Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and LPAL2[original query] |
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| Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.
Nature genetics 2009 Mar 41 (3): 283-5. Trégouët David-Alexandre, König Inke R, Erdmann Jeanette, Munteanu Alexandru, Braund Peter S, Hall Alistair S, Grosshennig Anika, Linsel-Nitschke Patrick, Perret Claire, DeSuremain Maylis, Meitinger Thomas, Wright Ben J, Preuss Michael, Balmforth Anthony J, Ball Stephen G, Meisinger Christa, Germain Cécile, Evans Alun, Arveiler Dominique, Luc Gérald, Ruidavets Jean-Bernard, Morrison Caroline, van der Harst Pim, Schreiber Stefan, Neureuther Katharina, Schäfer Arne, Bugert Peter, El Mokhtari Nour E, Schrezenmeir Jürgen, Stark Klaus, Rubin Diana, Wichmann H-Erich, Hengstenberg Christian, Ouwehand Willem, , , Ziegler Andreas, Tiret Laurence, Thompson John R, Cambien Francois, Schunkert Heribert, Samani Nilesh |
| Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk. Stroke; a journal of cerebral circulation 2011 Jan 42 (1): 2-9. Ronald James, Rajagopalan Ramakrishnan, Cerrato Felecia, Nord Alex S, Hatsukami Thomas, Kohler Ted, Marcovina Santica, Heagerty Patrick, Jarvik Gail |
| Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.
European heart journal 2012 Feb 33 (3): 325-34. Qi Qibin, Workalemahu Tsegaselassie, Zhang Cuilin, Hu Frank B, Qi |
| Genetic and clinical correlates of early-outgrowth colony-forming units.
Circulation. Cardiovascular genetics 2011 Jun 4 (3): 296-304. Shaw Stanley Y, Cheng Susan, Cupples L Adrienne, Larson Martin G, McCabe Elizabeth L, Ngwa Julius S, Wang Ying A, Martin Roderick P, Klein Rachael J, Hashmi Basma, Ajijola Olujimi A, Lau Evan, O'Donnell Christopher J, Vasan Ramachandran S, Cohen Kenneth S, Wang Thomas |
| Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study. Lipids in health and disease 2012 Oct 11 (1): 1. Lv X, Qiu J, Rao S, Zhang Y, Wang M, Liu F, Su D, Zuo X, Feng X, Xia M, Feng D, Yang Y, Ouyang P, Ling W, Ma W, Guo H, Li X, Li D |
| Two rare variants explain association with acute myocardial infarction in an extended genomic region including the apolipoprotein(A) gene. Annals of human genetics 2013 Jan 77 (1): 1. Koch W, Mueller JC, Schrempf M, Wolferstetter H, Kirchhofer J, Schömig A, Kastrati A |
| A Case-Control Study of the Relationship Between SLC22A3-LPAL2-LPA Gene Cluster Polymorphism and Coronary Artery Disease in the Han Chinese Population. Iranian Red Crescent medical journal 2016 Jun 18 (6): e35387. Song Zi-Kai, Cao Hong-Yan, Wu Hai-Di, Zhou Li-Ting, Qin Li |
| Functional Variant in the SLC22A3-LPAL2-LPA Gene Cluster Contributes to the Severity of Coronary Artery Disease. Arteriosclerosis, thrombosis, and vascular biology 2016 Jul . Wang Long, Chen Juan, Zeng Ying, Wei Jie, Jing Jinjin, Li Ge, Su Li, Tang Xiaojun, Wu Tangchun, Zhou |
| Effect of MEF2A and SLC22A3-LPAL2-LPA gene polymorphisms on warfarin sensitivity and responsiveness in Jordanian cardiovascular patients. PloS one 2023 11 18 (11): e0294226. Laith N Al-Eitan, Ayah Y Almasri, Adan H Alnaamneh, Ahmad Mihy |
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