These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
172 related articles for article (PubMed ID: 24332150)
1. Gene-environment interaction between SCN5A-1103Y and hypokalemia influences QT interval prolongation in African Americans: the Jackson Heart Study. Akylbekova EL; Payne JP; Newton-Cheh C; May WL; Fox ER; Wilson JG; Sarpong DF; Taylor HA; Maher JF Am Heart J; 2014 Jan; 167(1):116-122.e1. PubMed ID: 24332150 [TBL] [Abstract][Full Text] [Related]
2. A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans. Ilkhanoff L; Arking DE; Lemaitre RN; Alonso A; Chen LY; Durda P; Hesselson SE; Kerr KF; Magnani JW; Marcus GM; Schnabel RB; Smith JG; Soliman EZ; Reiner AP; Sotoodehnia N; J Cardiovasc Electrophysiol; 2014 Nov; 25(11):1150-7. PubMed ID: 25065297 [TBL] [Abstract][Full Text] [Related]
3. Patient-specific, re-engineered cardiomyocyte model confirms the circumstance-dependent arrhythmia risk associated with the African-specific common SCN5A polymorphism p.S1103Y: Implications for the increased sudden deaths observed in black individuals during the COVID-19 pandemic. Hamrick SK; John Kim CS; Tester DJ; Giudicessi JR; Ackerman MJ Heart Rhythm; 2022 May; 19(5):822-827. PubMed ID: 34979239 [TBL] [Abstract][Full Text] [Related]
4. Heritability in a SCN5A-mutation founder population with increased female susceptibility to non-nocturnal ventricular tachyarrhythmia and sudden cardiac death. Ter Bekke RMA; Isaacs A; Barysenka A; Hoos MB; Jongbloed JDH; Hoorntje JCA; Patelski ASM; Helderman-van den Enden ATJM; van den Wijngaard A; Stoll M; Volders PGA Heart Rhythm; 2017 Dec; 14(12):1873-1881. PubMed ID: 28782696 [TBL] [Abstract][Full Text] [Related]
5. Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Magnani JW; Brody JA; Prins BP; Arking DE; Lin H; Yin X; Liu CT; Morrison AC; Zhang F; Spector TD; Alonso A; Bis JC; Heckbert SR; Lumley T; Sitlani CM; Cupples LA; Lubitz SA; Soliman EZ; Pulit SL; Newton-Cheh C; O'Donnell CJ; Ellinor PT; Benjamin EJ; Muzny DM; Gibbs RA; Santibanez J; Taylor HA; Rotter JI; Lange LA; Psaty BM; Jackson R; Rich SS; Boerwinkle E; Jamshidi Y; Sotoodehnia N; ; ; Circ Cardiovasc Genet; 2014 Jun; 7(3):365-73. PubMed ID: 24951663 [TBL] [Abstract][Full Text] [Related]
6. Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans. Evans DS; Avery CL; Nalls MA; Li G; Barnard J; Smith EN; Tanaka T; Butler AM; Buxbaum SG; Alonso A; Arking DE; Berenson GS; Bis JC; Buyske S; Carty CL; Chen W; Chung MK; Cummings SR; Deo R; Eaton CB; Fox ER; Heckbert SR; Heiss G; Hindorff LA; Hsueh WC; Isaacs A; Jamshidi Y; Kerr KF; Liu F; Liu Y; Lohman KK; Magnani JW; Maher JF; Mehra R; Meng YA; Musani SK; Newton-Cheh C; North KE; Psaty BM; Redline S; Rotter JI; Schnabel RB; Schork NJ; Shohet RV; Singleton AB; Smith JD; Soliman EZ; Srinivasan SR; Taylor HA; Van Wagoner DR; Wilson JG; Young T; Zhang ZM; Zonderman AB; Evans MK; Ferrucci L; Murray SS; Tranah GJ; Whitsel EA; Reiner AP; ; Sotoodehnia N Hum Mol Genet; 2016 Oct; 25(19):4350-4368. PubMed ID: 27577874 [TBL] [Abstract][Full Text] [Related]
7. Persistent QT Prolongation in a Child with Gitelman Syndrome and SCN5A H558R Polymorphism. Tsukakoshi T; Lin L; Murakami T; Shiono J; Izumi I; Horigome H Int Heart J; 2018 Nov; 59(6):1466-1468. PubMed ID: 30305584 [TBL] [Abstract][Full Text] [Related]
8. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. Plant LD; Bowers PN; Liu Q; Morgan T; Zhang T; State MW; Chen W; Kittles RA; Goldstein SA J Clin Invest; 2006 Feb; 116(2):430-5. PubMed ID: 16453024 [TBL] [Abstract][Full Text] [Related]
9. A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome. Zumhagen S; Veldkamp MW; Stallmeyer B; Baartscheer A; Eckardt L; Paul M; Remme CA; Bhuiyan ZA; Bezzina CR; Schulze-Bahr E PLoS One; 2013; 8(6):e67963. PubMed ID: 23840796 [TBL] [Abstract][Full Text] [Related]
10. Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome. Van Norstrand DW; Tester DJ; Ackerman MJ Heart Rhythm; 2008 May; 5(5):712-5. PubMed ID: 18452875 [TBL] [Abstract][Full Text] [Related]
11. The common African American polymorphism SCN5A-S1103Y interacts with mutation SCN5A-R680H to increase late Na current. Cheng J; Tester DJ; Tan BH; Valdivia CR; Kroboth S; Ye B; January CT; Ackerman MJ; Makielski JC Physiol Genomics; 2011 May; 43(9):461-6. PubMed ID: 21385947 [TBL] [Abstract][Full Text] [Related]
12. Arrhythmias precede cardiomyopathy and remodeling of Ca Montnach J; Chizelle FF; Belbachir N; Castro C; Li L; Loussouarn G; Toumaniantz G; Carcouët A; Meinzinger AJ; Shmerling D; Benitah JP; Gómez AM; Charpentier F; Baró I J Mol Cell Cardiol; 2018 Oct; 123():13-25. PubMed ID: 30144447 [TBL] [Abstract][Full Text] [Related]
13. SCN5A variation is associated with electrocardiographic traits in the Jackson Heart Study. Jeff JM; Brown-Gentry K; Buxbaum SG; Sarpong DF; Taylor HA; George AL; Roden DM; Crawford DC Circ Cardiovasc Genet; 2011 Apr; 4(2):139-44. PubMed ID: 21325150 [TBL] [Abstract][Full Text] [Related]
14. Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:DeltaKPQ mutation. Windle JR; Geletka RC; Moss AJ; Zareba W; Atkins DL Ann Noninvasive Electrocardiol; 2001 Apr; 6(2):153-8. PubMed ID: 11333173 [TBL] [Abstract][Full Text] [Related]
15. Clinical correlates and heritability of QT interval duration in blacks: the Jackson Heart Study. Akylbekova EL; Crow RS; Johnson WD; Buxbaum SG; Njemanze S; Fox E; Sarpong DF; Taylor HA; Newton-Cheh C Circ Arrhythm Electrophysiol; 2009 Aug; 2(4):427-32. PubMed ID: 19808499 [TBL] [Abstract][Full Text] [Related]
17. H558R polymorphism in SCN5A is associated with Keshan disease and QRS prolongation in Keshan disease patients. Jiang S; Li FL; Dong Q; Liu HW; Fang CF; Shu C; Cheng H; Cui J; Ma HX; Chen DQ; Li H Genet Mol Res; 2014 Aug; 13(3):6569-76. PubMed ID: 25177937 [TBL] [Abstract][Full Text] [Related]
18. Sudden cardiac arrest associated with use of a non-cardiac drug that reduces cardiac excitability: evidence from bench, bedside, and community. Bardai A; Amin AS; Blom MT; Bezzina CR; Berdowski J; Langendijk PN; Beekman L; Klemens CA; Souverein PC; Koster RW; de Boer A; Tan HL Eur Heart J; 2013 May; 34(20):1506-16. PubMed ID: 23425522 [TBL] [Abstract][Full Text] [Related]
19. Electrocardiogram changes and atrial arrhythmias in individuals carrying sodium channel SCN5A D1275N mutation. Vanninen SUM; Nikus K; Aalto-Setälä K Ann Med; 2017 Sep; 49(6):496-503. PubMed ID: 28294644 [TBL] [Abstract][Full Text] [Related]
20. Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variant. Crotti L; Hu D; Barajas-Martinez H; De Ferrari GM; Oliva A; Insolia R; Pollevick GD; Dagradi F; Guerchicoff A; Greco F; Schwartz PJ; Viskin S; Antzelevitch C Heart Rhythm; 2012 Jul; 9(7):1104-12. PubMed ID: 22338672 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]