Serum fasting cortisol in relation to bone, and the role of genetic variations in the glucocorticoid receptor. by van Schoor, N, Dennison, E, Lips, P, Uitterlinden, A, Cooper, C

BMI-associated alleles do not constitute risk alleles for polycystic ovary syndrome independently of BMI: a case-control study by Louwers, Y, Rayner, N, Herrera, B, Stolk, L, Groves, C, Barber, T, Uitterlinden, A, Franks, S, Laven, J, McCarthy, M

Genetic variation underlying cognition and its relation with neurological outcomes and brain imaging by Knol, M, Heshmatollah, A, Cremers, L, Ikram, M, Uitterlinden, A, Van Duijn, C, Niessen, W, Vernooij, M, Ikram, M, Adams, H

GDF5 single-nucleotide polymorphism rs143383 is associated with lumbar disc degeneration in Northern European women. by Williams, F, Popham, M, Hart, D, de Schepper, E, Bierma-Zeinstra, S, Hofman, A, Uitterlinden, A, Arden, N, Cooper, C, Spector, T, Valdes, A, van Meurs, J

Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease by Robak, L, Jansen, I, Van Rooij, J, Uitterlinden, A, Kraaij, R, Jankovic, J, International Parkinson’S Disease Genomics Consortium (Ipdgc), Heutink, P, Shulman, J, Hu, M

GDF5 SNP rs143383 is associated with lumbar disc disease in northern European women. by Williams, F, Popham, M, Hart, D, de Schepper, E, Bierma-Zeinstra, S, Hofman, A, Uitterlinden, A, Arden, N, Cooper, C, Spector, T, Valdes, A, van Meurs, J

Relationship between gut microbiota and circulating metabolites in population-based cohorts by Vojinovic, D, Radjabzadeh, D, Kurilshikov, A, Amin, N, Wijmenga, C, Franke, L, Ikram, M, Uitterlinden, A, Zhernakova, A, Fu, J, Kraaij, R, van Duijn, C

Whole-genome linkage scan combined with exome sequencing identifies novel candidate genes for carotid intima-media thickness by Vojinovic, D, Kavousi, M, Ghanbari, M, Brouwer, R, Van Rooij, J, Van Den Hout, M, Kraaij, R, Van Ijcken, W, Uitterlinden, A, Van Duijn, C, Amin, N

Prediction model for knee osteoarthritis incidence, including clinical, genetic and biochemical risk factors. by Kerkhof, H, Bierma-Zeinstra, S, Arden, N, Metrustry, S, Castano-Betancourt, M, Hart, D, Hofman, A, Rivadeneira, F, Oei, E, Spector, T, Uitterlinden, A, Janssens, A, Valdes, A, van Meurs, J

Large scale prospective meta-analysis of BMD and fracture in relation to COLIA1 Sp1 polymorphism: The GENOMOS study. by Ralston, S, Uitterlinden, A, Balcells, S, Brandi, M, Carey, A, Langdahl, B, Lorenc, R, Nogues, X, Obermayer-Pietsch, B, Reeve, J, Reid, D, Pols, H, van Schoor, N, Ioannidis, J

LDL-RECEPTOR RELATED PROTEIN 5 GENE POLYMORPHISMS INFLUENCE THE NORMAL VARIATION OF BONE MINERAL DENSITY by Koay, A, Duncan, E, Ralston, S, Compston, J, Cooper, C, Keen, R, Langdahl, B, MacLelland, A, O'Riordan, J, Pols, H, Reid, D, Uitterlinden, A, Wass, J, Brown, M

PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton. by Vilariño-Güell, C, Miles, L, Duncan, E, Ralston, S, Compston, J, Cooper, C, Langdahl, B, Maclelland, A, Pols, H, Reid, D, Uitterlinden, A, Steer, C, Tobias, J, Wass, J, Brown, M

Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysms by van 't Hof, F, Vaucher, J, Holmes, M, de Wilde, A, Baas, A, Blankensteijn, J, Hofman, A, Kiemeney, L, Rivadeneira, F, Uitterlinden, A, Vermeulen, S, Rinkel, G, de Bakker, P, Ruigrok, Y

Large scale meta-analysis of urinary C-terminal telopeptide, serum cartilage oligomeric protein and matrix metalloprotease degraded type II collagen and their role in prevalence, i... by Valdes, A, Meulenbelt, I, Chassaing, E, Arden, N, Bierma-Zeinstra, S, Hart, D, Hofman, A, Karsdal, M, Kloppenburg, M, Kroon, H, Slagboom, E, Spector, T, Uitterlinden, A, van Meurs, J, Bay-Jensen, A

Large scale meta-analysis of urinary C-terminal telopeptide, serum cartilage oligomeric protein and matrix metalloprotease degraded type II collagen and their role in prevalence, i... by Valdes, A, Hart, D, Spector, T, Meulenbelt, I, Slagboom, E, Chassaing, E, Arden, N, Bierma-Zeinstra, S, Hofman, A, Uitterlinden, A, Karsdal, M, Bay-Jensen, A, Kloppenburg, M, Van Meurs, J, Kroon, H

META-ANALYSIS IDENTIFIES NOVEL GENES INFLUENCING LEVELS OF THE POTENTIAL OA BIOMARKERS SCOMP AND UCTX2 by Ramos, Y, van Meurs, J, Valdes, A, Metrustry, S, Hart, D, Arden, N, Kloppenburg, M, Lafeber, F, van Spil, E, Karsdal, M, Bay-Jensen, A, Spector, T, Uitterlinden, A, Slagboom, P, Meulenbelt, I

Assessment of cumulative evidence on genetic associations: interim guidelines. by Ioannidis, J, Boffetta, P, Little, J, O'Brien, T, Uitterlinden, A, Vineis, P, Balding, D, Chokkalingam, A, Dolan, S, Flanders, W, Higgins, J, McCarthy, M, McDermott, D, Page, G, Rebbeck, T, Seminara, D, Khoury, M

Influence of LRP5 polymorphisms on normal variation in BMD. by Koay, M, Woon, P, Zhang, Y, Miles, L, Duncan, E, Ralston, S, Compston, J, Cooper, C, Keen, R, Langdahl, B, MacLelland, A, O'Riordan, J, Pols, H, Reid, D, Uitterlinden, A, Wass, J, Brown, M

Loci for regulation of bone mineral density in men and women identified by genome wide linkage scan: the FAMOS study. by Ralston, S, Galwey, N, MacKay, I, Albagha, O, Cardon, L, Compston, J, Cooper, C, Duncan, E, Keen, R, Langdahl, B, McLellan, A, O'Riordan, J, Pols, H, Reid, D, Uitterlinden, A, Wass, J, Bennett, S

Cross-calibration of dual-energy X-ray densitometers for a large, multi-center genetic study of osteoporosis. by Reid, D, Mackay, I, Wilkinson, S, Miller, C, Schuette, D, Compston, J, Cooper, C, Duncan, E, Galwey, N, Keen, R, Langdahl, B, McLellan, A, Pols, H, Uitterlinden, A, O'Riordan, J, Wass, J, Ralston, S, Bennett, S