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The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

Basic research in cardiology, 2009-09, Vol.104 (5), p.511-522

2009

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Mental illness and cardiovascular health: observational and polygenic score analyses in a population-based cohort study

Psychological medicine, 2024-04, Vol.54 (5), p.1-939

2024

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Unique Cardiac Purkinje Fiber Transient Outward Current β-Subunit Composition: A Potential Molecular Link to Idiopathic Ventricular Fibrillation

Circulation research, 2013-05, Vol.112 (10), p.1310-1322

2013

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Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity

European journal of human genetics : EJHG, 2008-03, Vol.16 (3), p.350-357

2008

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Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6

Netherlands heart journal, 2011-06, Vol.19 (6), p.290-296

2011

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Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits

Biophysical reviews, 2018-08, Vol.10 (4), p.1053-1060

2018

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Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

Forensic science international, 2017-06, Vol.275, p.187-194

2017

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Cardiac dyssynchrony and response to cardiac resynchronisation therapy in heart failure: can genetic predisposition play a role?

Netherlands heart journal, 2016-01, Vol.24 (1), p.11-15

2016

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The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

Basic research in cardiology, 2009-09, Vol.104 (5), p.511-522

2009

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A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

Circulation research, 2003-01, Vol.92 (1), p.14-22

2003

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Contribution of Sodium Channel Mutations to Bradycardia and Sinus Node Dysfunction in LQT3 Families

Circulation research, 2003-05, Vol.92 (9), p.976-983

2003

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A sodium-channel mutation causes isolated cardiac conduction disease

Nature (London), 2001-02, Vol.409 (6823), p.1043-1047

2001

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Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System

Circulation research, 2003-02, Vol.92 (2), p.159-168

2003

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Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide

Netherlands heart journal, 2009-11, Vol.17 (11), p.422-428

2009

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Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation

Netherlands heart journal, 2007-06, Vol.15 (6), p.235-238

2007

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Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes

Circulation (New York, N.Y.), 2001-09, Vol.104 (10), p.1200-1205

2001

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Genetic predisposition for sudden cardiac death in myocardial ischaemia: the Arrhythmia Genetics in the NEtherlandS study

Netherlands heart journal, 2011-02, Vol.19 (2), p.96-100

2011

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Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

Circulation (New York, N.Y.), 2004-05, Vol.109 (20), p.2394-2397

2004

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Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction

Circulation (New York, N.Y.), 2006-01, Vol.113 (3), p.338-344

2006

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Right ventricular fibrosis and conduction delay in a patient with clinical signs of brugada syndrome : A combined electrophysiological, genetic, histopathologic, and computational study

Circulation (New York, N.Y.), 2005-11, Vol.112 (18), p.2769-2777

2005

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Genetics of cardiac arrhythmias

Heart (British Cardiac Society), 2005-10, Vol.91 (10), p.1352-1358

2005

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A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

Journal of molecular and cellular cardiology, 2005-06, Vol.38 (6), p.969-981

2005

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Genomics of cardiac electrical function

Briefings in functional genomics, 2014-01, Vol.13 (1), p.39-50

2014

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Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients

Journal of the American College of Cardiology, 2002-07, Vol.40 (2), p.350-356

2002

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The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

Mental illness and cardiovascular health: observational and polygenic score analyses in a population-based cohort study

Unique Cardiac Purkinje Fiber Transient Outward Current β-Subunit Composition: A Potential Molecular Link to Idiopathic Ventricular Fibrillation

Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity

Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6

Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

Cardiac dyssynchrony and response to cardiac resynchronisation therapy in heart failure: can genetic predisposition play a role?

The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

Contribution of Sodium Channel Mutations to Bradycardia and Sinus Node Dysfunction in LQT3 Families

A sodium-channel mutation causes isolated cardiac conduction disease

Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System

Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide

Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation

Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes

Genetic predisposition for sudden cardiac death in myocardial ischaemia: the Arrhythmia Genetics in the NEtherlandS study

Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction

Right ventricular fibrosis and conduction delay in a patient with clinical signs of brugada syndrome : A combined electrophysiological, genetic, histopathologic, and computational study

Genetics of cardiac arrhythmias

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

Genomics of cardiac electrical function

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients

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