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List of works by Arthur Wilde

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Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

scientific article
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).

scientific article published on August 2011
Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

scientific article published on 14 March 2012
Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

scientific article
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).

scientific article published on August 2011
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

scientific article
Proposed diagnostic criteria for the Brugada syndrome: consensus report

scientific article published in November 2002
Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

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

scientific article
Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry

scientific article published on 25 January 2010
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

scientific article
Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.

scientific article
Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia

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

scientific article published on 30 April 2007
Genetic variation in SCN10A influences cardiac conduction

scientific article
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

scientific article
Atlas of the clinical genetics of human dilated cardiomyopathy

scientific article (publication date: 7 May 2015)
Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

scientific article
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

scientific article
Brugada syndrome: report of the second consensus conference.

scientific article
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia

scientific article published on 01 October 2002
Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia

scientific article
Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

scientific article published on November 2005
Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives

scientific article published on 5 July 2005
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

scientific article published on 01 January 2012
Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?

scientific article published in August 2005
Cardiomyocytes derived from pluripotent stem cells recapitulate electrophysiological characteristics of an overlap syndrome of cardiac sodium channel disease

scientific article published on 30 May 2012
The pathophysiological mechanism underlying Brugada syndrome: depolarization versus repolarization

scientific article published on 24 July 2010
A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

scientific article published in January 2003
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

scientific article
A calcium sensor in the sodium channel modulates cardiac excitability

scientific article
Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

scientific article
Impact of genetics on the clinical management of channelopathies

scientific article published on 15 May 2013
Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome

scientific article published on 10 January 2005
Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients

scientific article published on 28 August 2006
Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system

scientific article published on February 2003
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading [...]

scientific article
Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel

scientific article
Proposed diagnostic criteria for the Brugada syndrome

scientific article
Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals

scientific article published in January 2011
Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features

scientific article
Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel

scientific article published on April 1, 2011
Brugada Syndrome

article from 2012
Genotype-phenotype aspects of type 2 long QT syndrome

scientific article
Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations

scientific article published on April 2008
Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD

scientific article
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study

scientific article (publication date: 14 June 2011)
Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise

scientific article published in June 2011
Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)

scientific article
A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

scientific article published on 01 July 2003

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