HuGE Literature Finder
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| 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 |
| Prothrombotic genotypes and risk of venous thromboembolism in occult cancer. Thrombosis research 2021 Jul 205 17-23. Skille Hanne, Paulsen Benedikte, Hveem Kristian, Severinsen Marianne T, Gabrielsen Maiken E, Kristensen Søren R, Næss Inger Anne, Hindberg Kristian, Tjønneland Anne, Brækkan Sigrid K, Hansen John-Bjar |
| 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, E Gabrielsen Maiken, 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 |
Novel exomic rare variants associated with venous thrombosis.
British journal of haematology 2020 Mar . Deguchi Hiroshi, Shukla Meenal, Hayat Mohammed, Torkamani Ali, Elias Darlene J, Griffin John |
| 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 |
| [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 |
| Genome-wide association study of peripheral artery disease in the Million Veteran Program.
Nature medicine 2019 Aug 25 (8): 1274-1279. Klarin Derek, Lynch Julie, Aragam Krishna, Chaffin Mark, Assimes Themistocles L, Huang Jie, Lee Kyung Min, Shao Qing, Huffman Jennifer E, Natarajan Pradeep, Arya Shipra, Small Aeron, Sun Yan V, Vujkovic Marijana, Freiberg Matthew S, Wang Lu, Chen Jinbo, Saleheen Danish, Lee Jennifer S, Miller Donald R, Reaven Peter, Alba Patrick R, Patterson Olga V, DuVall Scott L, Boden William E, Beckman Joshua A, Gaziano J Michael, Concato John, Rader Daniel J, Cho Kelly, Chang Kyong-Mi, Wilson Peter W F, O'Donnell Christopher J, Kathiresan Sekar, , Tsao Philip S, Damrauer Scott |
| A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process.
Journal of thrombosis and haemostasis : JTH 2019 Jul . Thibord Florian, Hardy Lise, Ibrahim-Kosta Manal, Saut Noémie, Pulcrano-Nicolas Anne-Sophie, Goumidi Louisa, Civelek Mete, Eriksson Per, Deleuze Jean-François, Le Goff Wilfried, Trégouët David-Alexandre, Morange Pierre-Emmanu |
| 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 |
| Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation. Scientific reports 2019 Mar 9 (1): 3750. Ibrahim-Kosta M, Suchon P, Couturaud F, Smadja D, Olaso R, Germain M, Saut N, Goumidi L, Derbois C, Thibord F, Debette S, Amouyel P, Deleuze J F, van Doorn P, Castoldi E, Patin E, Alessi M C, Trégouët D A, Morange P |
| 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 |
| 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 |
| Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss. Bosnian journal of basic medical sciences 2017 May . Mahmutbegovic Emir, Marjanovic Damir, Medjedovic Edin, Mahmutbegovic Nevena, Dogan Serkan, Valjevac Amina, Czerska Ewa, Pawi?ska-Matecka Anna, Madlani Agnieszka, Adler Grazy |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| A Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2015 Oct . Kalpage Hasini A, Sumathipala Dulika S, Goonasekara Hemali W, Dissanayake Vajira |
| 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 |
| Effects of MTHFR c.677C>T, F2 c.20210G>A and F5 Leiden Polymorphisms in Gastroschisis. Journal of investigative surgery : the official journal of the Academy of Surgical Research 2015 Sep 1-5. Makhmudi Akhmad, Sadewa Ahmad Hamim, Aryandono Teguh, Chatterjee Sumantra, Heij Hugo A, Gunad |
| Influence of CYP2C9 polymorphism on the fall in International Normalized Ratio in patients interrupting warfarin therapy before elective surgery. Journal of thrombosis and haemostasis : JTH 2015 Aug 13 (8): 1436-40. Abohelaika S, Wynne H, Avery P, Kamali |
| Genetic determinants of tissue factor pathway inhibitor plasma levels. Thrombosis and haemostasis 2015 Jul 114 (2): 245-57. Dennis J, Kassam I, Morange P-E, Trégouët D-A, Gagnon |
| 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 |
| Three novel variants in the coagulation factor V gene associated with deep venous thrombosis in Chilean patients with Amerindian ethnic background. Clinica chimica acta; international journal of clinical chemistry 2015 Apr 444 24-8. Guzmán Neftalí, Larama Giovanni, Ávila Andrés, Salazar Luis |
| 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 |
| [The association of hemostasis system genes with the development of ischemic stroke in patients under the age of 50 years]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 0 118 (9. Vyp. 2): 14-21. Kimelfeld E I, Koltsova E A, Petrova E A, Gudkova V V, Stahovskaya L V, Tupitsyna T V, Bondarenko E A, Slominsky P A, Limborska S |
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