Similar articles for PMID: 37071726

Year	Number of Results
1999	2
2000	1
2002	1
2003	2
2004	2
2005	6
2006	6
2007	3
2008	5
2009	6
2010	7
2011	12
2012	6
2013	10
2014	7
2015	6
2016	2
2017	4
2018	4
2019	1
2020	3
2021	4
2022	6
2023	5
2024	2

1

Elucidation of ALG10B as a Novel Long-QT Syndrome-Susceptibility Gene.

Zhou W, Ye D, Tester DJ, Bains S, Giudicessi JR, Haglund-Turnquist CM, Orland KM, January CT, Eckhardt LL, Maginot KR, Ackerman MJ. Zhou W, et al. Circ Genom Precis Med. 2023 Apr;16(2):e003726. doi: 10.1161/CIRCGEN.122.003726. Epub 2023 Feb 22. Circ Genom Precis Med. 2023. PMID: 37071726 Free PMC article.

2

Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant.

Tobert KE, Tester DJ, Zhou W, Haglund-Turnquist CM, Giudicessi JR, Ackerman MJ. Tobert KE, et al. Heart Rhythm. 2022 Jun;19(6):998-1007. doi: 10.1016/j.hrthm.2022.02.004. Epub 2022 Feb 7. Heart Rhythm. 2022. PMID: 35144019

3

Promise and Potential Peril With Lumacaftor for the Trafficking Defective Type 2 Long-QT Syndrome-Causative Variants, p.G604S, p.N633S, and p.R685P, Using Patient-Specific Re-Engineered Cardiomyocytes.

O'Hare BJ, John Kim CS, Hamrick SK, Ye D, Tester DJ, Ackerman MJ. O'Hare BJ, et al. Circ Genom Precis Med. 2020 Oct;13(5):466-475. doi: 10.1161/CIRCGEN.120.002950. Epub 2020 Sep 17. Circ Genom Precis Med. 2020. PMID: 32940533

4

Tbx20 controls the expression of the KCNH2 gene and of hERG channels.

Caballero R, Utrilla RG, Amorós I, Matamoros M, Pérez-Hernández M, Tinaquero D, Alfayate S, Nieto-Marín P, Guerrero-Serna G, Liu QH, Ramos-Mondragón R, Ponce-Balbuena D, Herron T, Campbell KF, Filgueiras-Rama D, Peinado R, López-Sendón JL, Jalife J, Delpón E, Tamargo J. Caballero R, et al. Proc Natl Acad Sci U S A. 2017 Jan 17;114(3):E416-E425. doi: 10.1073/pnas.1612383114. Epub 2017 Jan 3. Proc Natl Acad Sci U S A. 2017. PMID: 28049825 Free PMC article.

5

A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death.

Zhang Y, Zhou N, Jiang W, Peng J, Wan H, Huang C, Xie Z, Huang CL, Grace AA, Ma A. Zhang Y, et al. Eur J Pediatr. 2007 Sep;166(9):927-33. doi: 10.1007/s00431-006-0346-2. Epub 2006 Dec 14. Eur J Pediatr. 2007. PMID: 17171344

6

Disruption of protein quality control of the human ether-à-go-go related gene K⁺ channel results in profound long QT syndrome.

Ledford HA, Ren L, Thai PN, Park S, Timofeyev V, Sirish P, Xu W, Emigh AM, Priest JR, Perez MV, Ashley EA, Yarov-Yarovoy V, Yamoah EN, Zhang XD, Chiamvimonvat N. Ledford HA, et al. Heart Rhythm. 2022 Feb;19(2):281-292. doi: 10.1016/j.hrthm.2021.10.005. Epub 2021 Oct 9. Heart Rhythm. 2022. PMID: 34634443 Free PMC article.

7

Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome.

Bellin M, Casini S, Davis RP, D'Aniello C, Haas J, Ward-van Oostwaard D, Tertoolen LG, Jung CB, Elliott DA, Welling A, Laugwitz KL, Moretti A, Mummery CL. Bellin M, et al. EMBO J. 2013 Dec 11;32(24):3161-75. doi: 10.1038/emboj.2013.240. Epub 2013 Nov 8. EMBO J. 2013. PMID: 24213244 Free PMC article.

8

A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.

Liu L, Hayashi K, Kaneda T, Ino H, Fujino N, Uchiyama K, Konno T, Tsuda T, Kawashiri MA, Ueda K, Higashikata T, Shuai W, Kupershmidt S, Higashida H, Yamagishi M. Liu L, et al. Heart Rhythm. 2013 Jan;10(1):61-7. doi: 10.1016/j.hrthm.2012.09.053. Epub 2012 Sep 23. Heart Rhythm. 2013. PMID: 23010577

9

Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.

Tester DJ, Benton AJ, Train L, Deal B, Baudhuin LM, Ackerman MJ. Tester DJ, et al. Am J Cardiol. 2010 Oct 15;106(8):1124-8. doi: 10.1016/j.amjcard.2010.06.022. Am J Cardiol. 2010. PMID: 20920651 Free PMC article.

10

Long QT syndrome-associated mutations in intrauterine fetal death.

Crotti L, Tester DJ, White WM, Bartos DC, Insolia R, Besana A, Kunic JD, Will ML, Velasco EJ, Bair JJ, Ghidoni A, Cetin I, Van Dyke DL, Wick MJ, Brost B, Delisle BP, Facchinetti F, George AL, Schwartz PJ, Ackerman MJ. Crotti L, et al. JAMA. 2013 Apr 10;309(14):1473-82. doi: 10.1001/jama.2013.3219. JAMA. 2013. PMID: 23571586 Free PMC article.

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