Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: Sudden Infant Death and SCN5A[original query] |
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Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing. Heart rhythm : the official journal of the Heart Rhythm Society 2004 Nov 1 (5): 600-7. Ackerman Michael J, Splawski Igor, Makielski Jonathan C, Tester David J, Will Melissa L, Timothy Katherine W, Keating Mark T, Jones Gregg, Chadha Monica, Burrow Christopher R, Stephens J Claiborne, Xu Chuanbo, Judson Richard, Curran Mark |
A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. The Journal of clinical investigation 2006 Feb 116 (2): 430-5. Plant Leigh D, Bowers Peter N, Liu Qianyong, Morgan Thomas, Zhang Tingting, State Matthew W, Chen Weidong, Kittles Rick A, Goldstein Steve A |
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. Circulation 2007 Jan 115 (3): 361-7. Arnestad Marianne, Crotti Lia, Rognum Torleiv O, Insolia Roberto, Pedrazzini Matteo, Ferrandi Chiara, Vege Ashild, Wang Dao W, Rhodes Troy E, George Alfred L, Schwartz Peter |
Cardiac ion channel gene mutations in sudden infant death syndrome. Pediatric research 2008 Nov 64 (5): 482-7. Otagiri Tesshu, Kijima Kazuki, Osawa Motoki, Ishii Kuniaki, Makita Naomasa, Matoba Ryoji, Umetsu Kazuo, Hayasaka Kiyos |
Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome. Heart rhythm : the official journal of the Heart Rhythm Society 2008 May 5 (5): 712-5. Van Norstrand David W, Tester David J, Ackerman Michael |
Contribution of long-QT syndrome genetic variants in sudden infant death syndrome. Pediatric cardiology 2009 Mar . Millat G, Kugener B, Chevalier P, Chahine M, Huang H, Malicier D, Rodriguez-Lafrasse C, Rousson R |
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current. Circulation. Arrhythmia and electrophysiology 2009 Dec 2 (6): 667-76. Cheng Jianding, Van Norstrand David W, Medeiros-Domingo Argelia, Valdivia Carmen, Tan Bi-hua, Ye Bin, Kroboth Stacie, Vatta Matteo, Tester David J, January Craig T, Makielski Jonathan C, Ackerman Michael |
SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103Tyr. BMC medical genetics 2010 11 (1): 74. Killen Stacy A S, Kunic Jennifer, Wang Lily, Lewis Adele, Levy Bruce P, Ackerman Michael J, George Alfred |
Sudden infant death syndrome-associated mutations in the sodium channel beta subunits. Heart rhythm : the official journal of the Heart Rhythm Society 2010 Jun 7 (6): 771-8. Tan Bi-Hua, Pundi Kavitha N, Van Norstrand David W, Valdivia Carmen R, Tester David J, Medeiros-Domingo Argelia, Makielski Jonathan C, Ackerman Michael |
Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data. The Canadian journal of cardiology 2013 Sep 29 (9): 1104-9. Andreasen Charlotte, Refsgaard Lena, Nielsen Jonas B, Sajadieh Ahmad, Winkel Bo G, Tfelt-Hansen Jacob, Haunsø Stig, Holst Anders G, Svendsen Jesper H, Olesen Morten |
Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases. European journal of human genetics : EJHG 2015 Sep . Hertz Christin Loeth, Christiansen Sofie Lindgren, Larsen Maiken Kudahl, Dahl Morten, Ferrero-Miliani Laura, Weeke Peter Ejvind, Pedersen Oluf, Hansen Torben, Grarup Niels, Ottesen Gyda Lolk, Frank-Hansen Rune, Banner Jytte, Morling Nie |
[High incidence of sudden cardiac death in one family with type-3 long QT syndrome: molecular genetics and electrophysiology mechanism analysis]. Zhonghua xin xue guan bing za zhi 2015 Dec 43 (12): 1046-50. Zhou Hui, Li Zhang, Ali Raza Ghani, Zhu Wengen, Zhou Qiongqiong, Shen Yang, Xie Jinyan, Cao Qing, Wan Rong, Hu Jinzhu, Hong K |
Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea. Journal of Korean medical science 2018 8 33 (32): e200. Son Min-Jeong, Kim Min-Kyoung, Yang Kyung-Moo, Choi Byung-Ha, Lee Bong Woo, Yoo Seong |
Cardiac Genetic Predisposition in Sudden Infant Death Syndrome. Journal of the American College of Cardiology 2018 Mar 71 (11): 1217-1227. Tester David J, Wong Leonie C H, Chanana Pritha, Jaye Amie, Evans Jared M, FitzPatrick David R, Evans Margaret J, Fleming Peter, Jeffrey Iona, Cohen Marta C, Tfelt-Hansen Jacob, Simpson Michael A, Behr Elijah R, Ackerman Michael |
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