HuGE Literature Finder
Records 1-30
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Association of ABO haplotypes with the risk of venous thrombosis: impact on disease risks estimation.
Blood 2020 Dec . Goumidi Louisa, Thibord Florian, Wiggins Kerri L, Li-Gao Ruifang, Brown Michael R, van Hylckama Vlieg Astrid, Souto Juan Carlos, Soria Jose Manuel, Ibrahim-Kosta Manal, Saut Noémie, Daian-Bacq Delphine, Olaso Robert, Amouyel Philippe, Debette Stephanie, Boland Anne, Bailly Pascal, Morrison Alanna, Mook-Kanamori Dennis O, Deleuze Jean-François, Johnson Andrew D, de Vries Paul S, Sabater-Lleal Maria, Chiaroni Jacques, Smith Nicholas L, Rosendaal Frits R, Chasman Daniel I, Tregouet David, Morange Pierre-Emmanu |
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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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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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Polymorphism of the ABO gene associate with thrombosis risk in patients with paroxysmal nocturnal hemoglobinuria.
Oncotarget 2017 Nov 8 (54): 92411-92419. Long Zhangbiao, Du Yali, Li Hongmin, Han Bi |
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Prevalence of common hereditary risk factors for thrombophilia in Somalia and identification of a novel Gln544Arg mutation in coagulation factor V.
Journal of thrombosis and thrombolysis 2017 Sep . Abdi Abshir Ali, Osman Abdimaj |
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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Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance.
Journal of thrombosis and haemostasis : JTH 2016 09 14 (9): 1888-98. Ozel A B, McGee B, Siemieniak D, Jacobi P M, Haberichter S L, Brody L C, Mills J L, Molloy A M, Ginsburg D, Li J Z, Desch K |
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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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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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ABO blood type and ABO gene with susceptibility to deep vein thrombosis following orthopedic surgery: a case-control study in Chinese Han population.
Science China. Life sciences 2015 Apr 58 (4): 390-1. Sun Ye, Mao Ping, Lu JingWei, Dai Jin, Teng HuaJian, Jiang Qi |
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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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ABO blood group polymorphisms and risk for ischemic stroke and peripheral arterial disease.
Molecular biology reports 2014 Mar 41 (3): 1771-7. Sabino Adriano de Paula, Ribeiro Daniel Dias, Domingheti Caroline Pereira, Rios Danyelle Romana Alves, Dusse Luci Maria SantAna, Carvalho Maria das Graças, Fernandes Ana Pau |
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Lack of strong effect modification by NFE2L2/CYP3A5/ABO of the risk of venous thrombosis associated with oral hormone therapy.
Journal of thrombosis and haemostasis : JTH 2013 Aug 11 (8): 1617-9. Blondon M, Wiggins K L, Harrington L B, Psaty B M, Smith N |
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ABO blood groups and the risk of venous thrombosis in patients with inherited thrombophilia.
Blood transfusion = Trasfusione del sangue 2013 Apr 11 (2): 250-3. Spiezia Luca, Campello Elena, Bon Maria, Tison Tiziana, Milan Marta, Simioni Paolo, Prandoni Pao |
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Risk of venous thromboembolism and myocardial infarction associated with factor V Leiden and prothrombin mutations and blood type.
CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2013 Feb . Sode BF, Allin KH, Dahl M, Gyntelberg F, Nordestgaard BG |
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Genetic polymorphisms associated with carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study.
Physiological genomics 2013 Jan 45 (2): 79-88. Miller Virginia M, Petterson Tanya M, Jeavons Elysia N, Lnu Abhinita S, Rider David N, Heit John A, Cunningham Julie M, Huggins Gordon S, Hodis Howard N, Budoff Matthew J, Santoro Nanette, Hopkins Paul N, Lobo Rogerio A, Manson JoAnn E, Naftolin Frederick, Taylor Hugh S, Harman S Mitchell, de Andrade Mari |
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Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
Proceedings of the National Academy of Sciences of the United States of America 2013 Jan 110 (2): 588-93. Desch Karl C, Ozel Ayse B, Siemieniak David, Kalish Yossi, Shavit Jordan A, Thornburg Courtney D, Sharathkumar Anjali A, McHugh Caitlin P, Laurie Cathy C, Crenshaw Andrew, Mirel Daniel B, Kim Yoonhee, Cropp Cheryl D, Molloy Anne M, Kirke Peadar N, Bailey-Wilson Joan E, Wilson Alexander F, Mills James L, Scott John M, Brody Lawrence C, Li Jun Z, Ginsburg Dav |
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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 |
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ABO blood group and von Willebrand factor levels partially explained the incomplete penetrance of congenital thrombophilia.
Arteriosclerosis, thrombosis, and vascular biology 2012 Aug 32 (8): 2021-8. Cohen William, Castelli Christel, Alessi Marie-Christine, Aillaud Marie-Françoise, Bouvet Sophie, Saut Noémie, Brunet Dominique, Barthet Marie-Christine, Tregouet David-Alexandre, Lavigne Géraldine, Morange Pierre-Emmanu |
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Non-O blood type is the commonest genetic risk factor for VTE: results from a meta-analysis of the literature.
Seminars in thrombosis and hemostasis 2012 Jul 38 (5): 535-48. Dentali Francesco, Sironi Anna Paola, Ageno Walter, Turato Sara, Bonfanti Carlo, Frattini Francesco, Crestani Silvia, Franchini Massi |
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The association of non-O blood group and severity of liver fibrosis in patients with chronic hepatitis C infection.
Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2012 May 17 (5): 466-9. Shavakhi Ahmad, Hajalikhani Mehri, Minakari Mohammad, Norian Alireza, Riahi Rahil, Azarnia Mina, Liaghat Li |
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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 |
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Hemodialysis vascular access thrombosis: The role of factor V Leiden, prothrombin gene mutation and ABO blood groups.
Clinica chimica acta; international journal of clinical chemistry 2011 Feb 412 (5-6): 425-9. Rios Danyelle R A, Fernandes Ana P, Carvalho Maria G, Figueiredo Roberta C, Guimarães Daniela A M, Reis Daniberg R, Simões e Silva Ana C, Gomes Karina B, Dusse Luci M |
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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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Effect of genetic variations in syntaxin-binding protein-5 and syntaxin-2 on von Willebrand factor concentration and cardiovascular risk.
Circulation. Cardiovascular genetics 2010 Dec 3 (6): 507-12. van Loon Janine E, Leebeek Frank W G, Deckers Jaap W, Dippel Diederik W J, Poldermans Don, Strachan David P, Tang Weihong, O'Donnell Christopher J, Smith Nicholas L, de Maat Moniek P |
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von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels.
Journal of thrombosis and haemostasis : JTH 2010 Sep 8 (9): 1986-93. Hickson N, Hampshire D, Winship P, Goudemand J, Schneppenheim R, Budde U, Castaman G, Rodeghiero F, Federici A B, James P, Peake I, Eikenboom J, Goodeve A, |
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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 |
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ABO blood groups and genetic risk factors for thrombosis in Croatian population.
Croatian medical journal 2009 Dec 50 (6): 550-8. Jukic Irena, Bingulac-Popovic Jasna, Dogic Vesna, Babic Ivana, Culej Jelena, Tomicic Maja, Vuk Tomislav, Sarlija Dorotea, Balija Meli |
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- Page last updated:Apr 08, 2021
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