(Q38169914)

30 August 2017

Genetics of sudden cardiac death caused by ventricular arrhythmias (English)

1 reference

30 August 2017

Roos F Marsman

1

1 reference

30 August 2017

Hanno L Tan

series ordinal

2

1 reference

30 August 2017

Connie R Bezzina

series ordinal

3

1 reference

30 August 2017

language of work or name

English

0 references

publication date

10 December 2013

1 reference

Nature Reviews Cardiology

30 August 2017

1 reference

30 August 2017

11

1 reference

30 August 2017

2

1 reference

30 August 2017

96-111

1 reference

ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiolo

30 August 2017

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Out-of-hospital cardiac arrest in the 1990's: a population-based study in the Maastricht area on incidence, characteristics and survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Implantable cardioverter-defibrillators have reduced the incidence of resuscitation for out-of-hospital cardiac arrest caused by lethal arrhythmias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Systematic review of the incidence of sudden cardiac death in the United States

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Changing incidence of out-of-hospital ventricular fibrillation, 1980-2000.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Prospective study of sudden cardiac death among women in the United States.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Sudden cardiac death: epidemiology, transient risk, and intervention assessment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Epilepsy is a risk factor for sudden cardiac arrest in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Sudden death due to cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Sudden cardiac death in the United States, 1989 to 1998.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Incidence, causes, and survival trends from cardiovascular-related sudden cardiac arrest in children and young adults 0 to 35 years of age: a 30-year review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Sudden cardiac death in young people with apparently normal heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Molecular and genetic basis of sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Large-scale association analysis identifies new risk loci for coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Family history as a risk factor for primary cardiac arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Parental history is an independent risk factor for coronary artery disease: the Framingham Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Parental transmission of type 2 diabetes: the Framingham Offspring Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

The changing spectrum of arrhythmogenic (right ventricular) cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Inherited Cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Myofilament Ca sensitization increases cytosolic Ca binding affinity, alters intracellular Ca homeostasis, and causes pause-dependent Ca-triggered arrhythmia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Pharmacological targeting of long QT mutant sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to β-blocker therapy in type 1 long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Dominant-negative control of cAMP-dependent IKs upregulation in human long-QT syndrome type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genetic testing for inherited cardiac disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

An integrated map of genetic variation from 1,092 human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

High prevalence of genetic variants previously associated with Brugada syndrome in new exome data.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Disease-targeted sequencing: a cornerstone in the clinic

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A method and server for predicting damaging missense mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Paralogous annotation of disease-causing variants in long QT syndrome genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Distribution and intensity of constraint in mammalian genomic sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Molecular genetic testing and the future of clinical genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Rare-disease genetics in the era of next-generation sequencing: discovery to translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Calmodulin mutations associated with recurrent cardiac arrest in infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Rate, molecular spectrum, and consequences of human mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

NOS1AP is a genetic modifier of the long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Risk stratification in the long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Drug-induced prolongation of the QT interval

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Compound mutations: a common cause of severe long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genotype-phenotype aspects of type 2 long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genetic variation in SCN10A influences cardiac conduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Several common variants modulate heart rate, PR interval and QRS duration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genome-wide association study of PR interval

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Hey genes in cardiovascular development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common variants in cardiac ion channel genes are associated with sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Allelic variants of SCN5A and risk of sudden cardiac arrest in patients with coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Cardiac sodium channel gene variants and sudden cardiac death in women.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common beta-adrenergic receptor polymorphisms are not associated with risk of sudden cardiac death in patients with coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A common variant in the β2-adrenergic receptor and risk of sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Glycoprotein IIIa PlA1/A2 polymorphism and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genetic variation in angiotensin-converting enzyme-related pathways associated with sudden cardiac arrest risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A common missense variant in the neuregulin 1 gene is associated with both schizophrenia and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A common variant at 9p21 is associated with sudden and arrhythmic cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genome-wide association study identifies GPC5 as a novel genetic locus protective against sudden cardiac arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Human Coxsackie-Adenovirus Receptor Is Colocalized With Integrins αvβ3and αvβ5on the Cardiomyocyte Sarcolemma and Upregulated in Dilated Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Coxsackievirus and adenovirus receptor (CAR) mediates atrioventricular-node function and connexin 45 localization in the murine heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

The tight junction protein CAR regulates cardiac conduction and cell-cell communication

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

No evidence for an association between the rs2824292 variant at chromosome 21q21 and ventricular fibrillation during acute myocardial infarction in a German population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common genetic variation modulating cardiac ECG parameters and susceptibility to sudden cardiac death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Prolonged QTc interval and risk of sudden cardiac death in a population of older adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Determinants of prolonged QT interval and their contribution to sudden death risk in coronary artery disease: the Oregon Sudden Unexpected Death Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Significance of QRS complex duration in patients with heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genome-wide association analysis identifies multiple loci related to resting heart rate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genome-wide association studies of the PR interval in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common genetic variants, QT interval, and sudden cardiac death in a Finnish population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

SNPs identified as modulators of ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor ventricular fibrillation risk in this condition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Arrhythmogenic ion-channel remodeling in the heart: heart failure, myocardial infarction, and atrial fibrillation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Principles for the post-GWAS functional characterization of cancer risk loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genetics of human cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

An integrated encyclopedia of DNA elements in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

ChIP-seq accurately predicts tissue-specific activity of enhancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Large-scale discovery of enhancers from human heart tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Co-occupancy by multiple cardiac transcription factors identifies transcriptional enhancers active in heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

TBX5 drives Scn5a expression to regulate cardiac conduction system function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A tetrodotoxin-resistant voltage-gated sodium channel expressed by sensory neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Contactin-2 expression in the cardiac Purkinje fiber network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Long-range control of gene expression: emerging mechanisms and disruption in disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Neural Control of Heart Rate Is an Arrhythmia Risk Modifier in Long QT Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Heritability of Heart Rate Variability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

High Efficacy of β-Blockers in Long-QT Syndrome Type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

How Really Rare Are Rare Diseases?:

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

The ICD for primary prevention in patients with inherited cardiac diseases: indications, use, and outcome: a comparison with secondary prevention

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Sudden death and myocardial infarction in first degree relatives as predictors of primary cardiac arrest

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Predicting sudden death in the population: the Paris Prospective Study I

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Family history and the risk of sudden cardiac death as a manifestation of an acute coronary event

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Arrhythmogenic right ventricular cardiomyopathy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Low penetrance in the long-QT syndrome: clinical impact

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Common variants at ten loci influence QT interval duration in the QTGEN Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Beta2-adrenergic receptor genetic variants and risk of sudden cardiac death

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Platelet glycoprotein Ibalpha HPA-2 Met/VNTR B haplotype as a genetic predictor of myocardial infarction and sudden cardiac death

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

QT interval prolongation as predictor of sudden death in patients with myocardial infarction

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Electrocardiographic predictors of arrhythmic death and total mortality in the multicenter unsustained tachycardia trial

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Genetic and environmental sources of QT interval variability in Israeli families: the kibbutz settlements family study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Electrophysiological mechanisms of ventricular arrhythmias resulting from myocardial ischemia and infarction

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Functional Nav1.8 channels in intracardiac neurons: the link between SCN10A and cardiac electrophysiology

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Impact of onsite or dispatched automated external defibrillator use on survival after out-of-hospital cardiac arrest

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRCARDIO.2013.186

Human coxsackie-adenovirus receptor is colocalized with integrins alpha(v)beta(3) and alpha(v)beta(5) on the cardiomyocyte sarcolemma and upregulated in dilated cardiomyopathy: implications for cardiotropic viral infections

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24322550

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Family (parental) history and prevalence of hypertension. Results of a nationwide screening program

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24322550

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

How really rare are rare diseases?: the intriguing case of independent compound mutations in the long QT syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24322550

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRCARDIO.2013.186

1 reference

30 August 2017

1 reference