Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Atrial Fibrillation and GJA1[original query] |
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Connexin43 mutation causes heterogeneous gap junction loss and sudden infant death. Circulation 2012 Jan 125 (3): 474-81. Van Norstrand David W, Asimaki Angeliki, Rubinos Clio, Dolmatova Elena, Srinivas Miduturu, Tester David J, Saffitz Jeffrey E, Duffy Heather S, Ackerman Michael |
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation. Circulation 2014 Oct 130 (15): 1225-35. Sinner Moritz F, Tucker Nathan R, Lunetta Kathryn L, Ozaki Kouichi, Smith J Gustav, Trompet Stella, Bis Joshua C, Lin Honghuang, Chung Mina K, Nielsen Jonas B, Lubitz Steven A, Krijthe Bouwe P, Magnani Jared W, Ye Jiangchuan, Gollob Michael H, Tsunoda Tatsuhiko, Müller-Nurasyid Martina, Lichtner Peter, Peters Annette, Dolmatova Elena, Kubo Michiaki, Smith Jonathan D, Psaty Bruce M, Smith Nicholas L, Jukema J Wouter, Chasman Daniel I, Albert Christine M, Ebana Yusuke, Furukawa Tetsushi, Macfarlane Peter W, Harris Tamara B, Darbar Dawood, Dörr Marcus, Holst Anders G, Svendsen Jesper H, Hofman Albert, Uitterlinden Andre G, Gudnason Vilmundur, Isobe Mitsuaki, Malik Rainer, Dichgans Martin, Rosand Jonathan, Van Wagoner David R, , , Benjamin Emelia J, Milan David J, Melander Olle, Heckbert Susan R, Ford Ian, Liu Yongmei, Barnard John, Olesen Morten S, Stricker Bruno H C, Tanaka Toshihiro, Kääb Stefan, Ellinor Patrick |
Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation. Scientific reports 2018 Feb 8 (1): 3297. Wang Pengxia, Qin Weixi, Wang Pengyun, Huang Yufeng, Liu Ying, Zhang Rongfeng, Li Sisi, Yang Qin, Wang Xiaojing, Chen Feifei, Liu Jingqiu, Yang Bo, Cheng Xiang, Liao Yuhua, Wu Yanxia, Ke Tie, Tu Xin, Ren Xiang, Yang Yanzong, Xia Yunlong, Luo Xiaoping, Liu Mugen, Li He, Liu Jingyu, Xiao Yi, Chen Qiuyun, Xu Chengqi, Wang Qing |
A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation. The American journal of cardiology 2018 12 123 (5): 787-793. Mechakra Asma, Footz Tim, Walter Michael, Aránega Amelia, Hernández-Torres Francisco, Morel Elodie, Millat Gilles, Yang Yi-Qing, Chahine Mohamed, Chevalier Philippe, Christé Georg |
Association Between GJA1 rs13216675 T>C Polymorphism and Risk of Atrial Fibrillation: A Systematic Review and Meta-Analysis. Frontiers in cardiovascular medicine 2020 11 7 585268. Chen Xuejiao, Li Guowei, Zhang Junguo, Huang Xin, Ye Zebing, Zhao Yaho |
Minor allele of GJA1 gene polymorphism is associated with higher heart rate during atrial fibrillation. Scientific reports 2021 Jan 11 (1): 2549. Okamura Sho, Onohara Yuko, Ochi Hidenori, Tokuyama Takehito, Hironobe Naoya, Okubo Yosaku, Ikeuchi Yoshihiro, Miyauchi Shunsuke, Chayama Kazuaki, Kihara Yasuki, Nakano Yuki |
Identification of Cx43 variants predisposing to ventricular fibrillation in the acute phase of ST-elevation myocardial infarction. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2022 8 25 (1): 101-111. Chevalier Philippe, Moreau Adrien, Bessière Francis, Richard Sylvain, Chahine Mohamed, Millat Gilles, Morel Elodie, Paganelli Franck, Lesavre Nathalie, Placide Leslie, Montestruc François, Ankou Bénédicte, Puertas Rosa Doñate, Asatryan Babken, Delinière Antoine, |
GJA1 gene polymorphism is a genetic predictor of recurrence after pulmonary vein isolation in patients with paroxysmal atrial fibrillation. Heart rhythm 2022 Aug . Okamura Sho, Ochi Hidenori, Onohara Yuko, Nakashima Mika, Akiyama Rie, Tokuyama Takehito, Okubo Yousaku, Ikeuchi Yoshihiro, Miyauchi Shunsuke, Miyamoto Shogo, Oguri Naoto, Uotani Yukimi, Odake Yodo, Chayama Kazuaki, Kihara Yasuki, Nakano Yuki |
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- Page last updated:Apr 29, 2024
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