Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Atrial Fibrillation and NKX2-5[original query] |
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Mutational analysis of the PITX2 and NKX2-5 genes in patients with idiopathic atrial fibrillation. International journal of cardiology 2010 Nov 145 (2): 316-7. Boldt Leif-Hendrik, Posch Maximilian G, Perrot Andreas, Polotzki Michael, Rolf Sascha, Parwani Abdul S, Huemer Martin, Wutzler Alexander, Ozcelik Cemil, Haverkamp Wilhe |
Genome-wide association study of PR interval.
Nature genetics 2010 Feb 42 (2): 153-9. Pfeufer Arne, van Noord Charlotte, Marciante Kristin D, Arking Dan E, Larson Martin G, Smith Albert Vernon, Tarasov Kirill V, Müller Martina, Sotoodehnia Nona, Sinner Moritz F, Verwoert Germaine C, Li Man, Kao W H Linda, Köttgen Anna, Coresh Josef, Bis Joshua C, Psaty Bruce M, Rice Kenneth, Rotter Jerome I, Rivadeneira Fernando, Hofman Albert, Kors Jan A, Stricker Bruno H C, Uitterlinden André G, van Duijn Cornelia M, Beckmann Britt M, Sauter Wiebke, Gieger Christian, Lubitz Steven A, Newton-Cheh Christopher, Wang Thomas J, Magnani Jared W, Schnabel Renate B, Chung Mina K, Barnard John, Smith Jonathan D, Van Wagoner David R, Vasan Ramachandran S, Aspelund Thor, Eiriksdottir Gudny, Harris Tamara B, Launer Lenore J, Najjar Samer S, Lakatta Edward, Schlessinger David, Uda Manuela, Abecasis Gonçalo R, Müller-Myhsok Bertram, Ehret Georg B, Boerwinkle Eric, Chakravarti Aravinda, Soliman Elsayed Z, Lunetta Kathryn L, Perz Siegfried, Wichmann H-Erich, Meitinger Thomas, Levy Daniel, Gudnason Vilmundur, Ellinor Patrick T, Sanna Serena, Kääb Stefan, Witteman Jacqueline C M, Alonso Alvaro, Benjamin Emelia J, Heckbert Susan |
Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation. Clinics (São Paulo, Brazil) 2013 Jun 68 (6): 777-84. Xie Wen-Hui, Chang Cheng, Xu Ying-Jia, Li Ruo-Gu, Qu Xin-Kai, Fang Wei-Yi, Liu Xu, Yang Yi-Qi |
A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation. International journal of molecular medicine 2013 May 31 (5): 1119-26. Huang Ri-Tai, Xue Song, Xu Ying-Jia, Zhou Min, Yang Yi-Qi |
Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation. Heart rhythm : the official journal of the Heart Rhythm Society 2014 Jan 11 (1): 46-52. Weeke Peter, Parvez Babar, Blair Marcia, Short Laura, Ingram Christie, Kucera Gayle, Stubblefield Tanya, Roden Dan M, Darbar Dawo |
Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation. International journal of medical sciences 2014 11 (6): 554-63. Yu Hong, Xu Jia-Hong, Song Hao-Ming, Zhao Lan, Xu Wen-Jun, Wang Juan, Li Ruo-Gu, Xu Lei, Jiang Wei-Feng, Qiu Xing-Biao, Jiang Jin-Qi, Qu Xin-Kai, Liu Xu, Fang Wei-Yi, Jiang Jin-Fa, Yang Yi-Qi |
NKX2-6 mutation predisposes to familial atrial fibrillation. International journal of molecular medicine 2014 Dec 34 (6): 1581-90. Wang Jun, Zhang Dai-Fu, Sun Yu-Min, Li Ruo-Gu, Qiu Xing-Biao, Qu Xin-Kai, Liu Xu, Fang Wei-Yi, Yang Yi-Qi |
Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation. PLoS genetics 2015 Aug 11 (8): e1005393. Huang Yufeng, Wang Chuchu, Yao Yufeng, Zuo Xiaoyu, Chen Shanshan, Xu Chengqi, Zhang Hongfu, Lu Qiulun, Chang Le, Wang Fan, Wang Pengxia, Zhang Rongfeng, Hu Zhenkun, Song Qixue, Yang Xiaowei, Li Cong, Li Sisi, Zhao Yuanyuan, Yang Qin, Yin Dan, Wang Xiaojing, Si Wenxia, Li Xiuchun, Xiong Xin, Wang Dan, Huang Yuan, Luo Chunyan, Li Jia, Wang Jingjing, Chen Jing, Wang Longfei, Wang Li, Han Meng, Ye Jian, Chen Feifei, Liu Jingqiu, Liu Ying, Wu Gang, Yang Bo, Cheng Xiang, Liao Yuhua, Wu Yanxia, Ke Tie, Chen Qiuyun, Tu Xin, Elston Robert, Rao Shaoqi, Yang Yanzong, Xia Yunlong, Wang Qing |
TBX5 mutations contribute to early-onset atrial fibrillation in Chinese and Caucasians. Cardiovascular research 2016 Jan . Ma Ji-Fang, Yang Fan, Mahida Saagar N, Zhao Ling, Chen Xiaomin, Zhang Michael L, Sun Zhijun, Yao Yan, Zhang Yi-Xin, Zheng Gu-Yan, Dong Jie, Feng Ming-Jun, Zhang Rui, Sun Jian, Li Shuo, Wang Qun-Shan, Cao Huiqing, Benjamin Emelia J, Ellinor Patrick T, Li Yi-Gang, Tian Xiao- |
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
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 |
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