Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk-Reference-Cited by-同舟云学术

Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk

Published:2014-03-16 Issue:4 Volume:46 Page:345-351
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Holmen Oddgeir L,Zhang He,Fan Yanbo,Hovelson Daniel H,Schmidt Ellen M,Zhou Wei,Guo Yanhong,Zhang Ji,Langhammer Arnulf,Løchen Maja-Lisa,Ganesh Santhi K,Vatten Lars,Skorpen Frank,Dalen Håvard,Zhang Jifeng,Pennathur Subramaniam,Chen Jin,Platou Carl,Mathiesen Ellisiv B,Wilsgaard Tom,Njølstad Inger,Boehnke Michael,Chen Y Eugene,Abecasis Gonçalo R,Hveem Kristian,Willer Cristen J

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2926.pdf

Reference41 articles.

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4. Willer, C.J. et al. Discovery and refinement of loci associated with lipid levels. Nat. Genet. 45, 1274–1283 (2013).

5. Teslovich, T.M. et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466, 707–713 (2010).

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