HuGE Literature Finder
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| Characterization of the human ABO genotypes and their association to common inflammatory and cardiovascular disease in the UK Biobank. American journal of hematology 2021 Jul . Höglund Julia, Karlsson Torgny, Johansson Therese, Ek Weronica E, Johansson Å |
| 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 |
| Genetic Risk Profiling Associated with Recurrent Unprovoked Venous Thromboembolism. Genes 2021 Jun 12 (6): . Hodeib Hossam, Youssef Amira, Allam Alzahraa A, Selim Amal, Tawfik Mohamed A, Abosamak Mohammed F, Esam Ahmed, Abd Elghafar Mohamed S, Samir Sameh, ELshora Ola |
Genome-Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis.
Annals of neurology 2021 8 90 (5): 777-788. Ken-Dror Gie, Cotlarciuc Ioana, Martinelli Ida, Grandone Elvira, Hiltunen Sini, Lindgren Erik, Margaglione Maurizio, Duchez Veronique Le Cam, Triquenot Aude Bagan, Zedde Marialuisa, Mancuso Michelangelo, Ruigrok Ynte M, Marjot Thomas, Worrall Brad, Majersik Jennifer J, Metso Tiina M, Putaala Jukka, Haapaniemi Elena, Zuurbier Susanna M, Brouwer Matthijs C, Passamonti Serena M, Abbattista Maria, Bucciarelli Paolo, Mitchell Braxton D, Kittner Steven J, Lemmens Robin, Jern Christina, Pappalardo Emanuela, Costa Paolo, Colombi Marina, de Sousa Diana Aguiar, Rodrigues Sofia, Canhão Patrícia, Tkach Aleksander, Santacroce Rosa, Favuzzi Giovanni, Arauz Antonio, Colaizzo Donatella, Spengos Kostas, Hodge Amanda, Ditta Reina, Pezzini Alessandro, Debette Stephanie, Coutinho Jonathan M, Thijs Vincent, Jood Katarina, Pare Guillaume, Tatlisumak Turgut, Ferro José M, Sharma Pank |
| Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk 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 |
| Factor VIII pharmacokinetics associates with genetic modifiers of VWF and FVIII clearance in an adult hemophilia A population. Journal of thrombosis and haemostasis : JTH 2020 Nov . Ogiwara Kenichi, Swystun Laura L, Paine A Simonne, Kepa Sylvia, Choi Seon Jai, Rejtö Judit, Hopman Wilma, Pabinger Ingrid, Lillicrap Dav |
| 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 |
| 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 |
| Functional polymorphisms in the LDLR and pharmacokinetics of Factor VIII concentrates. Journal of thrombosis and haemostasis : JTH 2019 May . Lunghi Barbara, Bernardi Francesco, Martinelli Nicola, Frusconi Sabrina, Branchini Alessio, Linari Silvia, Marchetti Giovanna, Castaman Giancarlo, Morfini Massi |
| 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 |
| 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 |
| Joint effects of prothrombotic genotypes and body height on the risk of venous thromboembolism: the Tromsø study. Journal of thrombosis and haemostasis : JTH 2017 Nov . Horvei Lars D, Braekkan Sigrid K, Smith Erin N, Solomon Terry, Hindberg Kristian, Frazer Kelly A, Rosendaal Frits R, Hansen John-Bjar |
| 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 |
| 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 |
| Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations. Journal of thrombosis and haemostasis : JTH 2016 Dec . Loomans J I, van Velzen A S, Eckhardt C L, Peters M, Mäkipernaa A, Holmstrom M, Brons P P, Dors N, Haya S, Voorberg J, van der Bom J G, Fijnvandraat |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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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- Page last updated:Feb 03, 2023
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