HuGE Literature Finder
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| An NGS-based genotyping in LQTS; minor genes are no longer minor. Journal of human genetics 2020 Jul . Ohno Seiko, Ozawa Junichi, Fukuyama Megumi, Makiyama Takeru, Horie Mino |
| Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry. Circulation. Genomic and precision medicine 2020 Jun . Juang Jyh-Ming Jimmy, Liu Yen-Bin, Chen Ching-Yu Julius, Yu Qi-You, Chattopadhyay Amrita, Lin Lian-Yu, Chen Wen-Jone, Yu Chih-Chieh, Huang Hui-Chun, Ho Li-Ting, Lai Ling-Ping, Hwang Juey-Jen, Lin Ting-Tse, Liao Ming-Chun, Chen Jien-Jiun, Yeh Shih-Fan Sherri, Chuang Jing-Yuan, Yang Dun-Hui, Lin Jiunn-Lee, Lu Tzu-Pin, Chuang Eric Y, Ackerman Michael |
| Identification of Novel SCN5A Single Nucleotide Variants in Brugada Syndrome: A Territory-Wide Study From Hong Kong. Frontiers in physiology 2020 11 574590. Tse Gary, Lee Sharen, Liu Tong, Yuen Ho Chuen, Wong Ian Chi Kei, Mak Chloe, Mok Ngai Shing, Wong Wing T |
| 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 |
| Surveillance after cardiac arrest in patients with Brugada syndrome without an implantable defibrillator: An alarm effect of the previous syncope. International journal of cardiology 2016 May 218 69-74. Calvo David, Flórez Juan Pablo, Valverde Irene, Rubín José, Pérez Diego, Vasserot Mar Gonzalez, Rodríguez-Reguero Julián, Avanzas Pablo, de la Hera Jesús María, Gómez Juan, Coto Eliecer, Martínez-Camblor Pablo, Morís Cés |
| Influence of Pregnancy in Patients With Congenital Long QT Syndrome. Cardiology in review 2016 Mar . Garg Lohit, Garg Jalaj, Krishnamoorthy Parasuram, Ahnert Amy, Shah Neeraj, Dusaj Raman S, Bozorgnia Bab |
| Contribution of Cardiac Sodium Channel ß-Subunit Variants to Brugada Syndrome. Circulation journal : official journal of the Japanese Circulation Society 2015 Jul . Peeters Uschi, Scornik Fabiana, Riuró Helena, Pérez Guillermo, Komurcu-Bayrak Evrim, Van Malderen Sophie, Pappaert Gudrun, Tarradas Anna, Pagans Sara, Daneels Dorien, Breckpot Karine, Brugada Pedro, Bonduelle Maryse, Brugada Ramon, Van Dooren Son |
| Novel SCN10A variants associated with Brugada syndrome. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2015 Apr . Fukuyama Megumi, Ohno Seiko, Makiyama Takeru, Horie Mino |
| Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients. International heart journal 2015 56 (4): 450-3. Chang Ya-Sian, Yang Yi-Wen, Lin Yen-Nien, Lin Kuo-Hung, Chang Kuan-Cheng, Chang Jan-Gow |
| Prevalence and prognostic role of various conduction disturbances in patients with the Brugada syndrome. The American journal of cardiology 2013 Nov 112 (9): 1384-9. Maury Philippe, Rollin Anne, Sacher Frédéric, Gourraud Jean-Baptiste, Raczka Franck, Pasquié Jean-Luc, Duparc Alexandre, Mondoly Pierre, Cardin Christelle, Delay Marc, Derval Nicolas, Chatel Stéphanie, Bongard Vanina, Sadron Marie, Denis Arnaud, Davy Jean-Marc, Hocini Mélèze, Jaïs Pierre, Jesel Laurence, Haïssaguerre Michel, Probst Vince |
| Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
| A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome. Clinical genetics 2013 Jun 83 (6): 530-8. García-Molina E, Lacunza J, Ruiz-Espejo F, Sabater M, García-Alberola A, Gimeno J R, Cañizares F, García A, Martínez P, Valdés M, Tovar |
| L-type calcium channel mutations in Japanese patients with inherited arrhythmias. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (7): 1799-806. Fukuyama Megumi, Ohno Seiko, Wang Qi, Kimura Hiromi, Makiyama Takeru, Itoh Hideki, Ito Makoto, Horie Mino |
| Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5. Circulation journal : official journal of the Japanese Circulation Society 2012 Dec . Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N, Kimura A |
| Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing. BMC cardiovascular disorders 2012 12 (1): 95. Stattin Eva-Lena, Boström Ida Maria, Winbo Annika, Cederquist Kristina, Jonasson Jenni, Jonsson Björn-Anders, Diamant Ulla-Britt, Jensen Steen M, Rydberg Annika, Norberg An |
| Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing. The American journal of cardiology 2010 Oct 106 (8): 1124-8. Tester David J, Benton Amber J, Train Laura, Deal Barbara, Baudhuin Linnea M, Ackerman Michael |
| 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 |
| Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome. Frontiers of medicine in China 2007 Jul 1 (3): 312-5. Du Rong, Tian Li, Yuan Guohui, Li Jin, Ren Faxin, Gui Le, Li Wei, Zhang Shouyan, Kang Cailian, Yang Jung |
| Allelic variants of SCN5A and risk of sudden cardiac arrest in patients with coronary artery disease. Heart rhythm : the official journal of the Heart Rhythm Society 2006 Jun 3 (6): 697-700. Stecker Eric C, Sono Megan, Wallace Erin, Gunson Karen, Jui Jonathan, Chugh Sumeet |
| The long QT syndrome family of cardiac ion channelopathies: a HuGE review. Genetics in medicine : official journal of the American College of Medical Genetics 2006 Mar 8 (3): 143-55. Modell Stephen M, Lehmann Michael |
| Double SCN5A mutation underlying asymptomatic Brugada syndrome. Heart rhythm : the official journal of the Heart Rhythm Society 2005 Mar 2 (3): 285-92. Yokoi Hisataka, Makita Naomasa, Sasaki Koji, Takagi Yasuhiro, Okumura Yasuo, Nishino Tetsuo, Makiyama Takeru, Kitabatake Akira, Horie Minoru, Watanabe Ichiro, Tsutsui Hiroyu |
| Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations. Journal of the American College of Cardiology 2004 Mar 43 (5): 826-30. Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Simon F, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P |
| Modulating effects of age and gender on the clinical course of long QT syndrome by genotype. Journal of the American College of Cardiology 2003 Jul 42 (1): 103-9. Zareba Wojciech, Moss Arthur J, Locati Emanuela H, Lehmann Michael H, Peterson Derick R, Hall W Jackson, Schwartz Peter J, Vincent G Michael, Priori Silvia G, Benhorin Jesaia, Towbin Jeffrey A, Robinson Jennifer L, Andrews Mark L, Napolitano Carlo, Timothy Katherine, Zhang Li, Medina Aharon, |
| Beta-blocker therapy failures in symptomatic probands with genotyped long-QT syndrome. Pediatric cardiology 0 25 (5): 459-65. Chatrath R, Bell C M, Ackerman M |
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- Page last updated:May 24, 2022
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