PubMed (cited) for id: 607542

Year	Number of Results
1990	1
1993	1
1996	4
1997	9
1998	7
1999	11
2000	5
2001	4
2002	4
2003	5
2004	9
2005	5
2006	3
2007	1
2008	2
2009	3
2010	3
2013	3
2014	3
2015	1
2017	1
2024	0

1

Gating mechanisms underlying deactivation slowing by two KCNQ1 atrial fibrillation mutations.

Peng G, Barro-Soria R, Sampson KJ, Larsson HP, Kass RS. Peng G, et al. Sci Rep. 2017 Apr 6;7:45911. doi: 10.1038/srep45911. Sci Rep. 2017. PMID: 28383569 Free PMC article.

2

A new KCNQ1 mutation at the S5 segment that impairs its association with KCNE1 is responsible for short QT syndrome.

Moreno C, Oliveras A, de la Cruz A, Bartolucci C, Muñoz C, Salar E, Gimeno JR, Severi S, Comes N, Felipe A, González T, Lambiase P, Valenzuela C. Moreno C, et al. Cardiovasc Res. 2015 Sep 1;107(4):613-23. doi: 10.1093/cvr/cvv196. Epub 2015 Jul 13. Cardiovasc Res. 2015. PMID: 26168993

3

AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.

de Villiers CP, van der Merwe L, Crotti L, Goosen A, George AL Jr, Schwartz PJ, Brink PA, Moolman-Smook JC, Corfield VA. de Villiers CP, et al. Circ Cardiovasc Genet. 2014 Oct;7(5):599-606. doi: 10.1161/CIRCGENETICS.113.000580. Epub 2014 Aug 2. Circ Cardiovasc Genet. 2014. PMID: 25087618 Free PMC article.

4

Short QT syndrome manifesting with neonatal atrial fibrillation and bradycardia.

Villafañe J, Fischbach P, Gebauer R. Villafañe J, et al. Cardiology. 2014;128(3):236-40. doi: 10.1159/000360758. Epub 2014 May 9. Cardiology. 2014. PMID: 24818999 Review.

5

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

6

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.

7

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.

8

KCNE1 alters the voltage sensor movements necessary to open the KCNQ1 channel gate.

Osteen JD, Gonzalez C, Sampson KJ, Iyer V, Rebolledo S, Larsson HP, Kass RS. Osteen JD, et al. Proc Natl Acad Sci U S A. 2010 Dec 28;107(52):22710-5. doi: 10.1073/pnas.1016300108. Epub 2010 Dec 13. Proc Natl Acad Sci U S A. 2010. PMID: 21149716 Free PMC article.

9

Patient-specific induced pluripotent stem-cell models for long-QT syndrome.

Moretti A, Bellin M, Welling A, Jung CB, Lam JT, Bott-Flügel L, Dorn T, Goedel A, Höhnke C, Hofmann F, Seyfarth M, Sinnecker D, Schömig A, Laugwitz KL. Moretti A, et al. N Engl J Med. 2010 Oct 7;363(15):1397-409. doi: 10.1056/NEJMoa0908679. Epub 2010 Jul 21. N Engl J Med. 2010. PMID: 20660394 Free article.

10

Kcne2 deletion uncovers its crucial role in thyroid hormone biosynthesis.

Roepke TK, King EC, Reyna-Neyra A, Paroder M, Purtell K, Koba W, Fine E, Lerner DJ, Carrasco N, Abbott GW. Roepke TK, et al. Nat Med. 2009 Oct;15(10):1186-94. doi: 10.1038/nm.2029. Epub 2009 Sep 20. Nat Med. 2009. PMID: 19767733 Free PMC article.

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