KCNQ1mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1

Bijal Vyas; Ratna D. Puri; Narayanan Namboodiri; Mohan Nair; Deepak Sharma; Sireesha Movva; Renu Saxena; Shomu Bohora; Neeraj Aggarwal; Amit Vora; Jatinder Kumar; Tarandeep Singh; Ishwar C. Verma

doi:10.1002/ajmg.a.37636

KCNQ1mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.37636 ◽

2016 ◽

Vol 170 (6) ◽

pp. 1510-1519 ◽

Cited By ~ 6

Author(s):

Bijal Vyas ◽

Ratna D. Puri ◽

Narayanan Namboodiri ◽

Mohan Nair ◽

Deepak Sharma ◽

...

Keyword(s):

Long Qt Syndrome ◽

Autosomal Recessive ◽

Syndrome Type ◽

Long Qt ◽

Qt Syndrome

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Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia

Molecular Genetics & Genomic Medicine ◽

10.1002/mgg3.305 ◽

2017 ◽

Vol 5 (5) ◽

pp. 592-601 ◽

Cited By ~ 1

Author(s):

Amnah Y. Bdier ◽

Saleh Al-Ghamdi ◽

Prashant K. Verma ◽

Khalid Dagriri ◽

Bandar Alshehri ◽

...

Keyword(s):

Saudi Arabia ◽

Long Qt Syndrome ◽

Autosomal Recessive ◽

Syndrome Type ◽

Long Qt ◽

Qt Syndrome

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Systematic Evaluation of KCNQ1 variant using ACMG/AMP Guidelines and Risk Stratification in Long QT Syndrome Type 1: Expression of Concern

Circulation Genomic and Precision Medicine ◽

10.1161/hcg.0000000000000077 ◽

2020 ◽

Vol 13 (6) ◽

Keyword(s):

Risk Stratification ◽

Long Qt Syndrome ◽

Systematic Evaluation ◽

Syndrome Type ◽

Long Qt ◽

Qt Syndrome

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GW27-e1111 Renal sympathetic denervation prevents ventricular tachycardia in a canine model of drug-induced long-QT syndrome type 1

Journal of the American College of Cardiology ◽

10.1016/j.jacc.2016.07.240 ◽

2016 ◽

Vol 68 (16) ◽

pp. C65

Author(s):

Huang Bing ◽

Lilei Yu ◽

Hong Jiang

Keyword(s):

Ventricular Tachycardia ◽

Long Qt Syndrome ◽

Canine Model ◽

Renal Sympathetic Denervation ◽

Syndrome Type ◽

Long Qt ◽

Drug Induced ◽

Qt Syndrome ◽

Renal Sympathetic

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Generation and characterization of twelve human induced pluripotent stem cell (iPSC) lines from four familial long QT syndrome type 1 (LQT1) patients carrying KCNQ1 c.1201dupC mutation

Stem Cell Research ◽

10.1016/j.scr.2019.101650 ◽

2019 ◽

Vol 41 ◽

pp. 101650 ◽

Cited By ~ 2

Author(s):

Ning Ge ◽

Min Liu ◽

Yicheng Ding ◽

Janusz Krawczyk ◽

Veronica McInerney ◽

...

Keyword(s):

Stem Cell ◽

Long Qt Syndrome ◽

Pluripotent Stem Cell ◽

Induced Pluripotent Stem Cell ◽

Syndrome Type ◽

Long Qt ◽

Qt Syndrome ◽

Induced Pluripotent

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EP04.36: Fetal sinus bradycardia as the symptom of previously undiagnosed familial form of Long QT syndrome type 1 caused by mutation of KCNQ1 gene (c.926C>T)

Ultrasound in Obstetrics and Gynecology ◽

10.1002/uog.18386 ◽

2017 ◽

Vol 50 ◽

pp. 279-279

Author(s):

E. Klaskova ◽

E. Hostinska ◽

J. Petrkova ◽

J. Houda ◽

J. Navratil ◽

...

Keyword(s):

Long Qt Syndrome ◽

Sinus Bradycardia ◽

Syndrome Type ◽

Long Qt ◽

Kcnq1 Gene ◽

Familial Form ◽

Qt Syndrome

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Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1　― Modified Schwartz Score ―

Circulation Journal ◽

10.1253/circj.cj-17-1032 ◽

2018 ◽

Vol 82 (9) ◽

pp. 2269-2276 ◽

Cited By ~ 4

Author(s):

Junichi Ozawa ◽

Seiko Ohno ◽

Yusuke Fujii ◽

Takeru Makiyama ◽

Hiroshi Suzuki ◽

...

Keyword(s):

Differential Diagnosis ◽

Ventricular Tachycardia ◽

Long Qt Syndrome ◽

Catecholaminergic Polymorphic Ventricular Tachycardia ◽

Polymorphic Ventricular Tachycardia ◽

Syndrome Type ◽

Long Qt ◽

Qt Syndrome

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Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 population

2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society ◽

10.1109/embc.2014.6945158 ◽

2014 ◽

Author(s):

Vlasta Bari ◽

Andrea Marchi ◽

Giulia Girardengo ◽

Alfred L. George ◽

Paul A. Brink ◽

...

Keyword(s):

Empirical Mode Decomposition ◽

Long Qt Syndrome ◽

Syndrome Type ◽

Long Qt ◽

Short Scale ◽

Mode Decomposition ◽

Qt Syndrome ◽

Filtering Approach

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Association of a congenital long QT syndrome type 1 with Takotsubo cardiomyopathy

Clinical Case Reports ◽

10.1002/ccr3.567 ◽

2016 ◽

Vol 4 (8) ◽

pp. 789-792 ◽

Cited By ~ 1

Author(s):

Ibrahim El‐Battrawy ◽

Michael Behnes ◽

Martin Borggrefe ◽

Ibrahim Akin

Keyword(s):

Takotsubo Cardiomyopathy ◽

Long Qt Syndrome ◽

Syndrome Type ◽

Long Qt ◽

Qt Syndrome ◽

Congenital Long Qt Syndrome

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Modeling of the long-QT syndrome type 1 and 2

Proceedings of the 25th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (IEEE Cat. No.03CH37439) ◽

10.1109/iembs.2003.1279499 ◽

2004 ◽

Author(s):

C.E. Conrath ◽

R. Wilders ◽

H.J. Jongsma ◽

T. Opthof

Keyword(s):

Long Qt Syndrome ◽

Syndrome Type ◽

Long Qt ◽

Qt Syndrome

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A Common Mutation of Long QT Syndrome Type 1 in Japan

Circulation Journal ◽

10.1253/circj.cj-15-0342 ◽

2015 ◽

Vol 79 (9) ◽

pp. 2026-2030 ◽

Cited By ~ 10

Author(s):

Hideki Itoh ◽

Kenichi Dochi ◽

Wataru Shimizu ◽

Isabelle Denjoy ◽

Seiko Ohno ◽

...

Keyword(s):

Long Qt Syndrome ◽

Common Mutation ◽

Syndrome Type ◽

Long Qt ◽

Qt Syndrome

Download Full-text

KCNQ1mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1

Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia

Systematic Evaluation of KCNQ1 variant using ACMG/AMP Guidelines and Risk Stratification in Long QT Syndrome Type 1: Expression of Concern

GW27-e1111 Renal sympathetic denervation prevents ventricular tachycardia in a canine model of drug-induced long-QT syndrome type 1

Generation and characterization of twelve human induced pluripotent stem cell (iPSC) lines from four familial long QT syndrome type 1 (LQT1) patients carrying KCNQ1 c.1201dupC mutation

EP04.36: Fetal sinus bradycardia as the symptom of previously undiagnosed familial form of Long QT syndrome type 1 caused by mutation of KCNQ1 gene (c.926C>T)

Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1 ― Modified Schwartz Score ―

Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 population

Association of a congenital long QT syndrome type 1 with Takotsubo cardiomyopathy

Modeling of the long-QT syndrome type 1 and 2

A Common Mutation of Long QT Syndrome Type 1 in Japan

Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1　― Modified Schwartz Score ―