HuGE Literature Finder
Records
1
-
30
| Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. Nature genetics 2023 1 55 (3): 399-409. Ghouse Jonas, Tragante Vinicius, Ahlberg Gustav, Rand Søren A, Jespersen Jakob B, Leinøe Eva Birgitte, Vissing Christoffer Rasmus, Trudsø Linea, Jonsdottir Ingileif, Banasik Karina, Brunak Søren, Ostrowski Sisse R, Pedersen Ole B, Sørensen Erik, Erikstrup Christian, Bruun Mie Topholm, Nielsen Kaspar Rene, Køber Lars, Christensen Alex H, Iversen Kasper, Jones David, Knowlton Kirk U, Nadauld Lincoln, Halldorsson Gisli H, Ferkingstad Egil, Olafsson Isleifur, Gretarsdottir Solveig, Onundarson Pall T, Sulem Patrick, Thorsteinsdottir Unnur, Thorgeirsson Gudmundur, Gudbjartsson Daniel F, Stefansson Kari, Holm Hilma, Olesen Morten Salling, Bundgaard Henni |
| Joint Effect of Multiple Prothrombotic Genotypes and Mean Platelet Volume on the Risk of Incident Venous Thromboembolism. Thrombosis and haemostasis 2022 May . Jakobsen Lisa, Frischmuth Tobias, Brækkan Sigrid K, Hansen John-Bjarne, Morelli Vânia |
Whole exome sequencing identifies genetic variants in Chinese Han pregnant women with venous thromboembolism.
Thrombosis research 2022 Mar 211 49-55. Shen Yupei, Zhang Yan, Xiong Ying, Zhang Zhiping, Zhang Baohua, Li Aihong, Zhang Zhaofeng, Ding Jing, Du Jing, Che Y |
| Joint Effect of Multiple Prothrombotic Genotypes and Obesity on the Risk of Incident Venous Thromboembolism. Thrombosis and haemostasis 2021 5 122 (2): 267-276. Frischmuth Tobias, Hindberg Kristian, Gabrielsen Maiken E, Brumpton Ben, Hveem Kristian, Brækkan Sigrid K, Hansen John-Bjarne, Morelli Vânia |
| Predictive Ability of a Clinical-Genetic Risk Score for Venous Thromboembolism in Northern and Southern European Populations. TH open : companion journal to thrombosis and haemostasis 2021 7 5 (3): e303-e311. Salas Eduardo, Farm Maria, Pich Sara, Onelöv Liselotte, Guillen Kevin, Ortega Israel, Antovic Jovan P, Soria Jose Manu |
| The Higher Prevalence of Venous Thromboembolism in the Hungarian Roma Population Could Be Due to Elevated Genetic Risk and Stronger Gene-Environmental Interactions. Frontiers in cardiovascular medicine 2021 11 8 647416. Natae Shewaye Fituma, Kósa Zsigmond, Sándor János, Merzah Mohammed Abdulridha, Bereczky Zsuzsanna, Pikó Péter, Ádány Róza, Fiatal Szilv |
| Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event. Journal of thrombosis and haemostasis : JTH 2020 Jul . Skille Hanne, Paulsen Benedikte, Hveem Kristian, Gabrielsen Maiken E, Brumpton Ben, Hindberg Kristian, Gran Olga V, Rosendaal Frits R, Braekkan Sigrid K, Hansen John-Bjar |
| 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 |
| Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk: The Tromsø Study. Research and practice in thrombosis and haemostasis 2020 Feb 4 (2): 247-254. Sejrup Joakim K, Morelli Vania M, Løchen Maja-Lisa, Njølstad Inger, Mathiesen Ellisiv B, Wilsgaard Tom, Hansen John-Bjarne, Brækkan Sigrid |
| Impact of prothrombotic genotypes on the association between family history of myocardial infarction and venous thromboembolism. Journal of thrombosis and haemostasis : JTH 2019 May . Småbrekke Birgit, Rinde Ludvig B, Evensen Line H, Morelli Vania M, Hveem Kristian, Gabrielsen Maiken E, Njølstad Inger, Mathiesen Ellisiv B, Rosendaal Frits R, Braekkan Sigrid K, Hansen John-Bjar |
| 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 |
| Direct blood PCR: TaqMan-probe based detection of the venous thromboembolism associated mutations factor V Leiden and prothrombin c.20210G>A without DNA extraction. Clinica chimica acta; international journal of clinical chemistry 2018 11 488 221-225. Geiger Kathrin, Leiherer Andreas, Brandtner Eva-Maria, Fraunberger Peter, Drexel Heinz, Muendlein Ax |
| 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 |
| 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 |
| Genetic Determinants of Thrombin Generation and Their Relation to Venous Thrombosis: Results from the GAIT-2 Project. PloS one 2016 11 (1): e0146922. Martin-Fernandez Laura, Ziyatdinov Andrey, Carrasco Marina, Millon Juan Antonio, Martinez-Perez Angel, Vilalta Noelia, Brunel Helena, Font Montserrat, Hamsten Anders, Souto Juan Carlos, Soria José Manu |
| 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 |
| 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 |
| 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 |
| 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 |
| Multilocus genetic risk scores for venous thromboembolism risk assessment. Journal of the American Heart Association 2014 Oct 3 (5): e001060. Soria José Manuel, Morange Pierre-Emmanuel, Vila Joan, Souto Juan Carlos, Moyano Manel, Trégouët David-Alexandre, Mateo José, Saut Noémi, Salas Eduardo, Elosua Rober |
| Influence of single nucleotide polymorphisms on thrombin generation in factor V Leiden heterozygotes. Thrombosis and haemostasis 2014 Mar 111 (3): 438-46. Segers O, Simioni P, Tormene D, Castoldi |
| Haplotypes of TAFI gene and the risk of cerebral venous thrombosis--a case-control study. Thrombosis research 2013 Nov . Orikaza CM, Morelli VM, Matos MF, Lourenço DM |
| A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
Journal of thrombosis and haemostasis : JTH 2012 Aug 10 (8): 1521-31. Heit J A, Armasu S M, Asmann Y W, Cunningham J M, Matsumoto M E, Petterson T M, De Andrade |
| Site of venous thromboembolism and prothrombotic mutations according to body mass index. Results from the EDITH study. British journal of haematology 2011 Aug 154 (4): 486-91. Delluc Aurélien, Le Moigne Emmanuelle, Tromeur Cécile, Noel-Savina Elise, Couturaud Francis, Mottier Dominique, Le Gal Grégoire, Lacut Kari |
| Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism. Journal of thrombosis and haemostasis : JTH 2011 Jun 9 (6): 1133-42. Heit J A, Cunningham J M, Petterson T M, Armasu S M, Rider D N, DE Andrade |
| Genetic susceptibility, smoking, obesity and risk of venous thromboembolism. British journal of haematology 2010 Apr 149 (2): 273-9. Severinsen Marianne T, Overvad Kim, Johnsen Søren P, Dethlefsen Claus, Madsen Poul H, Tjønneland Anne, Kristensen Søren |
| Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancy. Journal of thrombosis and haemostasis : JTH 2010 Apr 8 (4): 707-13. Galanaud J P, Cochery-Nouvellon E, Alonso S, Chauleur C, Mercier E, Lissalde-Lavigne G, Fabbro-Peray P, Reny J L, Mares P, Dauzat M, Quere I, Gris J |
| Thrombin generation as an intermediate phenotype for venous thrombosis. Thrombosis and haemostasis 2010 1 103 (1): 114-22. Segers Olivier, van Oerle René van, ten Cate Hugo ten, Rosing Jan, Castoldi Elisabet |
| Rapid triplex asymmetric real-time PCR hybridization probe assay for the joint genotyping of F2, F5 and F12. Clinical biochemistry 2009 Aug 42 (12): 1317-24. Martínez-Serra J, Gutierrez A, Amat J C, Galmés B, Vila A, Julia M, López H, Bautista A M, Truyols C, Ros T, Navarro M, Canaro M, Díaz M, Besalduch |
| Prevalence of genetic thrombophilic polymorphisms in the Sri Lankan population--implications for association study design and clinical genetic testing services. Experimental and molecular pathology 2009 Jul . Dissanayake VH, Weerasekera LY, Gammulla CG, Jayasekara RW |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 31, 2023
- Content source: