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A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence

Journal of the American College of Cardiology, 2014-01, Vol.63 (3), p.259-266

2014

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Flecainide Therapy Reduces Exercise-Induced Ventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Journal of the American College of Cardiology, 2011-05, Vol.57 (22), p.2244-2254

2011

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Left Cardiac Sympathetic Denervation for Catecholaminergic Polymorphic Ventricular Tachycardia

The New England journal of medicine, 2008-05, Vol.358 (19), p.2024-2029

2008

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Editorial: Monogenic vs. Oligogenic Reclassification

Frontiers in genetics, 2021-12, Vol.12, p.821591-821591

2021

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Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes

Heart rhythm, 2016-10, Vol.13 (10), p.2012-2019

2016

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Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

Circulation (New York, N.Y.), 2006-04, Vol.113 (13), p.1650-1658

2006

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A Zebrafish Loss-of-Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ Function

Human mutation, 2016-02, Vol.37 (2), p.194-200

2016

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A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome

PloS one, 2013-06, Vol.8 (6), p.e67963

2013

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Sudden cardiac death in forensic medicine – Swiss recommendations for a multidisciplinary approach

Swiss medical weekly, 2015-06, Vol.145, p.w14129

2015

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Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy

Medicina (Kaunas, Lithuania), 2019-01, Vol.55 (1), p.17

2019

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ACTN2 variant associated with a cardiac phenotype suggestive of left-dominant arrhythmogenic cardiomyopathy

HeartRhythm case reports, 2020-01, Vol.6 (1), p.15-19

2020

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Discordance Between Germline and Blood Mosaicism in Calmodulinopathy

Circulation. Genomic and precision medicine, 2022-08, Vol.15 (4), p.101161CIRCGEN121003695-e003695

2022

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Molecular insight into heart development and congenital heart disease: An update review from the Arab countries

Trends in cardiovascular medicine, 2015-05, Vol.25 (4), p.291-301

2015

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Mechanistic insight into an exonic splice defect mutation from native induced pluripotent stem cell-derived cardiomyocytes

Heart rhythm, 2018-10, Vol.15 (10), p.1575-1576

Bhuiyan, Zahurul A.

2018

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Genetic Mosaicism in Calmodulinopathy

Circulation. Genomic and precision medicine, 2019-09, Vol.12 (9), p.375-385

2019

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Silent mutation in long QT syndrome: Pathogenicity prediction by computer simulation

Heart rhythm, 2012-02, Vol.9 (2), p.283-284

Bhuiyan, Zahurul A., MD, PhD

2012

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Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

European heart journal, 2019-09, Vol.40 (35), p.2964-2975

2019

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Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

Heart rhythm, 2008-04, Vol.5 (4), p.553-561

2008

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Genotype and clinical characteristics of congenital long QT syndrome in Thailand

Indian pacing and electrophysiology journal, 2018-09, Vol.18 (5), p.165-171

2018

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De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome

Clinical genetics, 2014-11, Vol.86 (5), p.492-495

2014

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A Novel Early Onset Lethal Form of Catecholaminergic Polymorphic Ventricular Tachycardia Maps to Chromosome 7p14-p22

Journal of cardiovascular electrophysiology, 2007-10, Vol.18 (10), p.1060-1066

2007

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SCN5A overlap syndromes: An open-minded approach

Heart rhythm, 2022-08, Vol.19 (8), p.1363-1368

2022

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SCN5A mutations in atrial fibrillation

Heart rhythm, 2010-12, Vol.7 (12), p.1870-1871

2010

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A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence

Flecainide Therapy Reduces Exercise-Induced Ventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Left Cardiac Sympathetic Denervation for Catecholaminergic Polymorphic Ventricular Tachycardia

TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

Editorial: Monogenic vs. Oligogenic Reclassification

Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardia

A Zebrafish Loss-of-Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ Function

A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome

Sudden cardiac death in forensic medicine – Swiss recommendations for a multidisciplinary approach

Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy

ACTN2 variant associated with a cardiac phenotype suggestive of left-dominant arrhythmogenic cardiomyopathy

Discordance Between Germline and Blood Mosaicism in Calmodulinopathy

Molecular insight into heart development and congenital heart disease: An update review from the Arab countries

Mechanistic insight into an exonic splice defect mutation from native induced pluripotent stem cell-derived cardiomyocytes

Genetic Mosaicism in Calmodulinopathy

Silent mutation in long QT syndrome: Pathogenicity prediction by computer simulation

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

Genotype and clinical characteristics of congenital long QT syndrome in Thailand

De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome

A Novel Early Onset Lethal Form of Catecholaminergic Polymorphic Ventricular Tachycardia Maps to Chromosome 7p14-p22

SCN5A overlap syndromes: An open-minded approach

SCN5A mutations in atrial fibrillation

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