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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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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 sodium channel and inherited arrhythmia syndromes

Cardiovascular research, 2001-02, Vol.49 (2), p.257-271

2001

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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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2023 ESC Guidelines for the management of cardiomyopathies Developed by the task force on the management of cardiomyopathies of the European Society of Cardiology (ESC)

European heart journal, 2023, Vol.44 (37), p.3503

2023

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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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Developmental aspects of cardiac arrhythmogenesis

Cardiovascular research, 2011-07, Vol.91 (2), p.243-251

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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Animal models and animal-free innovations for cardiovascular research: current status and routes to be explored. Consensus document of the ESC Working Group on Myocardial Function and the ESC Working Group on Cellular Biology of the Heart

Cardiovascular research, 2022-12, Vol.118 (15), p.3016-3051

2022

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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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Combined reduction of intercellular coupling and membrane excitability differentially affects transverse and longitudinal cardiac conduction

Cardiovascular research, 2009-07, Vol.83 (1), p.52-60

2009

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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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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

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

Cardiac sodium channel and inherited arrhythmia syndromes

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

2023 ESC Guidelines for the management of cardiomyopathies Developed by the task force on the management of cardiomyopathies of the European Society of Cardiology (ESC)

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

Developmental aspects of cardiac arrhythmogenesis

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

Animal models and animal-free innovations for cardiovascular research: current status and routes to be explored. Consensus document of the ESC Working Group on Myocardial Function and the ESC Working Group on Cellular Biology of the Heart

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

Combined reduction of intercellular coupling and membrane excitability differentially affects transverse and longitudinal cardiac conduction

Genetics of cardiac arrhythmias

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