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Lettre, G.* ; Jackson, A.U.* ; Gieger, C. ; Schumacher, F.R.* ; Berndt, S.I.* ; Sanna, S.* ; Eyheramendy, S. ; Voight, B.F.* ; Butler, J.L.* ; Guiducci, C.* ; Illig, T. ; Hackett, R.* ; Heid, I.M. ; Jacobs, K.B.* ; Lyssenko, V.* ; Uda, M* ; Diabetes Genetecs Initiative () ; FUSION Consortium (*) ; KORA Study Group () ; Prostate, Lung Colorectal and Ovarian Cancer Screening Tria (*) ; Nurses' Health Study (*) ; SardiNIA Study (*) ; Boehnke, M.* ; Chanock, S.J.* ; Groop, L.C.* ; Hu, F.B.* ; Isomaa, B.* ; Kraft, P.* ; Peltonen, L.* ; Salomaa, V.* ; Schlessinger, D.* ; Hunter, D.J.* ; Hayes, R.B.* ; Abecasis, G.R.* ; Wichmann, H.-E. ; Mohlke, K.L.* ; Hirschhorn, J.N.*

Identification of ten loci associated with height highlights new biological pathways in human growth.

Nat. Genet. 40, 584-591 (2008)
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Height is a classic polygenic trait, reflecting the combined influence of multiple as-yet-undiscovered genetic factors. We carried out a meta-analysis of genome-wide association study data of height from 15,821 individuals at 2.2 million SNPs, and followed up the strongest findings in >10,000 subjects. Ten newly identified and two previously reported loci were strongly associated with variation in height (P values from 4 x 10(-7) to 8 x 10(-22)). Together, these 12 loci account for approximately 2% of the population variation in height. Individuals with < or =8 height-increasing alleles and > or =16 height-increasing alleles differ in height by approximately 3.5 cm. The newly identified loci, along with several additional loci with strongly suggestive associations, encompass both strong biological candidates and unexpected genes, and highlight several pathways (let-7 targets, chromatin remodeling proteins and Hedgehog signaling) as important regulators of human stature. These results expand the picture of the biological regulation of human height and of the genetic architecture of this classical complex trait.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 1061-4036
e-ISSN 1546-1718
Zeitschrift Nature Genetics
Quellenangaben Band: 40, Heft: 5, Seiten: 584-591 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort New York, NY
Begutachtungsstatus Peer reviewed