HuGE Literature Finder
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Records 1-19
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Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders.
European journal of haematology 2019 Jul . Castaman Giancarlo, Giacomelli Sofia H, Biasoli Chiara, Contino Laura, Radossi Pao |
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Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes.
Journal of thrombosis and haemostasis : JTH 2018 Aug . de Haan H G, van Hylckama Vlieg A, Lotta L A, Gorski Marcin M, Bucciarelli P, Martinelli I, , Baglin T P, Peyvandi F, Rosendaal F |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
Human molecular genetics 2016 May 25 (9): 1867-74. Hinds David A, Buil Alfonso, Ziemek Daniel, Martinez-Perez Angel, Malik Rainer, Folkersen Lasse, Germain Marine, Mälarstig Anders, Brown Andrew, Soria Jose Manuel, Dichgans Martin, Bing Nan, Franco-Cereceda Anders, Souto Juan Carlos, Dermitzakis Emmanouil T, Hamsten Anders, Worrall Bradford B, Tung Joyce Y, , Sabater-Lleal Mar |
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Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis.
PloS one 2016 11 (3): e0151347. Gorski Marcin M, Lotta Luca A, Pappalardo Emanuela, de Haan Hugoline G, Passamonti Serena M, van Hylckama Vlieg Astrid, Martinelli Ida, Peyvandi Flo |
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Hypofibrinogenemia and the ?-Fibrinogen Thr312Ala Polymorphism may be Risk Factors for Early Pregnancy Loss.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2015 Jul . Kamimoto Yuki, Wada Hideo, Ikejiri Makoto, Nakatani Kaname, Sugiyama Takashi, Osato Kazuhiro, Murabayashi Nao, Habe Koji, Mizutani Hitoshi, Matsumoto Takeshi, Ohishi Kohshi, Ikeda Tomoa |
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Two symptomatic cases of dysfibrinogenemia in China: one with gamma-chain Arg275Cys mutation and another without detectable mutation in fibrinogen genes.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 Jul 26 (5): 564-71. Bin Qiong, Liang Fang, Ou Dan-yan, Cui Hai-rong, Luo Jian-mi |
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Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip.
Thrombosis and haemostasis 2013 Nov 110 (5): 995-1003. Gaunt T R, Zabaneh D, Shah S, Guyatt A, Ladroue C, Kumari M, Drenos F, Shah T, Talmud P J, Casas J P, Lowe G, Rumley A, Lawlor D A, Kivimaki M, Whittaker J, Hingorani A D, Humphries S E, Day I |
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Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes.
BMC medical genomics 2012 5 (1): 7. Lotta Luca A, Wang Mark, Yu Jin, Martinelli Ida, Yu Fuli, Passamonti Serena M, Consonni Dario, Pappalardo Emanuela, Menegatti Marzia, Scherer Steven E, Lewis Lora L, Akbar Humeira, Wu Yuanqing, Bainbridge Matthew N, Muzny Donna M, Mannucci Pier M, Gibbs Richard A, Peyvandi Flo |
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The fibrinogen gamma 10034C>T polymorphism is not associated with Peripheral Arterial Disease.
Thrombosis research 2010 Oct 126 (4): 350-2. Bahadori Babak, Uitz Elisabeth, Dehchamani Dadbeh, Pilger Ernst, Renner Wilfri |
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Gene variants associated with venous thrombosis: confirmation in the MEGA study.
Journal of thrombosis and haemostasis : JTH 2010 May 8 (5): 1132-4. Arellano A R, Bezemer I D, Tong C H, Catanese J J, Devlin J J, Reitsma P H, Bare L A, Rosendaal F |
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Fibrinogen alpha and gamma genes and factor VLeiden in children with thromboembolism: results from 2 family-based association studies.
Blood 2009 Aug 114 (9): 1947-53. Nowak-Göttl Ulrike, Weiler Hartmut, Hernandez Irene, Thedieck Sabine, Seehafer Tanja, Schulte Thomas, Stoll Moni |
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Prothrombotic genetic variants and atherosclerosis in patients with cerebral ischemia of arterial origin.
Atherosclerosis 2009 May 204 (1): 191-5. Pruissen D M O, Kappelle L J, Rosendaal F R, Algra A, |
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Genetic variation in fibrinogen; its relationship to fibrinogen levels and the risk of myocardial infarction and ischemic stroke.
Journal of thrombosis and haemostasis : JTH 2009 Mar 7 (3): 385-90. Siegerink B, Rosendaal F R, Algra |
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Fibrinogen Aalpha Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension.
The European respiratory journal 2008 Apr 31 (4): 736-41. Suntharalingam J, Goldsmith K, van Marion V, Long L, Treacy C M, Dudbridge F, Toshner M R, Pepke-Zaba J, Eikenboom J C J, Morrell N |
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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 |
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Functional polymorphisms of FGA, encoding alpha fibrinogen, are associated with susceptibility to venous thromboembolism in a Taiwanese population.
Human genetics 2006 Mar 119 (1-2): 84-91. Ko Yu-Lin, Hsu Lung-An, Hsu Tsu-Shiu, Tsai Chia-Ti, Teng Ming-Sheng, Wu Semon, Chang Chi-Jen, Lee Ying-Shiu |
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Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen gamma' levels.
Blood 2005 Dec 106 (13): 4176-83. Uitte de Willige Shirley, de Visser Marieke C H, Houwing-Duistermaat Jeanine J, Rosendaal Frits R, Vos Hans L, Bertina Rogier |
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[Pharmacogenetics of the local thrombolysis in patients with deep vein thrombosis].
Polskie Archiwum Medycyny Wewn?trznej 2005 Jul 114 (1): 644-51. Falkowski Aleksander, Kaczmarczyk Mariusz, Goracy Iwona, Górecka-Szyld Barbara, Poncyljusz Wojciech, Parczewski Mi?osz, Ciechanowicz Andrz |
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Analysis of prothrombotic mutations and polymorphisms in children who developed thrombosis in the perioperative period of congenital cardiac surgery.
Cardiology in the young 2005 Feb 15 (1): 19-25. Ozbek Namik, Ataç F Belgin, Yildirim Selman V, Verdi Hasibe, Yazici Canan, Yilmaz Ba?ak T, Tokel N Kür? |
- Page last reviewed:Jul 30, 2019
- Page last updated:Oct 10, 2019
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