Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Coronary artery disease and THBS1[original query] |
---|
Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients. Human genetics 2003 Dec 114 (1): 87-98. McCarthy Jeanette J, Meyer Joanne, Moliterno David J, Newby L Kristin, Rogers William J, Topol Eric J, |
Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary disease. American heart journal 2007 Dec 154 (6): 1035-42. Hlatky Mark A, Quertermous Thomas, Boothroyd Derek B, Priest James R, Glassford Alec J, Myers Richard M, Fortmann Stephen P, Iribarren Carlos, Tabor Holly K, Assimes Themistocles L, Tibshirani Robert J, Go Alan |
Polymorphisms associated with in vitro aspirin resistance are not associated with clinical outcomes in patients with coronary artery disease who report regular aspirin use. American heart journal 2011 Jul 162 (1): 166-72.e1. Voora Deepak, Horton John, Shah Svati H, Shaw Linda K, Newby L Krist |
Association between single nucleotide polymorphisms in thrombospondins genes and coronary artery disease: A meta-analysis. Thrombosis research 2015 Jul 136 (1): 45-51. Zhang Xiao-Jie, Wei Chun-Yan, Li Wen-Bo, Zhang Ling-Li, Zhou Ying, Wang Zhi-Hao, Tang Meng-Xiong, Zhang Wei, Zhang Yun, Zhong Mi |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: