HuGE Literature Finder
Records 1-30
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Prothrombotic genotypes and risk of major bleeding in patients with incident venous thromboembolism.
Thrombosis research 2020 Apr 191 82-89. Johnsen Håkon S, Bjøri Esben, Hindberg Kristian, Brækkan Sigrid K, Morelli Vânia M, Hansen John-Bjar |
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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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Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke.The TromsØ Study.
Journal of thrombosis and haemostasis : JTH 2019 Feb . Rinde Ludvig B, Morelli Vania M, Småbrekke Birgit, Mathiesen Ellisiv B, Løchen Maja-Lisa, Njølstad Inger, Wilsgaard Tom, Smith Erin, Rosendaal Frits R, Frazer Kelly A, Braekkan Sigrid K, Hansen John-Bjar |
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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 |
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Venous thromboembolism risk associated with ABO, F11 and FGG loci.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2018 Jul . Manco Licínio, Silva Catarina, Fidalgo Teresa, Martinho Patrícia, Sarmento Ana B, Ribeiro M Letíc |
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.
Circulation. Cardiovascular genetics 2017 Apr 10 (2): . Klarin Derek, Emdin Connor A, Natarajan Pradeep, Conrad Mark F, , Kathiresan Sek |
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Genetic risk factors for venous thrombosis in women using combined oral contraceptives: update of the PILGRIM study.
Clinical genetics 2016 Jul . Suchon Pierre, Frouh Fadi Al, Ibrahim Manal, Sarlon Gabrielle, Venton Geoffroy, Alessi Marie-Christine, Trégouët David-Alexandre, Morange Pierre-Emmanu |
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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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Prospective study of ?' fibrinogen and incident venous thromboembolism: The Longitudinal Investigation of Thromboembolism Etiology (LITE).
Thrombosis research 2016 Mar 139 44-9. Folsom Aaron R, Tang Weihong, George Kristen M, Heckbert Susan R, MacLehose Richard F, Cushman Mary, Pankow James |
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Thrombosis Related ABO, F5, MTHFR, and FGG Gene Polymorphisms in Morbidly Obese Patients.
Disease markers 2016 2016 7853424. Kupcinskiene Kristina, Murnikovaite Martyna, Varkalaite Greta, Juzenas Simonas, Trepenaitis Darius, Petereit Ruta, Maleckas Almantas, Kupcinskas Juozas, Macas Andri |
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Replication of a genetic risk score for venous thromboembolism in whites but not in African Americans.
Journal of thrombosis and haemostasis : JTH 2015 Nov . Folsom Aaron R, Tang Weihong, Weng Lu-Chen, Roetker Nicholas S, Cushman Mary, Basu Saonli, Pankow James |
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F11 is associated with recurrent VTE in women. A prospective cohort study.
Thrombosis and haemostasis 2015 Oct 115 (2): . Bruzelius M, Ljungqvist M, Bottai M, Bergendal A, Strawbridge R J, Holmström M, Silveira A, Kieler H, Hamsten A, Lärfars G, Odeberg |
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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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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 |
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Predicting venous thrombosis in women using a combination of genetic markers and clinical risk factors.
Journal of thrombosis and haemostasis : JTH 2015 Feb 13 (2): 219-27. Bruzelius M, Bottai M, Sabater-Lleal M, Strawbridge R J, Bergendal A, Silveira A, Sundström A, Kieler H, Hamsten A, Odeberg |
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Genetic variations associated with recurrent venous thrombosis.
Circulation. Cardiovascular genetics 2014 Dec 7 (6): 806-13. van Hylckama Vlieg Astrid, Flinterman Linda E, Bare Lance A, Cannegieter Suzanne C, Reitsma Pieter H, Arellano Andre R, Tong Carmen H, Devlin James J, Rosendaal Frits |
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Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia.
Thrombosis research 2014 Sep 134 (3): 659-63. Rovite Vita, Maurins Uidis, Megnis Kaspars, Vaivade Iveta, Pe?ulis Raitis, Rits Juris, Prave Sandra, Klovins Jan |
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Risk assessment of venous thrombosis in families with known hereditary thrombophilia: the MARseilles-NImes prediction model.
Journal of thrombosis and haemostasis : JTH 2014 Feb 12 (2): 138-146. Cohen W, Castelli C, Suchon P, Bouvet S, Aillaud M F, Brunet D, Barthet M C, Alessi M C, Trégouët D A, Morange P |
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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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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 |
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Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study.
British journal of haematology 2012 Nov . El-Galaly TC, Severinsen MT, Overvad K, Steffensen R, Vistisen AK, Tjønneland A, Kristensen SR |
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Genetic risk factors for thrombosis in systemic lupus erythematosus.
The Journal of rheumatology 2012 Aug 39 (8): 1603-10. Kaiser Rachel, Li Yonghong, Chang Monica, Catanese Joseph, Begovich Ann B, Brown Elizabeth E, Edberg Jeffrey C, McGwin Gerald, Alarcón Graciela S, Ramsey-Goldman Rosalind, Reveille John D, Vilá Luis M, Petri Michelle A, Kimberly Robert P, Taylor Kimberly E, Criswell Lindsey |
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Genetics of venous thrombosis: insights from a new genome wide association study.
PloS one 2011 6 (9): e25581. Germain Marine, Saut Noémie, Greliche Nicolas, Dina Christian, Lambert Jean-Charles, Perret Claire, Cohen William, Oudot-Mellakh Tiphaine, Antoni Guillemette, Alessi Marie-Christine, Zelenika Diana, Cambien François, Tiret Laurence, Bertrand Marion, Dupuy Anne-Marie, Letenneur Luc, Lathrop Mark, Emmerich Joseph, Amouyel Philippe, Trégouët David-Alexandre, Morange Pierre-Emmanu |
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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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Fibrinogen gamma gene 3'-end polymorphisms and risk of venous thromboembolism in the African-American and Caucasian population.
Thrombosis and haemostasis 2009 Jun 101 (6): 1078-84. Uitte de Willige Shirley, Pyle Meridith E, Vos Hans L, de Visser Marieke C H, Lally Cathy, Dowling Nicole F, Hooper W Craig, Bertina Rogier M, Austin Harla |
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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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The fibrinogen gamma (FGG) 10034C>T polymorphism is associated with venous thrombosis.
Thrombosis research 2007 121 (1): 33-6. Grünbacher Gerda, Weger Wolfgang, Marx-Neuhold Ernestine, Pilger Ernst, Köppel Herwig, Wascher Thomas, März Winfried, Renner Wilfri |
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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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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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- Page last updated:Jul 10, 2020
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