Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: Arrhythmia and KCNE1[original query] |
---|
Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias. Journal of cardiovascular electrophysiology 2001 Nov 12 (11): 1223-9. Kubota T, Horie M, Takano M, Yoshida H, Takenaka K, Watanabe E, Tsuchiya T, Otani H, Sasayama |
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 |
Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms. Journal of human genetics 2005 50 (9): 490-6. Lai Ling-Ping, Su Yi-Ning, Hsieh Fon-Jou, Chiang Fu-Tien, Juang Jyh-Ming, Liu Yen-Bin, Ho Yi-Lwun, Chen Wen-Jone, Yeh San-Jou, Wang Chun-Chieh, Ko Yu-Lin, Wu Tsu-Juey, Ueng Kwo-Chang, Lei Meng-Huan, Tsao Hsuan-Ming, Chen Shih-Ann, Lin Tin-Kwang, Wu Mei-Hwan, Lo Huey-Ming, Huang Shoei K Stephen, Lin Jiunn-L |
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 |
The association between SCN5A, KCNQ1 and KCNE1 gene polymorphisms and complex ventricular arrhythmias in survivors of myocardial infarction. Kardiologia polska 2008 Aug 66 (8): 845-53; discussion 854-5. Olszak-Wa?kiewicz Marlena, Kubik Leszek, Dziuk Miros?aw, Sid?o Ewa, Kucharczyk Krzysztof, Kaczanowski Rados? |
Single nucleotide polymorphisms and haplotype of four genes encoding cardiac ion channels in Chinese and their association with arrhythmia. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2008 Apr 13 (2): 180-90. Zhang Yu, Chang Bingxi, Hu Songnian, Wang Duenmei, Fang Quan, Huang Xianyong, Zeng Qiang, Qi Mi |
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 |
Common candidate gene variants are associated with QT interval duration in the general population. Journal of internal medicine 2009 Apr 265 (4): 448-58. Marjamaa A, Newton-Cheh C, Porthan K, Reunanen A, Lahermo P, Väänänen H, Jula A, Karanko H, Swan H, Toivonen L, Nieminen M S, Viitasalo M, Peltonen L, Oikarinen L, Palotie A, Kontula K, Salomaa |
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome. Journal of the American College of Cardiology 2009 Aug 54 (9): 812-9. Nishio Yukiko, Makiyama Takeru, Itoh Hideki, Sakaguchi Tomoko, Ohno Seiko, Gong Yin-Zhi, Yamamoto Satoshi, Ozawa Tomoya, Ding Wei-Guang, Toyoda Futoshi, Kawamura Mihoko, Akao Masaharu, Matsuura Hiroshi, Kimura Takeshi, Kita Toru, Horie Mino |
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 |
KCNE1 rs1805127 polymorphism increases the risk of atrial fibrillation: a meta-analysis of 10 studies. PloS one 2013 8 (7): e68690. Liang Chang, Li Xiankai, Xu Yawei, Chen Qingyong, Wu Yadong, Wang Wan, Li Weiming, Qiu Manta |
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 |
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 |
KCNE1 112G>a polymorphism and atrial fibrillation risk: a meta-analysis. Genetics and molecular research : GMR 2014 13 (4): 8367-77. Han H G, Wang H S, Yin Z, Jiang H, Fang M, Han |
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 |
Abnormal repolarization dynamics in a patient with KCNE1(G38S) who presented with torsades de pointes. Journal of electrocardiology 2015 Oct . Yamaguchi Yoshiaki, Mizumaki Koichi, Hata Yukiko, Inoue Hiros |
The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths. International journal of legal medicine 2016 Jul . Tzimas Iliana, Zingraf Jana-Christin, Bajanowski Thomas, Poetsch Micae |
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 |
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition. Circulation 2020 1 141 (6): 429-439. Roberts Jason D, Asaki S Yukiko, Mazzanti Andrea, Bos J Martijn, Tuleta Izabela, Muir Alison R, Crotti Lia, Krahn Andrew D, Kutyifa Valentina, Shoemaker M Benjamin, Johnsrude Christopher L, Aiba Takeshi, Marcondes Luciana, Baban Anwar, Udupa Sharmila, Dechert Brynn, Fischbach Peter, Knight Linda M, Vittinghoff Eric, Kukavica Deni, Stallmeyer Birgit, Giudicessi John R, Spazzolini Carla, Shimamoto Keiko, Tadros Rafik, Cadrin-Tourigny Julia, Duff Henry J, Simpson Christopher S, Roston Thomas M, Wijeyeratne Yanushi D, El Hajjaji Imane, Yousif Maisoon D, Gula Lorne J, Leong-Sit Peter, Chavali Nikhil, Landstrom Andrew P, Marcus Gregory M, Dittmann Sven, Wilde Arthur A M, Behr Elijah R, Tfelt-Hansen Jacob, Scheinman Melvin M, Perez Marco V, Kaski Juan Pablo, Gow Robert M, Drago Fabrizio, Aziz Peter F, Abrams Dominic J, Gollob Michael H, Skinner Jonathan R, Shimizu Wataru, Kaufman Elizabeth S, Roden Dan M, Zareba Wojciech, Schwartz Peter J, Schulze-Bahr Eric, Etheridge Susan P, Priori Silvia G, Ackerman Michael |
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
Circulation. Genomic and precision medicine 2021 Jul . Choi Seung Hoan, Jurgens Sean J, Haggerty Christopher M, Hall Amelia W, Halford Jennifer L, Morrill Valerie N, Weng Lu-Chen, Lagerman Braxton, Mirshahi Tooraj, Pettinger Mary, Guo Xiuqing, Lin Henry J, Alonso Alvaro, Soliman Elsayed Z, Kornej Jelena, Lin Honghuang, Moscati Arden, Nadkarni Girish N, Brody Jennifer A, Wiggins Kerri L, Cade Brian E, Lee Jiwon, Austin-Tse Christina, Blackwell Tom, Chaffin Mark D, Lee Christina J-Y, Rehm Heidi L, Roselli Carolina, , Redline Susan, Mitchell Braxton D, Sotoodehnia Nona, Psaty Bruce M, Heckbert Susan R, Loos Ruth J F, Vasan Ramachandran S, Benjamin Emelia J, Correa Adolfo, Boerwinkle Eric, Arking Dan E, Rotter Jerome I, Rich Stephen S, Whitsel Eric A, Perez Marco, Kooperberg Charles, Fornwalt Brandon K, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven A, |
Impact of rs1805127 and rs55742440 Variants on Atrial Remodeling in Hypertrophic Cardiomyopathy Patients with Atrial Fibrillation: A Romanian Cohort Study. International journal of molecular sciences 2023 12 24 (24): . Nicoleta-Monica Popa-Fotea, Nicoleta Oprescu, Alexandru Scafa-Udriste, Miruna Mihaela Mich |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: