Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Myocardial Infarction and MAF[original query] |
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| Pooled DNA resequencing of 68 myocardial infarction candidate genes in French canadians. Circulation. Cardiovascular genetics 2012 Oct 5 (5): 547-54. Beaudoin Mélissa, Lo Ken Sin, N'Diaye Amidou, Rivas Manuel A, Dubé Marie-Pierre, Laplante Nathalie, Phillips Michael S, Rioux John D, Tardif Jean-Claude, Lettre Guillau |
| BRCA2 variants and cardiovascular disease in a multi-ethnic study. BMC medical genetics 2012 13 56. Zbuk Kevin, Xie Changchun, Young Robin, Heydarpour Mahyar, Pare Guillaume, Davis A Darlene, Miller Ruby, Lanktree Matthew B, Saleheen Danish, Danesh John, Yusuf Salim, Engert James C, Hegele Robert A, Anand Sonia |
| [Clopidogrel metabolism related gene polymorphisms in Chinese patients with acute coronary syndrome]. Zhonghua xin xue guan bing za zhi 2012 Nov 40 (11): 11. Feng GX, Liang Y, Bai Y, Chen T, Liu X, Yang YM, Wang XY, Yang YJ, Zhu J |
| Whole-genome sequencing in French Canadians from Quebec. Human genetics 2016 Jul . Low-Kam Cécile, Rhainds David, Lo Ken Sin, Provost Sylvie, Mongrain Ian, Dubois Anick, Perreault Sylvie, Robinson John F, Hegele Robert A, Dubé Marie-Pierre, Tardif Jean-Claude, Lettre Guillau |
| Rare Variants in NOD1 Associated with Carotid Bifurcation Intima-Media Thickness in Dominican Republic Families. PloS one 2016 11 (12): e0167202. Dueker Nicole D, Beecham Ashley, Wang Liyong, Blanton Susan H, Guo Shengru, Rundek Tatjana, Sacco Ralph |
| Effect of carboxylesterase 1 S75N on clopidogrel therapy among acute coronary syndrome patients. Scientific reports 2017 8 7 (1): 7244. Xiao Fei-Yan, Luo Jian-Quan, Liu Min, Chen Bi-Lian, Cao Shan, Liu Zhao-Qian, Zhou Hong-Hao, Zhou Gan, Zhang W |
| Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons. Scientific reports 2017 Jun 7 (1): 4091. Hixson James E, Jun Goo, Shimmin Lawrence C, Wang Yizhi, Yu Guoqiang, Mao Chunhong, Warren Andrew S, Howard Timothy D, Heide Richard S Vander, Van Eyk Jennifer, Wang Yue, Herrington David |
| Variants in ANRIL gene correlated with its expression contribute to myocardial infarction risk. Oncotarget 2017 Jan . Cheng Jie, Cai Meng-Yun, Chen Yu-Ning, Li Zhi-Cheng, Tang Sai-Sai, Yang Xi-Li, Chen Can, Liu Xinguang, Xiong Xing-Do |
| Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. PloS one 2020 15 (11): e0230035. Hahn Julie, Fu Yi-Ping, Brown Michael R, Bis Joshua C, de Vries Paul S, Feitosa Mary F, Yanek Lisa R, Weiss Stefan, Giulianini Franco, Smith Albert Vernon, Guo Xiuqing, Bartz Traci M, Becker Diane M, Becker Lewis C, Boerwinkle Eric, Brody Jennifer A, Chen Yii-Der Ida, Franco Oscar H, Grove Megan, Harris Tamara B, Hofman Albert, Hwang Shih-Jen, Kral Brian G, Launer Lenore J, Markus Marcello R P, Rice Kenneth M, Rich Stephen S, Ridker Paul M, Rivadeneira Fernando, Rotter Jerome I, Sotoodehnia Nona, Taylor Kent D, Uitterlinden André G, Völker Uwe, Völzke Henry, Yao Jie, Chasman Daniel I, Dörr Marcus, Gudnason Vilmundur, Mathias Rasika A, Post Wendy, Psaty Bruce M, Dehghan Abbas, O'Donnell Christopher J, Morrison Alanna |
| New findings in the roles of Cyclin-dependent Kinase inhibitors 2B Antisense RNA 1 (CDKN2B-AS1) rs1333049 G/C and rs4977574 A/G variants on the risk to coronary heart disease. Bioengineered 2020 10 11 (1): 1084-1098. Yuan Wei, Zhang Wei, Zhang Wei, Ruan Zhong-Bao, Zhu Li, Liu Yu, Mi Yuan-Yuan, Zhang Li-Fe |
| The R93C Variant of PCSK9 Reduces the Risk of Premature MI in a Chinese Han Population. Frontiers in genetics 2022 4 13 875269. Yang Lincheng, Pu Tian, Zhang Yan, Yan Hua, Yu Haiyi, Gao W |
| Influence of the rs4238001 Genetic Polymorphism of the SR-B1 Gene on Serum Lipid Levels and Response to Rosuvastatin in Myocardial Infarction Iraqi Patients. Biochemical genetics 2023 12 . Shaimaa Y Abdulfattah, Huda Salman Alagely, Farah T Sama |
| Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts. Scientific reports 2023 12 13 (1): 21866. Amein K Al-Ali, Abdullah M Al-Rubaish, Rudaynah A Alali, Mohammed S Almansori, Mohammed A Al-Jumaan, Abdullah M Alshehri, Mohammed S Al-Madan, ChittiBabu Vatte, Tess Cherlin, Sylvia Young, Shefali S Verma, Grant Morahan, Bobby P C Koeleman, Brendan J Keati |
| Loss of Function in Protein Z (PROZ) is Associated with Increased Risk of Ischemic Stroke in the UK Biobank. Journal of thrombosis and haemostasis : JTH 2024 10 . Amelia K Haj, Justine Ryu, Sean J Jurgens, Sharjeel Chaudhry, Satoshi Koyama, Xin Wang, Seung Hoan Choi, Cody Hou, Simone Sanna-Cherchi, Christopher D Anderson, Patrick T Ellinor, Pavan K Bendapu |
| High Population Frequency of GNRHR p.Q106R in Malta: An Evaluation of Fertility and Hormone Profiles in Heterozygotes. Journal of the Endocrine Society 2024 1 8 (2): bvad172. Clayton John Axiak, Adrian Pleven, Ritienne Attard, Francesca Borg Carbott, Jean-Paul Ebejer, Ian Brincat, Karen Cassar, Mark Gruppetta, Josanne Vassallo, Stephanie Bezzina Wettinger, Rosienne Farrug |
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