Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity-Reference-Cited by-同舟云学术

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity

Published:2013-04-07 Issue:5 Volume:45 Page:513-517
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Wheeler Eleanor,Huang Ni,Bochukova Elena G,Keogh Julia M,Lindsay Sarah,Garg Sumedha,Henning Elana,Blackburn Hannah,Loos Ruth J F,Wareham Nick J,O'Rahilly Stephen,Hurles Matthew E,Barroso Inês,Farooqi I Sadaf

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2607.pdf

Reference26 articles.

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3. Zuk, O., Hechter, E., Sunyaev, S.R. & Lander, E.S. The mystery of missing heritability: genetic interactions create phantom heritability. Proc. Natl. Acad. Sci. USA 109, 1193–1198 (2012).

4. Cohen, J.C. et al. Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science 305, 869–872 (2004).

5. Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447, 661–678 (2007).

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