HuGE Literature Finder
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| Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome. European heart journal 2021 Jul . Ishikawa Taisuke, Kimoto Hiroki, Mishima Hiroyuki, Yamagata Kenichiro, Ogata Soshiro, Aizawa Yoshiyasu, Hayashi Kenshi, Morita Hiroshi, Nakajima Tadashi, Nakano Yukiko, Nagase Satoshi, Murakoshi Nobuyuki, Kowase Shinya, Ohkubo Kimie, Aiba Takeshi, Morimoto Shimpei, Ohno Seiko, Kamakura Shiro, Nogami Akihiko, Takagi Masahiko, Karakachoff Matilde, Dina Christian, Schott Jean-Jacques, Yoshiura Koh-Ichiro, Horie Minoru, Shimizu Wataru, Nishimura Kunihiro, Kusano Kengo, Makita Naoma |
| 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 |
| Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China. Mayo Clinic proceedings 2016 Oct . Zhang Liyong, Tester David J, Lang Di, Chen Yili, Zheng Jinxiang, Gao Rui, Corliss Robert F, Tang Shuangbo, Kyle John W, Liu Chao, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
52 Genetic Loci Influencing Myocardial Mass.
Journal of the American College of Cardiology 2016 Sep 68 (13): 1435-1448. van der Harst Pim, van Setten Jessica, Verweij Niek, Vogler Georg, Franke Lude, Maurano Matthew T, Wang Xinchen, Mateo Leach Irene, Eijgelsheim Mark, Sotoodehnia Nona, Hayward Caroline, Sorice Rossella, Meirelles Osorio, Lyytikäinen Leo-Pekka, Polašek Ozren, Tanaka Toshiko, Arking Dan E, Ulivi Sheila, Trompet Stella, Müller-Nurasyid Martina, Smith Albert V, Dörr Marcus, Kerr Kathleen F, Magnani Jared W, Del Greco M Fabiola, Zhang Weihua, Nolte Ilja M, Silva Claudia T, Padmanabhan Sandosh, Tragante Vinicius, Esko Tõnu, Abecasis Gonçalo R, Adriaens Michiel E, Andersen Karl, Barnett Phil, Bis Joshua C, Bodmer Rolf, Buckley Brendan M, Campbell Harry, Cannon Megan V, Chakravarti Aravinda, Chen Lin Y, Delitala Alessandro, Devereux Richard B, Doevendans Pieter A, Dominiczak Anna F, Ferrucci Luigi, Ford Ian, Gieger Christian, Harris Tamara B, Haugen Eric, Heinig Matthias, Hernandez Dena G, Hillege Hans L, Hirschhorn Joel N, Hofman Albert, Hubner Norbert, Hwang Shih-Jen, Iorio Annamaria, Kähönen Mika, Kellis Manolis, Kolcic Ivana, Kooner Ishminder K, Kooner Jaspal S, Kors Jan A, Lakatta Edward G, Lage Kasper, Launer Lenore J, Levy Daniel, Lundby Alicia, Macfarlane Peter W, May Dalit, Meitinger Thomas, Metspalu Andres, Nappo Stefania, Naitza Silvia, Neph Shane, Nord Alex S, Nutile Teresa, Okin Peter M, Olsen Jesper V, Oostra Ben A, Penninger Josef M, Pennacchio Len A, Pers Tune H, Perz Siegfried, Peters Annette, Pinto Yigal M, Pfeufer Arne, Pilia Maria Grazia, Pramstaller Peter P, Prins Bram P, Raitakari Olli T, Raychaudhuri Soumya, Rice Ken M, Rossin Elizabeth J, Rotter Jerome I, Schafer Sebastian, Schlessinger David, Schmidt Carsten O, Sehmi Jobanpreet, Silljé Herman H W, Sinagra Gianfranco, Sinner Moritz F, Slowikowski Kamil, Soliman Elsayed Z, Spector Timothy D, Spiering Wilko, Stamatoyannopoulos John A, Stolk Ronald P, Strauch Konstantin, Tan Sian-Tsung, Tarasov Kirill V, Trinh Bosco, Uitterlinden Andre G, van den Boogaard Malou, van Duijn Cornelia M, van Gilst Wiek H, Viikari Jorma S, Visscher Peter M, Vitart Veronique, Völker Uwe, Waldenberger Melanie, Weichenberger Christian X, Westra Harm-Jan, Wijmenga Cisca, Wolffenbuttel Bruce H, Yang Jian, Bezzina Connie R, Munroe Patricia B, Snieder Harold, Wright Alan F, Rudan Igor, Boyer Laurie A, Asselbergs Folkert W, van Veldhuisen Dirk J, Stricker Bruno H, Psaty Bruce M, Ciullo Marina, Sanna Serena, Lehtimäki Terho, Wilson James F, Bandinelli Stefania, Alonso Alvaro, Gasparini Paolo, Jukema J Wouter, Kääb Stefan, Gudnason Vilmundur, Felix Stephan B, Heckbert Susan R, de Boer Rudolf A, Newton-Cheh Christopher, Hicks Andrew A, Chambers John C, Jamshidi Yalda, Visel Axel, Christoffels Vincent M, Isaacs Aaron, Samani Nilesh J, de Bakker Paul I |
| Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases. International journal of legal medicine 2016 Feb . Neubauer Jacqueline, Haas Cordula, Bartsch Christine, Domingo-Medeiros Argelia, Berger Wolfga |
| 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 |
| Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder? Forensic science international 2014 Mar 236 38-45. Liu Chao, Tester David J, Hou Yiding, Wang Wen, Lv Guoli, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
| Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block. Circulation 2012 Sep 126 (12): 1469-77. Baruteau Alban-Elouen, Behaghel Albin, Fouchard Swanny, Mabo Philippe, Schott Jean-Jacques, Dina Christian, Chatel Stéphanie, Villain Elisabeth, Thambo Jean-Benoit, Marçon François, Gournay Véronique, Rouault Francis, Chantepie Alain, Guillaumont Sophie, Godart François, Martins Raphaël P, Delasalle Béatrice, Bonnet Caroline, Fraisse Alain, Schleich Jean-Marc, Lusson Jean-René, Dulac Yves, Daubert Jean-Claude, Le Marec Hervé, Probst Vince |
| Common variants in cardiac ion channel genes are associated with sudden cardiac death. Circulation. Arrhythmia and electrophysiology 2010 Jun 3 (3): 222-9. Albert Christine M, MacRae Calum A, Chasman Daniel I, VanDenburgh Martin, Buring Julie E, Manson JoAnn E, Cook Nancy R, Newton-Cheh Christoph |
| 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? |
| Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition. Heart rhythm : the official journal of the Heart Rhythm Society 2007 Feb 4 (2): 170-4. Chevalier Philippe, Bellocq Chloé, Millat Gilles, Piqueras Eric, Potet Franck, Schott Jean-Jacques, Baró Isabelle, Lemarec Hervé, Barhanin Jacques, Rousson Robert, Rodriguez-Lafrasse Clai |
| The electrocardiographic abnormalities in highly trained athletes compared to the genetic study related to causes of unexpected sudden cardiac death. Journal of medicine and life 0 2 (4): 361-72. Macarie C, Stoian Ioana, Dermengiu D, Barbarii Ligia, Piser Ileana Tepes, Chioncel O, Carp A, Stoian |
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- Page last updated:Oct 20, 2021
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