Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Death and SCN10A[original query] |
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Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
Nature genetics 2010 Dec 42 (12): 1068-76. Sotoodehnia Nona, Isaacs Aaron, de Bakker Paul I W, Dörr Marcus, Newton-Cheh Christopher, Nolte Ilja M, van der Harst Pim, Müller Martina, Eijgelsheim Mark, Alonso Alvaro, Hicks Andrew A, Padmanabhan Sandosh, Hayward Caroline, Smith Albert Vernon, Polasek Ozren, Giovannone Steven, Fu Jingyuan, Magnani Jared W, Marciante Kristin D, Pfeufer Arne, Gharib Sina A, Teumer Alexander, Li Man, Bis Joshua C, Rivadeneira Fernando, Aspelund Thor, Köttgen Anna, Johnson Toby, Rice Kenneth, Sie Mark P S, Wang Ying A, Klopp Norman, Fuchsberger Christian, Wild Sarah H, Mateo Leach Irene, Estrada Karol, Völker Uwe, Wright Alan F, Asselbergs Folkert W, Qu Jiaxiang, Chakravarti Aravinda, Sinner Moritz F, Kors Jan A, Petersmann Astrid, Harris Tamara B, Soliman Elsayed Z, Munroe Patricia B, Psaty Bruce M, Oostra Ben A, Cupples L Adrienne, Perz Siegfried, de Boer Rudolf A, Uitterlinden André G, Völzke Henry, Spector Timothy D, Liu Fang-Yu, Boerwinkle Eric, Dominiczak Anna F, Rotter Jerome I, van Herpen Gé, Levy Daniel, Wichmann H-Erich, van Gilst Wiek H, Witteman Jacqueline C M, Kroemer Heyo K, Kao W H Linda, Heckbert Susan R, Meitinger Thomas, Hofman Albert, Campbell Harry, Folsom Aaron R, van Veldhuisen Dirk J, Schwienbacher Christine, O'Donnell Christopher J, Volpato Claudia Beu, Caulfield Mark J, Connell John M, Launer Lenore, Lu Xiaowen, Franke Lude, Fehrmann Rudolf S N, te Meerman Gerard, Groen Harry J M, Weersma Rinse K, van den Berg Leonard H, Wijmenga Cisca, Ophoff Roel A, Navis Gerjan, Rudan Igor, Snieder Harold, Wilson James F, Pramstaller Peter P, Siscovick David S, Wang Thomas J, Gudnason Vilmundur, van Duijn Cornelia M, Felix Stephan B, Fishman Glenn I, Jamshidi Yalda, Stricker Bruno H Ch, Samani Nilesh J, Kääb Stefan, Arking Dan |
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 |
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome. Journal of the American College of Cardiology 2014 Jul 64 (1): 66-79. Hu Dan, Barajas-Martínez Hector, Pfeiffer Ryan, Dezi Fabio, Pfeiffer Jenna, Buch Tapan, Betzenhauser Matthew J, Belardinelli Luiz, Kahlig Kristopher M, Rajamani Sridharan, DeAntonio Harry J, Myerburg Robert J, Ito Hiroyuki, Deshmukh Pramod, Marieb Mark, Nam Gi-Byoung, Bhatia Atul, Hasdemir Can, Haïssaguerre Michel, Veltmann Christian, Schimpf Rainer, Borggrefe Martin, Viskin Sami, Antzelevitch Charl |
Carboplatin/taxane-induced gastrointestinal toxicity: a pharmacogenomics study on the SCOTROC1 trial. The pharmacogenomics journal 2015 Jul . He Y J, Winham S J, Hoskins J M, Glass S, Paul J, Brown R, Motsinger-Reif A, McLeod H |
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome. Human molecular genetics 2015 May 24 (10): 2757-63. Le Scouarnec Solena, Karakachoff Matilde, Gourraud Jean-Baptiste, Lindenbaum Pierre, Bonnaud Stéphanie, Portero Vincent, Duboscq-Bidot Laëtitia, Daumy Xavier, Simonet Floriane, Teusan Raluca, Baron Estelle, Violleau Jade, Persyn Elodie, Bellanger Lise, Barc Julien, Chatel Stéphanie, Martins Raphaël, Mabo Philippe, Sacher Frédéric, Haïssaguerre Michel, Kyndt Florence, Schmitt Sébastien, Bézieau Stéphane, Le Marec Hervé, Dina Christian, Schott Jean-Jacques, Probst Vincent, Redon Richa |
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. Cardiovascular research 2015 Jun 106 (3): 520-9. Behr Elijah R, Savio-Galimberti Eleonora, Barc Julien, Holst Anders G, Petropoulou Evmorfia, Prins Bram P, Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A, Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J, Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M, Bezzina Connie R, Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia, , Jamshidi Yal |
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 |
Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population. International journal of legal medicine 2016 Jun . Zhang Liyong, Zhou Feng, Huang Lei, Wu Qiuping, Zheng Jinxiang, Wu Yeda, Yin Kun, Cheng Jiandi |
GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations.
PloS one 2019 14 (6): e0217796. Swenson Brenton R, Louie Tin, Lin Henry J, Méndez-Giráldez Raúl, Below Jennifer E, Laurie Cathy C, Kerr Kathleen F, Highland Heather, Thornton Timothy A, Ryckman Kelli K, Kooperberg Charles, Soliman Elsayed Z, Seyerle Amanda A, Guo Xiuqing, Taylor Kent D, Yao Jie, Heckbert Susan R, Darbar Dawood, Petty Lauren E, McKnight Barbara, Cheng Susan, Bello Natalie A, Whitsel Eric A, Hanis Craig L, Nalls Mike A, Evans Daniel S, Rotter Jerome I, Sofer Tamar, Avery Christy L, Sotoodehnia No |
A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes. 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 2019 5 21 (9): 1410-1421. El-Battrawy Ibrahim, Albers Sebastian, Cyganek Lukas, Zhao Zhihan, Lan Huan, Li Xin, Xu Qiang, Kleinsorge Mandy, Huang Mengying, Liao Zhenxing, Zhong Rujia, Rudic Boris, Müller Jonas, Dinkel Hendrik, Lang Siegfried, Diecke Sebastian, Zimmermann Wolfram-Hubertus, Utikal Jochen, Wieland Thomas, Borggrefe Martin, Zhou Xiaobo, Akin Ibrah |
Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2020 Apr . Foddha Hajer, Bouzidi Nadia, Foddha Abdelhak, Chouchene Saoussen, Touhami Rahma, Leban Nadia, Maatoug Mohamed Faouzi, Gamra Habib, Ferchichi Salima, Chibani Jemni Ben, Khelil Amel H |
Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death. Heart rhythm 2023 2 . Isaacs Aaron, Barysenka Andrei, Ter Bekke Rachel M A, Helderman-van den Enden Apollonia T J M, van den Wijngaard Arthur, Volders Paul G A, Stoll Moni |
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