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

Wang TJ, Zhang F, Richards JB, Kestenbaum B, van Meurs JB, Berry D, Kiel DP, Streeten EA, Ohlsson C, Koller DL, Peltonen L, Cooper JD, O'Reilly PF, Houston DK, Glazer NL, Vandenput L, Peacock M, Shi J, Rivadeneira F, McCarthy MI, Anneli P, de Boer IH, Mangino M, Kato B, Smyth DJ, Booth SL, Jacques PF, Burke GL, Goodarzi M, Cheung CL, Wolf M, Rice K, Goltzman D, Hidiroglou N, Ladouceur M, Wareham NJ, Hocking LJ, Hart D, Arden NK, Cooper C, Malik S, Fraser WD, Hartikainen AL, Zhai G, Macdonald HM, Forouhi NG, Loos RJ, Reid DM, Hakim A, Dennison E, Liu Y, Power C, Stevens HE, Jaana L, Vasan RS, Soranzo N, Bojunga J, Psaty BM, Lorentzon M, Foroud T, Harris TB, Hofman A, Jansson JO, Cauley JA, Uitterlinden AG, Gibson Q, Järvelin MR, Karasik D, Siscovick DS, Econs MJ, Kritchevsky SB, Florez JC, Todd JA, Dupuis J, Hyppönen E, Spector TD
Lancet. 2010 376 (9736): 180-8

PMID: 20541252 · PMCID: PMC3086761 · DOI:10.1016/S0140-6736(10)60588-0

MeSH Terms (20)

Canada Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 11 Cohort Studies Dietary Supplements Europe European Continental Ancestry Group Genetic Predisposition to Disease Genome-Wide Association Study Heterozygote Homozygote Humans Immunoassay International Cooperation Linkage Disequilibrium Polymorphism, Single Nucleotide Seasons United States Vitamin D Vitamin D Deficiency

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