Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Arrhythmia and KCNJ2[original query] |
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| 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 |
| 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 |
| Phenotype variability in patients carrying KCNJ2 mutations. Circulation. Cardiovascular genetics 2012 Jun 5 (3): 344-53. Kimura Hiromi, Zhou Jun, Kawamura Mihoko, Itoh Hideki, Mizusawa Yuka, Ding Wei-Guang, Wu Jie, Ohno Seiko, Makiyama Takeru, Miyamoto Akashi, Naiki Nobu, Wang Qi, Xie Yu, Suzuki Tsugutoshi, Tateno Shigeru, Nakamura Yoshihide, Zang Wei-Jin, Ito Makoto, Matsuura Hiroshi, Horie Mino |
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval.
Heart rhythm : the official journal of the Heart Rhythm Society 2012 Jul 9 (7): 1099-103. Marjamaa Annukka, Oikarinen Lasse, Porthan Kimmo, Ripatti Samuli, Peloso Gina, Noseworthy Peter A, Viitasalo Matti, Nieminen Markku S, Toivonen Lauri, Kontula Kimmo, Peltonen Leena, Havulinna Aki S, Jula Antti, O'Donnell Christopher J, Newton-Cheh Christopher, Perola Markus, Salomaa Veik |
| 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 |
| 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 |
| 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- |
| 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 |
- Page last reviewed:Feb 1, 2024
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