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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 - 7 (of 7 Records)

Query Trace: Coronary artery disease and MTHFD1L[original query]
A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency.
Human mutation 2009 Dec 30 (12): 1650-6.
Parle-McDermott Anne, Pangilinan Faith, O'Brien Kirsty K, Mills James L, Magee Alan M, Troendle James, Sutton Marie, Scott John M, Kirke Peadar N, Molloy Anne M, Brody Lawrence
Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.
Annals of human genetics 2011 Jul 75 (4): 475-82.
Wang Annabel Z, Li Lin, Zhang Bin, Shen Gong-Qing, Wang Qing Kenne
Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome.
BMC medical genetics 2011 12 127.
Morgan Thomas M, House John A, Cresci Sharon, Jones Philip, Allayee Hooman, Hazen Stanley L, Patel Yesha, Patel Riyaz S, Eapen Danny J, Waddy Salina P, Quyyumi Arshed A, Kleber Marcus E, März Winfried, Winkelmann Bernhard R, Boehm Bernhard O, Krumholz Harlan M, Spertus John
Large scale association analysis identifies three susceptibility loci for coronary artery disease.
PloS one 2011 6 (12): e29427.
Saade Stephanie, Cazier Jean-Baptiste, Ghassibe-Sabbagh Michella, Youhanna Sonia, Badro Danielle A, Kamatani Yoichiro, Hager Jörg, Yeretzian Joumana S, El-Khazen Georges, Haber Marc, Salloum Angelique K, Douaihy Bouchra, Othman Raed, Shasha Nabil, Kabbani Samer, Bayeh Hamid El, Chammas Elie, Farrall Martin, Gauguier Dominique, Platt Daniel E, Zalloua Pierre A,
Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients.
PloS one 2014 9 (3): e89029.
Palmer Barry R, Slow Sandy, Ellis Katrina L, Pilbrow Anna P, Skelton Lorraine, Frampton Chris M, Palmer Suetonia C, Troughton Richard W, Yandle Tim G, Doughty Rob N, Whalley Gillian A, Lever Michael, George Peter M, Chambers Stephen T, Ellis Chris, Richards A Mark, Cameron Vicky
Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population.
Medicina (Kaunas, Lithuania) 2020 8 56 (9): .
Rodríguez-Arellano Martha Eunice, Solares-Tlapechco Jacqueline, Costa-Urrutia Paula, Cárdenas-Hernández Helios, Vallejo-Gómez Marajael, Granados Julio, Salas-Padilla Serg
Vitamin B-related Gene Polymorphisms and Cardiovascular Disease.
Endocrine, metabolic & immune disorders drug targets 2022 3 22 (10): 979-984.
Katsa Maria Efthymia, Gil Andrea Paola Roj
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