Article
Common variants in the GDF5-UQCC region are associated with variation in human height.
Nature genetics - 1 Feb 2008
Sanna Serena, Jackson Anne U, Nagaraja Ramaiah, Willer Cristen J, Chen Wei-Min, Bonnycastle Lori L, Shen Haiqing, Timpson Nicholas, Lettre Guillaume, Usala Gianluca, Chines Peter S, Stringham Heather M, Scott Laura J, Dei Mariano, Lai Sandra, Albai Giuseppe, Crisponi Laura, Naitza Silvia, Doheny Kimberly F, Pugh Elizabeth W, Ben-Shlomo Yoav, Ebrahim Shah, Lawlor Debbie A, Bergman Richard N, Watanabe Richard M, Uda Manuela, Tuomilehto Jaakko, Coresh Josef, Hirschhorn Joel N, Shuldiner Alan R, Schlessinger David, Collins Francis S, Davey Smith George, Boerwinkle Eric, Cao Antonio, Boehnke Michael, Abecasis Gonçalo R, Mohlke Karen L
Abstract excerpt
Identifying genetic variants that influence human height will advance our understanding of skeletal growth and development. Several rare genetic variants have been convincingly and reproducibly associated with height in mendelian syndromes, and common variants in the transcription factor gene HMGA2 are associated with variation in height in the general population. Here we report genome-wide association analyses,...
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