Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and meta-analysis and F5[original query] |
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| A field synopsis and meta-analysis of genetic association studies in peripheral arterial disease: The CUMAGAS-PAD database. American journal of epidemiology 2009 Jul 170 (1): 1-11. Zintzaras Elias, Zdoukopoulos Nik |
| The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease. Journal of thrombosis and haemostasis : JTH 2010 Oct 8 (10): 2116-21. Mannucci P M, Asselta R, Duga S, Guella I, Spreafico M, Lotta L, Merlini P A, Peyvandi F, Kathiresan S, Ardissino |
Multiple loci influencing hippocampal degeneration identified by genome scan.
Annals of neurology 2012 Jul 72 (1): 65-75. Melville Scott A, Buros Jacqueline, Parrado Antonio R, Vardarajan Badri, Logue Mark W, Shen Li, Risacher Shannon L, Kim Sungeun, Jun Gyungah, DeCarli Charles, Lunetta Kathryn L, Baldwin Clinton T, Saykin Andrew J, Farrer Lindsay A, |
| Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
American journal of human genetics 2012 Jul 91 (1): 152-62. Tang Weihong, Schwienbacher Christine, Lopez Lorna M, Ben-Shlomo Yoav, Oudot-Mellakh Tiphaine, Johnson Andrew D, Samani Nilesh J, Basu Saonli, Gögele Martin, Davies Gail, Lowe Gordon D O, Tregouet David-Alexandre, Tan Adrian, Pankow James S, Tenesa Albert, Levy Daniel, Volpato Claudia B, Rumley Ann, Gow Alan J, Minelli Cosetta, Yarnell John W G, Porteous David J, Starr John M, Gallacher John, Boerwinkle Eric, Visscher Peter M, Pramstaller Peter P, Cushman Mary, Emilsson Valur, Plump Andrew S, Matijevic Nena, Morange Pierre-Emmanuel, Deary Ian J, Hicks Andrew A, Folsom Aaron |
| A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Genetic epidemiology 2013 Jul 37 (5): 512-21. Tang Weihong, Teichert Martina, Chasman Daniel I, Heit John A, Morange Pierre-Emmanuel, Li Guo, Pankratz Nathan, Leebeek Frank W, Paré Guillaume, de Andrade Mariza, Tzourio Christophe, Psaty Bruce M, Basu Saonli, Ruiter Rikje, Rose Lynda, Armasu Sebastian M, Lumley Thomas, Heckbert Susan R, Uitterlinden André G, Lathrop Mark, Rice Kenneth M, Cushman Mary, Hofman Albert, Lambert Jean-Charles, Glazer Nicole L, Pankow James S, Witteman Jacqueline C, Amouyel Philippe, Bis Joshua C, Bovill Edwin G, Kong Xiaoxiao, Tracy Russell P, Boerwinkle Eric, Rotter Jerome I, Trégouët David-Alexandre, Loth Daan W, Stricker Bruno H Ch, Ridker Paul M, Folsom Aaron R, Smith Nicholas |
| Maternal genotype and severe preeclampsia: a HuGE review. American journal of epidemiology 2014 Aug 180 (4): 335-45. Fong Fiona M, Sahemey Manpreet K, Hamedi Golnessa, Eyitayo Rachel, Yates Derick, Kuan Valerie, Thangaratinam Shakila, Walton Robert |
| A genetic association study of D-dimer levels with 50K SNPs from a candidate gene chip in four ethnic groups. Thrombosis research 2014 Aug 134 (2): 462-7. Weng Lu-Chen, Tang Weihong, Rich Stephen S, Smith Nicholas L, Redline Susan, O'Donnell Christopher J, Basu Saonli, Reiner Alexander P, Delaney Joseph A, Tracy Russell P, Palmer Cameron D, Young Taylor, Yang Qiong, Folsom Aaron R, Cushman Ma |
| Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism.
American journal of human genetics 2015 Apr 96 (4): 532-42. Germain Marine, Chasman Daniel I, de Haan Hugoline, Tang Weihong, Lindström Sara, Weng Lu-Chen, de Andrade Mariza, de Visser Marieke C H, Wiggins Kerri L, Suchon Pierre, Saut Noémie, Smadja David M, Le Gal Grégoire, van Hylckama Vlieg Astrid, Di Narzo Antonio, Hao Ke, Nelson Christopher P, Rocanin-Arjo Ares, Folkersen Lasse, Monajemi Ramin, Rose Lynda M, Brody Jennifer A, Slagboom Eline, Aïssi Dylan, Gagnon France, Deleuze Jean-Francois, Deloukas Panos, Tzourio Christophe, Dartigues Jean-Francois, Berr Claudine, Taylor Kent D, Civelek Mete, Eriksson Per, , Psaty Bruce M, Houwing-Duitermaat Jeanine, Goodall Alison H, Cambien François, Kraft Peter, Amouyel Philippe, Samani Nilesh J, Basu Saonli, Ridker Paul M, Rosendaal Frits R, Kabrhel Christopher, Folsom Aaron R, Heit John, Reitsma Pieter H, Trégouët David-Alexandre, Smith Nicholas L, Morange Pierre-Emmanu |
| Discovery of coding genetic variants influencing diabetes-related serum biomarkers and their impact on risk of type 2 diabetes. The Journal of clinical endocrinology and metabolism 2015 Apr 100 (4): E664-71. Ahluwalia Tarunveer Singh, Allin Kristine Højgaard, Sandholt Camilla Helene, Sparsø Thomas Hempel, Jørgensen Marit Eika, Rowe Michael, Christensen Cramer, Brandslund Ivan, Lauritzen Torsten, Linneberg Allan, Husemoen Lise Lotte, Jørgensen Torben, Hansen Torben, Grarup Niels, Pedersen Ol |
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