Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 135 Records) |
Query Trace: FGB[original query] |
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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 |
Association of ?-fibrinogen polymorphisms and venous thromboembolism risk: A PRISMA-compliant meta-analysis. Medicine 2019 11 98 (48): e18204. Li Da, Zhang Xiaosong, Huang He, Zhang Hongga |
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 |
Evaluation of Cases with Myotonia Congenita for Cardiovascular Risk. Medeniyet medical journal 2020 8 34 (4): 374-379. Damar Ibrahim Halil, Eroz Rec |
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 |
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 |
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 |
Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia. International journal of hematology 2020 3 111 (6): 795-802. Simurda Tomas, Zolkova Jana, Kolkova Zuzana, Loderer Dusan, Dobrotova Miroslava, Skornova Ingrid, Brunclíkova Monika, Grendar Marian, Lasabova Zora, Stasko Jan, Kubisz Pet |
Relationship between fibrinogen level and its regulatory gene with Alzheimer's disease and vascular dementia. The Journal of international medical research 2020 2 48 (2): 300060520902578. Sun Yanan, Li Qi, Liu Wei, Zhang Bens |
Genetic association study of fatal pulmonary embolism. International journal of legal medicine 2020 10 135 (1): 143-151. Meißner Lisa, Schürmann Peter, Dörk Thilo, Hagemeier Lars, Klintschar Micha |
Genome-wide association study of high-sensitivity C-reactive protein, D-dimer, and interleukin-6 levels in multiethnic HIV+ cohorts.
AIDS (London, England) 2020 Oct . Sherman Brad T, Hu Xiaojun, Singh Kanal, Haine Lillian, Rupert Adam W, Neaton James D, Lundgren Jens D, Imamichi Tomozumi, Chang Weizhong, Lane H Clifford, |
Multiple sclerosis and genetic polymorphisms in fibrinogen-mediated hemostatic pathways: a case-control study. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 Sep . Abbadessa Gianmarco, Miele Giuseppina, Di Pietro Andrea, Sparaco Maddalena, Palladino Raffaele, Armetta Ignazio, D'Elia Giovanna, Trojsi Francesca, Signoriello Elisabetta, Lus Giacomo, Lavorgna Luigi, Bonavita Simo |
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 |
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 |
Certain Associations Between Iron Biomarkers and Total and ?' Fibrinogen and Plasma Clot Properties Are Mediated by Fibrinogen Genotypes. Frontiers in nutrition 2021 8 8 720048. Rautenbach Petro H, Nienaber-Rousseau Cornelie, de Lange-Loots Zelda, Pieters Marli |
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 |
Predictive value of C-reactive protein for radiographic spinal progression in axial spondyloarthritis in dependence on genetic determinants of fibrin clot formation and fibrinolysis. RMD open 2021 Jun 7 (2): . Hoppe Berthold, Schwedler Christian, Haibel Hildrun, Verba Maryna, Proft Fabian, Protopopov Mikhail, Heuft Hans-Gert, Rios Rodriguez Valeria, Edelmann Anke, Rudwaleit Martin, Sieper Joachim, Poddubnyy Den |
Quantile-dependent expressivity of serum C-reactive protein concentrations in family sets. PeerJ 2021 2 9 e10914. Williams Paul |
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 |
Fibrinogen ? chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism. European journal of clinical investigation 2021 Nov e13718. Klajmon Adrianna, Chmiel Jakub, Z?bczyk Micha?, Pociask El?bieta, Wypasek Ewa, Malinowski Krzysztof P, Undas Anetta, Natorska Joan |
The Correlation Between FGB Promoter Polymorphism and Clotting Function in Patients With Idiopathic Lower Extremity Deep Venous Thrombosis. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 0 27 1076029620967108. Han Shengbin, Yang Bin, Feng Yaoyu, Zhao Lingfeng, Feng Qun, Guan Hongxi, Song Donghui, Yin Fang, Zhuang |
Maternal Thrombophilic and Hypofibrinolytic Genetic Variants in Idiopathic Recurrent Pregnancy Loss: a Continuing Mystery. Reproductive sciences (Thousand Oaks, Calif.) 2022 Aug . Younis Mahmoud, Ali Mohamed A M, Ghareeb Doaa A, Youssef Rehab, Fathy Shadia |
Targeted genetic analysis unveils novel associations between ACE I/D and APO T158C polymorphisms with D-dimer levels in severe COVID-19 patients with pulmonary embolism. Journal of thrombosis and thrombolysis 2022 11 55 (1): 51-59. Fiorentino Giuseppe, Benincasa Giuditta, Coppola Antonietta, Franzese Monica, Annunziata Anna, Affinito Ornella, Viglietti Mario, Napoli Claud |
Betaine supplementation improves CrossFit performance and increases testosterone levels, but has no influence on Wingate power: randomized crossover trial. Journal of the International Society of Sports Nutrition 2023 7 20 (1): 2231411. Emilia Zawieja, Krzysztof Durkalec-Michalski, Marcin Sadowski, Natalia G?ówka, Agata Chmurzyns |
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 |
[Association of polymorphic variants of hemostatic system genes with the course of COVID-19]. Voprosy virusologii 2023 12 68 (5): 445-453. L I Nikolaeva, M D Stuchinskaya, A V Dedova, S G Nadezhda, I N Khlopova, I S Kruzhkova, L N Merkulova, L B Kisteneva, L V Kolobukhina, E A Mukasheva, K G Krasnoslobodtsev, S V Trushakova, A S Krepkaya, V V Kuprianov, N A Nikitenko, E A Khadorich, E M Burmistrov, I N Tyurin, N A Antipyat, E I Burtse |
The prevalence and linkage disequilibrium of 21 genetic variations related to thrombophilia, folate cycle, and hypertension in reproductive age women of Rostov region (Russia). Annals of human genetics 2023 11 . Oksana Yurievna Bordaeva, Ekaterina Grigorievna Derevyanchuk, Dema Alset, Maria Aleksandrovna Amelina, Tatiana Pavlovna Shkur |
Fibrinogen B ? promoter polymorphism may not be associated with pulmonary embolism. Phlebology 2023 11 2683555231216915. Wenxiang Chen, Shengbin Han, Jingzhe Xu, Shun Ding, Hongxi Gu |
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- Page last updated:Apr 22, 2024
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