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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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Cardiac sodium channel and inherited arrhythmia syndromes

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

2001

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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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Assessment of multi-trait analysis of GWAS (MTAG) for discovery of novel genetic variants and mechanistic insight in common cardiovascular diseases

European heart journal, 2023-11, Vol.44 (Supplement_2)

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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Bradycardia in a long QT type 2 family: coinciding KCNH2 and HCN4 variants

Cardiovascular research, 2024-05, Vol.120 (Supplement_1)

2024

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Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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New risk predictor of arrhythmias in patients with congenital Long-QT Syndrome

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Polygenic risk score for hypertrophic cardiomyopathy predicts population disease risk, penetrance in sarcomeric rare variant carriers and survival in cases

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Large-scale genetic and multi-omics analyses identify molecular pathways underlying dilated cardiomyopathy

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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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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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

Cardiac sodium channel and inherited arrhythmia syndromes

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

Assessment of multi-trait analysis of GWAS (MTAG) for discovery of novel genetic variants and mechanistic insight in common cardiovascular diseases

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

Bradycardia in a long QT type 2 family: coinciding KCNH2 and HCN4 variants

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

New risk predictor of arrhythmias in patients with congenital Long-QT Syndrome

Polygenic risk score for hypertrophic cardiomyopathy predicts population disease risk, penetrance in sarcomeric rare variant carriers and survival in cases

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome

Large-scale genetic and multi-omics analyses identify molecular pathways underlying dilated cardiomyopathy

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

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