Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome-Reference-Cited by-同舟云学术

Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome

Published:2011-09-29 Issue:1 Volume:12 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Morgan Thomas M,House John A,Cresci Sharon,Jones Philip,Allayee Hooman,Hazen Stanley L,Patel Yesha,Patel Riyaz S,Eapen Danny J,Waddy Salina P,Quyyumi Arshed A,Kleber Marcus E,März Winfried,Winkelmann Bernhard R,Boehm Bernhard O,Krumholz Harlan M,Spertus John A

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-12-127.pdf

Reference24 articles.

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2. Wellcome Trust Case Control Consortium: Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls. Nature. 2007, 447 (7145): 661-678. 10.1038/nature05911.

3. Dorn GW, Cresci S: Genome-wide association studies of coronary artery disease and heart failure: where are we going?. Pharmacogenomics. 2009, 10 (2): 213-223. 10.2217/14622416.10.2.213.

4. Erdmann J, Grosshennig A, Braund PS, Konig IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Tregouet DA, et al: New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet. 2009, 41 (3): 280-282. 10.1038/ng.307.

5. Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H, et al: Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet. 2009, 41 (3): 334-341. 10.1038/ng.327.

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