Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Myocardial Infarction and NPC1L1[original query] |
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Effect of naturally random allocation to lower low-density lipoprotein cholesterol on the risk of coronary heart disease mediated by polymorphisms in NPC1L1, HMGCR, or both: a 2 × 2 factorial Mendelian randomization study. Journal of the American College of Cardiology 2015 Apr 65 (15): 1552-61. Ference Brian A, Majeed Faisal, Penumetcha Raju, Flack John M, Brook Robert |
Common gene variants in ASGR1 gene locus associate with reduced cardiovascular risk in absence of pleiotropic effects. Atherosclerosis 2020 Jul 306 15-21. Ali Lubna, Cupido Arjen J, Rijkers Maaike, Hovingh G Kees, Holleboom Adriaan G, Dallinga-Thie Geesje M, Stroes Erik S G, van den Boogert Marjolein A |
Association of NPC1L1 and HMGCR Gene Polymorphisms with Major Adverse Cardiac and Cerebrovascular Events in Patients with Three-Vessel Disease. Human gene therapy 2020 Nov . Zhao Xueyan, Li Jiawen, Tang Xiaofang, Liu Ru, Xu Jingjing, Xu Lianjun, Jiang Lin, Huang Keyong, Tian Jian, Feng Xingxing, Wu Yajie, Zhang Yin, Wang Dong, Sun Kai, Xu Bo, Zhao Wei, Hui Rutai, Gao Runlin, Song Lei, Yuan Jinqi |
Effects of genetically proxied lipid-lowering drugs on acute myocardial infarction: a drug-target mendelian randomization study. Lipids in health and disease 2024 6 23 (1): 163. Wendi Xiao, Yueying Li, Zhenhuang Zhuang, Zimin Song, Wenxiu Wang, Ninghao Huang, Xue Dong, Jinzhu Jia, Zhonghua Liu, Yimin Zhao, Lu Qi, Tao Hua |
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