Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 92 Records) |
Query Trace: FGG[original query] |
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Polymorphism rs2066865 in the Fibrinogen Gamma Chain (FGG) Gene Increases Plasma Fibrinogen Concentration and Is Associated with an Increased Microvascular Thrombosis Rate. Medicina (Kaunas, Lithuania) 2019 9 55 (9): . Drizlionoka Karina, Zari?š J?nis, Ozoli?a Agnese, ?ikitina-Za?e Liene, Mamaja Biru |
Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations. Thrombosis research 2019 9 182 133-140. Wypasek Ewa, Klukowska Anna, Zdziarska Joanna, Zawilska Krystyna, Treli?ski Jacek, Iwaniec Teresa, Mital Andrzej, Pietrys Danuta, Sydor Wojciech, Neerman-Arbez Marguerite, Undas Anet |
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 |
Fibrinogen gamma gene rs2066865 and risk of cancer-related venous thromboembolism. Haematologica 2019 Oct . Paulsen Benedikte, Skille Hanne, Smith Erin N, Hveem Kristian, Gabrielsen Maiken E, Brækkan Sigrid K, Rosendaal Frits R, Frazer Kelly A, Gran Olga V, Hansen John-Bjar |
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 |
Mutations in inherited fibrinogen disorders correlated with clinical features in the Chinese population. Journal of thrombosis and thrombolysis 2020 9 51 (4): 1127-1131. Wan Yafang, Li Tian, Zhang Wei, Wang Liying, Zhang Yu, Liao Pu, Liu Shiqia |
Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations. International journal of laboratory hematology 2020 7 42 (5): 619-627. Tavasoli Behnaz, Safa Majid, Dorgalaleh Akbar, Ghasemi Jahan B, Rezaei Makhouri Farahnaz, Rezvani Mohammad R, Ahmadi Abbas, Tabibian Shadi, Jazebi Mohammad, Baghaipour Mohammad R, Zaker Farh |
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 |
Fibrinogen, factor XIII and ?-antiplasmin genotypes are associated with inflammatory activity and anti-citrullinated protein antibodies. Thrombosis research 2020 May 191 90-96. Hoppe Berthold, Schwedler Christian, Edelmann Anke, Pistioli Anneta, Poddubnyy Denis, Burmester Gerd-Rüdiger, Häupl Thom |
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 |
The joint effect of genetic risk factors and different types of combined oral contraceptives on venous thrombosis risk. British journal of haematology 2020 4 191 (1): 90-97. Khialani Deeksha, le Cessie Saskia, Lijfering Willem M, Cannegieter Suzanne C, Rosendaal Frits R, van Hylckama Vlieg Astr |
Evaluation of single nucleotide polymorphisms in 6 candidate genes and carotid intima-media thickness in community-dwelling residents. PloS one 2020 15 (3): e0230715. Wu Fang-Yang, Li Chia-Ing, Liao Li-Na, Liu Chiu-Shong, Lin Wen-Yuan, Lin Chih-Hsueh, Yang Chuan-Wei, Li Tsai-Chung, Lin Cheng-Chi |
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 |
Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population. Haemophilia : the official journal of the World Federation of Hemophilia 2021 8 27 (6): 1022-1027. Shen Ming-Ching, Wang Jiaan-Der, Tsai Woei, Lin Ching-Yeh, Lin Jen-Shiou, Kuo Su-Feng, Lin Po-Te, Huang Ying-Chih, Hung Mei-H |
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 |
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2021 7 60 (6): 103203. Mohsenian Samin, Seidizadeh Omid, Mirakhorli Mojgan, Jazebi Mohammad, Azarkeivan Azi |
Molecular classification of blood and bleeding disorder genes. NPJ genomic medicine 2021 Jul 6 (1): 62. Baz Batoul, Abouelhoda Mohamed, Owaidah Tarek, Dasouki Majed, Monies Dorota, Al Tassan Na |
Dysfibrinogenemia-Potential Impact of Genotype on Thrombosis or Bleeding. Seminars in thrombosis and hemostasis 2021 7 48 (2): 161-173. Bor Mustafa Vakur, Feddersen Søren, Pedersen Inge Søkilde, Sidelmann Johannes Jakobsen, Kristensen Søren Ris |
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 |
Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders. International journal of molecular sciences 2021 3 22 (5): . Szanto Timea, Lassila Riitta, Lemponen Marja, Lehtinen Elina, Neerman-Arbez Marguerite, Casini Alessand |
Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease. Journal of medical biochemistry 2021 Mar 40 (2): 138-149. Broni? Ana, Feren?ak Goran, Bernat Robert, Leni?ek-Krleža Jasna, Dumi? Jerka, Dabeli? San |
Association of Genetic Polymorphisms of Fibrinogen, Factor XIII A-Subunit and ?-Antiplasmin with Fibrinogen Levels in Pregnant Women. Life (Basel, Switzerland) 2021 12 11 (12): . Schwedler Christian, Heymann Guido, Bukreeva Larisa, Hoppe Bertho |
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 |
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 |
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 of 14?389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Human molecular genetics 2022 May . Pankratz Nathan, Wei Peng, Brody Jennifer A, Chen Ming-Huei, de Vries Paul S, Huffman Jennifer E, Stimson Mary Rachel, Auer Paul L, Boerwinkle Eric, Cushman Mary, de Maat Moniek P M, Folsom Aaron R, Franco Oscar H, Gibbs Richard A, Haagenson Kelly K, Hofman Albert, Johnsen Jill M, Kovar Christie L, Kraaij Robert, McKnight Barbara, Metcalf Ginger A, Muzny Donna, Psaty Bruce M, Tang Weihong, Uitterlinden André G, van Rooij Jeroen G J, Dehghan Abbas, O'Donnell Christopher J, Reiner Alex P, Morrison Alanna C, Smith Nicholas |
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 |
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. medRxiv : the preprint server for health sciences 2023 7 . Jennifer E Huffman, Jayna Nicolas, Julie Hahn, Adam S Heath, Laura M Raffield, Lisa R Yanek, Jennifer A Brody, Florian Thibord, Laura Almasy, Traci M Bartz, Lawrence F Bielak, Russell P Bowler, Germán D Carrasquilla, Daniel I Chasman, Ming-Huei Chen, David B Emmert, Mohsen Ghanbari, Jeffery Haessle, Jouke-Jan Hottenga, Marcus E Kleber, Ngoc-Quynh Le, Jiwon Lee, Joshua P Lewis, Ruifang Li-Gao, Jian'an Luan, Anni Malmberg, Massimo Mangino, Riccardo E Marioni, Angel Martinez-Perez, Nathan Pankratz, Ozren Polasek, Anne Richmond, Benjamin At Rodriguez, Jerome I Rotter, Maristella Steri, Pierre Suchon, Stella Trompet, Stefan Weiss, Marjan Zare, Paul Auer, Michael H Cho, Paraskevi Christofidou, Gail Davies, Eco de Geus, Jean-François Deleuze, Graciela E Delgado, Lynette Ekunwe, Nauder Faraday, Martin Gögele, Andreas Greinacher, Gao He, Tom Howard, Peter K Joshi, Tuomas O Kilpeläinen, Jari Lahti, Allan Linneberg, Silvia Naitza, Raymond Noordam, Ferran Paüls-Vergés, Stephen S Rich, Frits R Rosendaal, Igor Rudan, Kathleen A Ryan, Juan Carlos Souto, Frank Ja van Rooij, Heming Wang, Wei Zhao, Lewis C Becker, Andrew Beswick, Michael R Brown, Brian E Cade, Harry Campbell, Kelly Cho, James D Crapo, Joanne E Curran, Moniek Pm de Maat, Margaret Doyle, Paul Elliott, James S Floyd, Christian Fuchsberger, Niels Grarup, Xiuqing Guo, Sarah E Harris, Lifang Hou, Ivana Kolcic, Charles Kooperberg, Cristina Menni, Matthias Nauck, Jeffrey R O'Connell, Valeria Orrù, Bruce M Psaty, Katri Räikkönen, Jennifer A Smith, Jose Manuel Soria, David J Stott, Astrid van Hylckama Vlieg, Hugh Watkins, Gonneke Willemsen, Peter Wilson, Yoav Ben-Shlomo, John Blangero, Dorret Boomsma, Simon R Cox, Abbas Dehghan, Johan G Eriksson, Edoardo Fiorillo, Myriam Fornage, Torben Hansen, Caroline Hayward, M Arfan Ikram, J Wouter Jukema, Sharon Lr Kardia, Leslie A Lange, Winfried März, Rasika A Mathias, Braxton D Mitchell, Dennis O Mook-Kanamori, Pierre-Emmanuel Morange, Oluf Pedersen, Peter P Pramstaller, Susan Redline, Alexander Reiner, Paul M Ridker, Edwin K Silverman, Tim D Spector, Uwe Völker, Nick Wareham, James F Wilson, Jie Yao, , , David-Alexandre Trégouët, Andrew D Johnson, Alisa S Wolberg, Paul S de Vries, Maria Sabater-Lleal, Alanna C Morrison, Nicholas L Smi |
Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population. BMC medicine 2023 4 21 (1): 153. Zhu Zhang, Haobo Li, Haoyi Weng, Geyu Zhou, Hong Chen, Guoru Yang, Ping Zhang, Xiangyan Zhang, Yingqun Ji, Kejing Ying, Bo Liu, Qixia Xu, Yongjun Tang, Guangfa Zhu, Zhihong Liu, Shuyue Xia, Xiaohong Yang, Lixia Dong, Ling Zhu, Mian Zeng, Yadong Yuan, Yuanhua Yang, Nuofu Zhang, Xiaomao Xu, Wenyi Pang, Meng Zhang, Yu Zhang, Kaiyuan Zhen, Dingyi Wang, Jieping Lei, Sinan Wu, Shi Shu, Yunxia Zhang, Shuai Zhang, Qian Gao, Qiang Huang, Chao Deng, Xi Fu, Gang Chen, Wenxin Duan, Jun Wan, Wanmu Xie, Peng Zhang, Shengfeng Wang, Peiran Yang, Xianbo Zuo, Zhenguo Zhai, Chen Wang, |
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- Page last updated:Apr 22, 2024
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