95, 1, p. 49-65 17 p.

Fetal and Childhood Growth Patterns Associated with Bone Mass in School-Age Children: The Generation R Study

Heppe, D., Medina-Gomez, C., Jongste, J., Raat, H.Steegers, E.Hofman, B.Rivadeneira, F. & Jaddoe, V., 2014, In: Journal of Bone and Mineral Research. 29, 12, p. 2584-2593 10 p.

Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants

Valk, R., Duijts, L., Timpson, N., Salam, M., Standl, M., Curtin, J., Genuneit, J., Kerhof, M., Kreiner-Moller, E., Caceres, A., Gref, A., Liang, L., Taal, R., Bouzigon, E., Demenais, F., Nadif, R., Ober, C., Thompson, E., Estrada Gil, K. & Hofman, B. & 38 others, , 2014, In: Journal of Allergy and Clinical Immunology. 134, 1, p. 46-55 10 p.

Gene-Age Interactions in Blood Pressure Regulation: A Large-Scale Investigation with the CHARGE, Global BPgen, and ICBP Consortia

Simino, J., Shi, G., Bis, J., Chasman, D., Ehret, G., Gu, X., Guo, X., Hwang, S., Sijbrands, E. J. G., Smith, A., Verwoert, G., Bragg-Gresham, J., Cadby, G., Chen, P., Cheng, C., Corre, T., de Boer, R., Goel, A., Johnson, T. & Khor, C. & 83 others, , 2014, In: American Journal of Human Genetics. 95, 1, p. 24-38 15 p.

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

Moayyeri, A., Hsu, Y., Karasik, D., Estrada Gil, K., Xiao, S., Nielson, C., Srikanth, P., Giroux, S., Wilson, S., Zheng, H., Smith, A., Pye, S., Leo, P., Teumer, A., Hwang, J., Ohlsson, C., McGuigan, F., Minster, R., Hayward, C. & Olmos, J. & 110 others, , 2014, In: Human Molecular Genetics. 23, 11, p. 3054-3068 15 p.

Genetic taste blindness to bitter and body composition in childhood: a Mendelian randomization design

Bouthoorn, S., van Lenthe, F., Jong, J., Taal, R., Wijtzes, A., Hofman, B.Jaddoe, V., Glymour, M., Rivadeneira, F. & Raat, H., 2014, In: International Journal of Obesity. 38, 7, p. 1005-1010 6 p.

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

Hysi, P., Cheng, C., Springelkamp, H., Macgregor, S., Bailey, J., Wojciechowski, R., Vitart, V., Nag, A., Hewitt, A., Hohn, R., Venturini, C., Mirshahi, A., Ramdas, W., Thorleifsson, G., Vithana, E., Khor, C., Stefansson, A., Liao, J., Haines, J. & Amin, N. & 70 others, , 2014, In: Nature Genetics. 46, 10, p. 1126-1130 5 p.

Genome-wide association analysis identifies six new loci associated with forced vital capacity

Loth, D., Artigas, M., Gharib, S., Wain, L., Franceschini, N., Koch, B., Pottinger, T., Smith, A., Duan, Q., Oldmeadow, C., Lee, M., Strachan, D., James, A., Huffman, J., Vitart, V., Ramasamy, A., Wareham, N., Kaprio, J., Wang, X. & Trochet, H. & 140 others, , 2014, In: Nature Genetics. 46, 7, p. 669-677 9 p.

Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age

Deelen, J., Beekman, M., Uh, H., Broer, L., Ayers, K., Tan, Q., Kamatani, Y., Bennet, A., Tamm, R., Trompet, S., Guobjartsson, D., Flachsbart, F., Rose, G., Viktorin, A., Fischer, K., Nygaard, M., Cordell, H., Crocco, P., van den Akker, E. & Bohringer, S. & 67 others, , 2014, In: Human Molecular Genetics. 23, 16, p. 4420-4432 13 p.

Genome-wide association study for radiographic vertebral fractures: A potential role for the 16q24 BMD locus

Oei – Oei, L., Estrada Gil, K., Duncan, E., Christiansen, C., Liu, C., Langdahl, B., Obermayer-Pietsch, B., Riancho, J., Prince, R., Schoor, N., McCloskey, E., Hsu, Y., Evangelou, E., Ntzani, E., Evans, D., Alonso, N., Husted, L., Valero, C., Hernandez, J. & Lewis, J. & 34 others, , 2014, In: Bone. 59, p. 20-27 8 p.

Genome-Wide Association Study of Height-Adjusted BMI in Childhood Identifies Functional Variant in ADCY3

Stergiakouli, E., Gaillard, R., Tavare, J., Balthasar, N., Loos, R., Taal, R., Evans, D., Rivadeneira, F., St Pourcain, B., Uitterlinden, A., Kemp, J., Hofman, B., Ring, S., Cole, T., Jaddoe, V., Smith, G. & Timpson, N., 2014, In: Obesity. 22, 10, p. 2252-2259 8 p.

Genome-Wide Meta-Analysis of Myopia and Hyperopia Provides Evidence for Replication of 11 Loci

Simpson, C., Wojciechowski, R., Oexle, K., Murgia, F., Portas, L., Li, X., Verhoeven, V., Vitart, V., Schache, M., Hosseini, S., Hysi, P., Raffel, L., Cotch, M., Chew, E., Klein, B., Klein, R., Wong, T., Duijn, C., Mitchell, P. & Saw, S. & 33 others, , 2014, In: PLoS One (print). 9, 9

.Health in children: A conceptual framework for use in healthy ageing research

Felix, J.Voortman, T., Hooven, E., Sajjad, A., Leermakers, L., Tharner, A., Jong, J., Duijts, L., Verhulst, F., Jongste, J., Tiemeier, H., Hofman, B.Rivadeneira, F.Moll, H.Raat, H.Jaddoe, V. & Franco Duran, O., 2014, In: Maturitas. 77, 1, p. 47-51 5 p.

Health in children: A conceptual framework for use in healthy ageing research.

Felix, J.Voortman, T., Hooven, E., Sajjad, A., Leermakers, L., Tharner, A., Kiefte-de Jong, J., Duijts, L., Verhulst, F., Jongste, J., Tiemeier, H., Hofman, B.Rivadeneira, F.Moll, H.Jaddoe, V. & Franco Duran, O., 2014, In: Maturitas. 77, 1, p. 47-51 5 p.

Identification of Novel Genetic Loci Associated with Thyroid Peroxidase Antibodies and Clinical Thyroid Disease

Medici, M., Porcu, E., Pistis, G., Teumer, A., Brown, S., Jensen, R., Rawal, R., Roef, G., Plantinga, T., Vermeulen, S., Lahti, J., Simmonds, M., Husemoen, L., Freathy, R., Shields, B., Pietzner, D., Nagy, R., Broer, L.Chaker, L. & Korevaar, T. & 98 others, , 2014, In: PLoS Genetics (print). 10, 2

Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’

Deelen, P., Menelaou, A., Leeuwen, E., Kanterakis, A., Dijk, F., Medina-Gomez, C., Francioli, L., Hottenga, J., Karssen, L., Estrada Gil, K., Kreiner-Moller, E., Rivadeneira, F., van Setten, J., Gutierrez-Achury, J., Westra, H., Franke, L., van Enckevort, D., Dijkstra, M., Byelas, H. & Duijn, C. & 3 others, , 2014, In: European Journal of Human Genetics. 22, 11, p. 1321-1326 6 p.

Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function

Tang, W., Kowgier, M., Loth, D., Artigas, M., Joubert, B., Hodge, E., Gharib, S., Smith, A., Ruczinski, I., Gudnason, V., Mathias, R., Harris, T., Hansel, N., Launer, L., Barnes, K., Hansen, J., Albrecht, E., Aldrich, M., Allerhand, M. & Barr, R. & 61 others, , 2014, In: PLoS One (print). 9, 7

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

Springelkamp, H., Hohn, R., Mishra, A., Hysi, P., Khor, C., Loomis, S., Bailey, J., Gibson, J., Thorleifsson, G., Janssen, S., Luo, X., Ramdas, W., Vithana, E., Nongpiur, M., Montgomery, G., Xu, L., Mountain, J., Gharahkhani, P., Lu, Y. & Amin, N. & 57 others, , 2014, In: Nature Communications. 5

Multistage genome-wide association meta-analyses identified two new loci for bone mineral density

Zhang, L., Choi, H., Estrada Gil, K., Leo, P., Li, J., Pei, Y., Zhang, Y., Lin, Y., Shen, H., Liu, Y., Liu, Y., Zhao, Y., Zhang, J., Tian, Q., Wang, Y., Han, Y., Ran, S., Hai, R., Zhu, X. & Wu, S. & 36 others, , 2014, In: Human Molecular Genetics. 23, 7, p. 1923-1933 11 p.

 

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Perry, J., Day, F., Elks, C., Sulem, P., Thompson, D., Ferreira, T., He, C., Chasman, D., Esko, T., Thorleifsson, G., Albrecht, E., Ang, W., Corre, T., Cousminer, D., Feenstra, B., Franceschini, N., Ganna, A., Johnson, A., Kjellqvist, S. & Lunetta, K. & 178 others, , 2014, In: Nature. 514, 7520, p. 92-+

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

Postmus, I., Trompet, S., Deshmukh, H., Barnes, M., Li, X., Warren, H., Chasman, D., Zhou, K., Arsenault, B., Donnelly, L., Wiggins, K., Avery, C., Griffin, P., Feng, Q., Taylor, K., Li, G., Evans, D., Smith, A., de Keyser, T. & Johnson, A. & 83 others, , 2014, In: Nature Communications. 5

Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment

Kemp, J., Medina-Gomez, C., Estrada Gil, K., St Pourcain, B., Heppe, D., Warrington, N., Oei – Oei, L., Ring, S., Kruithof, C., Timpson, N., Wolber, L., Reppe, S., Gautvik, K., Grundberg, E., Ge, B., van der Eerden, B.van de Peppel, J., Hibbs, M., Ackert-Bicknell, C. & Choi, K. & 13 others, , 2014, In: PLoS Genetics (print). 10, 6

Prediction model for knee osteoarthritis incidence, including clinical, genetic and biochemical risk factors

Kerkhof, H., Bierma – Zeinstra, S., Arden, N., Metrustry, S., Castano-Betancourt, M., Hart, D., Hofman, B.Rivadeneira, F.Oei, E., Spector, T., Uitterlinden, A., Janssens, C., Valdes, A. & van Meurs, J., 2014, In: Annals of the Rheumatic Diseases. 73, 12, p. 2116-2121 6 p.

Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31

Styrkarsdottir, U., Thorleifsson, G., Helgadottir, H., Bomer, N., Metrustry, S., Bierma – Zeinstra, S., Strijbosch, A., Evangelou, E., Hart, D., Beekman, M., Jonasdottir, A., Sigurdsson, A., Eiriksson, F., Thorsteinsdottir, M., Frigge, M., Kong, A., Gudjonsson, S., Magnusson, O., Masson, G. & Hofman, B. & 16 others, , 2014, In: Nature Genetics. 46, 5, p. 498-502 5 p.

Stratified medicine approaches for the treatment of musculoskeletal disorders

Hocking, L. & Rivadeneira, F., 2014, In: Current Opinion in Pharmacology. 16, p. 127-132 6 p.

Susceptibility to Chronic Mucus Hypersecretion, a Genome Wide Association Study

Dijkstra, A., Smolonska, J., van den Berge, M., Wijmenga, C., Zanen, P., Luinge, M., Platteel, M., Lammers, J., Dahlback, M., Tosh, K., Hiemstra, P., Sterk, P., Spira, A., Vestbo, J., Nordestgaard, B., Benn, M., Nielsen, S., Dahl, M., Verschuren, W. & Picavet, H. & 33 others, , 2014, In: PLoS One (print). 9, 4

The association between plasma homocysteine levels and bone quality and bone mineral density parameters in older persons

Enneman, A., Swart, K., Zillikens, M. C., Boon – van Dijk, S., Wijngaarden, J., Brouwer-Brolsma, E., Dhonukshe-Rutten, R., Hofman, B.Rivadeneira, F., van der Cammen, T. J. M., Lips, P., de Groot, C., Uitterlinden, A.van Meurs, J., Schoor, N. & van der Velde, N., 2014, In: Bone. 63, p. 141-146 6 p.

The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels

Leeuwen, E., Smouter, F., Kam-Thong, T., Karbalai, N., Smith, A., Harris, T., Launer, L., Sitlani, C., Li, G., Brody, J., Bis, J., White, C., Jaiswal, A., Oostra, B., Hofman, B.Rivadeneira, F.Uitterlinden, A., Boerwinkle, E., Ballantyne, C. & Gudnason, V. & 8 others, , 2014, In: PLoS One (print). 9, 10

The Generation R Study: Biobank update 2015

Kruithof, C., Kooijman, M., Duijn, C., Franco Duran, O., Jongste, J., Klaver, C.Mackenbach, J.Moll, H.Raat, H.Rings, E.Rivadeneira, F.Steegers, E., Tiemeier, H., Uitterlinden, A., Verhulst, F., Wolvius, E.Hofman, B. & Jaddoe, V., 2014, In: European Journal of Epidemiology. 29, 12, p. 911-927 17 p.

The Genome of the Netherlands: design, and project goals

Boomsma, D., Wijmenga, C., Slagboom, E., Swertz, M., Karssen, L., Abdellaoui, A., Ye, K., Guryev, V., Vermaat, M., Dijk, F., Francioli, L., Hottenga, J., Laros, J., Li, Q., Li, Y., Cao, H., Chen, R., Du, Y., Li, N. & Cao, S. & 32 others, , 2014, In: European Journal of Human Genetics. 22, 2, p. 221-227 7 p.

Whole-genome sequence variation, population structure and demographic history of the Dutch population

Francioli, L., Menelaou, A., Pulit, S., Dijk, F., Palamara, P., Elbers, C., Neerincx, P., Ye, K., Guryev, V., Kloosterman, W., Deelen, P., Abdellaoui, A., Leeuwen, E., Oven, M., Vermaat, M., Li, M., Laros, J., Karssen, L., Kanterakis, A. & Amin, N. & 64 others, , 2014, In: Nature Genetics. 46, 8, p. 818-825 8 p.

 

2013

TRPV4 deficiency causes sexual dimorphism in bone metabolism and osteoporotic fracture risk

van der Eerden, B. C. J., Oei, L., Roschger, P., Fratzl-Zelman, N., Hoenderop, J. G. J., van Schoor, N. M., Pettersson-Kymmer, U., Schreuders-Koedam, M., Uitterlinden, A. G.Hofman, A., Suzuki, M., Klaushofer, K., Ohlsson, C., Lips, P. J. A., Rivadeneira, F., Bindels, R. J. M. & van Leeuwen, J. P. T. M., Dec 2013, In: Bone. 57, 2, p. 443-454 12 p.

Genetic Determinants of Osteoporosis

Uitterlinden, A. G., Zillikens, M. C. & Rivadeneira, F., Jun 2013, Osteoporosis: Fourth Edition. Elsevier Inc., p. 563-604 42 p.

Genetic variants of FOXP3 influence graft survival in kidney transplant patients

Engela, A. U., Boer, K.Roodnat, J. I.Peeters, A. M. A.Eilers, P. H., Kal-van Gestel, J. A., Rivadeneira, F.Weimar, W. & Baan, C. C., Jun 2013, In: Human Immunology. 74, 6, p. 751-757 7 p.

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Consortium for Refractive Error and Myopia (CREAM)DCCT/EDIC Research GroupWellcome Trust Case Control Consortium 2 (WTCCC2)the Fuchs’ genetics multi-center study groupVerhoeven, V., Buitendijk, G., Verkerk, A. J. M. H., Karssen, L. C., Uitterlinden, A.Rivadeneira, F.Vingerling, J. R.Hofman, A., Oostra, B. A., Amin, N., van Duijn, C. M. & Klaver, C., Mar 2013, In: Nature Genetics. 45, 3, p. 314-318 5 p.

 

A genome-wide association study of early menopause and the combined impact of identified variants

Perry, J., Corre, T., Esko, T., Chasman, D., Fischer, K., Franceschini, N., He, C., Kutalik, Z., Mangino, M., Rose, L., Smith, A., Stolk, L., Sulem, P., Weedon, M., Zhuang, W., Arnold, A., Ashworth, A., Bergmann, S., Buring, J. & Burri, A. & 46 others, , 2013, In: Human Molecular Genetics. 22, 7, p. 1465-1472 8 p.

A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function

Porcu, E., Medici, M., Pistis, G., Volpato, C., Wilson, S., Cappola, A., Bos, S., Deelen, J., Heijer, M., Freathy, R., Lahti, J., Liu, C., Lopez, L., Nolte, I., O’Connell, J., Tanaka, T., Trompet, S., Arnold, A., Bandinelli, S. & Beekman, M. & 74 others, , 2013, In: PLoS Genetics (print). 9, 2

 

Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent

Fernandez-Rhodes, L., Demerath, E., Cousminer, D., Tao, R., Dreyfus, J., Esko, T., Smith, A., Gudnason, V., Harris, T., Launer, L., McArdle, P., Yerges-Armstrong, L., Elks, C., Strachan, D., Kutalik, Z., Vollenweider, P., Feenstra, B., Boyd, H., Metspalu, A. & Mihailov, E. & 55 others, , 2013, In: American Journal of Epidemiology. 178, 3, p. 451-460 10 p.

Association of lumbar disc degeneration with osteoporotic fractures; the Rotterdam study and meta-analysis from systematic review

Castano Betancourt, M., Oei – Oei, L., Rivadeneira, F.de Schepper, E.Hofman, B.Bierma – Zeinstra, S., Pols, H., Uitterlinden, A. & van Meurs, J., 2013, In: Bone. 57, 1, p. 284-289 6 p.

Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium

Grove, M., Yu, B., Cochran, B., Haritunians, T., Bis, J., Taylor, K., Hansen, M., Borecki, I., Cupples, L., Fornage, M., Gudnason, V., Harris, T., Kathiresan, S., Kraaij, R., Launer, L., Levy, D., Liu, Y., Mosley, T., Peloso, G. & Psaty, B. & 10 others, , 2013, In: PLoS One (print). 8, 7

 

Bone parameters across different types of hip osteoarthritis and their relationship to osteoporotic fracture risk

Castano Betancourt, M., Rivadeneira, F.Bierma – Zeinstra, S., Kerkhof, H., Hofman, B.Uitterlinden, A. & van Meurs, J., 2013, In: Arthritis & Rheumatism. 65, 3, p. 693-700 8 p.

 

Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease

van Meurs, J., Pare, G., Schwartz, S., Hazra, A., Tanaka, T., Vermeulen, S., Cotlarciuc, I., Yuan, X., Malarstig, A., Bandinelli, S., Bis, J., Morn, H., Brown, M., Chen, C., Chen, Y., Clarke, R., Dehghan, A., Erdmann, J., Ferrucci, L. & Hamsten, A. & 38 others, , 2013, In: American Journal of Clinical Nutrition. 98, 3, p. 668-676 9 p.

 

Common variants associated with plasma triglycerides and risk for coronary artery disease

Do, R., Willer, C., Schmidt, E., Sengupta, S., Gao, C., Peloso, G., Gustafsson, S., Kanoni, S., Ganna, A., Chen, J., Buchkovich, M., Mora, S., Beckmann, J., Bragg-Gresham, J., Chang, H., Demirkan, A., den Hertog, H., Donnelly, L., Ehret, G. & Esko, T. & 243 others, , 2013, In: Nature Genetics. 45, 11, p. 1345-+

Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function

Parsa, A., Fuchsberger, C., Kottgen, A., O’Seaghdha, C., Pattaro, C., de Andrade, M., Chasman, D., Teumer, A., Endlich, K., Olden, M., Chen, M., Tin, A., Kim, Y., Taliun, D., Li, M., Feitosa, M., Gorski, M., Yang, Q., Hundertmark, C. & Foster, M. & 139 others, , 2013, In: Journal of the American Society of Nephrology. 24, 12, p. 2105-2117 13 p.

 

Discovery and refinement of loci associated with lipid levels

Willer, C., Schmidt, E., Sengupta, S., Peloso, G., Gustafsson, S., Kanoni, S., Ganna, A., Chen, J., Buchkovich, M., Mora, S., Beckmann, J., Bragg-Gresham, J., Chang, H., Demirkan, A., den Hertog, H., Do, R., Donnelly, L., Ehret, G., Esko, T. & Feitosa, M. & 239 others, , 2013, In: Nature Genetics. 45, 11, p. 1274-+

 

Early growth genetics C. New loci associated with birgh weight identify genetic links between intrauterine growth and adult height and metabolism

Horikoshi, M., Yaghootkar, H., Mook, D., Sovio, U., Taal, R., Hennig, B., Bradfield, J., St Pourcain, B., Evans, D., Charoen, P., Kaakinen, M., Cousminer, D., Lehtimaki, T., Kreiner-Moller, E., Warrington, N., Bustamante, M., Feenstra, B., Berry, D., Thiering, E. & Pfab, T. & 128 others, , 2013, In: Nature Genetics. 45, p. 76-82 7 p.

 

Education influences the role of genetics in myopia

Verhoeven, V., Buitendijk, G., Rivadeneira, F.Uitterlinden, A.Vingerling, H.Hofman, B. & Klaver, C., 2013, In: European Journal of Epidemiology. 28, 12, p. 973-980 8 p.

 

Fast linear mixed model computations for genome-wide association studies with longitudinal data

Sikorska, K., Rivadeneira, F.Groenen, P.Hofman, B.Uitterlinden, A.Eilers, P. & Lesaffre, E., 2013, In: Statistics in Medicine. 32, 1, p. 165-180 16 p.

 

Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways

Deelen, J., Uh, H., Monajemi, R., van Heemst, D., Thijssen, P., Bohringer, S., van den Akker, E., de Craen, A., Rivadeneira, F.Uitterlinden, A., Westendorp, R., Goeman, J., Slagboom, P., Houwing-Duistermaat, J. & Beekman, M., 2013, In: Age. 35, 1, p. 235-249 15 p.

 

Genetic determinants of mortality. Can findings from genome-wide association studies explain variation in human mortality?

Ganna, A., Rivadeneira, F.Hofman, B.Uitterlinden, A., Magnusson, P., Pedersen, N., Ingelsson, E. & Tiemeier, H., 2013, In: Human Genetics. 132, 5, p. 553-561 9 p.

Genetic Loci for Retinal Arteriolar Microcirculation

Sim, X., Jensen, R., Ikram, K., Cotch, M., Li, X., Macgregor, S., Xie, J., Smith, A., Boerwinkle, E., Mitchell, P., Klein, R., Klein, B., Glazer, N., Lumley, T., McKnight, B., Psaty, B., de Jong, P., Hofman, B.Rivadeneira, F. & Uitterlinden, A. & 36 others, , 2013, In: PLoS One (print). 8, 6, e65804.

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Kottgen, A., Albrecht, E., Teumer, A., Vitart, V., Krumsiek, J., Hundertmark, C., Pistis, G., Ruggiero, D., O’ Seaghdha, C., Haller, T., Yang, Q., Tanaka, T., Johnson, A., Kutalik, Z., Smith, A., Shi, J., Struchalin, M., Middelberg, R., Brown, M. & Gaffo, A. & 203 others, , 2013, In: Human Genetics. 45, 2, p. 154-11 142 p., 145.

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

Garcia-Closas, M., Couch, F., Lindstrom, S., Michailidouo, K., Schmidt, M. K., Brook, M., Orr, N., Rhie, S., Riboli, E., Feigelson, H., Le Marchand, L., Buring, J., Eccles, D., Miron, P., Fasching, P., Brauch, H., Chang-Claude, J., Carpenter, J., Godwin, A. & Nevanlinna, H. & 250 others, , 2013, In: Nature Genetics. 45, 4, p. 392-398 7 p.

 

Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region

Peters, M., Broer, L., Willemen, H., Eiriksdottir, G., Hocking, L., Holliday, K., Horan, M., Meulenbelt, I., Neogi, T., Popham, M., Schmidt, C., Soni, A., Valdes, A., Amin, N., Dennison, E., Eijkelkamp, N., Harris, T., Hart, D., Hofman, B. & Huygen, F. & 32 others, , 2013, In: Annals of the Rheumatic Diseases. 72, 3, p. 427-436 10 p.

Genome-Wide Association Study of Retinopathy in Individuals without Diabetes

Jensen, R., Sim, X., Li, X., Cotch, M., Ikram, K., Holliday, E., Eiriksdottir, G., Harris, T., Jonasson, F., Klein, B., Launer, L., Smith, A., Boerwinkle, E., Cheung, N., Hewitt, A., Liew, G., Mitchell, P., Wang, J., Attia, J. & Scott, R. & 29 others, , 2013, In: PLoS One (print). 8, 2

 

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Berndt, S., Gustafsson, S., Magi, R., Ganna, A., Wheeler, E., Feitosa, M., Justice, A., Monda, K., Croteau-Chonka, D., Day, F., Esko, T., Fall, T., Ferreira, T., Gentilini, D., Jackson, A., Luan, J., Randall, J., Vedantam, S., Willer, C. & Winkler, T. & 302 others, , 2013, In: Nature Genetics. 45, 5, p. 501-U69

 

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

Rietveld, N., Medland, S., Derringer, J., Yang, J., Esko, T., Martin, N., Westra, H., Shakhbazov, K., Abdellaoui, A., Agrawal, A., Albrecht, E., Alizadeh, B., Amin, N., Barnard, J., Baumeister, S., Benke, K., Bielak, L., Boatman, J., Boyle, P. & Davies, G. & 184 others, , 2013, In: Science. 240, 6139, p. 1467-1471 5 p.

High Bone Mineral Density and Fracture Risk in Type 2 Diabetes as Skeletal Complications of Inadequate Glucose Control The Rotterdam Study

Oei – Oei, L., Zillikens, M. C., Dehghan, A., Buitendijk, G., Castano Betancourt, M., Estrada Gil, K., Stolk, L., Oei, E.van Meurs, J.Janssen, J. A. M. J. L.Hofman, B.van Leeuwen, H., Witteman, J., Pols, H., Uitterlinden, A.Klaver, C., Franco Duran, O. & Rivadeneira, F., 2013, In: Diabetes Care. 36, 6, p. 1619-1628 10 p.

Hunting osteoporosis susceptibility genes: bigger is better but diverse is also welcome

Rivadeneira, F., 2013, In: Endocrine. 43, 1, p. 6-7 2 p.

Identification of Genetic Loci Associated With Helicobacter pylori Serologic Status

Mayerle, J., den Hoed, C., Schurmann, C., Stolk, L., Homuth, G., Peters, M., Capelle, L., Zimmermann, K., Rivadeneira, F., Gruska, S., Volzke, H., de Vries, A., Volker, U., Teumer, A., van Meurs, J., Steinmetz, I., Nauck, M., Ernst, F., Weiss, F. & Hofman, B. & 6 others, , 2013, In: JAMA – Journal of the American Medical Association. 309, 18, p. 1912-1920 9 p.

 

Impact of Inherited Genetic Variants Associated With Lipid Profile, Hypertension, and Coronary Artery Disease on the Risk of Intracranial and Abdominal Aortic Aneurysms

van ‘t Hof, F., Ruigrok, Y., Baas, A., Kiemeney, L., Vermeulen, S., Uitterlinden, A.Hofman, B.Rivadeneira, F., Rinkel, G. & de Bakker, P., 2013, In: Circulation-cardiovascular genetics. 6, 3, p. 264-270 7 p.

 

Maternal first-trimester diet and childhood bone mass: the Generation R Study

Heppe, D., Medina-Gomez, C., Hofman, B., Franco Duran, O., Rivadeneira, F. & Jaddoe, V., 2013, In: American Journal of Clinical Nutrition. 98, 1, p. 224-232 9 p.

 

Meta-Analysis of Genome-Wide Association Studies Identifies Six New Loci for Serum Calcium Concentrations

O’Seaghdha, C., Wu, H., Yang, Q., Kapur, K., Guessous, I., Zuber, A., Kottgen, A., Stoudmann, C., Teumer, A., Kutalik, Z., Mangino, M., Dehghan, A., Zhang, W., Eiriksdottir, G., Li, G., Tanaka, T., Portas, L., Lopez, L., Hayward, C. & Lohman, K. & 89 others, , 2013, In: PLoS Genetics (print). 9, 9, e1003796.

 

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

Stambolian, D., Wojciechowski, R., Oexle, K., Pirastu, M., Li, X., Raffel, L., Cotch, M., Chew, E., Klein, B., Klein, R., Wong, T., Simpson, C., Klaver, C., Duijn, C., Verhoeven, V., Baird, P., Vitart, V., Paterson, A., Mitchell, P. & Saw, S. & 41 others, , 2013, In: Human Molecular Genetics. 22, 13, p. 2754-2764 11 p.

Multiethnic Meta-Analysis of Genome-Wide Association Studies in > 100 000 Subjects Identifies 23 FibrinogenAssociated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease

Sabater-Lleal, M., Huang, J., Chasman, D., Naitza, S., Dehghan, A., Johnson, A., Teumer, A., Reiner, A., Folkersen, L., Basu, S., Rudnicka, A., Trompet, S., Malarstig, A., Baumert, J., Bis, J., Guo, X., Hottenga, J., Shin, S., Lopez, L. & Lahti, J. & 125 others, , 2013, In: Circulation. 128, 12, p. 1310-1324 15 p.

 

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

Horikoshi, M., Yaghootkar, H., Mook, D., Sovio, U., Taal, R., Hennig, B., Bradfield, J., St Pourcain, B., Evans, D., Charoen, P., Kaakinen, M., Cousminer, D., Lehtimaki, T., Kreiner-Moller, E., Warrington, N., Bustamante, M., Feenstra, B., Berry, D., Thiering, E. & Pfab, T. & 127 others, , 2013, In: Nature Genetics. 45, 1, p. 76-U115

 

Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

Cheng, C., Schache, M., Ikram, K., Young, T., Guggenheim, J., Vitart, V., Macgregor, S., Verhoeven, V., Barathi, V., Liao, J., Hysi, P., Bailey-Wilson, J., St Pourcain, B., Kemp, J., McMahon, G., Timpson, N., Evans, D., Montgomery, G., Mishra, A. & Wang, Y. & 88 others, , 2013, In: American Journal of Human Genetics. 93, 2, p. 264-277 14 p.

Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects

Williams, F., Bansal, A., van Meurs, J., Bell, J., Meulenbelt, I., Suri, P., Rivadeneira, F., Sambrook, P., Hofman, B.Bierma – Zeinstra, S., Menni, C., Kloppenburg, M., Slagboom, P., Hunter, D., MacGregor, A., Uitterlinden, A. & Spector, T., 2013, In: Annals of the Rheumatic Diseases. 72, 7, p. 1141-1148 8 p.

 

Osteoporosis Genes Identified by Genome-wide Association Studies

Rivadeneira, F. & Uitterlinden, A., 2013, Genetics of Bone Biology and Skeletal Disease. Thakker, R. (ed.). p. 243-256 14 p.

 

Polymorphisms in genes within the IGF-axis influence antenatal and postnatal growth

Parmar, P., Marsch, J., Taal, R., Kowgier, M., Uitterlinden, A.Rivadeneira, F., Briollais, L., Newham, J., Hofman, B., Lye, S., Steegers, E., Duijn, C., Palmer, L., Jaddoe, V. & Pennell, C., 2013, In: Journal of Developmental Origins of Health and Disease. 4, 2, p. 157-169 13 p.

 

Quant Multi-functionality of computer-aided quantitative vertebral fracture morphometry analyses

Oei – Oei, L., Ly, F., El Saddy, S., Makurthou, A., Hofman, B.van Rooij, F.Uitterlinden, A., Zillikens, M. C., Rivadeneira, F. & Oei, E., 2013, In: Quantitative Imaging in Medicine and Surgery. 3, 5, p. 249-255 7 p.

 

Review of radiological scoring methods of osteoporotic vertebral fractures for clinical and research settings

Oei – Oei, L., Rivadeneira, F., Ly, F., Breda, S., Zillikens, M. C., Hofman, B.Uitterlinden, A.Krestin, G. & Oei, E., 2013, In: European Radiology. 23, 2, p. 476-486 11 p.

Scheuermann Disease Evaluation of Radiological Criteria and Population Prevalence

Makurthou, A., Oei – Oei, L., El Saddy, S., Breda, S., Castano Betancourt, M., Hofman, B.van Meurs, J.Uitterlinden, A.Rivadeneira, F. & Oei, E., 2013, In: Spine. 38, 19, p. 1690-1694 5 p.

 

Serum testosterone levels in males are not associated with entrepreneurial behavior in two independent observational studies

van der Loos, M., Haring, R., Rietveld, N., Baumeister, S., Groenen, P.Hofman, B., Jong, F., Koellinger, P., Kohlmann, T., Nauck, M., Rivadeneira, F.Uitterlinden, A.van Rooij, F., Wallaschofski, H. & Thurik, R., 2013, In: Physiology & Behavior. 119, p. 110-114 5 p.

 

Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits

Randall, J., Winkler, T., Kutalik, Z., Berndt, S., Jackson, A., Monda, K., Kilpelainen, T., Esko, T., Magi, R., Li, S., Workalemahu, T., Feitosa, M., Croteau-Chonka, D., Day, F., Fall, T., Ferreira, T., Gustafsson, S., Locke, A., Mathieson, I. & Scherag, A. & 244 others, , 2013, In: PLoS Genetics (print). 9, 6

Systematic identification of trans eQTLs as putative drivers of known disease associations

Westra, H., Peters, M., Esko, T., Yaghootkar, H., Schurmann, C., Kettunen, J., Christiansen, M., Fairfax, B., Schramm, K., Powell, J., Zhernakova, A., Zhernakova, D., Veldink, J., van den Berg, L., Karjalainen, J., Withoff, S., Uitterlinden, A.Hofman, B.Rivadeneira, F. & ‘t Hoen, P. & 39 others, , 2013, In: Nature Genetics. 45, 10, p. 1238-U195

The contribution of hip geometry to the prediction of hip osteoarthritis

Castano Betancourt, M., van Meurs, J.Bierma – Zeinstra, S.Rivadeneira, F.Hofman, B., Weinans, H., Uitterlinden, A. & Waarsing, J., 2013, In: Osteoarthritis and Cartilage. 21, 10, p. 1530-1536 7 p.

 

The effect of thiazide and loop diuretics on urinary levels of free deoxypyridinoline: an osteoclastic bone-resorption marker

Ruiter, R., Oei – Oei, L., Visser, L., Peltenburg, H., Hofman, B., Zillikens, M. C., Uitterlinden, A.Rivadeneira, F. & Stricker, B., 2013, In: Journal of Clinical Pharmacy and Therapeutics. 38, 3, p. 225-229 5 p.

 

The Molecular Genetic Architecture of Self-Employment

van der Loos, M., Rietveld, N., Eklund, N., Koellinger, P., Rivadeneira, F., Abecasis, G., Ankra-Badu, G., Baumeister, S., Benjamin, D., Biffar, R., Blankenberg, S., Boomsma, D., Cesarini, D., Cucca, F., de Geus, E., Dedoussis, G., Deloukas, P., Dimitriou, M., Eiriksdottir, G. & Eriksson, J. & 48 others, , 2013, In: PLoS One (print). 8, 4, p. e60542

The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis

Fall, T., Hagg, S., Magi, R., Ploner, A., Fischer, K., Horikoshi, M., Sarin, A., Thorleifsson, G., Ladenvall, C., Kals, M., Kuningas, M., Draisma, H., Ried, J., van Zuydam, N., Huikari, V., Mangino, M., Sonestedt, E., Benyamin, B., Nelson, C. & Rivera, N. & 105 others, , 2013, In: PLoS Medicine (print). 10, 6

 

2012

Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson’s disease

Keller, M. F., Saad, M., groep, Bras, J., Bettella, F., Nicolaou, N., Simón-Sánchez, J., Mittag, F., Büchel, F., Sharma, M., Gibbs, J. R., Schulte, C., Moskvina, V., Durr, A., Holmans, P., Kilarski, L. L., Guerreiro, R., Hernandez, D. G., Brice, A. & Ylikotila, P. & 18 others, , 15 Nov 2012, In: Human Molecular Genetics. 21, 22, p. 4996-5009 14 p.

 

Identification of new susceptibility loci for osteoarthritis (arcOGEN): A genome-wide association study

Zeggini, E., Panoutsopoulou, K., groep, Southam, L., Rayner, N. W., Day-Williams, A. G., Lopes, M. C., Boraska, V., Esko, T., Evangelou, E., Hofman, A., Houwing-Duistermaat, J. J., Ingvarsson, T., Jonsdottir, I., Jonsson, H., Kerkhof, H. J. M., Kloppenburg, M., Bos, S. D., Mangino, M. & Metrustry, S. & 31 others, , Sept 2012, In: The Lancet. 380, 9844, p. 815-823 9 p.

 

Degree of glucose control is related to fracture risk in women with type 2 diabetes mellitus: The Rotterdam study

Oei, L., Zillikens, M. C., Dehghan, A., Castano-Betancourt, M. C., Estrada, K., Stolk, L., Oei, E. H. G.van Meurs, J. B.Hofman, A.Sijbrands, E. J. G.Janssen, J. A. M. J. L., Witteman, J. C., van Leeuwen, J. P. T. M.Uitterlinden, A. G. & Rivadeneira, F., May 2012, In: Bone. 50, supplement 1, p. S29-S29 1 p.

 

A de novo 14q12q13.3 interstitial deletion in a patient affected by a severe neurodevelopmental disorder of unknown origin

Fonseca, D., Prada, C., Siza, L., Angel, D., Gomez, Y., Restrepo, C., Douben, H.Rivadeneira, F.de Klein, A. & Laissue, P., 2012, In: American Journal of Medical Genetics Part A. 158A, 3, p. 689-693 5 p.

 

A Genetic Epidemiologic Study of Candidate Genes Involved in the Optic Nerve Head Morphology

Gasten, A., Ramdas, W.Broer, L., Koolwijk, L., Ikram, K., de Jong, P., Aulchenko, Y., Wolfs, R. C. W.Hofman, B.Rivadeneira, F.Uitterlinden, A., Oostra, B., Lemij, H., Klaver, C., Jansonius, N., Vingerling, H. & Duijn, C., 2012, In: Investigative Ophthalmology & Visual Science. 53, 3, p. 1485-1491 7 p.

A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies

Brautbar, A., Pompeii, L., Dehghan, A., Ngwa, J., Nambi, V., Virani, S., Rivadeneira, F.Uitterlinden, A.Hofman, B., Witteman, J., Pencina, M., Folsom, A., Cupples, L., Ballantyne, C. & Boerwinkle, E., 2012, In: Atherosclerosis. 223, 2, p. 421-426 6 p.

A genome-wide association meta-analysis identifies new childhood obesity loci

Bradfield, J., Taal, R., Timpson, N., Scherag, A., Lecoeur, C., Warrington, N., Hypponen, E., Holst, C., Valcarcel, B., Thiering, E., Salem, R., Schumacher, F., Cousminer, D., Sleiman, P., Zhao, J., Berkowitz, R., Vimaleswaran, K., Jarick, I., Pennell, C. & Evans, D. & 61 others, , 2012, In: Nature Genetics. 44, 5, p. 526-+

 

A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone-Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation

Coviello, A., Haring, R., Wellons, M., Vaidya, D., Lehtimaki, T., Keildson, S., Lunetta, K., He, C., Fornage, M., Lagou, V., Mangino, M., Onland-Moret, N., Chen, B., Eriksson, J., Garcia, M., Mei, Y., Koster, A., Lohman, K., Lyytikainen, L. & Petersen, A. & 79 others, , 2012, In: PLoS Genetics (print). 8, 7

A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans

Liu, F., Lijn, F., Schurmann, C., Zhu, G., Chakravarty, M., Hysi, P., Wollstein, A., Lao Grueso, O., de Bruijne, M.Ikram, A.van der Lugt, A.Rivadeneira, F.Uitterlinden, A.Hofman, B.Niessen, W., Homuth, G., de Zubicaray, G., McMahon, K., Thompson, P. & Daboul, A. & 14 others, , 2012, In: PLoS Genetics (print). 8, 9, e1002932.

A Large-Scale Population-Based Analysis of Common Genetic Variation in the Thyroid Hormone Receptor Alpha Locus and Bone

Medici, M.Rivadeneira, F., Deure, W., Hofman, B.van Meurs, J., Styrkarsdottir, U., Duijn, C., Spector, T., Kiel, D., Uitterlinden, A., Visser, T. & Peeters, R., 2012, In: Thyroid. 22, 2, p. 223-224 2 p.

 

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11

Siddiq, A., Couch, F., Chen, G., Lindstrom, S., Eccles, D., Millikan, R., Michailidou, K., Stram, D., Beckmann, L., Rhie, S., Ambrosone, C., Aittomaki, K., Amiano, P., Apicella, C., Baglietto, L., Bandera, E., Beckmann, M., Berg, C., Bernstein, L. & Blomqvist, C. & 120 others, , 2012, In: Human Molecular Genetics. 21, 24, p. 5373-5384 12 p.

 

Assessment of gene-by-sex interaction effect on bone mineral density

Liu, C., Estrada Gil, K., Yerges-Armstrong, L., Amin, N., Evangelou, E., Li, G., Minster, R., Carless, M., Kammerer, C., Oei – Oei, L., Zhou, Y., Alonso, N., Dailiana, Z., Eriksson, J., Garcia-Giralt, N., Giroux, S., Husted, L., Khusainova, R., Koromila, T. & Kung, A. & 70 others, , 2012, In: Journal of Bone and Mineral Research. 27, 10, p. 2051-2064 14 p.

Association between bone mineral density and type 2 diabetes mellitus: a meta-analysis of observational studies

Ma, L., Oei – Oei, L., Jiang, L., Estrada Gil, K., Chen, H., Wang, Z., Yu, Q., Zillikens, M. C., Gao, X. & Rivadeneira, F., 2012, In: European Journal of Epidemiology. 27, 5, p. 319-332 14 p.

 

Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies

Murabito, J., White, C., Kavousi, M., Sun, Y., Feitosa, M., Nambi, V., Lamina, C., Schillert, A., Coassin, S., Bis, J., Broer, L., Crawford, D., Franceschini, N., Frikke-Schmidt, R., Haun, M., Holewijn, S., Huffman, J., Hwang, S., Kiechl, S. & Kollerits, B. & 109 others, , 2012, In: Circulation-cardiovascular genetics. 5, 1, p. 100-112 13 p.

Common Genetic Determinants of Intraocular Pressure and Primary Open-Angle Glaucoma

Koolwijk, L., Ramdas, W.Ikram, K., Jansonius, N., Pasutto, F., Hysi, P., Macgregor, S., Janssen, S., Hewitt, A., Viswanathan, A., Brink, J., Hosseini, S., Amin, N., Despriet, D., Willemse-Assink, J., Kramer, R., Rivadeneira, F., Struchalin, M., Aulchenko, Y. & Weisschuh, N. & 29 others, , 2012, In: PLoS Genetics (print). 8, 5

 

Common Genetic Variation in the 3 ‘-BCL11B Gene Desert Is Associated With Carotid-Femoral Pulse Wave Velocity and Excess Cardiovascular Disease Risk The AortaGen Consortium

Mitchell, G., Verwoert, G., Tarasov, K., Isaacs, A., Smith, A., Yasmin, Rietzschel, E., Tanaka, T., Liu, Y., Parsa, A., Najjar, S., O’Shaughnessy, K., Sigurdsson, S., De Buyzere, M., Larson, M., Sie, M., Andrews, J., Post, W., Mattace Raso, F. U. S. & McEniery, C. & 55 others, , 2012, In: Circulation-cardiovascular genetics. 5, 1, p. 81-90 10 p.

Common variants at 12q15 and 12q24 are associated with infant head circumference

Taal, R., St Pourcain, B., Thiering, E., Das, S., Mook, D., Warrington, N., Kaakinen, M., Kreiner-Moller, E., Bradfield, J., Freathy, R., Geller, F., Guxens Junyent, M., Cousminer, D., Kerkhof, M., Timpson, N., Ikram, A., Beilin, L., Bonnelykke, K., Buxton, J. & Charoen, P. & 65 others, , 2012, In: Nature Genetics. 44, 5, p. 532-538 7 p.

 

Common variants at 6q22 and 17q21 are associated with intracranial volume

Ikram, A., Fornage, M., Smith, A., Seshadri, S., Schmidt, R., Debette, S., Vrooman, H., Sigurdsson, S., Ropele, S., Taal, R., Mook, D., Coker, L., Longstreth, W., Niessen, W., DeStefano, A., Beiser, A., Zijdenbos, A., Struchalin, M., Jack, C. & Rivadeneira, F. & 109 others, , 2012, In: Nature Genetics. 44, 5, p. 539-+

 

Common variants at 6q22 and 17q21 are associated with intracranial volume (vol 44, pg 539, 2012)

Ikram, A., Fornage, M., Smith, A., Seshadri, S., Schmidt, R., Debette, S., Vrooman, H., Sigurdsson, S., Ropele, S., Taal, R., Mook, D., Coker, L., Longstreth, W., Niessen, W., DeStefano, A., Beiser, A., Zijdenbos, A., Struchalin, M., Jack, C. & Rivadeneira, F. & 36 others, , 2012, In: Nature Genetics. 44, 6, p. 732-732 1 p.

Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies

Grallert, H., Dupuis, J., Bis, J., Dehghan, A., Barbalic, M., Baumert, J., Lu, C., Smith, N., Uitterlinden, A., Roberts, R., Khuseyinova, N., Schnabel, R., Rice, K., Rivadeneira, F., Hoogeveen, R., Fontes, J., Meisinger, C., Keaney, J., Lemaitre, R. & Aulchenko, Y. & 25 others, , 2012, In: European Heart Journal. 33, 2, p. 238-251 14 p.

 

Evidence of Inbreeding Depression on Human Height

McQuillan, R., Eklund, N., Pirastu, N., Kuningas, M., McEvoy, B., Esko, T., Corre, T., Davies, G., Kaakinen, M., Lyytikainen, L., Kristiansson, K., Havulinna, A., Gogele, M., Vitart, V., Tenesa, A., Aulchenko, Y., Hayward, C., Johansson, A., Boban, M. & Ulivi, S. & 73 others, , 2012, In: PLoS Genetics (print). 8, 7, e1002655.

 

FTO genotype is associated with phenotypic variability of body mass index

Yang, J., Loos, R., Powell, J., Medland, S., Speliotes, E., Chasman, D., Rose, L., Thorleifsson, G., Steinthorsdottir, V., Magi, R., Waite, L., Smith, A., Yerges-Armstrong, L., Monda, K., Hadley, D., Mahajan, A., Li, G., Kapur, K., Vitart, V. & Huffman, J. & 151 others, , 2012, In: Nature. 490, p. 267-272 6 p.

 

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Freilinger, T., Anttila, V., de Vries, B., Malik, R., Kallela, M., Terwindt, G., Pozo-Rosich, P., Winsvold, B., Nyholt, D., van Oosterhout, W., Artto, V., Todt, U., Hamalainen, E., Fernandez-Morales, J., Louter, M., Kaunisto, M., Schoenen, J., Raitakari, O., Lehtimaki, T. & Vila-Pueyo, M. & 23 others, , 2012, In: Nature Genetics. 44, 7, p. 777-U205

Genome-wide association analysis identifies three new breast cancer susceptibility loci

Ghoussaini, M., Fletcher, O., Michailidou, K., Turnbull, C., Schmidt, M. K., Dicks, E., Dennis, J., Wang, Q., Humphreys, M., Luccarini, C., Baynes, C., Conroy, D., Maranian, M., Ahmed, S., Driver, K., Johnson, N., Orr, N., Silva, I., Waisfisz, Q. & Meijers-Heijboer, H. & 162 others, , 2012, In: Nature Genetics. 44, 3, p. 312-U120

 

Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function

Pattaro, C., Kottgen, A., Teumer, A., Garnaas, M., Boger, C., Fuchsberger, C., Olden, M., Chen, M., Tin, A., Taliun, D., Li, M., Gao, X., Gorski, M., Yang, Q., Hundertmark, C., Foster, M., O’Seaghdha, C., Glazer, N., Isaacs, A. & Liu, C. & 146 others, , 2012, In: PLoS Genetics (print). 8, 3

 

Genome-wide association and functional studies identify the DOT1L gene to be involved in cartilage thickness and hip osteoarthritis

Betancourt, M., Cailotto, F., Kerkhof, H., Cornelis, F., Doherty, S., Hart, D., Hofman, B., Luyten, F., Maciewicz, R., Mangino, M., Metrustry, S., Muir, K., Peters, M., Rivadeneira, F., Wheeler, M., Zhang, W., Arden, N., Spector, T., Uitterlinden, A. & Doherty, M. & 3 others, , 2012, In: Proceedings of the National Academy of Sciences of the U.S.A.. 109, 21, p. 8218-8223 6 p.

 

Genome-Wide Association Studies Identify CHRNA5/3 and HTR4 in the Development of Airflow Obstruction

Wilk, J., Shrine, N., Loehr, L., Zhao, J., Manichaikul, A., Lopez, L., Smith, A., Heckbert, S., Smolonska, J., Tang, W., Loth, D., Curjuric, I., Hui, J., Cho, M., Latourelle, J., Henry, A., Aldrich, M., Bakke, P., Beaty, T. & Bentley, A. & 59 others, , 2012, In: American Journal of Respiratory and Critical Care Medicine. 186, 7, p. 622-632 11 p.

 

Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations

Demirkan, A., Duijn, C., Ugocsai, P., Isaacs, A., Pramstaller, P., Liebisch, G., Wilson, J., Johansson, A., Rudan, I., Aulchenko, Y., Kirichenko, A., Janssens, C., Jansen, R., Gnewuch, C., Domingues, F., Pattaro, C., Wild, S., Jonasson, I., Polasek, O. & Zorkoltseva, I. & 34 others, , 2012, In: PLoS Genetics (print). 8, 2

 

Genome-Wide Association Study of Vascular Dementia

Schrijvers, E., Schurmann, B., Koudstaal, P., van den Bussche, H., Duijn, C., Hentschel, F., Heun, R., Hofman, B., Jessen, F., Kolsch, H., Kornhuber, J., Peters, O., Rivadeneira, F., Ruether, E., Uitterlinden, A., Riedel-Heller, S., Dichgans, M., Wiltfang, J., Maier, W. & Breteler, M. & 1 others, , 2012, In: Stroke. 43, 2, p. 315-319 5 p.

 

Genome-Wide Joint Meta-Analysis of SNP and SNP-by-Smoking Interaction Identifies Novel Loci for Pulmonary Function

Hancock, D., Artigas, M., Gharib, S., Henry, A., Manichaikul, A., Ramasamy, A., Loth, D., Imboden, M., Koch, B., McArdle, W., Smith, A., Smolonska, J., Sood, A., Tang, W., Wilk, J., Zhai, G., Zhao, J., Aschard, H., Burkart, K. & Curjuric, I. & 70 others, , 2012, In: PLoS Genetics (print). 8, 12

 

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

Estrada Gil, K., Styrkarsdottir, U., Evangelou, E., Hsu, Y., Duncan, E., Ntzani, E., Oei – Oei, L., Albagha, O., Amin, N., Kemp, J., Koller, D., Li, G., Liu, C., Minster, R., Moayyeri, A., Vandenput, L., Willner, D., Xiao, S., Yerges-Armstrong, L. & Zheng, H. & 161 others, , 2012, In: Nature Genetics. 44, 5, p. 491-+

 

Genome-wide meta-analysis of common variant differences between men and women

Boraska, V., Jeroncic, A., Colonna, V., Southam, L., Nyholt, D., Rayner, N., Perry, J., Toniolo, D., Albrecht, E., Ang, W., Bandinelli, S., Barbalic, M., Barroso, I., Beckmann, J., Biffar, R., Boomsma, D., Campbell, H., Corre, T., Erdmann, J. & Esko, T. & 107 others, , 2012, In: Human Molecular Genetics. 21, 21, p. 4805-4815 11 p.

 

Genome-Wide Profiling of Blood Pressure in Adults and Children

Taal, R., Verwoert, G., Demirkan, A., Janssens, C., Rice, K., Ehret, G., Smith, A., Verhaaren, B., Witteman, J., Hofman, B.Vernooij, M.Uitterlinden, A.Rivadeneira, F.Ikram, A., Levy, D., Heijden, B., Jaddoe, V. & Duijn, C., 2012, In: Hypertension. 59, 2, p. 241-247 7 p.

 

Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk

Sanchez-Juan, P., Bishop, M., Aulchenko, Y., Brandel, J., Rivadeneira, F., Struchalin, M., Lambert, J., Amouyel, P., Combarros, O., Sainz, J., Carracedo, A., Uitterlinden, A.Hofman, B., Zerr, I., Kretzschmar, H., Laplanche, J., Knight, R., Will, R. & Duijn, C., 2012, In: Neurobiology of Aging. 33, 7

 

Gremlin 1, frizzled-related protein, and Dkk-1 are key regulators of human articular cartilage homeostasis

Leijten, J., Emons, J., Sticht, C., van Gool, S., Decker, E., Uitterlinden, A., Rappold, G., Hofman, B.Rivadeneira, F., Scherjon, S., Wit, J., van Meurs, J., van Blitterswijk, C. & Karperien, M., 2012, In: Arthritis & Rheumatism. 64, 10, p. 3302-3312 11 p.

 

How to deal with the early GWAS data when imputing and combining different arrays is necessary

Uh, H., Deelen, J., Beekman, M., Helmer, Q., Rivadeneira, F., Hottenga, J., Boomsma, D., Hofman, B.Uitterlinden, A., Slagboom, P., Bohringer, S. & Houwing-Duistermaat, J., 2012, In: European Journal of Human Genetics. 20, 5, p. 572-576 5 p.

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

Chasman, D., Fuchsberger, C., Pattaro, C., Teumer, A., Boger, C., Endlich, K., Olden, M., Chen, M., Tin, A., Taliun, D., Li, M., Gao, X., Gorski, M., Yang, Q., Hundertmark, C., Foster, M., O’Seaghdha, C., Glazer, N., Isaacs, A. & Liu, C. & 144 others, , 2012, In: Human Molecular Genetics. 21, 24, p. 5329-5343 15 p.

 

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Scott, R., Lagou, V., Welch, R., Wheeler, E., Montasser, M., Luan, J., Magi, R., Strawbridge, R., Rehnberg, E., Gustafsson, S., Kanoni, S., Rasmussen-Torvik, L., Yengo, L., Lecoeur, C., Shungin, D., Sanna, S., Sidore, C., Johnson, P., Jukema, J. & Johnson, T. & 194 others, , 2012, In: Nature Genetics. 44, 9, p. 991-+

 

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

Verhoeven, V., Hysi, P., Saw, S., Vitart, V., Mirshahi, A., Guggenheim, J., Cotch, M., Yamashiro, K., Baird, P., Mackey, D., Wojciechowski, R., Ikram, K., Hewitt, A., Duggal, P., Janmahasatian, S., Khor, C., Fan, Q., Zhou, X., Young, T. & Tai, E. & 75 others, , 2012, In: Human Genetics. 131, 9, p. 1467-1480 14 p.

 

Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS

Diekstra, F., Saris, C., van Rheenen, W., Franke, L., Jansen, R., van Es, M., Van Vught, P., Blauw, H., Groen, E., Horvath, S., Estrada Gil, K., Rivadeneira, F.Hofman, B.Uitterlinden, A., Robberecht, W., Andersen, P., Melki, J., Meininger, V., Hardiman, O. & Landers, J. & 8 others, , 2012, In: PLoS One (print). 7, 4

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

Ellinor, P., Lunetta, K., Albert, C., Glazer, N., Ritchie, M., Smith, A., Arking, D., Muller-Nurasyid, M., Krijthe, B., Lubitz, S., Bis, J., Chung, M., Doerr, M., Ozaki, K., Roberts, J., Smith, J., Pfeufer, A., Sinner, M., Lohman, K. & Ding, J. & 69 others, , 2012, In: Nature Genetics. 44, 6, p. 670-U88

 

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

Paternoster, L., Standl, M., Chen, C., Ramasamy, A., Bonnelykke, K., Duijts, L., Ferreira, M., Alves, A., Thyssen, J., Albrecht, E., Baurecht, H., Feenstra, B., Sleiman, P., Hysi, P., Warrington, N., Curjuric, I., Myhre, R., Curtin, J., Groen-Blokhuis, M. & Kerkhof, M. & 89 others, , 2012, In: Nature Genetics. 44, 2, p. 187-192 6 p.

 

Meta-Analysis of Genome-Wide Scans for Total Body BMD in Children and Adults Reveals Allelic Heterogeneity and Age-Specific Effects at the WNT16 Locus

Medina-Gomez, C., Kemp, J., Estrada Gil, K., Eriksson, J., Liu, J., Reppe, S., Evans, D., Heppe, D., Vandenput, L., Herrera, L., Ring, S., Kruithof, C., Timpson, N., Zillikens, M. C., Olstad, O., Zheng, H., Richards, J., Pourcain, B., Hofman, B. & Jaddoe, V. & 8 others, , 2012, In: PLoS Genetics (print). 8, 7

 

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

Horikoshi, M., Yaghootkar, H., Mook, D., Sovio, U., Taal, R., Hennig, B., Bradfield, J., St Pourcain, B., Evans, D., Charoen, P., Kaakinen, M., Cousminer, D., Lehtimaki, T., Kreiner-Moller, E., Warrington, N., Bustamante, M., Feenstra, B., Berry, D., Thiering, E. & Pfab, T. & 127 others, , 2012, In: Nature Genetics. 45, 1, p. 76-82 7 p.

 

Reproductive aging-associated common genetic variants and the risk of breast cancer

He, C., Chasman, D., Dreyfus, J., Hwang, S., Ruiter, R., Sanna, S., Buring, J., Fernandez-Rhodes, L., Franceschini, N., Hankinson, S., Hofman, B., Lunetta, K., Palmieri, G., Porcu, E., Rivadeneira, F., Rose, L., Splansky, G., Stolk, L., Uitterlinden, A. & Chanock, S. & 6 others, , 2012, In: Breast Cancer Research. 14, 2

 

The association between plasma homocysteine levels, methylation capacity and incident osteoporotic fractures

Enneman, A., van der Velde, N., Jonge, R., Heil, S., Stolk, L., Hofman, B.Rivadeneira, F., Zillikens, M. C., Uitterlinden, A. & van Meurs, J., 2012, In: Bone. 50, 6, p. 1401-1405 5 p.

 

The Generation R Study: design and cohort update 2012

Jaddoe, V., Duijn, C., Franco Duran, O., Heijden, B., van IIzendoorn, M., Jongste, J., van der Lugt, A.Mackenbach, J.Moll, H.Raat, H.Rivadeneira, F.Steegers, E., Tiemeier, H., Uitterlinden, A., Verhulst, F. & Hofman, B., 2012, In: European Journal of Epidemiology. 27, 9, p. 739-756 18 p.

2011

Common genetic determinants of vitamin D insufficiency: A genome-wide association study

The SUNLIGHT consortium, Feb 2011, In: Obstetrical and Gynecological Survey. 66, 2, p. 91-93 3 p.

 

Common genetic variants are significant risk factors for early menopause: results from the Breakthrough Generations Study

Murray, A., Bennett, C. E., Perry, J. R. B., Weedon, M. N., Jacobs, P. A., Morris, D. H., Orr, N., Schoemaker, M. J., Jones, M., Ashworth, A., Swerdlow, A. J. & ReproGen Consortium, 1 Jan 2011, In: Human Molecular Genetics. 20, 1, p. 186-92 7 p.

 

A child with a deletion in the monocarboxylate transporter 8 gene: 7-year follow-up and effects of thyroid hormone treatment

Zung, A., Visser, T., Uitterlinden, A.Rivadeneira, F. & Friesema, E., 2011, In: European Journal of Endocrinology. 165, 5, p. 823-830 8 p.

 

A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

Surakka, I., Isaacs, A., Karssen, L., Laurila, P., Middelberg, R., Tikkanen, E., Ried, J., Lamina, C., Mangino, M., Igl, W., Hottenga, J., Lagou, V., van der Harst, P., Leach, I., Esko, T., Kutalik, Z., Wainwright, N., Struchalin, M., Sarin, A. & Kangas, A. & 58 others, , 2011, In: PLoS Genetics (print). 7, 10

 

Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD

Boger, C., Gorski, M., Li, M., Hoffmann, M., Huang, C., Yang, Q., Teumer, A., Krane, V., O’Seaghdha, C., Kutalik, Z., Wichmann, H., Haak, T., Boes, E., Coassin, S., Coresh, J., Kollerits, B., Haun, M., Paulweber, B., Kottgen, A. & Li, G. & 19 others, , 2011, In: PLoS Genetics (print). 7, 9

 

Association of heat shock proteins with Parkinson’s disease

Broer, L.Koudstaal, P.Amin, N.Rivadeneira, F.Uitterlinden, A.Hofman, B., Oostra, B., Breteler, M., Ikram, A. & Duijn, C., 2011, In: European Journal of Epidemiology. 26, 12, p. 933-935 3 p.

 

Association of HSP70 and its Co-Chaperones with Alzheimer’s Disease

Broer, L., Ikram, A., Schuur, M., DeStefano, A., Bis, J., Liu, F.Rivadeneira, F.Uitterlinden, A., Beiser, A., Longstreth, W., Hofman, B., Aulchenko, Y., Seshadri, S., Fitzpatrick, A., Oostra, B., Breteler, M. & Duijn, C., 2011, In: Journal of Alzheimers Disease. 25, 1, p. 93-102 10 p.

A Variant in MCF2L Is Associated with Osteoarthritis

Day-Williams, A., Southam, L., Panoutsopoulou, K., Rayner, N., Esko, T., Estrada Gil, K., Helgadottir, H., Hofman, B., Ingvarsson, T., Jonsson, H., Keis, A., Kerkhof, H., Thorleifsson, G., Arden, N., Carr, A., Chapman, K., Deloukas, P., Loughlin, J., McCaskie, A. & Ollier, W. & 25 others, , 2011, In: American Journal of Human Genetics. 89, 3, p. 446-450 5 p.

 

Candidate gene studies and the quest for the entrepreneurial gene

van der Loos, M., Koellinger, P., Groenen, P.Rietveld, N.Rivadeneira, F.van Rooij, F.Uitterlinden, A.Hofman, B. & Thurik, R., 2011, In: Small Business Economics. 37, 3, p. 269-275 7 p.

Clinical Implications of Old and New Genes for Open-Angle Glaucoma

Ramdas, W., Koolwijk, L., Cree, A., Janssens, C., Amin, N., de Jong, P., Wolfs, R. C. W., Gibson, J., Kirwan, J., Hofman, B.Rivadeneira, F., Oostra, B., Uitterlinden, A., Ennis, S., Lotery, A., Lemij, H., Klaver, C.Vingerling, H., Jansonius, N. & Duijn, C., 2011, In: Ophthalmology. 118, 12, p. 2389-2397 9 p.

 

Common genetic variants associated with open-angle glaucoma

Ramdas, W., Koolwijk, L., Lemij, H., Pasutto, F., Cree, A., Thorleifsson, G., Janssen, S., Jacoline, T., Amin, N.Rivadeneira, F.Wolfs, R. C. W., Walters, G., Jonasson, F., Weisschuh, N., Mardin, C., Gibson, J., Zegers, R., Hofman, B., de Jong, P. & Uitterlinden, A. & 13 others, , 2011, In: Human Molecular Genetics. 20, 12, p. 2464-2471 8 p.

De genetica van ondernemerschap

van der Loos, M., Groenen, P.Hofman, B., Koellinger, P., Rivadeneira, F.van Rooij, F.Thurik, R. & Uitterlinden, A., 2011, In: Economisch-Statistische Berichten. 96, 4609s, p. 30-36 7 p.

 

Eight Common Genetic Variants Associated with Serum DHEAS Levels Suggest a Key Role in Ageing Mechanisms

Zhai, G., Teumer, A., Stolk, L., Perry, J., Vandenput, L., Coviello, A., Koster, A., Bell, J., Bhasin, S., Eriksson, J., Eriksson, A., Ernst, F., Ferrucci, L., Frayling, T., Glass, D., Grundberg, E., Haring, R., Hedman, A., Hofman, B. & Kiel, D. & 26 others, , 2011, In: PLoS Genetics (print). 7, 4

 

Genetic architecture of open angle glaucoma and related determinants

Ramdas, W.Amin, N., Koolwijk, L., Janssens, C., Demirkan, A., de Jong, P., Aulchenko, Y., Wolfs, R. C. W.Hofman, B.Rivadeneira, F.Uitterlinden, A., Oostra, B., Lemij, H., Klaver, C.Vingerling, H., Jansonius, N. & Duijn, C., 2011, In: Journal of Medical Genetics. 48, 3, p. 190-196 7 p.

 

Genetic Determinants of Serum Testosterone Concentrations in Men

Ohlsson, C., Wallaschofski, H., Lunetta, K., Stolk, L., Perry, J., Koster, A., Petersen, A., Eriksson, J., Lehtimaki, T., Huhtaniemi, I., Hammond, G., Maggio, M., Coviello, A., Ferrucci, L., Heier, M., Hofman, B., Holliday, K., Jansson, J., Kahonen, M. & Karasik, D. & 39 others, , 2011, In: PLoS Genetics (print). 7, 10

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

Ehret, G., Munroe, P., Rice, K., Bochud, M., Johnson, A., Chasman, D., Smith, A., Tobin, M., Verwoert, G., Hwang, S., Pihur, V., Vollenweider, P., O’Reilly, P., Amin, N., Bragg-Gresham, J., Teumer, A., Glazer, N., Launer, L., Zhao, J. & Aulchenko, Y. & 326 others, , 2011, In: Nature. 478, 7367, p. 103-109 7 p.

 

Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile

Kilpelainen, T., Zillikens, M. C., Stancakova, A., Finucane, F., Ried, J., Langenberg, C., Zhang, W., Beckmann, J., Luan, J., Vandenput, L., Styrkarsdottir, U., Zhou, Y., Smith, A., Zhao, J., Amin, N., Vedantam, S., Shin, S., Haritunians, T., Fu, M. & Feitosa, M. & 97 others, , 2011, In: Nature Genetics. 43, 8, p. 753-U58

 

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function

Artigas, M., Loth, D., Wain, L., Gharib, S., Obeidat, M., Tang, W., Zhai, G., Zhao, J., Smith, A., Huffman, J., Albrecht, E., Jackson, C., Evans, D., Cadby, G., Fornage, M., Manichaikul, A., Lopez, L., Johnson, T., Aldrich, M. & Aspelund, T. & 149 others, , 2011, In: Nature Genetics. 43, 11, p. 1082-U70

 

Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area

Khor, C., Ramdas, W., Vithana, E., Cornes, B., Sim, X., Tay, W., Saw, S., Zheng, Y., Lavanya, R., Wu, R., Wang, J., Mitchell, P., Uitterlinden, A.Rivadeneira, F., Teo, Y., Chia, K., Seielstad, M., Hibberd, M., Vingerling, H. & Klaver, C. & 5 others, , 2011, In: Human Molecular Genetics. 20, 9, p. 1864-1872 9 p.

 

Genome-wide association study confirms extant PD risk loci among the Dutch

Simon-Sanchez, J., van Hilten, J., van de Warrenburg, B., Post, B., Berendse, H., Arepalli, S., Hernandez, D., de Bie, R., Velseboer, D., Scheffer, H., Bloem, B., van Dijk, K., Rivadeneira, F.Hofman, B.Uitterlinden, A., Rizzu, P., Bochdanovits, Z., Singleton, A. & Heutink, P., 2011, In: European Journal of Human Genetics. 19, 6, p. 655-661 7 p.

 

Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited

Deelen, J., Beekman, M., Uh, H., Helmer, Q., Kuningas, M., Christiansen, L., Kremer, D., van der Breggen, R., Suchiman, H., Lakenberg, N., van den Akker, E., Passtoors, W., Tiemeier, H., van Heemst, D., de Craen, A., Rivadeneira, F., de Geus, E., Perola, M., van der Ouderaa, F. & Gunn, D. & 8 others, , 2011, In: Aging Cell. 10, 4, p. 686-698 13 p.

 

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Wain, L., Verwoert, G., O’Reilly, P., Shi, G., Johnson, T., Johnson, A., Bochud, M., Rice, K., Henneman, P., Smith, A., Ehret, G., Amin, N., Larson, M., Mooser, V., Hadley, D., Dorr, M., Bis, J., Aspelund, T., Esko, T. & Janssens, C. & 204 others, , 2011, In: Nature Genetics. 43, 10, p. 1005-U122

Genome-Wide Association Study Using Extreme Truncate Selection Identifies Novel Genes Affecting Bone Mineral Density and Fracture Risk

Duncan, E., Danoy, P., Kemp, J., Leo, P., McCloskey, E., Nicholson, G., Eastell, R., Prince, R., Eisman, J., Jones, G., Sambrook, P., Reid, I., Dennison, E., Wark, J., Richards, J., Uitterlinden, A., Spector, T., Esapa, C., Cox, R. & Brown, S. & 27 others, , 2011, In: PLoS Genetics (print). 7, 4

 

High prevalence of vertebral fractures despite normal bone mineral density in patients with long-term controlled acromegaly

Wassenaar, M., Biermasz, N., Hamdy, N., Zillikens, M. C., van Meurs, J.Rivadeneira, F.Hofman, B.Uitterlinden, A., Stokkel, M., Roelfsema, F., Kloppenburg, M., Kroon, H., Romijn, J. & Pereira, A., 2011, In: European Journal of Endocrinology. 164, 4, p. 475-483 9 p.

 

Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals

Arking, D., Junttila, M., Goyette, P., Huertas-Vazquez, A., Eijgelsheim, M., Blom, M., Newton-Cheh, C., Reinier, K., Teodorescu, C., Uy-Evanado, A., Carter-Monroe, N., Kaikkonen, K., Kortelainen, M., Boucher, G., Lagace, C., Moes, A., Zhao, X., Kolodgie, F., Rivadeneira, F. & Hofman, B. & 41 others, , 2011, In: PLoS Genetics (print). 7, 6

 

Large common deletions associate with mortality at old age

Kuningas, M., Estrada Gil, K., Hsu, Y., Nandakumar, K., Uitterlinden, A., Lunetta, K., Duijn, C., Karasik, D., Hofman, B., Murabito, J., Rivadeneira, F., Kiel, D. & Tiemeier, H., 2011, In: Human Molecular Genetics. 20, 21, p. 4290-4296 7 p.

Large-scale meta-analysis of interleukin-1 beta and interleukin-1 receptor antagonist polymorphisms on risk of radiographic hip and knee osteoarthritis and severity of knee osteoarthritis

Kerkhof, H., Doherty, M., Arden, N., Abramson, S., Attur, M., Bos, S., Cooper, C., Dennison, E., Doherty, S., Evangelou, E., Hart, D., Hofman, B., Javaid, K., Kerna, I., Kisand, K., Kloppenburg, M., Krasnokutsky, S., Maciewicz, R., Meulenbelt, I. & Muir, K. & 13 others, , 2011, In: Osteoarthritis and Cartilage. 19, 3, p. 265-271 7 p.

 

Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chrmosome 7q22

Evangelou, E., Valdes, A., Kerkhof, H., Styrkarsdottir, U., Zhu, Y., Meulenbelt, I., Lories, R., Karassa, F., Tylzanowski, P., Bos, S., Akune, T., Arden, N., Carr, A., Chapman, K., Cupples, L., Le Dai, J., Deloukas, P., Doherty, S., Engstrom, G. & Gonzalez, A. & 49 others, , 2011, In: Annals of the Rheumatic Diseases. 70, 2, p. 349-355 7 p.

 

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

Bis, J., Kavousi, M., Franceschini, N., Isaacs, A., Abecasis, G., Schminke, U., Post, W., Smith, A., Cupples, L., Markus, H., Schmidt, R., Huffman, J., Lehtimaki, T., Baumert, J., Munzel, T., Heckbert, S., Dehghan, A., North, K., Oostra, B. & Bevan, S. & 73 others, , 2011, In: Nature Genetics. 43, 10, p. 940-U40

 

Mild Hyponatremia as a Risk Factor for Fractures: The Rotterdam Study

Hoorn, E.Rivadeneira, F.van Meurs, J.Ziere, B.Stricker, B.Hofman, B., Pols, H., Zietse, R.Uitterlinden, A. & Zillikens, M. C., 2011, In: Journal of Bone and Mineral Research. 26, 8, p. 1822-1828 7 p.

Recommendations for standardization and phenotype definitions in genetic studies of osteoarthritis: the TREAT-OA consortium

Kerkhof, H., Meulenbelt, I., Akune, T., Arden, N., Aromaa, A., Bierma – Zeinstra, S., Carr, A., Cooper, C., Le Dai, J., Doherty, M., Doherty, S., Felson, D., Gonzalez, A., Gordon, A., Harilainen, A., Hart, D., Hauksson, V., Heliovaara, M., Hofman, B. & Ikegawa, S. & 30 others, , 2011, In: Osteoarthritis and Cartilage. 19, 3, p. 254-264 11 p.

 

Replication Study of Chr17q25 With Cerebral White Matter Lesion Volume

Verhaaren, B., Boer, R., Vernooij, M.Rivadeneira, F.Uitterlinden, A.Hofman, B.Krestin, G.van der Lugt, A.Niessen, W., Breteler, M. & Ikram, A., 2011, In: Stroke. 42, 11, p. 3297-3299 3 p.

 

The GDF5 rs143383 polymorphism is associated with osteoarthritis of the knee with genome-wide statistical significance

Valdes, A., Evangelou, E., Kerkhof, H., Doherty, S., Kisand, K., Tamm, A., Kerna, I., Uitterlinden, A.Hofman, B.Rivadeneira, F., Cooper, C., Dennison, E., Zhang, W., Muir, K., Ioannidis, J., Wheeler, M., Maciewicz, R., van Meurs, J., Arden, N. & Spector, T. & 1 others, , 2011, In: Annals of the Rheumatic Diseases. 70, 5, p. 873-U308

 

2010

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Elks, C. E., Perry, J. R. B., Sulem, P., Chasman, D. I., Franceschini, N., He, C., Lunetta, K. L., Visser, J. A., Byrne, E. M., Cousminer, D. L., Gudbjartsson, D. F., Esko, T., Feenstra, B., GIANT Consortium, Hottenga, J.-J., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M. & Marongiu, M. & 31 others, , Dec 2010, In: Nature Genetics. 42, 12, p. 1077-1085 9 p.

17 Osteoporosis

Uitterlinden, A. G.Van Meurs, J. B. J. & Rivadeneira, F., 1 May 2010, 

 

A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22

Kerkhof, H. J. M., Lories, R. J., Meulenbelt, I., Jonsdottir, I., Valdes, A. M., Arp, P., Ingvarsson, T., Jhamai, M., Jonsson, H., Stolk, L., Thorleifsson, G., Zhai, G., Zhang, F., Zhu, Y., Van Der Breggen, R., Carr, A., Doherty, M., Doherty, S., Felson, D. T. & Gonzalez, A. & 22 others, , Feb 2010, In: Arthritis and Rheumatism. 62, 2, p. 499-510 12 p.

 

A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14

Solouki, M., Verhoeven, V., Duijn, C., Verkerk, A., Ikram, K., Hysi, P., Despriet, D., Koolwijk, L., Ho, L., Ramdas, W., Czudowska, M., Kuijpers, R.Amin, N., Struchalin, M., Aulchenko, Y., Rij, Riemslag, F., Young, T., Mackey, D. & Spector, T. & 15 others, , 2010, In: Nature Genetics. 42, 10, p. 897-901 5 p.

A Genome-Wide Association Study of Optic Disc Parameters

Ramdas, W., Koolwijk, L., Ikram, K., Jansonius, N., de Jong, P., Bergen, A., Isaacs, A., Amin, N., Aulchenko, Y., Wolfs, R. C. W.Hofman, B.Rivadeneira, F., Oostra, B., Uitterlinden, A., Hysi, P., Hammond, C., Lemij, H., Vingerling, H.Klaver, C. & Duijn, C., 2010, In: PLoS Genetics (print). 6, 6

 

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

Blauw, H., Al-Chalabi, A., Andersen, P., Van Vught, P., Diekstra, F., van Es, M., Saris, C., Groen, E., van Rheenen, W., Koppers, M., van ‘t Slot, R., Strengman, E., Estrada Gil, K., Rivadeneira, F.Hofman, B.Uitterlinden, A., Kiemeney, L., Vermeulen, S., Birve, A. & Waibel, S. & 20 others, , 2010, In: Human Molecular Genetics. 19, 20, p. 4091-4099 9 p.

 

A Meta-analysis of Four Genome-Wide Association Studies of Survival to Age 90 Years or Older: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

Newman, A., Walter, S., Lunetta, K., Garcia, M., Slagboom, P., Christensen, K., Arnold, A., Aspelund, T., Aulchenko, Y., Benjamin, E., Christiansen, L., D’Agostino, R., Fitzpatrick, A., Franceschini, N., Glazer, N., Gudnason, V., Hofman, B., Kaplan, R., Karasik, D. & Kelly-Hayes, M. & 23 others, , 2010, In: Journals of Gerontology Series A-Biological Sciences and Medical Sciences. 65, 5, p. 478-487 10 p.

An Integration of Genome-Wide Association Study and Gene Expression Profiling to Prioritize the Discovery of Novel Susceptibility Loci for Osteoporosis-Related Traits

Hsu, Y., Zillikens, M. C., Wilson, S., Farber, C., Demissie, S., Soranzo, N., Bianchi, E., Grundberg, E., Liang, L., Richards, J., Estrada Gil, K., Zhou, Y., van Nas, A., Moffatt, M., Zhai, G., Hofman, B.van Meurs, J., Pols, H., Price, R. & Nilsson, O. & 10 others, , 2010, In: PLoS Genetics (print). 6, 6, e1000977.

 

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Speliotes, E., Willer, C., Berndt, S., Monda, K., Thorleifsson, G., Jackson, A., Allen, H., Lindgren, C., Luan, J., Magi, R., Randall, J., Vedantam, S., Winkler, T., Qi, L., Workalemahu, T., Heid, I., Steinthorsdottir, V., Stringham, H., Weedon, M. & Wheeler, E. & 355 others, , 2010, In: Nature Genetics. 42, 11, p. 937-U53

Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry A Prospective Meta-Analysis From the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

Smith, N., Felix, J., Morrison, A., Demissie, S., Glazer, N., Loehr, L., Cupples, L., Dehghan, A., Lumley, T., Rosamond, W., Lieb, W., Rivadeneira, F., Bis, J., Folsom, A., Benjamin, E., Aulchenko, Y., Haritunians, T., Couper, D., Murabito, J. & Wang, Y. & 18 others, , 2010, In: Circulation-cardiovascular genetics. 3, 3, p. 256-U79

Common genetic determinants of vitamin D insufficiency: a genome-wide association study

Wang, T., Zhang, F., Richards, J., Kestenbaum, B., van Meurs, J., Berry, D., Kiel, D., Streeten, E., Ohlsson, C., Koller, D., Peltonen, L., Cooper, J., O’Reilly, P., Houston, D., Glazer, N., Vandenput, L., Peacock, M., Shi, J., Rivadeneira, F. & McCarthy, M. & 56 others, , 2010, In: Lancet (UK). 376, 9736, p. 180-188 9 p.

 

Common Genetic Variants Associate with Serum Phosphorus Concentration

Kestenbaum, B., Glazer, N., Kottgen, A., Felix, J., Hwang, S., Liu, Y., Lohman, K., Kritchevsky, S., Hausman, D., Petersen, A., Gieger, C., Ried, J., Meitinger, T., Strom, T., Wichmann, H., Campbell, H., Hayward, C., Rudan, I., Boer, I. & Psaty, B. & 19 others, , 2010, In: Journal of the American Society of Nephrology. 21, 7, p. 1223-1232 10 p.

 

Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis

Kerkhof, H., Meulenbelt, I., Carr, A., Gonzalez, A., Hart, D., Hofman, B., Kloppenburg, M., Lane, N., Loughlin, J., Nevitt, M., Pols, H., Rivadeneira, F., Slagboom, E., Spector, T., Stolk, L., Tsezou, A., Uitterlinden, A., Valdes, A. & van Meurs, J., 2010, In: BMC Medical Genetics. 11

 

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

Sotoodehnia, N., Isaacs, A., de Bakker, P., Dorr, M., Newton-Cheh, C., Nolte, I., van der Harst, P., Muller, M., Eijgelsheim, M., Alonso, A., Hicks, A., Padmanabhan, S., Hayward, C., Smith, A., Polasek, O., Giovannone, S., Fu, J., Magnani, J., Marciante, K. & Pfeufer, A. & 79 others, , 2010, In: Nature Genetics. 42, 12, p. 1068-1076 9 p.

Digital Quantification of Human Eye Color Highlights Genetic Association of Three New Loci

Liu, F., Wollstein, A., Hysi, P., Ankra-Badu, G., Spector, T., Park, D., Larsson, M., Duffy, D., Montgomery, G., Mackey, D., Walsh, S., Lao Grueso, O., Hofman, B.Rivadeneira, F.Vingerling, H.Uitterlinden, A., Martin, N., Hammond, C., Kayser, M. & Zhu, G., 2010, In: PLoS Genetics (print). 6, 5

 

Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo

Ikram, K., Xueling, S., Jensen, R., Cotch, M., Hewitt, A., Ikram, A., Wang, J., Klein, R., Klein, B., Breteler, M., Cheung, N., Liew, G., Mitchell, P., Uitterlinden, A.Rivadeneira, F.Hofman, B., de Jong, P., Duijn, C., Kao, L. & Cheng, C. & 37 others, , 2010, In: PLoS Genetics (print). 6, 10, p. e1001184

 

Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease

Seshadri, S., Fitzpatrick, A., Ikram, A., DeStefano, A., Gudnason, V., Boada, M., Bis, J., Smith, A., Carassquillo, M., Lambert, J., Harold, D., Schrijvers, E., Ramirez-Lorca, R., Debette, S., Longstreth, W., Janssens, C., Pankratz, V., Dartigues, J., Hollingworth, P. & Aspelund, T. & 42 others, , 2010, In: JAMA – Journal of the American Medical Association. 303, 18, p. 1832-1840 9 p.

 

Genome-wide assocation studies in economics and entrepreneurship research: promises and limitations

Koellinger, P., van der Loos, M., Groenen, P.Thurik, R.Rivadeneira, F.van Rooij, F.Uitterlinden, A. & Hofman, B., 2010, In: Small Business Economics. 35, 1, p. 1-18 18 p.

Genome-wide association analysis identifies multiple loci related to resting heart rate

Eijgelsheim, M., Newton-Cheh, C., Sotoodehnia, N., de Bakker, P., Muller, M., Morrison, A., Smith, A., Isaacs, A., Sanna, S., Dorr, M., Navarro, P., Fuchsberger, C., Nolte, I., de Geus, E., Estrada Gil, K., Hwang, S., Bis, J., Ruckert, I., Alonso, A. & Launer, L. & 54 others, , 2010, In: Human Molecular Genetics. 19, 19, p. 3885-3894 10 p.

 

Genome-Wide Association Studies of MRI-Defined Brain Infarcts Meta-Analysis From the CHARGE Consortium

Debette, S., Bis, J., Fornage, M., Schmidt, H., Ikram, A., Sigurdsson, S., Heiss, G., Struchalin, M., Smith, A., van der Lugt, A., DeCarli, C., Lumley, T., Knopman, D., Enzinger, C., Eiriksdottir, G., Koudstaal, P., DeStefano, A., Psaty, B., Dufouil, C. & Catellier, D. & 33 others, , 2010, In: Stroke. 41, 2, p. 210-217 8 p.

 

Genome-wide association study of PR interval

Pfeufer, A., Noord, C., Marciante, K., Arking, D., Larson, M., Smith, A., Tarasov, K., Muller, M., Sotoodehnia, N., Sinner, M., Verwoert, G., Li, M., Kao, W., Kottgen, A., Coresh, J., Bis, J., Psaty, B., Rice, K., Rotter, J. & Rivadeneira, F. & 45 others, , 2010, In: Nature Genetics. 42, 2, p. 153-U89

Genomic Variation Associated With Mortality Among Adults of European and African Ancestry With Heart Failure The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

Morrison, A., Felix, J., Cupples, L., Glazer, N., Loehr, L., Dehghan, A., Demissie, S., Bis, J., Rosamond, W., Aulchenko, Y., Wang, Y., Haritunians, T., Folsom, A., Rivadeneira, F., Benjamin, E., Lumley, T., Couper, D., Stricker, B., O’Donnell, C. & Rice, K. & 14 others, , 2010, In: Circulation-cardiovascular genetics. 3, 3, p. 248-U64

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Allen, H., Estrada Gil, K., Lettre, G., Berndt, S., Weedon, M., Rivadeneira, F., Willer, C., Jackson, A., Vedantam, S., Raychaudhuri, S., Ferreira, T., Wood, A., Weyant, R., Segre, A., Speliotes, E., Wheeler, E., Soranzo, N., Park, J., Yang, J. & Gudbjartsson, D. & 270 others, , 2010, In: Nature. 467, 7317, p. 832-838 7 p.

Interactions between dietary vitamin E intake and SIRT1 genetic variation influence body mass index

Zillikens, M. C., van Meurs, J.Rivadeneira, F.Hofman, B., Oostra, B., Sijbrands, E. J. G., Witteman, J., Pols, H., Duijn, C. & Uitterlinden, A., 2010, In: American Journal of Clinical Nutrition. 91, 5, p. 1387-1393 7 p.

Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function

Hancock, D., Eijgelsheim, M., Wilk, J., Gharib, S., Loehr, L., Marciante, K., Franceschini, N., van Durme, Y., Chen, T., Barr, R., Schabath, M., Couper, D., Brusselle, G., Psaty, B., Duijn, C., Rotter, J., Uitterlinden, A.Hofman, B., Punjabi, N. & Rivadeneira, F. & 8 others, , 2010, In: Nature Genetics. 42, 1, p. 45-U61

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Heid, I., Jackson, A., Randall, J., Winkler, T., Qi, L., Steinthorsdottir, V., Thorleifsson, G., Zillikens, M. C., Speliotes, E., Magi, R., Workalemahu, T., White, C., Bouatia-Naji, N., Harris, T., Berndt, S., Ingelsson, E., Willer, C., Weedon, M., Luan, J. & Vedantam, S. & 280 others, , 2010, In: Nature Genetics. 42, 11, p. 949-U160

Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk Factors

Yang, Q., Kottgen, A., Dehghan, A., Smith, A., Glazer, N., Chen, M., Chasman, D., Aspelund, T., Eiriksdottir, G., Harris, T., Launer, L., Nalls, M., Hernandez, D., Arking, D., Boerwinkle, E., Grove, M., Li, M., Kao, W., Chonchol, M. & Haritunians, T. & 21 others, , 2010, In: Circulation-cardiovascular genetics. 3, 6, p. 523-530 8 p.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Dupuis, J., Langenberg, C., Prokopenko, I., Saxena, R., Soranzo, N., Jackson, A., Wheeler, E., Glazer, N., Bouatia-Naji, N., Gloyn, A., Lindgren, C., Magi, R., Morris, A., Randall, J., Johnson, T., Elliott, P., Rybin, D., Thorleifsson, G., Steinthorsdottir, V. & Henneman, P. & 283 others, , 2010, In: Nature Genetics. 42, 2, p. 105-U32

 

New loci associated with kidney function and chronic kidney disease

Kottgen, A., Pattaro, C., Boger, C., Fuchsberger, C., Olden, M., Glazer, N., Parsa, A., Gao, X., Yang, Q., Smith, A., O’Connell, J., Li, M., Schmidt, H., Tanaka, T., Isaacs, A., Ketkar, S., Hwang, S., Johnson, A., Dehghan, A. & Teumer, A. & 112 others, , 2010, In: Nature Genetics. 42, 5, p. 376-U34

 

Serum C reactive protein levels and genetic variation in the CRP gene are not associated with the prevalence, incidence or progression of osteoarthritis independent of body mass index

Kerkhof, H., Bierma – Zeinstra, S., Castano Betancourt, M., de Maat, M.Hofman, B., Pols, H., Rivadeneira, F., Witteman, J., Uitterlinden, A. & van Meurs, J., 2010, In: Annals of the Rheumatic Diseases. 69, 11, p. 1976-1982 7 p.

 

The Complement Component 5 Gene and Age-Related Macular Degeneration

Baas, D., Ho, L., Ennis, S., Merriam, J., Tanck, M., Uitterlinden, A., de Jong, P., Cree, A., Griffiths, H., Rivadeneira, F.Hofman, B., Duijn, C., Smith, R., Barile, G., Gorgels, T., Vingerling, H.Klaver, C., Lotery, A., Allikmets, R. & Bergen, A., 2010, In: Ophthalmology. 117, 3, p. 500-511 12 p.

The Role of Body Mass Index, Insulin, and Adiponectin in the Relation Between Fat Distribution and Bone Mineral Density

Zillikens, M. C., Uitterlinden, A.van Leeuwen, H., Berends, A., Henneman, P., van Dijk, K., Oostra, B., Duijn, C., Pols, H. & Rivadeneira, F., 2010, In: Calcified Tissue International. 86, 2, p. 116-125 10 p.

The T-13910C Polymorphism in the Lactase Phlorizin Hydrolase Gene Is Associated With Differences in Serum Calcium Levels and Calcium Intake

Koek, N., van Meurs, J.van der Eerden, B.Rivadeneira, F., Zillikens, M. C., Hofman, B., Obermayer-Pietsch, B., Lips, P., Pols, H., Uitterlinden, A. & van Leeuwen, H., 2010, In: Journal of Bone and Mineral Research. 25, 9, p. 1980-1987 8 p.

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

Freathy, R., Mook, D., Sovio, U., Prokopenko, I., Timpson, N., Berry, D., Warrington, N., Widen, E., Hottenga, J., Kaakinen, M., Lange, L., Bradfield, J., Kerkhof, M., Marsh, J., Magi, R., Chen, C., Lyon, H., Kirin, M., Adair, L. & Aulchenko, Y. & 63 others, , 2010, In: Nature Genetics. 42, 5, p. 430-U73

 

2009

Genetic variation in the GDF5 region is associated with osteoarthritis, height, hip axis length and fracture risk: The Rotterdam study

Vaes, R. B. A., Rivadeneira, F., Kerkhof, J. M., Hofman, A., Pols, H. A. P., Uitterlinden, A. G. & Van Meurs, J. B. J., Nov 2009, In: Annals of the Rheumatic Diseases. 68, 11, p. 1754-1760 7 p.

Tissue effect on genetic control of transcript isoform variation

Kwan, T., Grundberg, E., Koka, V., Ge, B., Lam, K. C. L., Dias, C., Kindmark, A., Mallmin, H., Ljunggren, Ö., Rivadeneira, F., Estrada, K., Van Meurs, J. B.Uitterlinden, A., Karlsson, M., Ohlsson, C., Mellström, D., Nilsson, O., Pastinen, T. & Majewski, J., 14 Aug 2009, In: PLoS Genetics. 5, 8, e1000608.

 

Gender specific effects of the calcium channel TRPV4 on osteoporotic fracture risk and osteoblast-osteoclast coupling

van der Eerden, B. C. J., Schreuders-Koedam, M., Rivadeneira, F.van Meurs, J. B., Hoenderop, J. G. J., Weinans, H., Suzuki, M., Bindels, R. J. M., Uitterlinden, A. G. & van Leeuwen, J. P. T. M., Jun 2009, In: Bone. 44, 2, p. S214 1 p., OC07.

Genome-wide association scan meta-analysis identifies three loci influencing adiposity and fat distribution

Lindgren, C. M., Heid, I. M., groep, Randall, J. C., Lamina, C., Steinthorsdottir, V., Qi, L., Speliotes, E. K., Thorleifsson, G., Willer, C. J., Herrera, B. M., Jackson, A. U., Lim, N., Scheet, P., Soranzo, N., Amin, N., Aulchenko, Y. S., Chambers, J. C., Drong, A. & Luan, J. N. A. & 31 others, , Jun 2009, In: PLoS Genetics. 5, 6, e1000508.

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

GIANT Consortium, Jan 2009, In: Nature Genetics. 41, 1, p. 25-34 10 p.

 

A genome-wide association study of acenocoumarol maintenance dosage

Teichert, M., Eijgelsheim, M., Rivadeneira, F.Uitterlinden, A.van Schaik, R.Hofman, B., de Smet, P., Gelder, T.Visser, L. & Stricker, B., 2009, In: Human Molecular Genetics. 18, 19, p. 3758-3768 11 p.

 

A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation

Estrada Gil, K., Krawczak, M., Schreiber, S., Duijn, J., Stolk, L., van Meurs, J.Liu, F., Penninx, B., Smit, J., Vogelzangs, N., Hottenga, J., Willemsen, G., de Geus, E., Lorentzon, M., von Eller-Eberstein, H., Lips, P., Schoor, N., Pop, V., de Keijzer, J. & Hofman, B. & 8 others, , 2009, In: Human Molecular Genetics. 18, 18, p. 3516-3524 9 p.

 

An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population

Lu, T., Lao Grueso, O., Nothnagel, M., Junge, O., Freitag-Wolf, S., Caliebe, A., Balascakova, M., Bertranpetit, J., Bindoff, L., Comas, D., Holmlund, G., Kouvatsi, A., Macek, M., Mollet, I., Nielsen, F., Parson, W., Palo, J., Ploski, R., Sajantila, A. & Tagliabracci, A. & 14 others, , 2009, In: European Journal of Human Genetics. 17, 7, p. 967-975 9 p.

Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

Dehghan, A., Yang, Q., Peters, A., Basu, S., Bis, J., Rudnicka, A., Kavousi, M., Chen, M., Baumert, J., Lowe, G., McKnight, B., Tang, W., de Maat, M., Larson, M., Eyhermendy, S., McArdie, W., Lumley, T., Pankow, J., Hofman, B. & Massaro, J. & 21 others, , 2009, In: Circulation-cardiovascular genetics. 2, 2, p. 125-133 9 p.

Body composition by dual-energy X-ray absorptiometry in women with previous pre-eclampsia or small-for-gestational-age offspring

Berends, A., Zillikens, M. C., de Groot, C., Rivadeneira, F., Oostra, B., Duijn, C. & Steegers, E., 2009, In: Bjog-An International Journal of Obstetrics and Gynaecology. 116, 3, p. 442-450 9 p.

 

Building the evidence for using genetic information to improve health and prevent disease

Uitterlinden, A.van Meurs, J. & Rivadeneira, F., 2009, Human genome epidemiology. Khoury, Gwinn, Bradley, Little, Higgins & Ioannidis (eds.). Oxford: Oxford University Press

 

Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture

Richards, J., Kavvoura, F., Rivadeneira, F., Styrkarsdottir, U., Estrada Gil, K., Halldorsson, B., Hsu, Y., Zillikens, M. C., Wilson, S., Mullin, B., Amin, N., Aulchenko, Y., Cupples, L., Deloukas, P., Demissie, S., Hofman, B., Kong, A., Karasik, D., van Meurs, J. & Oostra, B. & 14 others, , 2009, In: Annals of Internal Medicine. 151, 8, p. 528-U32

 

Common variants at ten loci influence QT interval duration in the QTGEN Study

Newton-Cheh, C., Eijgelsheim, M., Rice, K., de Bakker, P., Yin, X., Estrada Gil, K., Bis, J., Marciante, K., Rivadeneira, F., Noseworthy, P., Sotoodehnia, N., Smith, N., Rotter, J., Kors, J., Witteman, J., Hofman, B., Heckbert, S., O’Donnell, C., Uitterlinden, A. & Psaty, B. & 3 others, , 2009, In: Nature Genetics. 41, 4, p. 399-406 8 p.

 

 

Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

Johansson, A., Marroni, F., Hayward, C., Franklin, C., Kirichenko, A., Jonasson, I., Hicks, A., Vitart, V., Isaacs, A., Axenovich, T., Campbell, S., Dunlop, M., Floyd, J., Hastie, N., Hofman, B., Knott, S., Kolcic, I., Pichler, I., Polasek, O. & Rivadeneira, F. & 15 others, , 2009, In: Human Molecular Genetics. 18, 2, p. 373-380 8 p.

 

Dual energy X-ray absorptiometry analysis contributes to the prediction of hip osteoarthritis progression

Betancourt, M., van der Linden, J., Rivadeneira, F.Rozendaal, R.Bierma – Zeinstra, S. & Weinans, H., 2009, In: Arthritis Research & Therapy. 11, 6, p. 162

Genetic Variants Associated With Cardiac Structure and Function A Meta-analysis and Replication of Genome-wide Association Data

Vasan, R., Glazer, N., Felix, J., Lieb, W., Wild, P., Felix, S., Watzinger, N., Larson, M., Smith, N., Dehghan, A., Grosshennig, A., Schillert, A., Teumer, A., Schmidt, R., Kathiresan, S., Lumley, T., Aulchenko, Y., Konig, I., Zeller, T. & Homuth, G. & 48 others, , 2009, In: JAMA – Journal of the American Medical Association. 302, 2, p. 168-178 11 p.

Genome-wide association meta-analysis for total serum bilirubin levels

Johnson, A., Kavousi, M., Smith, A., Chen, M., Dehghan, A., Aspelund, T., Lin, J., Duijn, C., Harris, T., Cupples, L., Uitterlinden, A., Launer, L., Hofman, B.Rivadeneira, F.Stricker, B., Yang, Q., O’Donnell, C., Gudnason, V. & Witteman, J., 2009, In: Human Molecular Genetics. 18, 14, p. 2700-2710 11 p.

 

Genomewide Association Studies of Stroke

Ikram, A., Seshadri, S., Bis, J., Fornage, M., DeStefano, A., Aulchenko, Y., Debette, S., Lumley, T., Folsom, A., Medici – van den Herik, E.Bos, M., Beiser, A., Cushman, M., Launer, L., Shahar, E., Struchalin, M., Du, Y., Glazer, N., Rosamond, W. & Rivadeneira, F. & 26 others, , 2009, In: New England Journal of Medicine. 360, 17, p. 1718-1728 11 p.

 

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

van Es, M., Veldink, J., Saris, C., Blauw, H., Van Vught, P., Birve, A., Lemmens, R., Schelhaas, H., Groen, E., Huisman, M., van der Kooi, A., Visser, M., Dahlberg, C., Estrada Gil, K., Rivadeneira, F.Hofman, B., Zwarts, M., van Doormaal, P., Rujescu, D. & Strengman, E. & 34 others, , 2009, In: Nature Genetics. 41, 10, p. 1083-U53

Genome-wide association study of blood pressure and hypertension

Levy, D., Ehret, G., Rice, K., Verwoert, G., Launer, L., Dehghan, A., Glazer, N., Morrison, A., Johnson, A., Aspelund, T., Aulchenko, Y., Lumley, T., Kottgen, A., Vasan, R., Rivadeneira, F., Eiriksdottir, G., Guo, X., Arking, D., Mitchell, G. & Mattace Raso, F. U. S. & 24 others, , 2009, In: Nature Genetics. 41, 6, p. 677-687 11 p.

 

GRIMP: a web- and grid-based tool for high-speed analysis of large-scale genome-wide association using imputed data

Estrada Gil, K., Abuseiris, A., Grosveld, F.Uitterlinden, A., Knoch, T. & Rivadeneira, F., 2009, In: Bioinformatics. 25, 20, p. 2750-2752 3 p.

Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration

Eijgelsheim, M., Aarnoudse, A., Rivadeneira, F.Kors, J., Witteman, J., Hofman, B., Duijn, C., Uitterlinden, A. & Stricker, B., 2009, In: Human Molecular Genetics. 18, 2, p. 347-357 11 p.

 

Loci at chromosomes 13, 19 and 20 influence age at natural menopause

Stolk, L., Zhai, G., van Meurs, J.Verbiest, M.Visser, J., Estrada Gil, K., Rivadeneira, F., Williams, F., Cherkas, L., Deloukas, P., Soranzo, N., Keyzer, J., Pop, V., Lips, P., Lebrun, C., van der Schouw, Y., Grobbee, D., Witteman, J., Hofman, B. & Pols, H. & 3 others, , 2009, In: Nature Genetics. 41, 6, p. 645-647 3 p.

Low prevalence of NOD2 SNPs in Behcet’s disease suggests protective association in Caucasians

Kappen, J., Wallace, G., Stolk, L., Rivadeneira, F.Uitterlinden, A.van Daele, P., Laman, J., Kuijpers, R., Baarsma, G., Stanford, M., Fortune, F., Madanat, W., van Hagen, P. M. & van Laar, J., 2009, In: Rheumatology. 48, 11, p. 1375-1377 3 p.

Meta-analysis of genome-wide association data identifies two loci influencing age at menarche

Perry, J., Stolk, L., Franceschini, N., Lunetta, K., Zhai, G., McArdle, P., Smith, A., Aspelund, T., Bandinelli, S., Boerwinkle, E., Cherkas, L., Eiriksdottir, G., Estrada Gil, K., Ferrucci, L., Folsom, A., Garcia, M., Gudnason, V., Hofman, B., Karasik, D. & Kiel, D. & 19 others, , 2009, In: Nature Genetics. 41, 6, p. 648-650 3 p.

 

Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size

Soranzo, N., Rivadeneira, F., Chinappen-Horsley, U., Malkina, I., Richards, J., Hammond, N., Stolk, L., Nica, A., Inouye, M., Hofman, B., Stephens, J., Wheeler, E., Arp, P., Gwilliam, R., Jhamai, P., Potter, S., Chaney, A., Ghori, M., Ravindrarajah, R. & Ermakov, S. & 18 others, , 2009, In: PLoS Genetics (print). 5, 4

 

Multiple loci associated with indices of renal function and chronic kidney disease

Kottgen, A., Glazer, N., Dehghan, A., Hwang, S., Katz, R., Li, M., Yang, Q., Gudnason, V., Launer, L., Harris, T., Smith, A., Arking, D., Astor, B., Boerwinkle, E., Ehret, G., Ruczinski, I., Scharpf, R., Chen, Y., de Boer, I. & Haritunians, T. & 19 others, , 2009, In: Nature Genetics. 41, 6, p. 712-717 6 p.

NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium

Heard-Costa, N., Zillikens, M. C., Monda, K., Johansson, A., Harris, T., Fu, M., Haritunians, T., Feitosa, M., Aspelund, T., Eiriksdottir, G., Garcia, M., Launer, L., Smith, A., Mitchell, B., McArdle, P., Shuldiner, A., Bielinski, S., Boerwinkle, E., Brancati, F. & Demerath, E. & 41 others, , 2009, In: PLoS Genetics (print). 5, 6

 

Population genomics in a disease targeted primary cell model

Grundberg, E., Kwan, T., Ge, B., Lam, K., Koka, V., Kindmark, A., Mallmin, H., Dias, J., Verlaan, D., Ouimet, M., Sinnett, D., Rivadeneira, F., Estrada Gil, K., Hofman, B., van Meurs, J., Uitterlinden, A., Beaulieu, P., Graziani, A., Harmsen, E. & Ljunggren, O. & 5 others, , 2009, In: Genome Research. 19, 11, p. 1942-1952 11 p.

Practical Operationalizations of Risk Factors for Fracture in Older Women: Results From Two Longitudinal Studies

Pluijm, S., Steyerberg, E., Kuchuk, N., Rivadeneira, F., Looman, C., Schoor, N., Koes, B.Mackenbach, J., Lips, P. & Pois, H., 2009, In: Journal of Bone and Mineral Research. 24, 3, p. 534-542 9 p.

Simple Risk Score for the Assessment of Absolute Fracture Risk in General Practice Based on Two Longitudinal Studies

Pluijm, S., Koes, B., de Laet, C., Schoor, N., Kuchuk, N., Rivadeneira, F.Mackenbach, J., Lips, P., Pols, H. & Steyerberg, E., 2009, In: Journal of Bone and Mineral Research. 24, 5, p. 768-774 7 p.

SIRT1 genetic variation and mortality in type 2 diabetes: interaction with smoking and dietary niacin

Zillikens, M. C., van Meurs, J.Sijbrands, E. J. G.Rivadeneira, F., Dehghan, A., van Leeuwen, H.Hofman, B., Duijn, C., Witteman, J., Uitterlinden, A. & Pols, H., 2009, In: Free Radical Biology and Medicine. 46, 6, p. 836-841 6 p.

SIRT1 Genetic Variation Is Related to BMI and Risk of Obesity

Zillikens, M. C., van Meurs, J.Rivadeneira, F.Amin, N.Hofman, B., Oostra, B., Sijbrands, E. J. G., Witteman, J., Pols, H., Duijn, C. & Uitterlinden, A., 2009, In: Diabetes. 58, 12, p. 2828-2834 7 p.

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

Rivadeneira, F., Styrkarsdottir, U., Estrada Gil, K., Halldorsson, B., Hsu, Y., Richards, J., Zillikens, M. C., Kavvoura, F., Amin, N., Aulchenko, Y., Cupples, L., Deloukas, P., Demissie, S., Grundberg, E., Hofman, B., Kong, A., Karasik, D., van Meurs, J., Oostra, B. & Pastinen, T. & 15 others, , 2009, In: Nature Genetics. 41, 11, p. 1199-U58

 

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

Benjamin, E., Rice, K., Arking, D., Pfeufer, A., Noord, C., Smith, A., Schnabel, R., Bis, J., Boerwinkle, E., Sinner, M., Dehghan, A., Lubitz, S., D’Agostino, R., Lumley, T., Ehret, G., Heeringa, J., Aspelund, T., Newton-Cheh, C., Larson, M. & Marciante, K. & 36 others, , 2009, In: Nature Genetics. 41, 8, p. 879-881 3 p.

 

2008

Gender Specific Effects of TRPV4 on Osteoblast-Osteoclast Coupling and Risk of Osteoporotic Fractures

van der Eerden, B. C. J.Koedam, M.Rivadeneira, F.van Meurs, J. B. J., Hoenderop, J. G. J., Weinans, H., Suzuki, M., Bindels, R. J. M., Uitterlinden, A. G. & van Leeuwen, J. P. T. M., 13 Aug 2008, In: Journal of Bone and Mineral Research. 23, supplement 1, p. S200-S200 1 p., SA355.

Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: The GENOMOS study

APOSS investigatorsDOPS investigatorsEPOS investigatorsEPOLOS investigatorsFAMOS investigatorsLASA investigatorsERGO investigators, Langdahl, B. L., Uitterlinden, A. G., Ralston, S. H., Trikalinos, T. A., Balcells, S., Brandi, M. L., Scollen, S., Lips, P., Lorenc, R., Obermayer-Pietsch, B., Reid, D. M., Armas, J. B. & Arp, P. P. & 25 others, , May 2008, In: Bone. 42, 5, p. 969-981 13 p.

Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene

Kayser, M.Liu, F., Janssens, C., Rivadeneira, F., Lao Grueso, O., Duijn, J., Vermeulen, M., Arp, P., Jhamai, M., van Ijcken, W., Dunnen, J., Heath, S., Zelenika, D., Despriet, D., Klaver, C.Vingerling, H., de Jong, P., Hofman, B., Aulchenko, Y. & Uitterlinden, A. & 2 others, , 8 Feb 2008, In: American Journal of Human Genetics. 82, 2, p. 411-423 13 p.

Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study

Dehghan, A., Kottgen, A., Yang, Q., Hwang, S., Kao, W., Rivadeneira, F., Boerwinkle, E., Levy, D., Hofman, B., Astor, B., Benjamin, E., Duijn, C., Witteman, J., Coresh, J. & Fox, C., 2008, In: Lancet (UK). 372, 9654, p. 1953-1961 9 p.

 

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study

Richards, J., Rivadeneira, F., Inouye, M., Pastinen, T., Soranzo, N., Wilson, S., Andrew, T., Falchi, M., Gwilliam, R., Ahmadi, K., Valdes, A., Arp, P., Whittaker, P., Verlaan, D., Jhamai, M., Kumanduri, V., Moorhouse, M., van Meurs, J.Hofman, B. & Pols, H. & 8 others, , 2008, In: Lancet (UK). 371, 9623, p. 1505-1512 8 p.

 

Correlation between genetic and geographic structure in Europe

Lao Grueso, O., Lu, T., Nothnagel, M., Junge, O., Freitag-Wolf, S., Caliebe, A., Balascakova, M., Bertranpetit, J., Bindoff, L., Comas, D., Hoimlund, G., Kouvatsi, A., Macek, M., Mollet, I., Parson, W., Palo, J., Ploski, R., Sajantila, A., Tagliabracci, A. & Gether, U. & 13 others, , 2008, In: Current Biology. 18, 16, p. 1241-1248 8 p.

 

Effects of serum TSH and FT4 levels and the TSHR-Asp727Glu polymorphism on bone: the Rotterdam Study

Deure, W., Uitterlinden, A.Hofman, B.Rivadeneira, F., Pols, H., Peeters, R. & Visser, T., 2008, In: Clinical Endocrinology. 68, 2, p. 175-181 7 p.

Estrogen receptor alpha polymorphisms and postmenopausal breast cancer risk

Gonzalez Zuloeta Ladd, A., Vasquez, A., Rivadeneira, F., Siemes, C., Hofman, B.Stricker, B., Pols, H., Uitterlinden, A. & Duijn, C., 2008, In: Breast Cancer Research and Treatment. 107, 3, p. 415-419 5 p.

Fractures are not in genes – Authors’ reply

Richards, J. B., Rivadeneira, F.Uitterlinden, A. G. & Spector, T. D., 2008, In: The Lancet. 372, 9648, p. 1460 1 p.

 

Genetic Determinants of Osteoporosis

Uitterlinden, A. G.Rivadeneira, F.van Leeuwen, H. P. T. M.van Meurs, J. B. J. & Pols, H. A. P., 2008, Osteoporosis, Two-Volume Set. Third edition ed. Academic Press, Vol. I. p. 759-798 40 p.

 

Genome-wide association for loci influencing entrepreneurial behavior: The Rotterdam Study

Groenen, P.Hofman, B., Koellinger, P., van der Loos, M., Rivadeneira, F.van Rooij, F.Thurik, R. & Uitterlinden, A., 2008, In: Behavior Genetics. 38, 6, p. 628-629 2 p.

 

Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis

van Meurs, J., Trikalinos, T., Ralston, S., Balcells, S., Brandi, M., Brixen, K., Kiel, D., Langdahl, B., Lips, P., Ljunggren, O., Lorenc, R., Obermayer-Pietsch, B., Ohlsson, C., Pettersson, U., Reid, D., Rousseau, F., Scollen, S., van Hul, W., Agueda, L. & Akesson, K. & 23 others, , 2008, In: JAMA – Journal of the American Medical Association. 299, 11, p. 1277-1290 14 p.

 

Large-scale analysis of association between polymorphisms in the transfonning growth factor beta 1 gene (TGFB1) and osteoporosis: The GENOMOS study

Langdahl, B., Uitterlinden, A., Ralston, S., Trikalinos, T., Balcells, S., Brandi, M., Scollen, S., Lips, P., Lorenc, R., Obermayer-Pietsch, B., Reid, D., Armas, J., Arp, P., Bassiti, A., Bustamante, M., Husted, L., Carey, A., Cano, R., Dobnig, H. & Dunning, A. & 18 others, , 2008, In: Bone. 42, 5, p. 969-981 13 p.

 

Low dietary riboflavin but not folate predicts increased fracture risk in postmenopausal women homozygous for the MTHFR 677 T allele

Yazdan Panah, M., Uitterlinden, A., Zillikens, M. C., Jhamai, M., Rivadeneira, F.Hofman, B., Jonge, R., Lindemans, J., Pols, H. & van Meurs, J., 2008, In: Journal of Bone and Mineral Research. 23, 1, p. 86-94 9 p.

 

Radiographic osteoarthritis at three joint sites and FRZB, LRP5, and LRP6 polymorphisms in two population-based cohorts.

Kerkhof, H., Uitterlinden, A., Valdes, A., Hart, D., Rivadeneira, F., Jhamai, M., Hofman, B., Pols, H., Bierma – Zeinstra, S., Spector, T. & van Meurs, J., 2008, In: Osteoarthritis and Cartilage. 16, 10, p. 1141-1149 9 p.

 

Sex-specific genetic effects influence variation in body composition

Zillikens, M. C., Yazdan Panah, M., Pardo, L.Rivadeneira, F., Aulchenko, Y., Oostra, B., Uitterlinden, A., Pols, H. & Duijn, C., 2008, In: Diabetologia. 51, 12, p. 2233-2241 9 p.

2007

The-1997 G/T and sp1 polymorphisms in the collagen type I alpha1 (COLIA1) gene in relation to changes in femoral neck bone mineral density and the risk of fracture in the elderly: The Rotterdam study

Yazdan Panah, M., Rivadeneira, F.van Meurs, J., Zillikens, M. C., Arp, P., Hofman, B., Duijn, C., Pols, H. & Uitterlinden, A., 7 Jun 2007, In: Calcified Tissue International. 81, 1, p. 18-25 8 p.

Gender differences in calcium homeostasis: A reflection of aging?

Koek, W. N. H., van der Eerden, B. C. J., de Rijke, Y. B., Rivadeneira, F., Zillikens, M. C., Pols, H. A. P. & van Leeuwen, J. P. T. M., May 2007, In: Calcified Tissue International. 80, p. S163 1 p., P471-M.

 

A polymorphism in the AMH type II receptor gene is associated with age at menopause in interaction with parity

Kevenaar, M., Themmen, A., Rivadeneira, F.Uitterlinden, A.Laven, J., Schoor, N., Lips, P., Pols, H. & Visser, J., 2007, In: Human Reproduction. 22, 9, p. 2382-2388 7 p.

 

Effect of dietary B vitamins on BMD and risk of fracture in elderly men and women: The Rotterdam Study

Yazdan Panah, M., Zillikens, M. C., Rivadeneira, F., de Jong, R., Lindemans, J., Uitterlinden, A., Pols, H. & van Meurs, J., 2007, In: Bone. 41, 6, p. 987-994 8 p.

 

Femoral neck BMD is a strong predictor of hip fracture susceptibility in elderly men and women because it detects cortical bone instability: The Rotterdam study

Rivadeneira, F., Zillikens, M. C., de Laet, C., Hofman, B.Uitterlinden, A., Beck, T. & Pols, H., 2007, In: Journal of Bone and Mineral Research. 22, 11, p. 1781-1790 10 p.

 

Genome-wide association study identifies novel breast cancer susceptibility loci

Easton, D., Pooley, K., Dunning, A., Pharoah, P., Thompson, D., Ballinger, D., Struewing, J., Morrison, J., Field, H., Luben, R., Wareham, N., Ahmed, S., Healey, C., Bowman, R., Meyer, K., Haiman, C., Kolonel, L., Henderson, B., Le Marchand, L. & Brennan, P. & 79 others, , 2007, In: Nature. 447, 7148, p. 1087-U7

 

Vitamin D receptor gene haplotype is associated with body height and bone size

Fang, Y., van Meurs, J.Rivadeneira, F., Schoor, N., van Leeuwen, J., Lips, P., Pols, H. & Uitterlinden, A., 2007, In: Journal of Clinical Endocrinology and Metabolism. 92, 4, p. 1491-1501 11 p.

2006

Estrogen receptor beta (ESR2) polymorphisms in interaction with estrogen receptor alpha (ESR1) and insulin-like growth factor I (IGF1) variants influence the risk of fracture in postmenopausal women

Rivadeneira, F.van Meurs, J., Kant, J., Zillikens, M. C., Stolk, L., Beck, T., Arp, P., Schuit, S., Hofman, B., Houwing-Duistermaat, J., Duijn, C., van Leeuwen, H., Pols, H. & Uitterlinden, A., Sept 2006, In: Journal of Bone and Mineral Research. 21, 9, p. 1443-1456 14 p.

 

The association between common vitamin D receptor gene variations and osteoporosis: A participant-level meta-analysis

APOSS investigatorsEPOS investigatorsEPOLOS investigatorsFAMOS investigatorsLASA investigatorsRotterdam Study investigatorsUitterlinden, A., Ralston, S. H., Brandi, M. L., Carey, A. H., Grinberg, D., Langdahl, B. L., Lips, P., Lorenc, R., Obermayer-Pietsch, B., Reeve, J., Reid, D. M., Amedei, A., Bassiti, A. & Bustamante, M. & 21 others, , 15 Aug 2006, In: Annals of Internal Medicine. 145, 4, p. 255-264 10 p.

BMP-2 gene polymorphisms and osteoporosis: The Rotterdam Study

Medici, M.van Meurs, J.Rivadeneira, F., Zhao, H., Arp, P., Hofman, B., Pols, H. & Uitterlinden, A., 2006, In: Journal of Bone and Mineral Research. 21, 6, p. 845-854 10 p.

 

Common genetic variation of the low-density lipoprotein receptor-related protein 5 and 6 genes determines fracture risk in elderly white men

van Meurs, J.Rivadeneira, F.Jhamai, M., Hugens, W., Hofman, B.van Leeuwen, H., Pols, H. & Uitterlinden, A., 2006, In: Journal of Bone and Mineral Research. 21, 1, p. 141-150 10 p.

 

Heritability of fasting glucose levels in a young genetically isolated population

Santos, R., Zillikens, M. C., Rivadeneira, F., Pols, H., Oostra, B., Duijn, C. & Aulchenko, Y., 2006, In: Diabetologia. 49, 4, p. 667-672 6 p.

Identifying genetic risk factors for osteoporosis

Uitterlinden, A.van Meurs, J.Rivadeneira, F. & Pols, H., 2006, In: The Journal of Musculoskeletal Neuronal Interactions. 6, p. 16-26 11 p.

Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: The GENOMOS study (vol 3, pg 223, 2006)

Ralston, S., Uitterlinden, A., Brandi, M., Balcells, S., Langdahl, B., Lips, P., Lorenc, R., Obermayer-Pietsch, B., Scollen, S., Bustamante, M., Husted, L., Carey, A., Diez-Perez, A., Dunning, A., Falchetti, A., Karczmarewicz, E., Kruk, M., van Leeuwen, H.van Meurs, J. & Mangion, J. & 11 others, , 2006, In: PLoS Medicine (print). 3, 5, p. 704-704 1 p.

 

The Role of Genetic Variation in Osteoporosis

Uitterlinden, A. G.van Meurs, J. B. J.Rivadeneira, F.van Leeuwen, J. P. T. M. & Pols, H. A. P., 2006, Dynamics of Bone and Cartilage Metabolism: Principles and Clinical Applications. 2 ed. Elsevier Inc., p. 471-485 15 p.

Vitamin D receptor gene BsmI and TaqI polymorphisms and fracture risk: A meta-analysis

Fang, Y., Rivadeneira, F.van Meurs, J., Pols, H., Ioannidis, J. & Uitterlinden, A., 2006, In: Bone. 39, 4, p. 938-945 8 p.

 

2005

Promoter and 3 ‘-untranslated-region haplotypes in the vitamin D receptor gene predispose to osteoporotic fracture: The Rotterdam study

Fang, Y., van Meurs, J., d’Alesio, A., Jhamai, M., Zhao, H., Rivadeneira, F.Hofman, B.van Leeuwen, H., Jehan, F., Pols, H. & Uitterlinden, A., 2005, In: American Journal of Human Genetics. 77, 5, p. 807-823 17 p.

 

2004

Osteoporosis: from genes to phenotypes

Rivadeneira, F., 10 Nov 2004, Erasmus Universiteit Rotterdam (EUR). 196 p.

 

A polymorphic CA repeat in the IGF-I gene is associated with gender-specific differences in body height, but has no effect on the secular trend in body height

Rietveld, I., Janssen, J. A. M. J. L.van Rossum, L., Houwing-Duistermaat, J., Rivadeneira, F.Hofman, B., Pols, H., Duijn, C. & Lamberts, S. W. J., 2004, In: Clinical Endocrinology. 61, p. 195-203 9 p.

Insulin-like growth factor I gene promoter polymorphism, collagen type IIa1 (COL2A1) gene, and the prevalence of radiographic osteoarthritis: the Rotterdam Study

Zhai, G., Rivadeneira, F., Houwing-Duistermaat, J., Meulenbelt, I., Bijkerk, C., Hofman, B.van Meurs, J.Uitterlinden, A., Pols, H., Slagboom, P. & Duijn, C., 2004, In: Annals of the Rheumatic Diseases. 63, p. 544-548 5 p.

Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites

Uitterlinden, A., Arp, P., Paeper, B., Charmley, P., Proll, S., Rivadeneira, F., Fang, Y., van Meurs, J., Britschgi, T., Latham, J., Chatzman, R., Pols, H. & Brunkow, M., 2004, In: American Journal of Human Genetics. 75, 6, p. 1032-1045 14 p.

 

The influence of an insulin-like growth factor I gene promoter polymorphism on hip bone geometry and the risk of nonvertebral fracture in the elderly: the Rotterdam Study

Rivadeneira, F., Houwing-Duistermaat, J., Beck, T., Janssen, J. A. M. J. L.Hofman, B., Pols, H., Duijn, C. & Uitterlinden, A., 2004, In: Journal of Bone and Mineral Research. 19, 8, p. 1280-1290 11 p.

2003

Association between an insulin-like growth factor I gene promoter polymorphism and bone mineral density in the elderly: the Rotterdam Study

Rivadeneira, F., Houwing-Duistermaat, J., Vaessen, N., Drop, J., Hofman, B., Pols, H., Duijn, C. & Uitterlinden, A., 2003, In: Journal of Clinical Endocrinology and Metabolism. 88, 8, p. 3878-3884 7 p.

 

2011

The Alliance for Better Bone Health Iain T Boyle Award – European Calcified Tissue Society

2015

World’s Most Influential Scientific Minds – Thomson Reuters Highly Cited Researcher

Fuller Albright Award – American Society for Bone and Mineral Research

2023
Medicine in Netherlands Leader Award – Research.com

Genetics in Netherlands Leader Award – Research.com

2022

Genetics and Molecular Biology in Netherlands Leader Award – Research.com

European Research Council Advance Grand(ERC, LEGENDARE,101021500)

Bone Fragility In Diabetes in Europe – towards a persona Lised medIcine approach (FIDELIO-ITN);

GEnomics of MusculoSkeletal traits TranslatiOnal Network – GEMSTONE(CA18139 Cost Action);

From genetic discoveries to clinical applications – comprehensive phenotyping of the musculoskeletal system (ZonMW VIDI-016-136-367);

 Pleiotropy and Phenomics of Musculoskeletal Aging – (NIH-NIAAMS);

Genetic Factors of Osteoporosis – (GEFOS) (EC-FP7-HEALTH- F2-2008-201865);