Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia-Reference-Cited by-同舟云学术

Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia

Published:2017-12 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Han Yi,Dorajoo Rajkumar^ORCID,Chang Xuling,Wang Ling,Khor Chiea-Chuen^ORCID,Sim Xueling,Cheng Ching-Yu,Shi Yuan,Tham Yih Chung,Zhao Wanting,Chee Miao Ling,Sabanayagam Charumathi^ORCID,Chee Miao Li,Tan Nicholas,Wong Tien Yin,Tai E-Shyong,Liu Jianjun,Goh Daniel Y. T.,Yuan Jian-Min,Koh Woon-Puay,van Dam Rob M.,Low Adrian F.,Chan Mark Yan-Yee,Friedlander Yechiel,Heng Chew-Kiat

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-18214-z.pdf

Reference70 articles.

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3. CARDIoGRAMplusC4D Consortium. A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet 47, 1121–1130 (2015).

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5. Kathiresan, S. et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 41, 334–341 (2009).

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