Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 67 Records) |
Query Trace: F11[original query] |
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High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study. Haemophilia : the official journal of the World Federation of Hemophilia 2017 Sep . Esteban J, de la Morena-Barrio M E, Salloum-Asfar S, Padilla J, Miñano A, Roldán V, Soria J M, Vidal F, Corral J, Vicente |
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 M M, Bucciarelli P, Martinelli I, Baglin T P, Peyvandi F, Rosendaal F R, |
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 determinants of activity and antigen levels of contact system factors. Journal of thrombosis and haemostasis : JTH 2018 Oct . Rohmann J L, de Haan H G, Algra A, Vossen C Y, Rosendaal F R, Siegerink |
Common Risk Factors Add to Inherited Thrombophilia to Predict Venous Thromboembolism Risk in Families. TH open : companion journal to thrombosis and haemostasis 2019 Jan 3 (1): e28-e35. Suchon Pierre, Resseguier Noemie, Ibrahim Manal, Robin Alexia, Venton Geoffroy, Barthet Marie-Christine, Brunet Dominique, Saut Noemie, Alessi Marie-Christine, Trégouët David A, Morange Pierre |
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 |
Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population. Thrombosis research 2019 5 179 37-44. Fiatal Szilvia, Pikó Péter, Kósa Zsigmond, Sándor János, Ádány Ró |
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 |
Heterozygote carriers of mutations in the F11 gene, encoding Factor XI, have normal coagulation by thromboelastography during pregnancy. International journal of obstetric anesthesia 2019 12 42 57-60. Ciampa E J, Liu N, Stiles J, Carani J L, Li Y, Hess P |
Candidate single nucleotide polymorphisms and thromboembolism in acute lymphoblastic leukemia - A NOPHO ALL2008 study. Thrombosis research 2019 Nov 184 92-98. Jarvis Kirsten Brunsvig, LeBlanc Marissa, Tulstrup Morten, Nielsen Rikke Linnemann, Albertsen Birgitte Klug, Gupta Ramneek, Huttunen Pasi, Jónsson Ólafur Gisli, Rank Cecilie Utke, Ranta Susanna, Ruud Ellen, Saks Kadri, Trakymiene Sonata Saulyte, Tuckuviene Ruta, Schmiegelow Kje |
Congenital factor XI deficiency, complete genotype and phenotype of two Iranian families. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2019 10 30 (8): 409-412. Dorgalaleh Akbar, Gholaminezhad Masoume, Shiravand Yavar, Naderi Majid, Safa Maj |
A large-scale exome array analysis of venous thromboembolism.
Genetic epidemiology 2019 Jan . Lindström Sara, Brody Jennifer A, Turman Constance, Germain Marine, Bartz Traci M, Smith Erin N, Chen Ming-Huei, Puurunen Marja, Chasman Daniel, Hassler Jeffrey, Pankratz Nathan, Basu Saonli, Guan Weihua, Gyorgy Beata, Ibrahim Manal, Empana Jean-Philippe, Olaso Robert, Jackson Rebecca, Braekkan Sigrid K, McKnight Barbara, Deleuze Jean-Francois, O'Donnell Cristopher J, Jouven Xavier, Frazer Kelly A, Psaty Bruce M, Wiggins Kerri L, Taylor Kent, Reiner Alexander P, Heckbert Susan R, Kooperberg Charles, Ridker Paul, Hansen John-Bjarne, Tang Weihong, Johnson Andrew D, Morange Pierre-Emmanuel, Trégouët David A, Kraft Peter, Smith Nicholas L, Kabrhel Christopher, |
The Correlation Between Abnormal Uterine Artery Flow in the First Trimester and Genetic Thrombophilic Alteration: A Prospective Case-Controlled Pilot Study. Diagnostics (Basel, Switzerland) 2020 Aug 10 (9): . Vedmedovska Natalija, Bokucava Diana, Kivite-Urtane Anda, Rovite Vita, Zake-Nikitina Liene, Klovins Janis, Fodina Violeta, Donders Gilbert G |
COVID-19-Related Coagulopathy-Is Transferrin a Missing Link? Diagnostics (Basel, Switzerland) 2020 8 10 (8): . McLaughlin Katie-May, Bechtel Marco, Bojkova Denisa, Münch Christian, Ciesek Sandra, Wass Mark N, Michaelis Martin, Cinatl Jindri |
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 |
Determining the association of thrombophilic gene polymorphisms with recurrent pregnancy loss in Iranian women. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2020 6 36 (12): 1082-1085. Khorshidi Fatemeh, Hajizadeh Sonia, Choobineh Hamid, Alizadeh Shaban, Sharifi Mohammad Jafar, Kavosh Zeinab, Omidkhoda Azad |
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 |
Congenital factor XI deficiency caused by a novel F11 missense variant: a case report. Croatian medical journal 2020 3 61 (1): 62-65. Gotovac Jer?i? Kristina, Blažekovi? Antonela, Han?evi? Mirea, Bili? Ervina, Borove?ki Fr |
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 |
Implications of venous thromboembolism GWAS reported genetic makeup in the clinical outcome of ovarian cancer patients. The pharmacogenomics journal 2020 Nov . Tavares Valéria, Pinto Ricardo, Assis Joana, Coelho Sara, Brandão Mariana, Alves Sara, Pereira Deolinda, Medeiros R |
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 |
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 |
Monogenic Causes of Apparently Idiopathic Perinatal Intracranial Hemorrhage. Annals of neurology 2021 2 89 (4): 813-822. Hausman-Kedem Moran, Malinger Gustavo, Modai Shira, Kushner Steven A, Shiran Shelly I, Ben-Sira Liat, Roth Jonathan, Constantini Shlomi, Fattal-Valevski Aviva, Ben-Shachar Sh |
The Risk of Venous Thromboembolism Attributed to Established Prothrombotic Genotypes. Thrombosis and haemostasis 2021 Nov . Evensen Line H, Arnesen Carl Arne Løchen, Rosendaal Frits R, Gabrielsen Maiken E, Brumpton Ben M, Hveem Kristian, Hansen John-Bjarne, Brækkan Sigrid |
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 |
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 |
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature 2022 10 611 (7934): 115-123. Mishra Aniket, Malik Rainer, Hachiya Tsuyoshi, Jürgenson Tuuli, Namba Shinichi, Posner Daniel C, Kamanu Frederick K, Koido Masaru, Le Grand Quentin, Shi Mingyang, He Yunye, Georgakis Marios K, Caro Ilana, Krebs Kristi, Liaw Yi-Ching, Vaura Felix C, Lin Kuang, Winsvold Bendik Slagsvold, Srinivasasainagendra Vinodh, Parodi Livia, Bae Hee-Joon, Chauhan Ganesh, Chong Michael R, Tomppo Liisa, Akinyemi Rufus, Roshchupkin Gennady V, Habib Naomi, Jee Yon Ho, Thomassen Jesper Qvist, Abedi Vida, Cárcel-Márquez Jara, Nygaard Marianne, Leonard Hampton L, Yang Chaojie, Yonova-Doing Ekaterina, Knol Maria J, Lewis Adam J, Judy Renae L, Ago Tetsuro, Amouyel Philippe, Armstrong Nicole D, Bakker Mark K, Bartz Traci M, Bennett David A, Bis Joshua C, Bordes Constance, Børte Sigrid, Cain Anael, Ridker Paul M, Cho Kelly, Chen Zhengming, Cruchaga Carlos, Cole John W, de Jager Phil L, de Cid Rafael, Endres Matthias, Ferreira Leslie E, Geerlings Mirjam I, Gasca Natalie C, Gudnason Vilmundur, Hata Jun, He Jing, Heath Alicia K, Ho Yuk-Lam, Havulinna Aki S, Hopewell Jemma C, Hyacinth Hyacinth I, Inouye Michael, Jacob Mina A, Jeon Christina E, Jern Christina, Kamouchi Masahiro, Keene Keith L, Kitazono Takanari, Kittner Steven J, Konuma Takahiro, Kumar Amit, Lacaze Paul, Launer Lenore J, Lee Keon-Joo, Lepik Kaido, Li Jiang, Li Liming, Manichaikul Ani, Markus Hugh S, Marston Nicholas A, Meitinger Thomas, Mitchell Braxton D, Montellano Felipe A, Morisaki Takayuki, Mosley Thomas H, Nalls Mike A, Nordestgaard Børge G, O'Donnell Martin J, Okada Yukinori, Onland-Moret N Charlotte, Ovbiagele Bruce, Peters Annette, Psaty Bruce M, Rich Stephen S, Rosand Jonathan, Sabatine Marc S, Sacco Ralph L, Saleheen Danish, Sandset Else Charlotte, Salomaa Veikko, Sargurupremraj Muralidharan, Sasaki Makoto, Satizabal Claudia L, Schmidt Carsten O, Shimizu Atsushi, Smith Nicholas L, Sloane Kelly L, Sutoh Yoichi, Sun Yan V, Tanno Kozo, Tiedt Steffen, Tatlisumak Turgut, Torres-Aguila Nuria P, Tiwari Hemant K, Trégouët David-Alexandre, Trompet Stella, Tuladhar Anil Man, Tybjærg-Hansen Anne, van Vugt Marion, Vibo Riina, Verma Shefali S, Wiggins Kerri L, Wennberg Patrik, Woo Daniel, Wilson Peter W F, Xu Huichun, Yang Qiong, Yoon Kyungheon, , , , , , , , , , , , , , , , Millwood Iona Y, Gieger Christian, Ninomiya Toshiharu, Grabe Hans J, Jukema J Wouter, Rissanen Ina L, Strbian Daniel, Kim Young Jin, Chen Pei-Hsin, Mayerhofer Ernst, Howson Joanna M M, Irvin Marguerite R, Adams Hieab, Wassertheil-Smoller Sylvia, Christensen Kaare, Ikram Mohammad A, Rundek Tatjana, Worrall Bradford B, Lathrop G Mark, Riaz Moeen, Simonsick Eleanor M, Kõrv Janika, França Paulo H C, Zand Ramin, Prasad Kameshwar, Frikke-Schmidt Ruth, de Leeuw Frank-Erik, Liman Thomas, Haeusler Karl Georg, Ruigrok Ynte M, Heuschmann Peter Ulrich, Longstreth W T, Jung Keum Ji, Bastarache Lisa, Paré Guillaume, Damrauer Scott M, Chasman Daniel I, Rotter Jerome I, Anderson Christopher D, Zwart John-Anker, Niiranen Teemu J, Fornage Myriam, Liaw Yung-Po, Seshadri Sudha, Fernández-Cadenas Israel, Walters Robin G, Ruff Christian T, Owolabi Mayowa O, Huffman Jennifer E, Milani Lili, Kamatani Yoichiro, Dichgans Martin, Debette Stephan |
A combination of strongly associated prothrombotic single nucleotide polymorphisms could efficiently predict venous thrombosis risk. Frontiers in cardiovascular medicine 2023 9 10 1224462. Shewaye Fituma Natae, Mohammed Abdulridha Merzah, János Sándor, Róza Ádány, Zsuzsanna Bereczky, Szilvia Fiat |
Venous thromboembolism-related genetic determinant F11 rs4253417 is a potential prognostic factor in ischaemic stroke. Molecular and cellular probes 2023 6 70 101917. Valéria Tavares, Joana Assis, Ricardo Pinto, Margarida Freitas-Silva, Rui Medeir |
Factor XI in Carriers of Antiphospholipid Antibodies: Elevated Levels Associated with Symptomatic Thrombotic Cases, While Low Levels Linked to Asymptomatic Cases. International journal of molecular sciences 2023 11 24 (22): . Javier Pagán-Escribano, Javier Corral, Antonia Miñano, José Padilla, Vanessa Roldán, María Julia Hernández-Vidal, Jesús Lozano, Isabel de la Morena-Barrio, Vicente Vicente, María Luisa Lozano, María Teresa Herranz, María Eugenia de la Morena-Barr |
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