HuGE Literature Finder
Records 1-25
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Relationship between SCN5A gene H558R polymorphism and atrial fibrillation in Tibetan and Han nationalities at high altitude.
Medicine 2021 Mar 100 (12): e25229. Liu Jiang, Yao Fengcai, Han Kaiyue, Chai Jinping, Tian Dekuan, Zhang Jinwei, Wang Rong, Li Wei, Shen Yanmei, Ma Yuanfeng, Geng Sang, Su Xiaoli |
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Correlations of SCN5A gene polymorphisms with onset of atrial fibrillation.
European review for medical and pharmacological sciences 2019 Aug 23 (16): 7089-7097. Wang X-J, Ding P, Wang F-Z, Liu |
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.
Circulation. Cardiovascular genetics 2017 Aug 10 (4): . Christophersen Ingrid E, Magnani Jared W, Yin Xiaoyan, Barnard John, Weng Lu-Chen, Arking Dan E, Niemeijer Maartje N, Lubitz Steven A, Avery Christy L, Duan Qing, Felix Stephan B, Bis Joshua C, Kerr Kathleen F, Isaacs Aaron, Müller-Nurasyid Martina, Müller Christian, North Kari E, Reiner Alex P, Tinker Lesley F, Kors Jan A, Teumer Alexander, Petersmann Astrid, Sinner Moritz F, Buzkova Petra, Smith Jonathan D, Van Wagoner David R, Völker Uwe, Waldenberger Melanie, Peters Annette, Meitinger Thomas, Limacher Marian C, Wilhelmsen Kirk C, Psaty Bruce M, Hofman Albert, Uitterlinden Andre, Krijthe Bouwe P, Zhang Zhu-Ming, Schnabel Renate B, Kääb Stefan, van Duijn Cornelia, Rotter Jerome I, Sotoodehnia Nona, Dörr Marcus, Li Yun, Chung Mina K, Soliman Elsayed Z, Alonso Alvaro, Whitsel Eric A, Stricker Bruno H, Benjamin Emelia J, Heckbert Susan R, Ellinor Patrick |
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Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.
Heart rhythm 2017 Jan . Ishikawa Taisuke, Ohno Seiko, Murakami Takashi, Yoshida Kentaro, Mishima Hiroyuki, Fukuoka Tetsuya, Kimoto Hiroki, Sakamoto Risa, Ohkusa Takafumi, Aiba Takeshi, Nogami Akihiko, Sumitomo Naokata, Shimizu Wataru, Yoshiura Koh-Ichiro, Horigome Hitoshi, Horie Minoru, Makita Naoma |
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A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.
PloS one 2017 12 (1): e0170193. Jabbari Reza, Glinge Charlotte, Jabbari Javad, Risgaard Bjarke, Winkel Bo Gregers, Terkelsen Christian Juhl, Tilsted Hans-Henrik, Jensen Lisette Okkels, Hougaard Mikkel, Haunsø Stig, Engstrøm Thomas, Albert Christine M, Tfelt-Hansen Jac |
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PR Interval Associated Genes, Atrial Remodeling and Rhythm Outcome of Catheter Ablation of Atrial Fibrillation-A Gene-Based Analysis of GWAS Data.
Frontiers in genetics 2017 8 224. Husser Daniela, Büttner Petra, Stübner Dorian, Ueberham Laura, Platonov Pyotr G, Dinov Borislav, Arya Arash, Hindricks Gerhard, Bollmann Andre |
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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 |
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Brugada syndrome risk loci seem protective against atrial fibrillation.
European journal of human genetics : EJHG 2014 Dec 22 (12): 1357-61. Andreasen Laura, Nielsen Jonas B, Darkner Stine, Christophersen Ingrid E, Jabbari Javad, Refsgaard Lena, Thiis Jens J, Sajadieh Ahmad, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Schmitt Nicole, Olesen Morten |
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A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans.
Journal of cardiovascular electrophysiology 2014 Nov 25 (11): 1150-7. Ilkhanoff Leonard, Arking Dan E, Lemaitre Rozenn N, Alonso Alvaro, Chen Lin Y, Durda Peter, Hesselson Stephanie E, Kerr Kathleen F, Magnani Jared W, Marcus Gregory M, Schnabel Renate B, Smith J Gustav, Soliman Elsayed Z, Reiner Alexander P, Sotoodehnia Nona, |
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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 |
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Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Circulation 2013 Apr 127 (13): 1377-85. Ritchie Marylyn D, Denny Joshua C, Zuvich Rebecca L, Crawford Dana C, Schildcrout Jonathan S, Bastarache Lisa, Ramirez Andrea H, Mosley Jonathan D, Pulley Jill M, Basford Melissa A, Bradford Yuki, Rasmussen Luke V, Pathak Jyotishman, Chute Christopher G, Kullo Iftikhar J, McCarty Catherine A, Chisholm Rex L, Kho Abel N, Carlson Christopher S, Larson Eric B, Jarvik Gail P, Sotoodehnia Nona, , Manolio Teri A, Li Rongling, Masys Daniel R, Haines Jonathan L, Roden Dan |
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High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.
Circulation. Cardiovascular genetics 2012 Aug 5 (4): 450-9. Olesen Morten S, Yuan Lei, Liang Bo, Holst Anders G, Nielsen Nikolaj, Nielsen Jonas B, Hedley Paula L, Christiansen Michael, Olesen Søren-Peter, Haunsø Stig, Schmitt Nicole, Jespersen Thomas, Svendsen Jesper |
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Common genetic variants associated with sudden cardiac death: the FinSCDgen study.
PloS one 2012 7 (7): e41675. Lahtinen Annukka M, Noseworthy Peter A, Havulinna Aki S, Jula Antti, Karhunen Pekka J, Kettunen Johannes, Perola Markus, Kontula Kimmo, Newton-Cheh Christopher, Salomaa Veik |
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Polymorphism H558R in the human cardiac sodium channel SCN5A gene is associated with atrial fibrillation.
The Journal of international medical research 2011 39 (5): 5. Chen L, Zhang W, Fang C, Jiang S, Shu C, Cheng H, Li F, Li H |
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SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism.
Journal of the American College of Cardiology 2011 May 57 (21): 2160-8. McNair William P, Sinagra Gianfranco, Taylor Matthew R G, Di Lenarda Andrea, Ferguson Debra A, Salcedo Ernesto E, Slavov Dobromir, Zhu Xiao, Caldwell John H, Mestroni Luisa, |
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Mutations in sodium channel ß-subunit SCN3B are associated with early-onset lone atrial fibrillation.
Cardiovascular research 2011 Mar 89 (4): 786-93. Olesen Morten S, Jespersen Thomas, Nielsen Jonas B, Liang Bo, Møller Daniel V, Hedley Paula, Christiansen Michael, Varró András, Olesen Søren-Peter, Haunsø Stig, Schmitt Nicole, Svendsen Jesper |
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Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.
Biochemical and biophysical research communications 2010 Jul 398 (1): 98-104. Wang Pengyun, Yang Qinbo, Wu Xiaofen, Yang Yanzong, Shi Lisong, Wang Chuchu, Wu Gang, Xia Yunlong, Yang Bo, Zhang Rongfeng, Xu Chengqi, Cheng Xiang, Li Sisi, Zhao Yuanyuan, Fu Fenfen, Liao Yuhua, Fang Fang, Chen Qiuyun, Tu Xin, Wang Qing |
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Genome-wide association study of PR interval.
Nature genetics 2010 Feb 42 (2): 153-9. Pfeufer Arne, van Noord Charlotte, Marciante Kristin D, Arking Dan E, Larson Martin G, Smith Albert Vernon, Tarasov Kirill V, Müller Martina, Sotoodehnia Nona, Sinner Moritz F, Verwoert Germaine C, Li Man, Kao W H Linda, Köttgen Anna, Coresh Josef, Bis Joshua C, Psaty Bruce M, Rice Kenneth, Rotter Jerome I, Rivadeneira Fernando, Hofman Albert, Kors Jan A, Stricker Bruno H C, Uitterlinden André G, van Duijn Cornelia M, Beckmann Britt M, Sauter Wiebke, Gieger Christian, Lubitz Steven A, Newton-Cheh Christopher, Wang Thomas J, Magnani Jared W, Schnabel Renate B, Chung Mina K, Barnard John, Smith Jonathan D, Van Wagoner David R, Vasan Ramachandran S, Aspelund Thor, Eiriksdottir Gudny, Harris Tamara B, Launer Lenore J, Najjar Samer S, Lakatta Edward, Schlessinger David, Uda Manuela, Abecasis Gonçalo R, Müller-Myhsok Bertram, Ehret Georg B, Boerwinkle Eric, Chakravarti Aravinda, Soliman Elsayed Z, Lunetta Kathryn L, Perz Siegfried, Wichmann H-Erich, Meitinger Thomas, Levy Daniel, Gudnason Vilmundur, Ellinor Patrick T, Sanna Serena, Kääb Stefan, Witteman Jacqueline C M, Alonso Alvaro, Benjamin Emelia J, Heckbert Susan |
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Atrial electrophysiological and structural remodeling in high-risk patients with Brugada syndrome: assessment with electrophysiology and echocardiography.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 7 (2): 218-24. Toh Norihisa, Morita Hiroshi, Nagase Satoshi, Taniguchi Manabu, Miura Daiji, Nishii Nobuhiro, Nakamura Kazufumi, Ohe Tohru, Kusano Kengo F, Ito Hiros |
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Mutations in sodium channel ß1- and ß2-subunits associated with atrial fibrillation.
Circulation. Arrhythmia and electrophysiology 2009 Jun 2 (3): 268-75. Watanabe Hiroshi, Darbar Dawood, Kaiser Daniel W, Jiramongkolchai Kim, Chopra Sameer, Donahue Brian S, Kannankeril Prince J, Roden Dan |
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A genotype-dependent intermediate ECG phenotype in patients with persistent lone atrial fibrillation genotype ECG-phenotype correlation in atrial fibrillation.
Circulation. Arrhythmia and electrophysiology 2009 Feb 2 (1): 1. Husser D, Stridh M, Sörnmo L, Roden DM, Darbar D, Bollmann A |
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Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.
Circulation 2008 Apr 117 (15): 1927-35. Darbar Dawood, Kannankeril Prince J, Donahue Brian S, Kucera Gayle, Stubblefield Tanya, Haines Jonathan L, George Alfred L, Roden Dan |
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Atrial fibrillation in patients with Brugada syndrome relationships of gene mutation, electrophysiology, and clinical backgrounds.
Journal of the American College of Cardiology 2008 Mar 51 (12): 1169-75. Kusano Kengo F, Taniyama Makiko, Nakamura Kazufumi, Miura Daiji, Banba Kimikazu, Nagase Satoshi, Morita Hiroshi, Nishii Nobuhiro, Watanabe Atsuyuki, Tada Takeshi, Murakami Masato, Miyaji Kohei, Hiramatsu Shigeki, Nakagawa Koji, Tanaka Masamichi, Miura Aya, Kimura Hideo, Fuke Soichiro, Sumita Wakako, Sakuragi Satoru, Urakawa Shigemi, Iwasaki Jun, Ohe Toh |
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A common polymorphism in SCN5A is associated with lone atrial fibrillation.
Clinical pharmacology and therapeutics 2007 Jan 81 (1): 35-41. Chen LY, Ballew JD, Herron KJ, Rodeheffer RJ, Olson TM |
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Cx40 polymorphism in human atrial fibrillation.
Advances in cardiology 2006 42 (): 284-91. Hauer Richard N W, Groenewegen W Antoinette, Firouzi Mehran, Ramanna Hemanth, Jongsma Habo |
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- Page last updated:Sep 22, 2021
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