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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Myocardial Infarction and LRP8[original query]
An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.
American journal of human genetics 2007 Oct 81 (4): 780-91.
Shen Gong-Qing, Li Lin, Girelli Domenico, Seidelmann Sara B, Rao Shaoqi, Fan Chun, Park Jeong Euy, Xi Quansheng, Li Jing, Hu Ying, Olivieri Oliviero, Marchant Kandice, Barnard John, Corrocher Roberto, Elston Robert, Cassano June, Henderson Susan, Hazen Stanley L, Plow Edward F, Topol Eric J, Wang Qing
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.
Journal of molecular medicine (Berlin, Germany) 2008 Oct 86 (10): 1163-70.
Lieb Wolfgang, Zeller Tanja, Mangino Massimo, Götz Anika, Braund Peter, Wenzel Juergen J, Horn Christian, Proust Carole, Linsel-Nitschke Patrick, Amouyel Philippe, Bruse Petra, Arveiler Dominique, König Inke R, Ferrières Jean, Ziegler Andreas, Balmforth Anthony J, Evans Alun, Ducimetière Pierre, Cambien Francois, Hengstenberg Christian, Stark Klaus, Hall Alistair S, Schunkert Heribert, Blankenberg Stefan, Samani Nilesh J, Erdmann Jeanette, Tiret Lauren
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study.
BMC medical genetics 2009 10 41.
Martinelli Nicola, Olivieri Oliviero, Shen Gong-Qing, Trabetti Elisabetta, Pizzolo Francesca, Busti Fabiana, Friso Simonetta, Bassi Antonella, Li Lin, Hu Ying, Pignatti Pier Franco, Corrocher Roberto, Wang Qing Kenneth, Girelli Domeni
Genetic variant R952Q in LRP8 is associated with increased plasma triglyceride levels in patients with early-onset CAD and MI.
Annals of human genetics 2012 May 76 (3): 193-9.
Shen Gong-Qing, Li Lin, Wang Qing
Multi-allelic haplotype association identifies novel information different from single-SNP analysis: a new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI.
Gene 2013 May 521 (1): 78-81.
Shen Gong-Qing, Girelli Domenico, Li Lin, Olivieri Oliviero, Martinelli Nicola, Chen Qiuyun, Topol Eric J, Wang Qing
A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.
Circulation. Cardiovascular genetics 2014 Aug 7 (4): 514-20.
Shen Gong-Qing, Girelli Domenico, Li Lin, Rao Shaoqi, Archacki Stephen, Olivieri Oliviero, Martinelli Nicola, Park Jeong Euy, Chen Qiuyun, Topol Eric J, Wang Qing
TG haplotype in the LRP8 is associated with myocardial infarction in south Indian population.
Gene 2017 10 642 225-229.
Asif Muhammed, Bhat Shivarama, Nizamuddin Sheikh, Mustak Mohammed
Identification of Genetic Variants Associated With Myocardial Infarction in Saudi Arabia.
The heart surgery forum 2020 Jul 23 (4): E517-E523.
Ai-Ghalayini Kamal W, Salama Mohammed A, Al Mahdi Hadia Bassam, Al-Harthi Sameer, Alhejily Wesam A, Alasnag Mirvat A, Tasbhji Noura O, Al-Quwaie Diana A H, Deloukas Panos, Edris Sher
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