Common variants in the GDF5-UQCC region are associated with variation in human height

Serena Sanna, Anne U. Jackson, Ramaiah Nagaraja, Cristen J. Willer, Wei Min Chen, Lori L. Bonnycastle, Haiqing Shen, Nicholas Timpson, Guillaume Lettre, Gianluca Usala, Peter S. Chines, Heather M. Stringham, Laura J. Scott, Mariano Dei, Sandra Lai, Giuseppe Albai, Laura Crisponi, Silvia Naitza, Kimberly F. Doheny, Elizabeth W. PughYoav Ben-Shlomo, Shah Ebrahim, Debbie A. Lawlor, Richard N. Bergman, Richard M. Watanabe, Manuela Uda, Jaakko Tuomilehto, Josef Coresh, Joel N. Hirschhorn, Alan R. Shuldiner, David Schlessinger, Francis S. Collins, George Davey Smith, Eric Boerwinkle, Antonio Cao, Michael Boehnke, Gonçalo R. Abecasis, Karen L. Mohlke

Research output: Contribution to journalArticlepeer-review

Abstract

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, using genotyped and imputed markers, of 6,669 individuals from Finland and Sardinia, and follow-up analyses in an additional 28,801 individuals. We show that common variants in the osteoarthritis- associated locus GDF5-UQCC contribute to variation in height with an estimated additive effect of 0.44 cm (overall P < 10-15). Our results indicate that there may be a link between the genetic basis of height and osteoarthritis, potentially mediated through alterations in bone growth and development.

Original languageEnglish (US)
Pages (from-to)198-203
Number of pages6
JournalNature genetics
Volume40
Issue number2
DOIs
StatePublished - Feb 2008

ASJC Scopus subject areas

  • Genetics

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