Author:
Liu Jimmy Z.,Medland Sarah E.,Wright Margaret J.,Henders Anjali K.,Heath Andrew C.,Madden Pamela A. F.,Duncan Alexis,Montgomery Grant W.,Martin Nicholas G.,McRae Allan F.
Abstract
AbstractHuman height and body mass index are influenced by a large number of genes, each with small effects, along with environment. To identify common genetic variants associated with these traits, we performed genome-wide association studies in 11,536 individuals composed of Australian twins, family members, and unrelated individuals at ∼550,000 genotyped SNPs. We identified a single genome-wide significant variant for height (Pvalue = 1.06 × 10–9) located inHHIP, a well-replicated height-associated gene. Suggestive levels of association were found for other known genes associated with height (Pvalues < 1 × 10–6):ADAMTSL3,EFEMP1,GPR126, andHMGA2; and BMI (Pvalues < 1 × 10–4):FTOandMC4R. Together, these variants explain less than 2% of total phenotypic variation for height and 0.5% for BMI.
Publisher
Cambridge University Press (CUP)
Subject
Genetics(clinical),Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Cited by
56 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献