Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 114 Records) |
Query Trace: FGA[original query] |
---|
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 |
BRCA Mutations, Homologous DNA Repair Deficiency, Tumor Mutational Burden, and Response to Immune Checkpoint Inhibition in Recurrent Ovarian Cancer. JCO precision oncology 2020 9 4 . Liu Ying L, Selenica Pier, Zhou Qin, Iasonos Alexia, Callahan Margaret, Feit Noah Z, Boland Julia, Vazquez-Garcia Ignacio, Mandelker Diana, Zehir Ahmet, Burger Robert A, Powell Daniel J, Friedman Claire, Cadoo Karen, Grisham Rachel, Konner Jason A, O'Cearbhaill Roisin E, Aghajanian Carol, Reis-Filho Jorge S, Weigelt Britta, Zamarin Dmitr |
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 |
Relation of ?-Antiplasmin Genotype and Genetic Determinants of Fibrinogen Synthesis and Fibrin Clot Formation with Vascular Endothelial Growth Factor Level in Axial Spondyloarthritis. International journal of molecular sciences 2020 Dec 21 (24): . 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 |
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 |
Aotearoa New Zealand M?ori and Pacific Population-amplified Gout Risk Variants: CLNK Is a Separate Risk Gene at the SLC2A9 Locus. The Journal of rheumatology 2021 Jul . Ji Aichang, Shaukat Amara, Takei Riku, Bixley Matthew, Cadzow Murray, Topless Ruth K, Major Tanya J, Phipps-Green Amanda, Merriman Marilyn E, Hindmarsh Jennie Harré, Stamp Lisa K, Dalbeth Nicola, Li Changgui, Merriman Tony |
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 |
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 |
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 |
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 |
Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism.
Thrombosis and haemostasis 2021 Feb . Herrera-Rivero Marisol, Stoll Monika, Hegenbarth Jana-Charlotte, Rühle Frank, Limperger Verena, Junker Ralf, Franke André, Hoffmann Per, Shneyder Maria, Stach Michael, Nowak-Göttl Ulri |
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 |
Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese Cohort. Frontiers in genetics 2021 12 12 746082. Xiang Huifen, Wang Chunyan, Pan Hong, Hu Qian, Wang Ruyi, Xu Zuying, Li Tengyan, Su Yezhou, Ma Xu, Cao Yunxia, Wang Binb |
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 |
Mutational analysis of 16 STR markers in the Slovak population. Annals of human biology 2022 7 49 (5-6): 248-253. ?ervenák Zdenko, ?ervenák Filip, Baldovi? Marian, Patlevi?ová Andrea, Masnicová So |
Could routine forensic STR genotyping data leak personal phenotypic information? Forensic science international 2022 4 335 111311. Yang Jiawen, Chen Ji, Ji Qiang, Li Kai, Deng Chuwei, Kong Xiaochao, Xie Sumei, Zhan Wenxuan, Mao Zhengsheng, Zhang Beilei, Yu Yanfang, Li Ding, Cao Yue, Ye Ke, Liu Qingfan, Wu Maowang, Chen Feng, Chen Pe |
Utility of Circulating Cell-Free DNA in Assessing Microsatellite Instability and Loss of Heterozygosity in Breast Cancer Using Human Identification Approach. Genes 2022 4 13 (4): . Al Sharhan Norah A, Messaoudi Safia A, Babu Saranya R, Chaudhary AbdulRauf B, Alsharm Abdullah A, Alrefaei Abdulmajeed F, Kadasah Sultan, Abu-Elmagd Muhammad, Assidi Mourad, Buhmeida Abdelbaset, Carracedo Ángel, Almawi Wassim |
Association between FGA gene polymorphisms and coronary artery lesion in Kawasaki disease. Frontiers in medicine 2023 8 10 1193303. Xingzhu Liu, Yanfei Chen, Yanfei Yang, Zhongjian Su, Feng Wang, Chenghao Zhanghuang, Yuqin Wu, Xing Zha |
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 |
Comprehensive analysis of necroptosis-related lncRNA signature with potential implications in tumor heterogeneity and prediction of prognosis in clear cell renal cell carcinoma. European journal of medical research 2023 7 28 (1): 236. Hang Lin, Lingzhi Qu, Guanqiu Chen, Chunfang Zhang, Liqing Lu, Yongheng Ch |
Optimizing cancer immunotherapy response prediction by tumor aneuploidy score and fraction of copy number alterations. NPJ precision oncology 2023 6 7 (1): 54. Tian-Gen Chang, Yingying Cao, Eldad D Shulman, Uri Ben-David, Alejandro A Schäffer, Eytan Rupp |
An Exploratory Study Using Next-Generation Sequencing to Identify Prothrombotic Variants in Patients with Cerebral Vein Thrombosis. International journal of molecular sciences 2023 5 24 (9): . Robert Anton Kramer, Robert Zimmermann, Julian Strobel, Susanne Achenbach, Armin Michael Ströbel, Holger Hackstein, David Alexander Christian Messerer, Sabine Schneid |
Germline VWF/MPRIP and somatoplasm FGA variants synergically confer susceptibility to non-traumatic osteonecrosis of the femoral head. Scientific reports 2023 2 13 (1): 3112. Wang Dawei, Gu Longchao, Zheng Juan, Zhang Qiang, Xu Qi, Li Rongrong, Song Da, Ha Chengzhi, Zhang Qianqian, Yin Han, Xu Mingtao, Wang Hongmin, Li Wei, Yuan Zhengfeng, Yang Cuncun, Gu Minglia |
Allelic frequencies of 22 short tandem repeats loci and tri-allelic patterns of Penta D and TPOX identified in Gabonese population. Scientific reports 2023 11 13 (1): 19938. Elisabeth Lendoye, Landry Erick Mombo, Marie-Andree N'Negue Ep Mezui-Mbeng, Opheelia Makoyo Komba, Edgard Brice Ngoungou, Felix Ovono Abessolo, Joel Fleury Djoba Siawaya, Juliane Alt-Mör |
Construction and validation of a prognostic model for gastrointestinal stromal tumors based on copy number alterations and clinicopathological characteristics. Frontiers in oncology 2023 1 12 1055174. Zhao Heng, Song Nuohan, Feng Hao, Lei Qiang, Zheng Yingying, Liu Jing, Liu Chunyan, Chai Zhengb |
Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2024 1 . Tomas Simurda, Rita Marchi, Alessandro Casini, Marguerite Neerman-Arbez, Miroslava Drotarova, Ingrid Skornova, Jana Zolkova, Zuzana Kolkova, Dusan Loderer, Monika Brunclikova, Kristina Maria Belakova, Jan Stas |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: