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7. Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. Behr ER; Savio-Galimberti E; Barc J; Holst AG; Petropoulou E; Prins BP; Jabbari J; Torchio M; Berthet M; Mizusawa Y; Yang T; Nannenberg EA; Dagradi F; Weeke P; Bastiaenan R; Ackerman MJ; Haunso S; Leenhardt A; Kääb S; Probst V; Redon R; Sharma S; Wilde A; Tfelt-Hansen J; Schwartz P; Roden DM; Bezzina CR; Olesen M; Darbar D; Guicheney P; Crotti L; ; Jamshidi Y Cardiovasc Res; 2015 Jun; 106(3):520-9. PubMed ID: 25691538 [TBL] [Abstract][Full Text] [Related]
8. Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest. Andreasen L; Ghouse J; Skov MW; Have CT; Ahlberg G; Rasmussen PV; Linneberg A; Pedersen O; Platonov PG; Haunsø S; Svendsen JH; Hansen T; Kanters JK; Olesen MS Front Physiol; 2018; 9():894. PubMed ID: 30042696 [No Abstract] [Full Text] [Related]
9. Genetic modifier of the QTc interval associated with early-onset atrial fibrillation. Andreasen L; Nielsen JB; Christophersen IE; Holst AG; Sajadieh A; Tveit A; Haunsø S; Svendsen JH; Schmitt N; Olesen MS Can J Cardiol; 2013 Oct; 29(10):1234-40. PubMed ID: 24074973 [TBL] [Abstract][Full Text] [Related]
10. Common and rare variants in SCN10A modulate the risk of atrial fibrillation. Jabbari J; Olesen MS; Yuan L; Nielsen JB; Liang B; Macri V; Christophersen IE; Nielsen N; Sajadieh A; Ellinor PT; Grunnet M; Haunsø S; Holst AG; Svendsen JH; Jespersen T Circ Cardiovasc Genet; 2015 Feb; 8(1):64-73. PubMed ID: 25691686 [TBL] [Abstract][Full Text] [Related]
11. Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC. Martin RI; Babaei MS; Choy MK; Owens WA; Chico TJ; Keenan D; Yonan N; Koref MS; Keavney BD J Mol Cell Cardiol; 2015 Aug; 85():207-14. PubMed ID: 26073630 [TBL] [Abstract][Full Text] [Related]
12. Association of Genetic Variants at the 4q25 Locus with Atrial Fibrillation in Indian Population. Bhanushali A; Nair A; Jagdale G; Suvarna T; Das BR J Clin Lab Anal; 2017 Jan; 31(1):. PubMed ID: 27346453 [TBL] [Abstract][Full Text] [Related]
13. Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci. Ishikawa T; Masuda T; Hachiya T; Dina C; Simonet F; Nagata Y; Tanck MWT; Sonehara K; Glinge C; Tadros R; Khongphatthanayothin A; Lu TP; Higuchi C; Nakajima T; Hayashi K; Aizawa Y; Nakano Y; Nogami A; Morita H; Ohno S; Aiba T; Krijger Juárez C; Mauleekoonphairoj J; Poovorawan Y; Gourraud JB; Shimizu W; Probst V; Horie M; Wilde AAM; Redon R; Juang JJ; Nademanee K; Bezzina CR; Barc J; Tanaka T; Okada Y; Schott JJ; Makita N Eur Heart J; 2024 Jul; 45(26):2320-2332. PubMed ID: 38747976 [TBL] [Abstract][Full Text] [Related]
14. Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction. Foddha H; Bouzidi N; Foddha A; Chouchene S; Touhami R; Leban N; Maatoug MF; Gamra H; Ferchichi S; Chibani JB; Khelil AH Adv Clin Exp Med; 2020 Apr; 29(4):423-429. PubMed ID: 32330377 [TBL] [Abstract][Full Text] [Related]
15. Novel SCN10A variants associated with Brugada syndrome. Fukuyama M; Ohno S; Makiyama T; Horie M Europace; 2016 Jun; 18(6):905-11. PubMed ID: 25842276 [TBL] [Abstract][Full Text] [Related]
16. Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci. Lee JY; Kim TH; Yang PS; Lim HE; Choi EK; Shim J; Shin E; Uhm JS; Kim JS; Joung B; Oh S; Lee MH; Kim YH; Pak HN Eur Heart J; 2017 Sep; 38(34):2586-2594. PubMed ID: 28460022 [TBL] [Abstract][Full Text] [Related]
17. Genetic loci associated with atrial fibrillation: relation to left atrial structure in the Framingham Heart Study. Magnani JW; Yin X; McManus DD; Chuang ML; Cheng S; Lubitz SA; Arora G; Manning WJ; Ellinor PT; Benjamin EJ J Am Heart Assoc; 2014 Apr; 3(2):e000616. PubMed ID: 24695651 [TBL] [Abstract][Full Text] [Related]
18. The rs6771157 C/G polymorphism in SCN10A is associated with the risk of atrial fibrillation in a Chinese Han population. Fang Z; Jiang Y; Wang Y; Lin Y; Liu Y; Zhao L; Xu Y; Toorabally MB; He S; Zhang F Sci Rep; 2016 Oct; 6():35212. PubMed ID: 27725708 [TBL] [Abstract][Full Text] [Related]
19. Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years. Olesen MS; Holst AG; Jabbari J; Nielsen JB; Christophersen IE; Sajadieh A; Haunsø S; Svendsen JH Can J Cardiol; 2012; 28(2):191-5. PubMed ID: 22336519 [TBL] [Abstract][Full Text] [Related]
20. Genetic and Metabolic Determinants of Atrial Fibrillation in a General Population Sample: The CHRIS Study. Emmert DB; Vukovic V; Dordevic N; Weichenberger CX; Losi C; D'Elia Y; Volpato C; Hernandes VV; Gögele M; Foco L; Pontali G; Mascalzoni D; Domingues FS; Paulmichl R; Pramstaller PP; Pattaro C; Rossini A; Rainer J; Fuchsberger C; De Bortoli M Biomolecules; 2021 Nov; 11(11):. PubMed ID: 34827661 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]