PubMed (cited) for id: 607554

Year	Number of Results
1997	1
2003	1
2005	1
2008	1
2009	2
2010	1
2013	3
2014	1
2024	0

1

A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.

Hasegawa K, Ohno S, Ashihara T, Itoh H, Ding WG, Toyoda F, Makiyama T, Aoki H, Nakamura Y, Delisle BP, Matsuura H, Horie M. Hasegawa K, et al. Heart Rhythm. 2014 Jan;11(1):67-75. doi: 10.1016/j.hrthm.2013.09.073. Epub 2013 Oct 1. Heart Rhythm. 2014. PMID: 24096004

2

Long QT genetics manifesting as atrial fibrillation.

Guerrier K, Czosek RJ, Spar DS, Anderson J. Guerrier K, et al. Heart Rhythm. 2013 Sep;10(9):1351-3. doi: 10.1016/j.hrthm.2013.07.012. Epub 2013 Jul 11. Heart Rhythm. 2013. PMID: 23851063 No abstract available.

3

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation.

Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP. Bartos DC, et al. J Cardiovasc Electrophysiol. 2013 May;24(5):562-9. doi: 10.1111/jce.12068. Epub 2013 Jan 25. J Cardiovasc Electrophysiol. 2013. PMID: 23350853 Free PMC article.

4

Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation.

Abraham RL, Yang T, Blair M, Roden DM, Darbar D. Abraham RL, et al. J Mol Cell Cardiol. 2010 Jan;48(1):181-90. doi: 10.1016/j.yjmcc.2009.07.020. Epub 2009 Jul 30. J Mol Cell Cardiol. 2010. PMID: 19646991 Free PMC article.

5

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation.

Das S, Makino S, Melman YF, Shea MA, Goyal SB, Rosenzweig A, Macrae CA, Ellinor PT. Das S, et al. Heart Rhythm. 2009 Aug;6(8):1146-53. doi: 10.1016/j.hrthm.2009.04.015. Epub 2009 Apr 15. Heart Rhythm. 2009. PMID: 19632626 Free PMC article.

6

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome.

Johnson JN, Tester DJ, Perry J, Salisbury BA, Reed CR, Ackerman MJ. Johnson JN, et al. Heart Rhythm. 2008 May;5(5):704-9. doi: 10.1016/j.hrthm.2008.02.007. Epub 2008 Feb 8. Heart Rhythm. 2008. PMID: 18452873 Free PMC article.

7

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

Napolitano C, Priori SG, Schwartz PJ, Bloise R, Ronchetti E, Nastoli J, Bottelli G, Cerrone M, Leonardi S. Napolitano C, et al. JAMA. 2005 Dec 21;294(23):2975-80. doi: 10.1001/jama.294.23.2975. JAMA. 2005. PMID: 16414944

8

KCNQ1 gain-of-function mutation in familial atrial fibrillation.

Chen YH, Xu SJ, Bendahhou S, Wang XL, Wang Y, Xu WY, Jin HW, Sun H, Su XY, Zhuang QN, Yang YQ, Li YB, Liu Y, Xu HJ, Li XF, Ma N, Mou CP, Chen Z, Barhanin J, Huang W. Chen YH, et al. Science. 2003 Jan 10;299(5604):251-4. doi: 10.1126/science.1077771. Science. 2003. PMID: 12522251

9

Identification of a genetic locus for familial atrial fibrillation.

Brugada R, Tapscott T, Czernuszewicz GZ, Marian AJ, Iglesias A, Mont L, Brugada J, Girona J, Domingo A, Bachinski LL, Roberts R. Brugada R, et al. N Engl J Med. 1997 Mar 27;336(13):905-11. doi: 10.1056/NEJM199703273361302. N Engl J Med. 1997. PMID: 9070470 Free article.

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