Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Syndrome and HEY2[original query] |
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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Nature genetics 2013 Sep 45 (9): 1044-9. Bezzina Connie R, Barc Julien, Mizusawa Yuka, Remme Carol Ann, Gourraud Jean-Baptiste, Simonet Floriane, Verkerk Arie O, Schwartz Peter J, Crotti Lia, Dagradi Federica, Guicheney Pascale, Fressart Véronique, Leenhardt Antoine, Antzelevitch Charles, Bartkowiak Susan, Borggrefe Martin, Schimpf Rainer, Schulze-Bahr Eric, Zumhagen Sven, Behr Elijah R, Bastiaenen Rachel, Tfelt-Hansen Jacob, Olesen Morten Salling, Kääb Stefan, Beckmann Britt M, Weeke Peter, Watanabe Hiroshi, Endo Naoto, Minamino Tohru, Horie Minoru, Ohno Seiko, Hasegawa Kanae, Makita Naomasa, Nogami Akihiko, Shimizu Wataru, Aiba Takeshi, Froguel Philippe, Balkau Beverley, Lantieri Olivier, Torchio Margherita, Wiese Cornelia, Weber David, Wolswinkel Rianne, Coronel Ruben, Boukens Bas J, Bézieau Stéphane, Charpentier Eric, Chatel Stéphanie, Despres Aurore, Gros Françoise, Kyndt Florence, Lecointe Simon, Lindenbaum Pierre, Portero Vincent, Violleau Jade, Gessler Manfred, Tan Hanno L, Roden Dan M, Christoffels Vincent M, Le Marec Hervé, Wilde Arthur A, Probst Vincent, Schott Jean-Jacques, Dina Christian, Redon Richa |
| 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 |
| Common Variant Near HEY2 Has a Protective Effect on Ventricular Fibrillation Occurrence in Brugada Syndrome by Regulating the Repolarization Current. Circulation. Arrhythmia and electrophysiology 2016 Jan 9 (1): . Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Toshishige Masaaki, Tokuyama Takehito, Matsumura Hiroya, Kawazoe Hiroshi, Tomomori Shunsuke, Sairaku Akinori, Watanabe Yoshikazu, Ikenaga Hiroki, Motoda Chikaaki, Suenari Kazuyoshi, Hayashida Yasufumi, Miki Daiki, Oda Nozomu, Kishimoto Shinji, Oda Noboru, Yoshida Yukihiko, Tashiro Satoshi, Chayama Kazuaki, Kihara Yasu |
| The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity. Circulation research 2017 Aug 121 (5): 537-548. Veerman Christiaan C, Podliesna Svitlana, Tadros Rafik, Lodder Elisabeth M, Mengarelli Isabella, de Jonge Berend, Beekman Leander, Barc Julien, Wilders Ronald, Wilde Arthur A M, Boukens Bastiaan J, Coronel Ruben, Verkerk Arie O, Remme Carol Ann, Bezzina Connie |
| Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest. Frontiers in physiology 2018 9 894. Andreasen Laura, Ghouse Jonas, Skov Morten W, Have Christian T, Ahlberg Gustav, Rasmussen Peter V, Linneberg Allan, Pedersen Oluf, Platonov Pyotr G, Haunsø Stig, Svendsen Jesper H, Hansen Torben, Kanters Jørgen K, Olesen Morten |
| Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
Heart rhythm 2020 Jun . Makarawate Pattarapong, Glinge Charlotte, Khongphatthanayothin Apichai, Walsh Roddy, Mauleekoonphairoj John, Amnueypol Montawatt, Prechawat Somchai, Wongcharoen Wanwarang, Krittayaphong Rungroj, Anannab Alisara, Lichtner Peter, Meitinger Thomas, Tjong Fleur V Y, Lieve Krystien V V, Amin Ahmad S, Sahasatas Dujdao, Ngarmukos Tachapong, Wichadakul Duangdao, Payungporn Sunchai, Sutjaporn Boosamas, Wandee Pharawee, Poovorawan Yong, Tfelt-Hansen Jacob, Tanck Michael W T, Tadros Rafik, Wilde Arthur A M, Bezzina Connie R, Veerakul Gumpanart, Nademanee Koonlaw |
- Page last reviewed:Feb 1, 2024
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