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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 31, 2023. (Total: 217454Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Atrial Fibrillation and GATA4[original query]
Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation.
European journal of medical genetics 0 53 (4): 201-3.
Posch Maximilian G, Boldt Leif-Hendrik, Polotzki Michael, Richter Silke, Rolf Sascha, Perrot Andreas, Dietz Rainer, Ozcelik Cemil, Haverkamp Wilhe
Novel GATA4 mutations in lone atrial fibrillation.
International journal of molecular medicine 2011 Dec 28 (6): 1025-32.
Jiang Jin-Qi, Shen Fang-Fang, Fang Wei-Yi, Liu Xu, Yang Yi-Qi
GATA4 loss-of-function mutations in familial atrial fibrillation.
Clinica chimica acta; international journal of clinical chemistry 2011 Jun .
Yang YQ, Wang MY, Zhang XL, Tan HW, Shi HF, Jiang WF, Wang XH, Fang WY, Liu X
Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation.
Molecular biology reports 2012 Aug 39 (8): 8127-35.
Wang Jun, Sun Yu-Min, Yang Yi-Qi
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. GWAS Catalog
Nature genetics 2018 Jul .
Nielsen Jonas B, Thorolfsdottir Rosa B, Fritsche Lars G, Zhou Wei, Skov Morten W, Graham Sarah E, Herron Todd J, McCarthy Shane, Schmidt Ellen M, Sveinbjornsson Gardar, Surakka Ida, Mathis Michael R, Yamazaki Masatoshi, Crawford Ryan D, Gabrielsen Maiken E, Skogholt Anne Heidi, Holmen Oddgeir L, Lin Maoxuan, Wolford Brooke N, Dey Rounak, Dalen Håvard, Sulem Patrick, Chung Jonathan H, Backman Joshua D, Arnar David O, Thorsteinsdottir Unnur, Baras Aris, O'Dushlaine Colm, Holst Anders G, Wen Xiaoquan, Hornsby Whitney, Dewey Frederick E, Boehnke Michael, Kheterpal Sachin, Mukherjee Bhramar, Lee Seunggeun, Kang Hyun M, Holm Hilma, Kitzman Jacob, Shavit Jordan A, Jalife José, Brummett Chad M, Teslovich Tanya M, Carey David J, Gudbjartsson Daniel F, Stefansson Kari, Abecasis Gonçalo R, Hveem Kristian, Willer Cristen
ISL1 loss-of-function variation causes familial atrial fibrillation.
European journal of medical genetics 2020 8 63 (11): 104029.
Wu Shao-Hui, Wang Xin-Hua, Xu Ying-Jia, Gu Jia-Ning, Yang Chen-Xi, Qiao Qi, Guo Xiao-Juan, Guo Yu-Han, Qiu Xing-Biao, Jiang Wei-Feng, Yang Yi-Qi
A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve.
Genetics and molecular biology 2020 12 43 (4): e20200142.
Jiang Wei-Feng, Xu Ying-Jia, Zhao Cui-Mei, Wang Xin-Hua, Qiu Xing-Biao, Liu Xu, Wu Shao-Hui, Yang Yi-Qi
Ethnic similarities in genetic polymorphisms associated with atrial fibrillation: Far East Asian vs European populations. GWAS Catalog
European journal of clinical investigation 2021 5 51 (9): e13584.
Hong Myunghee, Ebana Yusuke, Shim Jaemin, Choi Eue-Keun, Lim Hong Euy, Hwang Inseok, Yu Hee Tae, Kim Tae-Hoon, Uhm Jae-Sun, Joung Boyoung, Oh Seil, Lee Moon-Hyoung, Kim Young-Hoon, Jee Sun Ha, Pak Hui-N
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