259 related articles for article (PubMed ID: 25691538)
1. 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]
2. Common variants in SCN10A gene associated with Brugada syndrome.
Huang Y; Chen XM; Barajas-Martinez H; Jiang H; Antzelevitch C; Hu D
Hum Mol Genet; 2021 Dec; 31(2):157-165. PubMed ID: 34312669
[TBL] [Abstract][Full Text] [Related]
3. Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome.
Hu D; Barajas-Martínez H; Pfeiffer R; Dezi F; Pfeiffer J; Buch T; Betzenhauser MJ; Belardinelli L; Kahlig KM; Rajamani S; DeAntonio HJ; Myerburg RJ; Ito H; Deshmukh P; Marieb M; Nam GB; Bhatia A; Hasdemir C; Haïssaguerre M; Veltmann C; Schimpf R; Borggrefe M; Viskin S; Antzelevitch C
J Am Coll Cardiol; 2014 Jul; 64(1):66-79. PubMed ID: 24998131
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants.
Monasky MM; Micaglio E; Vicedomini G; Locati ET; Ciconte G; Giannelli L; Giordano F; Crisà S; Vecchi M; Borrelli V; Ghiroldi A; D'Imperio S; Di Resta C; Benedetti S; Ferrari M; Santinelli V; Anastasia L; Pappone C
Europace; 2019 Oct; 21(10):1550-1558. PubMed ID: 31292628
[TBL] [Abstract][Full Text] [Related]
6. A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes.
El-Battrawy I; Albers S; Cyganek L; Zhao Z; Lan H; Li X; Xu Q; Kleinsorge M; Huang M; Liao Z; Zhong R; Rudic B; Müller J; Dinkel H; Lang S; Diecke S; Zimmermann WH; Utikal J; Wieland T; Borggrefe M; Zhou X; Akin I
Europace; 2019 Sep; 21(9):1410-1421. PubMed ID: 31106349
[TBL] [Abstract][Full Text] [Related]
7. Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
Makarawate P; Glinge C; Khongphatthanayothin A; Walsh R; Mauleekoonphairoj J; Amnueypol M; Prechawat S; Wongcharoen W; Krittayaphong R; Anannab A; Lichtner P; Meitinger T; Tjong FVY; Lieve KVV; Amin AS; Sahasatas D; Ngarmukos T; Wichadakul D; Payungporn S; Sutjaporn B; Wandee P; Poovorawan Y; Tfelt-Hansen J; Tanck MWT; Tadros R; Wilde AAM; Bezzina CR; Veerakul G; Nademanee K
Heart Rhythm; 2020 Dec; 17(12):2145-2153. PubMed ID: 32619740
[TBL] [Abstract][Full Text] [Related]
8. Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.
Zhang L; Zhou F; Huang L; Wu Q; Zheng J; Wu Y; Yin K; Cheng J
Int J Legal Med; 2017 Jan; 131(1):53-60. PubMed ID: 27272739
[TBL] [Abstract][Full Text] [Related]
9. SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation.
Savio-Galimberti E; Weeke P; Muhammad R; Blair M; Ansari S; Short L; Atack TC; Kor K; Vanoye CG; Olesen MS; LuCamp ; Yang T; George AL; Roden DM; Darbar D
Cardiovasc Res; 2014 Nov; 104(2):355-63. PubMed ID: 25053638
[TBL] [Abstract][Full Text] [Related]
10. Distinct Features of Probands With Early Repolarization and Brugada Syndromes Carrying SCN5A Pathogenic Variants.
Zhang ZH; Barajas-Martínez H; Xia H; Li B; Capra JA; Clatot J; Chen GX; Chen X; Yang B; Jiang H; Tse G; Aizawa Y; Gollob MH; Scheinman M; Antzelevitch C; Hu D
J Am Coll Cardiol; 2021 Oct; 78(16):1603-1617. PubMed ID: 34649698
[TBL] [Abstract][Full Text] [Related]
11. High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia.
Hasdemir C; Payzin S; Kocabas U; Sahin H; Yildirim N; Alp A; Aydin M; Pfeiffer R; Burashnikov E; Wu Y; Antzelevitch C
Heart Rhythm; 2015 Jul; 12(7):1584-94. PubMed ID: 25998140
[TBL] [Abstract][Full Text] [Related]
12. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Bezzina CR; Barc J; Mizusawa Y; Remme CA; Gourraud JB; Simonet F; Verkerk AO; Schwartz PJ; Crotti L; Dagradi F; Guicheney P; Fressart V; Leenhardt A; Antzelevitch C; Bartkowiak S; Borggrefe M; Schimpf R; Schulze-Bahr E; Zumhagen S; Behr ER; Bastiaenen R; Tfelt-Hansen J; Olesen MS; Kääb S; Beckmann BM; Weeke P; Watanabe H; Endo N; Minamino T; Horie M; Ohno S; Hasegawa K; Makita N; Nogami A; Shimizu W; Aiba T; Froguel P; Balkau B; Lantieri O; Torchio M; Wiese C; Weber D; Wolswinkel R; Coronel R; Boukens BJ; Bézieau S; Charpentier E; Chatel S; Despres A; Gros F; Kyndt F; Lecointe S; Lindenbaum P; Portero V; Violleau J; Gessler M; Tan HL; Roden DM; Christoffels VM; Le Marec H; Wilde AA; Probst V; Schott JJ; Dina C; Redon R
Nat Genet; 2013 Sep; 45(9):1044-9. PubMed ID: 23872634
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome.
Tambi R; Abdel Hameid R; Bankapur A; Nassir N; Begum G; Alsheikh-Ali A; Uddin M; Berdiev BK
Am J Physiol Heart Circ Physiol; 2021 May; 320(5):H1935-H1948. PubMed ID: 33797273
[TBL] [Abstract][Full Text] [Related]
15. Variant Intronic Enhancer Controls
Man JCK; Bosada FM; Scholman KT; Offerhaus JA; Walsh R; van Duijvenboden K; van Eif VWW; Bezzina CR; Verkerk AO; Boukens BJ; Barnett P; Christoffels VM
Circulation; 2021 Jul; 144(3):229-242. PubMed ID: 33910361
[TBL] [Abstract][Full Text] [Related]
16. Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Le Scouarnec S; Karakachoff M; Gourraud JB; Lindenbaum P; Bonnaud S; Portero V; Duboscq-Bidot L; Daumy X; Simonet F; Teusan R; Baron E; Violleau J; Persyn E; Bellanger L; Barc J; Chatel S; Martins R; Mabo P; Sacher F; Haïssaguerre M; Kyndt F; Schmitt S; Bézieau S; Le Marec H; Dina C; Schott JJ; Probst V; Redon R
Hum Mol Genet; 2015 May; 24(10):2757-63. PubMed ID: 25650408
[TBL] [Abstract][Full Text] [Related]
17. Familial Brugada Syndrome Associated With a Complete Deletion of the SCN5A and SCN10A Genes.
Trujillo-Quintero JP; Gutiérrez-Agulló M; Ochoa JP; Martínez-Martínez JG; de Uña D; García-Fernández A
Rev Esp Cardiol (Engl Ed); 2019 Feb; 72(2):176-178. PubMed ID: 29650450
[No Abstract] [Full Text] [Related]
18. Common Coding Variants in
Macri V; Brody JA; Arking DE; Hucker WJ; Yin X; Lin H; Mills RW; Sinner MF; Lubitz SA; Liu CT; Morrison AC; Alonso A; Li N; Fedorov VV; Janssen PM; Bis JC; Heckbert SR; Dolmatova EV; Lumley T; Sitlani CM; Cupples LA; Pulit SL; Newton-Cheh C; Barnard J; Smith JD; Van Wagoner DR; Chung MK; Vlahakes GJ; O'Donnell CJ; Rotter JI; Margulies KB; Morley MP; Cappola TP; Benjamin EJ; Muzny D; Gibbs RA; Jackson RD; Magnani JW; Herndon CN; Rich SS; Psaty BM; Milan DJ; Boerwinkle E; Mohler PJ; Sotoodehnia N; Ellinor PT
Circ Genom Precis Med; 2018 May; 11(5):e001663. PubMed ID: 29752399
[TBL] [Abstract][Full Text] [Related]
19. Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.
Huang L; Wu KH; Zhang L; Wang Q; Tang S; Wu Q; Jiang PH; Lin JJ; Guo J; Wang L; Loh SH; Cheng J
J Am Heart Assoc; 2018 Jan; 7(1):. PubMed ID: 29306897
[TBL] [Abstract][Full Text] [Related]
20. Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Te Riele AS; James CA; Murray B; Tichnell C; Amat-Alarcon N; Burks K; Tandri H; Calkins H; Polydefkis M; Judge DP
J Cardiovasc Transl Res; 2016 Feb; 9(1):87-9. PubMed ID: 26733327
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]