Similar articles for PMID: 29202755

Year	Number of Results
2003	2
2004	1
2006	2
2007	3
2008	2
2009	5
2010	8
2011	6
2012	11
2013	15
2014	18
2015	22
2016	18
2017	12
2018	23
2019	20
2020	21
2021	25
2022	18
2023	7
2024	0

1

H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters.

Matsumura H, Nakano Y, Ochi H, Onohara Y, Sairaku A, Tokuyama T, Tomomori S, Motoda C, Amioka M, Hironobe N, Toshishige M, Takahashi S, Imai K, Sueda T, Chayama K, Kihara Y. Matsumura H, et al. J Biomed Sci. 2017 Dec 4;24(1):91. doi: 10.1186/s12929-017-0397-x. J Biomed Sci. 2017. PMID: 29202755 Free PMC article.

2

Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.

Veltmann C, Barajas-Martinez H, Wolpert C, Borggrefe M, Schimpf R, Pfeiffer R, Cáceres G, Burashnikov E, Antzelevitch C, Hu D. Veltmann C, et al. J Am Heart Assoc. 2016 Jul 5;5(7):e003379. doi: 10.1161/JAHA.116.003379. J Am Heart Assoc. 2016. PMID: 27381756 Free PMC article.

3

Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?

Daimi H, Khelil AH, Neji A, Ben Hamda K, Maaoui S, Aranega A, Be Chibani J, Franco D. Daimi H, et al. Biomed J. 2019 Aug;42(4):252-260. doi: 10.1016/j.bj.2019.03.003. Epub 2019 Sep 12. Biomed J. 2019. PMID: 31627867 Free PMC article.

4

Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters.

Rudic B, Schimpf R, Veltmann C, Doesch C, Tülümen E, Schoenberg SO, Borggrefe M, Papavassiliu T. Rudic B, et al. Europace. 2016 Sep;18(9):1411-9. doi: 10.1093/europace/euv300. Epub 2015 Oct 28. Europace. 2016. PMID: 26511399

5

Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.

Pambrun T, Mercier A, Chatelier A, Patri S, Schott JJ, Le Scouarnec S, Chahine M, Degand B, Bois P. Pambrun T, et al. Heart Rhythm. 2014 Aug;11(8):1393-400. doi: 10.1016/j.hrthm.2014.04.026. Epub 2014 Apr 21. Heart Rhythm. 2014. PMID: 24768612

6

SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families.

Wijeyeratne YD, Tanck MW, Mizusawa Y, Batchvarov V, Barc J, Crotti L, Bos JM, Tester DJ, Muir A, Veltmann C, Ohno S, Page SP, Galvin J, Tadros R, Muggenthaler M, Raju H, Denjoy I, Schott JJ, Gourraud JB, Skoric-Milosavljevic D, Nannenberg EA, Redon R, Papadakis M, Kyndt F, Dagradi F, Castelletti S, Torchio M, Meitinger T, Lichtner P, Ishikawa T, Wilde AAM, Takahashi K, Sharma S, Roden DM, Borggrefe MM, McKeown PP, Shimizu W, Horie M, Makita N, Aiba T, Ackerman MJ, Schwartz PJ, Probst V, Bezzina CR, Behr ER. Wijeyeratne YD, et al. Circ Genom Precis Med. 2020 Dec;13(6):e002911. doi: 10.1161/CIRCGEN.120.002911. Epub 2020 Nov 9. Circ Genom Precis Med. 2020. PMID: 33164571 Free PMC article.

7

Brugada syndrome disease phenotype explained in apparently benign sodium channel mutations.

Hoshi M, Du XX, Shinlapawittayatorn K, Liu H, Chai S, Wan X, Ficker E, Deschênes I. Hoshi M, et al. Circ Cardiovasc Genet. 2014 Apr;7(2):123-31. doi: 10.1161/CIRCGENETICS.113.000292. Epub 2014 Feb 26. Circ Cardiovasc Genet. 2014. PMID: 24573164 Free PMC article.

8

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. Makarawate P, et al. Heart Rhythm. 2020 Dec;17(12):2145-2153. doi: 10.1016/j.hrthm.2020.06.027. Epub 2020 Jun 30. Heart Rhythm. 2020. PMID: 32619740

9

SCN5A Genetic Polymorphisms Associated With Increased Defibrillator Shocks in Brugada Syndrome.

Makarawate P, Chaosuwannakit N, Vannaprasaht S, Sahasthas D, Koo SH, Lee EJD, Tassaneeyakul W, Barajas-Martinez H, Hu D, Sawanyawisuth K. Makarawate P, et al. J Am Heart Assoc. 2017 Jun 5;6(6):e005009. doi: 10.1161/JAHA.116.005009. J Am Heart Assoc. 2017. PMID: 28584071 Free PMC article.

10

A novel microsatellite polymorphism of sodium channel beta1-subunit gene (SCN1B) may underlie abnormal cardiac excitation manifested by coved-type ST-elevation compatible with Brugada syndrome in Japanese.

Ogawa R, Kishi R, Takagi A, Sakaue I, Takahashi H, Matsumoto N, Masuhara K, Nakazawa K, Kobayashi S, Miyake F, Echizen H. Ogawa R, et al. Int J Clin Pharmacol Ther. 2010 Feb;48(2):109-19. doi: 10.5414/cpp48109. Int J Clin Pharmacol Ther. 2010. PMID: 20137763

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