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Records 1-12

Query Trace: Atrial Fibrillation and KCNH2[orginal query]

Genetic variants of potassium voltage-gated channel genes (KCNQ1, KCNH2, and KCNE1) affected the risk of atrial fibrillation in elderly patients. Genetic testing and molecular biomarkers 2015 Jul 19 (7): 359-65. Li Li, Shen Chao, Yao Zhaohui, Liang Jinjun, Huang Congx Similar articles in PubMed
Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation. Circulation. Arrhythmia and electrophysiology 2015 Jun . Hayashi Kenshi, Konno Tetsuo, Tada Hayato, Tani Satoyuki, Liu Li, Fujino Noboru, Nohara Atsushi, Hodatsu Akihiko, Tsuda Toyonobu, Tanaka Yoshihiro, Kawashiri Masa-Aki, Ino Hidekazu, Makita Naomasa, Yamagishi Masaka Similar articles in PubMed
Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population. Journal of the American Heart Association 2015 May 4 (5): . Chen Shanshan, Wang Chuchu, Wang Xiaojing, Xu Chengqi, Wu Manman, Wang Pengxia, Tu Xin, Wang Qing Similar articles in PubMed
Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation. Heart rhythm : the official journal of the Heart Rhythm Society 2014 Feb 11 (2): 246-51. Olesen Morten S, Andreasen Laura, Jabbari Javad, Refsgaard Lena, Haunsø Stig, Olesen Søren-Peter, Nielsen Jonas B, Schmitt Nicole, Svendsen Jesper Similar articles in PubMed
Single nucleotide polymorphisms in proximity to K-channel genes are associated with decreased longitudinal QTc variance. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2014 Jan 19 (1): 63-9. Mints Yuliya, Zipunnikov Vadim, Khurram Irfan, Calkins Hugh, Nazarian Sam Similar articles in PubMed
Genetic modifier of the QTc interval associated with early-onset atrial fibrillation. The Canadian journal of cardiology 2013 Oct 29 (10): 1234-40. Andreasen Laura, Nielsen Jonas B, Christophersen Ingrid E, Holst Anders Gaarsdal, Sajadieh Ahmad, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Schmitt Nicole, Olesen Morten Similar articles in PubMed
Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis. Journal of internal medicine 2012 Dec 272 (6): 573-82. Smith J G, Almgren P, Engström G, Hedblad B, Platonov P G, Newton-Cheh C, Melander Similar articles in PubMed
Impact of ancestry and common genetic variants on QT interval in African Americans. Circulation. Cardiovascular genetics 2012 Dec 5 (6): 647-55. Smith J Gustav, Avery Christy L, Evans Daniel S, Nalls Michael A, Meng Yan A, Smith Erin N, Palmer Cameron, Tanaka Toshiko, Mehra Reena, Butler Anne M, Young Taylor, Buxbaum Sarah G, Kerr Kathleen F, Berenson Gerald S, Schnabel Renate B, Li Guo, Ellinor Patrick T, Magnani Jared W, Chen Wei, Bis Joshua C, Curb J David, Hsueh Wen-Chi, Rotter Jerome I, Liu Yongmei, Newman Anne B, Limacher Marian C, North Kari E, Reiner Alexander P, Quibrera P Miguel, Schork Nicholas J, Singleton Andrew B, Psaty Bruce M, Soliman Elsayed Z, Solomon Allen J, Srinivasan Sathanur R, Alonso Alvaro, Wallace Robert, Redline Susan, Zhang Zhu-Ming, Post Wendy S, Zonderman Alan B, Taylor Herman A, Murray Sarah S, Ferrucci Luigi, Arking Dan E, Evans Michele K, Fox Ervin R, Sotoodehnia Nona, Heckbert Susan R, Whitsel Eric A, Newton-Cheh Christopher, Similar articles in PubMed
[Genetic predisposition to development of atrial fibrillation in patients with hypertensive disease]. Kardiologiia 2010 50 (5): 19-24. Gorshkova E S, Minushkina L O, Brovkin A N, Brazhnik V A, Nosikov V V, Zate?shchikov D Similar articles in PubMed
Genetic polymorphism of KCNH2 confers predisposition of acquired atrial fibrillation in Chinese. Journal of cardiovascular electrophysiology 2009 Oct 20 (10): 1158-62. Wang Qun-Shan, Wang Xiao-Feng, Chen Xing-Dong, Yu Jie-Fei, Wang Jun, Sun Jian, Lu Shang-Biao, Shen Mu-Yao, Lu Ming, Li Yi-Gang, Jin Similar articles in PubMed
The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG). European heart journal 2008 Apr 29 (7): 907-14. Sinner Moritz F, Pfeufer Arne, Akyol Mahmut, Beckmann Britt-Maria, Hinterseer Martin, Wacker Annette, Perz Siegfried, Sauter Wiebke, Illig Thomas, Näbauer Michael, Schmitt Claus, Wichmann H-Erich, Schömig Albert, Steinbeck Gerhard, Meitinger Thomas, Kääb Stef Similar articles in PubMed
The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study. European heart journal 2007 Feb 28 (3): 305-9. Akyol Mahmut, Jalilzadeh Shapour, Sinner Moritz F, Perz Siegfried, Beckmann Britt M, Gieger Christian, Illig Thomas, Wichmann H-Erich, Meitinger Thomas, Kääb Stefan, Pfeufer Ar Similar articles in PubMed

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