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Arthur A.M. Wilde

Researcher Next ID · RN-030051

Researcher · Medicine

Amsterdam University of the Arts

Amsterdam, Netherlands

Not currently recruitingFunding unknown
Works count
1,184
Citation count
78,373
H-index
150
i10-index
610

Research interests

Medicine
Biochemistry, Genetics and Molecular Biology
Cardiac electrophysiology and arrhythmias
Ion channel regulation and function
Cardiac Arrhythmias and Treatments
Cardiac pacing and defibrillation studies
Cardiovascular Effects of Exercise

Publications

  • 2023 ESC Guidelines for the management of cardiomyopathies

    European Heart Journal · 2023 · https://doi.org/10.1093/eurheartj/ehad194

  • Subcutaneous or Transvenous Defibrillator Therapy

    New England Journal of Medicine · 2020 · 10.1056/nejmoa1915932

  • 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy

    Heart Rhythm · 2019 · https://doi.org/10.1016/j.hrthm.2019.05.007

  • J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge

    Heart Rhythm · 2016 · 10.1016/j.hrthm.2016.05.024

  • Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members

    Circulation Cardiovascular Genetics · 2015 · 10.1161/circgenetics.114.001003

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

    Nature Genetics · 2013 · 10.1038/ng.2712

  • HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

    Heart Rhythm · 2013 · https://doi.org/10.1016/j.hrthm.2013.05.014

  • Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes

    EP Europace · 2013 · https://doi.org/10.1093/europace/eut272

  • Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

    Journal of the American College of Cardiology · 2012 · https://doi.org/10.1016/j.jacc.2011.08.078

  • Phospholamban R14del Mutation in Patients Diagnosed with Dilated Cardiomyopathy or Arrhythmogenic Right Ventricular Cardiomyopathy: Evidence Supporting the Concept of Arrhythmogenic Cardiomyopathy

    European Journal of Heart Failure · 2012 · 10.1093/eurjhf/hfs119

  • HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

    Heart Rhythm · 2011 · https://doi.org/10.1016/j.hrthm.2011.05.020

  • Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome

    Circulation · 2010 · 10.1161/circulationaha.109.887026

  • An Entirely Subcutaneous Implantable Cardioverter–Defibrillator

    New England Journal of Medicine · 2010 · 10.1056/nejmoa0909545

  • An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

    Heart Rhythm · 2009 · 10.1016/j.hrthm.2009.09.069

  • Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

    Nature Medicine · 2009 · 10.1038/nm.1942

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

    Heart Rhythm · 2009 · 10.1016/j.hrthm.2009.05.021

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

    Journal of Clinical Investigation · 2008 · https://doi.org/10.1172/jci33891

  • Familial Sudden Death Is an Important Risk Factor for Primary Ventricular Fibrillation

    Circulation · 2006 · https://doi.org/10.1161/circulationaha.105.606145

  • Brugada Syndrome: Report of the Second Consensus Conference

    Circulation · 2005 · https://doi.org/10.1161/01.cir.0000152479.54298.51

  • Mutation in the KCNQ1 Gene Leading to the Short QT-Interval Syndrome

    Circulation · 2004 · 10.1161/01.cir.0000130409.72142.fe

  • Proposed Diagnostic Criteria for the Brugada Syndrome

    Circulation · 2002 · 10.1161/01.cir.0000034169.45752.4a

  • Genotype-Phenotype Correlation in the Long-QT Syndrome

    Circulation · 2001 · https://doi.org/10.1161/01.cir.103.1.89

  • A Single Na + Channel Mutation Causing Both Long-QT and Brugada Syndromes

    Circulation Research · 1999 · 10.1161/01.res.85.12.1206

  • Cardiac conduction defects associate with mutations in SCN5A

    Nature Genetics · 1999 · 10.1038/12618

  • Reentry as a cause of ventricular tachycardia in patients with chronic ischemic heart disease: electrophysiologic and anatomic correlation.

    Circulation · 1988 · 10.1161/01.cir.77.3.589

Current projects

    No projects listed.