Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia-Reference-Cited by-同舟云学术

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

Published:2010-07-25 Issue:8 Volume:42 Page:684-687
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Johansen Christopher T,Wang Jian,Lanktree Matthew B,Cao Henian,McIntyre Adam D,Ban Matthew R,Martins Rebecca A,Kennedy Brooke A,Hassell Reina G,Visser Maartje E,Schwartz Stephen M,Voight Benjamin F,Elosua Roberto,Salomaa Veikko,O'Donnell Christopher J,Dallinga-Thie Geesje M,Anand Sonia S,Yusuf Salim,Huff Murray W,Kathiresan Sekar,Hegele Robert A

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.628.pdf

Reference27 articles.

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2. Willer, C.J. et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat. Genet. 40, 161–169 (2008).

3. Sabatti, C. et al. Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat. Genet. 41, 35–46 (2009).

4. Aulchenko, Y.S. et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat. Genet. 41, 47–55 (2009).

5. Kathiresan, S. et al. Common variants at 30 loci contribute to polygenic dyslipidemia. Nat. Genet. 41, 56–65 (2009).

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