Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Arrhythmia and KCNE2[original query] |
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| KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science (New York, N.Y.) 2003 1 299 (5604): 251-4. Chen Yi-Han, Xu Shi-Jie, Bendahhou Said, Wang Xiao-Liang, Wang Ying, Xu Wen-Yuan, Jin Hong-Wei, Sun Hao, Su Xiao-Yan, Zhuang Qi-Nan, Yang Yi-Qing, Li Yue-Bin, Liu Yi, Xu Hong-Ju, Li Xiao-Fei, Ma Ning, Mou Chun-Ping, Chen Zhu, Barhanin Jacques, Huang W |
| Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. Circulation 2007 Jan 115 (3): 361-7. Arnestad Marianne, Crotti Lia, Rognum Torleiv O, Insolia Roberto, Pedrazzini Matteo, Ferrandi Chiara, Vege Ashild, Wang Dao W, Rhodes Troy E, George Alfred L, Schwartz Peter |
| Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation. Heart rhythm : the official journal of the Heart Rhythm Society 2008 Mar 5 (3): 427-35. Ravn Lasse S, Aizawa Yoshiyasu, Pollevick Guido D, Hofman-Bang Jacob, Cordeiro Jonathan M, Dixen Ulrik, Jensen Gorm, Wu Yuesheng, Burashnikov Elena, Haunso Stig, Guerchicoff Alejandra, Hu Dan, Svendsen Jesper H, Christiansen Michael, Antzelevitch Charl |
| Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates. The Canadian journal of cardiology 2010 Apr 26 (4): 208-12. Subbiah Rajesh N, Gollob Michael H, Gula Lorne J, Davies Robert W, Leong-Sit Peter, Skanes Allan C, Yee Raymond, Klein George J, Krahn Andrew |
| Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance. Journal of the American College of Cardiology 2010 12 57 (1): 40-7. Barc Julien, Briec François, Schmitt Sébastien, Kyndt Florence, Le Cunff Martine, Baron Estelle, Vieyres Claude, Sacher Frédéric, Redon Richard, Le Caignec Cédric, Le Marec Hervé, Probst Vincent, Schott Jean-Jacqu |
| Cardiac ion channel gene mutations in Greek long QT syndrome patients. Journal of applied genetics 2010 51 (4): 515-8. Kotta C-M, Anastasakis A, Gatzoulis K, Papagiannis J, Geleris P, Stefanadis |
| The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study. Journal of negative results in biomedicine 2011 10 (1): 12. Hedley Paula L, Haundrup Ole, Andersen Paal S, Aidt Frederik H, Jensen Morten, Moolman-Smook Johanna C, Bundgaard Henning, Christiansen Micha |
| Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation. Biomarkers in medicine 2014 8 (4): 557-70. Nielsen Jonas Bille, Bentzen Bo Hjorth, Olesen Morten Salling, David Jens-Peter, Olesen Søren-Peter, Haunsø Stig, Svendsen Jesper Hastrup, Schmitt Nico |
| Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome. Journal of the American College of Cardiology 2014 Apr 63 (14): 1430-7. Weeke Peter, Mosley Jonathan D, Hanna David, Delaney Jessica T, Shaffer Christian, Wells Quinn S, Van Driest Sara, Karnes Jason H, Ingram Christie, Guo Yan, Shyr Yu, Norris Kris, Kannankeril Prince J, Ramirez Andrea H, Smith Joshua D, Mardis Elaine R, Nickerson Deborah, George Alfred L, Roden Dan |
| 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 |
| Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation? Circulation. Arrhythmia and electrophysiology 2017 8 10 (8): . Roberts Jason D, Krahn Andrew D, Ackerman Michael J, Rohatgi Ram K, Moss Arthur J, Nazer Babak, Tadros Rafik, Gerull Brenda, Sanatani Shubhayan, Wijeyeratne Yanushi D, Baruteau Alban-Elouen, Muir Alison R, Pang Benjamin, Cadrin-Tourigny Julia, Talajic Mario, Rivard Lena, Tester David J, Liu Taylor, Whitman Isaac R, Wojciak Julianne, Conacher Susan, Gula Lorne J, Leong-Sit Peter, Manlucu Jaimie, Green Martin S, Hamilton Robert, Healey Jeff S, Lopes Coeli M, Behr Elijah R, Wilde Arthur A, Gollob Michael H, Scheinman Melvin |
| The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. Molecular genetics & genomic medicine 2019 Jul e835. Liu Xiumin, Li Yujie, Zhang Huan, Ji Yuqiang, Zhao Zhao, Wang Chang |
| Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy. BMC cardiovascular disorders 2019 Jul 19 (1): 174. Raju Hariharan, Ware James S, Skinner Jonathan R, Hedley Paula L, Arno Gavin, Love Donald R, van der Werf Christian, Tfelt-Hansen Jacob, Winkel Bo Gregers, Cohen Marta C, Li Xinzhong, John Shibu, Sharma Sanjay, Jeffery Steve, Wilde Arthur A M, Christiansen Michael, Sheppard Mary N, Behr Elijah |
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