Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Thrombosis and F7[original query] |
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| Common genetic variation in five thrombosis genes and relations to plasma hemostatic protein level and cardiovascular disease risk. Arteriosclerosis, thrombosis, and vascular biology 2006 Jun 26 (6): 1405-12. Kathiresan Sekar, Yang Qiong, Larson Martin G, Camargo Amy L, Tofler Geoffrey H, Hirschhorn Joel N, Gabriel Stacey B, O'Donnell Christopher |
| Perioperative genomic profiles using structure-specific oligonucleotide probes. Clinical medicine & research 2009 Sep 7 (3): 69-84. Hogan Kirk J, Burmester James K, Caldwell Michael D, Hogan Quinn H, Coursin Douglas B, Green Dawn N, Selzer Rebecca M R, Broderick Thomas P, Rusy Deborah A, Poroli Mark, Lutz Anna L, Sanders Allison M, Oldenburg Mary C, Koelbl James A, de Arruda-Indig Monika, Halsey Jennifer L, Day Stephen P, Domanico Michael |
| Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men. Journal of thrombosis and haemostasis : JTH 2010 Nov 8 (11): 2394-403. Ken-Dror G, Drenos F, Humphries S E, Talmud P J, Hingorani A D, Kivimäki M, Kumari M, Bauer K A, Morrissey J H, Ireland H |
Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium.
Circulation 2010 Mar 121 (12): 1382-92. Smith Nicholas L, Chen Ming-Huei, Dehghan Abbas, Strachan David P, Basu Saonli, Soranzo Nicole, Hayward Caroline, Rudan Igor, Sabater-Lleal Maria, Bis Joshua C, de Maat Moniek P M, Rumley Ann, Kong Xiaoxiao, Yang Qiong, Williams Frances M K, Vitart Veronique, Campbell Harry, Mälarstig Anders, Wiggins Kerri L, Van Duijn Cornelia M, McArdle Wendy L, Pankow James S, Johnson Andrew D, Silveira Angela, McKnight Barbara, Uitterlinden Andre G, , Aleksic Nena, Meigs James B, Peters Annette, Koenig Wolfgang, Cushman Mary, Kathiresan Sekar, Rotter Jerome I, Bovill Edwin G, Hofman Albert, Boerwinkle Eric, Tofler Geoffrey H, Peden John F, Psaty Bruce M, Leebeek Frank, Folsom Aaron R, Larson Martin G, Spector Timothy D, Wright Alan F, Wilson James F, Hamsten Anders, Lumley Thomas, Witteman Jacqueline C M, Tang Weihong, O'Donnell Christopher |
| Association of coagulation-related and inflammation-related genes and factor VIIc levels with stroke: the Cardiovascular Health Study. Journal of thrombosis and haemostasis : JTH 2011 Feb 9 (2): 267-74. Zakai N A, Lange L, Longstreth W T, O'Meara E S, Kelley J L, Fornage M, Nikerson D, Cushman M, Reiner A |
| Decanucleotide insertion polymorphism of F7 significantly influences the risk of thrombosis in patients with essential thrombocythemia. European journal of haematology 2014 Aug 93 (2): 103-11. Buxhofer-Ausch Veronika, Olcaydu Damla, Gisslinger Bettina, Schalling Martin, Frantal Sophie, Thiele Jürgen, Müllauer Leonhard, Kvasnicka Hans-Michael, Watzke Herbert, Kralovics Robert, Gisslinger Hei |
| 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 |
| Associations of activated coagulation factor VII and factor VIIa-antithrombin levels with genome-wide polymorphisms and cardiovascular disease risk. Journal of thrombosis and haemostasis : JTH 2017 Nov . Olson N C, Raffield L M, Lange L A, Lange E M, Longstreth W T, Chauhan G, Debette S, Seshadri S, Reiner A P, Tracy R |
| Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis. Haemophilia : the official journal of the World Federation of Hemophilia 2018 11 25 (1): 127-135. Saes Joline L, Simons Annet, de Munnik Sonja A, Nijziel Marten R, Blijlevens Nicole M A, Jongmans Marjolijn C, van der Reijden Bert A, Smit Yolba, Brons Paul P, van Heerde Waander L, Schols Saskia E |
| [Hemostatic Gene Polymorphisms in Acute Coronary Syndrome with Nonobstructive Coronary Atherosclerosis]. Kardiologiia 2019 Oct 59 (10): 14-22. Fedorova S B, Kulagina I V, Ryabov V |
| Polymorphisms of F2 (G20210A), F5 (G1691A), F 7 (G10976A), F 13(G13T), FGB, ITGA2, ITGB3, PAI-I genes and its association with thrombotic complications in patients suffering from Takayasu aortoarteritis of Urals population. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2021 Sep 49 (6): 448-455. Borodina Irina, Salavatova Gezel, Shardina Lub |
| Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism. Clinica chimica acta; international journal of clinical chemistry 2021 5 519 247-254. Athar Mohammad, Ghita Ibrahim S, Albagenny Amani A, Abduljaleel Zainularifeen, Shadab Ghulam, Elsendiony Ahmed, Halawani Saeed H, Alkazmi Mohammad M, Alquthami Khalid, Alkhuzae Mohammad M, Althebyani Abdulaziz A, Bogari Neda M, Dannoun Anas, Al-Allaf Faisal |
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