Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Stroke and THBD[original query] |
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| Combined effects of thrombosis pathway gene variants predict cardiovascular events. PLoS genetics 2007 Jul 3 (7): e120. Auro Kirsi, Alanne Mervi, Kristiansson Kati, Silander Kaisa, Kuulasmaa Kari, Salomaa Veikko, Peltonen Leena, Perola Mark |
| An interactive association of common sequence variants in the neuropeptide Y gene with susceptibility to ischemic stroke. Stroke; a journal of cerebral circulation 2007 Oct 38 (10): 2663-9. Lee Chaeyoung, Kong Minyou |
| [Polymorphic markers Ala455Val of the THBD gene and Arg353Gln of the F7 gene and association with unfavorable outcomes of coronary atherosclerosis in patients with a history of acute ischemic heart disease]. Genetika 2011 Oct 47 (10): 1386-92. Pushkov A A, Blagodatskikh K A, Nikitin A G, Agapkina Iu V, Brovkin A N, Chudakova D A, Evdokimova M A, Ase?cheva O Iu, Osmolovskaia V S, Minushkina L O, Baklanova T N, Talyzin P A, Donetskaia O P, Tereshchenko S N, Dzhaiani N A, Akatova E A, Glezer M G, Galiavich A S, Zakirova V B, Koziolova N A, Iagoda A V, Boeva O I, Horolets E V, Shlyk S V, Volkova E G, Margarian M P, Guz' I O, Konstantinov V O, Sidorenko B A, Zate?shchikov D A, Nosikov V |
| A Prothrombotic Score Based on Genetic Polymorphisms of the Hemostatic System Differs in Patients with Ischemic Stroke, Myocardial Infarction, or Peripheral Arterial Occlusive Disease. Frontiers in cardiovascular medicine 2017 4 39. Herm Juliane, Hoppe Berthold, Siegerink Bob, Nolte Christian H, Koscielny Jürgen, Haeusler Karl Geo |
| Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke. PloS one 2018 13 (11): e0206554. Cole John W, Xu Huichun, Ryan Kathleen, Jaworek Thomas, Dueker Nicole, McArdle Patrick, Gaynor Brady, Cheng Yu-Ching, O'Connell Jeffrey, Bevan Steve, Malik Rainer, Ahmed Naveed Uddin, Amouyel Philippe, Anjum Sheraz, Bis Joshua C, Crosslin David, Danesh John, Engelter Stefan T, Fornage Myriam, Frossard Philippe, Gieger Christian, Giese Anne-Katrin, Grond-Ginsbach Caspar, Ho Weang Kee, Holliday Elizabeth, Hopewell Jemma, Hussain M, Iqbal W, Jabeen S, Jannes Jim, Kamal Ayeesha, Kamatani Yoichiro, Kanse Sandip, Kloss Manja, Lathrop Mark, Leys Didier, Lindgren Arne, Longstreth W T, Mahmood Khalid, Meisinger Christa, Metso Tiina M, Mosley Thomas, Müller-Nurasyid Martina, Norrving Bo, Parati Eugenio, Peters Annette, Pezzini Alessandro, Quereshi I, Rasheed Asif, Rauf A, Salam T, Shen Jess, S?owik Agnieszka, Stanne Tara, Strauch Konstantin, Tatlisumak Turgut, Thijs Vincent N, Tiedt Steffen, Traylor Matthew, Waldenberger Melanie, Walters Matthew, Zhao Wei, Boncoraglio Giorgio, Debette Stéphanie, Jern Christina, Levi Christopher, Markus Hugh, Meschia James, Rolfs Arndt, Rothwell Peter, Saleheen Danish, Seshadri Sudha, Sharma Pankaj, Sudlow Cathie, Worrall Bradford, , , Stine O Colin, Kittner Steven J, Mitchell Braxton |
| Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease. Blood advances 2020 May 4 (9): 1978-1986. Srisuwananukorn Andrew, Raslan Rasha, Zhang Xu, Shah Binal N, Han Jin, Gowhari Michel, Molokie Robert E, Gordeuk Victor R, Saraf Santosh |
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