A. Wilde

Michael J Ackerman, Stephan Willems, Silvia G Priori, 2011, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

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

Marielle Alders, Abdelaziz Sefiani, A. Wilde, 2014, Journal of the American College of Cardiology.

Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy.

A. Wilde, M. P. van den Berg, F. Asselbergs, 2021, JACC. Clinical electrophysiology.

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) expert consensus on risk assessment in cardiac arrhythmias: use the right tool for the right outcome, in the right population

G. Hindricks, E. Kaufman, T. Chao, 2020, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site.

E. Kaufman, C. January, E. Behr, 2019, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands.

V. Regitz-Zagrosek, A. Wilde, F. T. ten Cate, 2003, European heart journal.

Brugada syndrome: report of the second consensus conference.

Wataru Shimizu, Josep Brugada, Martin Borggrefe, 2005, Heart rhythm.

Learning From Mistakes: The Case of Clinical Electrophysiology: A Perspective on Evidence-Based Rhythmology

P. Coumel, A. Wilde, 2001, Circulation.

Homozygous premature truncation of the HERG protein : the human HERG knockout.

A. Wilde, T. Hoorntje, N. Sreeram, 1999, Circulation.

Stop-codon and C-terminal nonsense mutations are associated with a lower risk of cardiac events in patients with long QT syndrome type 1.

A. Moss, W. Zareba, W. Shimizu, 2016, Heart rhythm.

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

H. Huikuri, S. Viskin, H. Morita, 2016, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

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

H. Huikuri, S. Viskin, H. Morita, 2016, Journal of arrhythmia.

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

H. Huikuri, S. Viskin, H. Morita, 2016, Heart rhythm.

Arrhythmogenic Right Ventricular Cardiomyopathy.

H. Calkins, A. Wilde, A. Krahn, 2022, JACC. Clinical electrophysiology.

Novel KCNQ1 and HERG missense mutations in Dutch long‐QT families

H. Smeets, A. Wilde, H. Smeets, 1999, Human mutation.

Mutations in Conserved Amino Acids in the KCNQ1 Channel and Risk of Cardiac Events in Type‐1 Long‐QT Syndrome

A. Moss, J. Towbin, W. Zareba, 2009, Journal of cardiovascular electrophysiology.

Arrhythmogenic Cardiomyopathy

A. Wilde, V. Proost, 2020, Electrocardiography of Inherited Arrhythmias and Cardiomyopathies.

Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life- Threatening Events: Implications for Mutation-Specific Response to Beta- Blocker Therapy in Type-1 Long QT Syndrome Running title: Barsheshet et al.; Mutations in Cytoplasmic Loops of KCNQ1 Channel

E. Kaufman, A. Moss, J. Towbin, 2012 .

Idiopathic ventricular fibrillation in two infants, not always idiopathic on follow-up.

A. Wilde, N. Blom, P. Chockalingam, 2009, Heart rhythm.

Title: Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic

S. Viskin, A. Wilde, M. Horie, 2022 .

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

Michael J. Ackerman, Pyotr G. Platonov, Wojciech Zareba, 2011, Journal of the American College of Cardiology.

Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome.

E. Kaufman, A. Moss, J. Towbin, 2013, Heart rhythm.

Clinical utility gene card for: Long-QT syndrome

E. Schulze-Bahr, A. Wilde, S. Kääb, 2021, European Journal of Human Genetics.

Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events

S. Priori, E. Behr, A. Mazzanti, 2021, Circulation. Genomic and precision medicine.

Tissues attached to retrieved leadless pacemakers: histopathologic evaluation of tissue composition in relation to implantation time and complications.

A. Wilde, A. C. van der Wal, R. Knops, 2021, Heart rhythm.

Incidence and predictors of implantable cardioverter-defibrillator therapy and its complications in idiopathic ventricular fibrillation patients.

P. Doevendans, P. Postema, A. Wilde, 2019, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .

Predictive genetic testing for cardiovascular diseases: Impact on carrier children

A. Wilde, E. Smets, E. Mollema, 2008, American journal of medical genetics. Part A.

A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q

A. Moorman, A. Wilde, B. Mulder, 2011, European Journal of Human Genetics.

Efficacy and Safety of Appropriate Shocks and Antitachycardia Pacing in Transvenous and Subcutaneous Implantable Defibrillators: Analysis of All Appropriate Therapy in the PRAETORIAN Trial

P. Lambiase, P. Neužil, E. Behr, 2021, Circulation.

Beneficial Effects of Cardiomyopathy-Associated Genetic Variants on Physical Performance: A Hypothesis-Generating Scoping Review

Y. Pinto, A. Wilde, R. L. Lekanne Deprez, 2021, Cardiology.

Penetrance of Hypertrophic Cardiomyopathy in Children Who Are Mutation Positive

A. Wilde, N. Blom, I. Christiaans, 2017, The Journal of pediatrics.

Laminopathy presenting as familial atrial fibrillation.

A. Wilde, S. Kääb, C. Reithmann, 2010, International journal of cardiology.

Optimal echocardiographic assessment of myocardial dysfunction for arrhythmic risk stratification in phospholamban mutation carriers

A. Wilde, R. D. de Boer, M. P. van den Berg, 2021, European heart journal. Cardiovascular Imaging.

Desmosomal mutations across the fence.

A. Wilde, Z. Bhuiyan, 2011, Heart rhythm.

De Novo Mutation in the SCN5A Gene Associated With Early Onset of Sudden Infant Death

G. Breithardt, W. Haverkamp, M. Borggrefe, 2001, Circulation.

Congenital Long QT Syndrome.

P. Postema, A. Wilde, A. Krahn, 2008, JACC. Clinical electrophysiology.

Sex Hormones and Repolarization Dynamics during the Menstrual Cycle in Women with Congenital Long QT Syndrome.

Derick R. Peterson, P. Kudenchuk, T. Rea, 2022, Heart rhythm.

Phenotypic Variability in Caucasian and Japanese Patients with Matched LQT1 Mutations

A. Moss, W. Zareba, W. Shimizu, 2008, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance.

A. Wilde, D. Tester, M. Ackerman, 2019, Circulation. Genomic and precision medicine.

Prevalence of Mitral Annulus Disjunction and Mitral Valve Prolapse in Patients With Idiopathic Ventricular Fibrillation

P. Postema, A. Wilde, R. Nijveldt, 2022, Journal of the American Heart Association.

Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients.

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

Comparing clinical performance of current implantable cardioverter-defibrillator implantation recommendations in arrhythmogenic right ventricular cardiomyopathy

H. Calkins, A. Wilde, K. Zeppenfeld, 2021, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Effectiveness and safety of mexiletine in patients at risk for (recurrent) ventricular arrhythmias: a systematic review

P. Postema, A. Wilde, C. Hollak, 2022, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

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

R. Redon, E. Behr, D. Roden, 2013, Nature Genetics.

The Brugada Numbers (reply to letter)

R. Hauer, S. Priori, J. Towbin, 2003 .

De novo mutation in the KCNQ1 gene causal to Jervell and Lange‐Nielsen syndrome

J. Al-Aama, A. Wilde, Z. Bhuiyan, 2014, Clinical genetics.

A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product*

A. Wilde, D. Escande, S. Demolombe, 1998, The Journal of Biological Chemistry.

Importance of Dedicated Units for the Management of Patients With Inherited Arrhythmia Syndromes.

T. Potpara, E. Behr, A. Wilde, 2021, Circulation. Genomic and precision medicine.

Diagnosis, family screening, and treatment of inherited arrhythmogenic diseases in Europe: results of the European Heart Rhythm Association Survey.

T. Potpara, E. Behr, A. Wilde, 2020, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Profile of patients with Brugada syndrome presenting with their first documented arrhythmic event: Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

Zhengrong, E. Behr, C. Napolitano, 2018 .

Comprehensive Open Reading Frame Mutational Analysis of the RYR2-Encoded Ryanodine Receptor/Calcium Channel in Patients Diagnosed Previously with Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome

A. Wilde, D. Tester, M. Ackerman, 2009 .

mutation analysis for the long QT syndrome The use of genotype-phenotype correlations in

A. Wilde, M. Alders, I. M. Langen, 2006 .

Genotype-Phenotype Correlation in the Long-QT Syndrome

G. Breithardt, S. Priori, A. Moss, 2001 .

E. Kaufman, A. Moss, J. Towbin, 2012 .

Somatic mosaicism contributes to phenotypic variation in Timothy syndrome

A. Wilde, A. Rope, M. Tristani-Firouzi, 2011, American journal of medical genetics. Part A.

Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation.

A. Moorman, A. Wilde, T. Opthof, 2001, Cardiovascular research.

Pregnancy in women with Brugada syndrome: Is there an increased arrhythmia risk? A case‐series report

A. Wilde, S. Clur, S. N. van der Crabben, 2021, Journal of cardiovascular electrophysiology.

Ethnic Differences in Patients with Brugada Syndrome and Arrhythmic Events: New Insights from SABRUS.

S. Priori, E. Behr, A. Mazzanti, 2019, Heart rhythm.

Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome.

S. Priori, E. Behr, A. Mazzanti, 2019, Journal of the American College of Cardiology.

Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

S. Priori, E. Behr, C. Napolitano, 2019, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients

S. Priori, E. Behr, C. Napolitano, 2017, Circulation. Arrhythmia and electrophysiology.

Oral Contraceptives and their Effect on Arrhythmogenesis in Long-QT Syndrome; Does it Matter?

A. Wilde, A. Vink, 2021, Heart rhythm.

HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency.

H. Smeets, A. Wilde, A. Paulussen, 2005, Cardiovascular research.

Addressing the diagnostic and therapeutic challenges in inheritable arrhythmia syndromes : with emphasis on the pediatric population

A. Wilde, N. Blom, S. Clur, 2012 .

Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel

T. Callis, A. Wilde, Jamie D. Kapplinger, 2015, Journal of Cardiovascular Translational Research.

Screening, diagnosis and follow-up of Brugada syndrome in children: a Dutch expert consensus statement

A. Wilde, N. Blom, F. van den Heuvel, 2022, Netherlands Heart Journal.

The diagnostic and therapeutic aspects of loss-of-function cardiac sodium channelopathies in children.

A. Wilde, N. Blom, T. Paul, 2012, Heart rhythm.

The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome

A. Wilde, N. Blom, N. Hofman, 2009, Pediatric Cardiology.

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

H. Tan, A. Wilde, S. Kääb, 2007, European heart journal.

IKs in heart and hearing, the ear can do with less than the heart.

A. Wilde, Z. Bhuiyan, 2013, Circulation. Cardiovascular genetics.

UvA-DARE ( Digital Academic Repository ) The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome

A. Wilde, N. Blom, N. Hofman, 2010 .

Stop-codon and C-terminus nonsense mutations are associated with lower risk of cardiac events in Long QT Syndrome Type 1 patients

A. Moss, W. Shimizu, A. Wilde, 2016 .

SCN5A-related cardiac channelopathy

C. Dina, A. Wilde, F. Charpentier, 2012 .

KVLQT1, the rhythm of imprinting

A. Wilde, M. Mannens, 1997, Nature Genetics.

Clinical Assessment of the Pathogenicity of Unknown Variants in Long‐QT Syndrome: Does the Pendulum Swing Back?

A. Wilde, E. Lodder, 2012, Journal of cardiovascular electrophysiology.

Erratum: HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies (Europace (2011) 13 (1077-1109) DOI: 10.1093/europace/eur245)

H. Calkins, P. Ellinor, S. Priori, 2012 .

A Phenotype-Enhanced Variant Classification Framework to Decrease the Burden of Missense Variants of Uncertain Significance in Type 1 Long QT Syndrome.

A. Wilde, D. Tester, M. Ackerman, 2021, Heart rhythm.

Diagnosis of Congenital Long QT Syndrome: Do All Clinically Suspected Patients Warrant Genetic Testing?

A. Wilde, N. Blom, N. Hofman, 2012 .

[Congenital long QT syndrome].

A. Wilde, E. O. Robles de Medina, M. Creanza, 2022, Nederlands tijdschrift voor geneeskunde.

Brugada syndrome: report of the second consensus conference.

Wataru Shimizu, Josep Brugada, Martin Borggrefe, 2005, Heart rhythm.

Age of First Arrhythmic Event in Brugada Syndrome: Data from the Survey on Arrhythmic Events in Brugada Syndrome (SABRUS) in 678 Patients Age of First Arrhythmic Event in Brugada Syndrome

E. Behr, C. Napolitano, J. Brugada, 2020 .

Long QT syndrome: a double hit hurts more.

A. Wilde, 2010, Heart rhythm.

Does function trump bioinformatics in Brugada syndrome-associated SCN5A mutation calling? Patients, computers, and patches

A. Wilde, Cheng-I Wu, 2021, European heart journal.

Ion Channels, the QT Interval, and Arrhythmias

A. Wilde, A. Wilde, M. W. Veldkamp, 1997, Pacing and clinical electrophysiology : PACE.

Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia

A. Wilde, P. Verma, Z. Bhuiyan, 2017, Molecular genetics & genomic medicine.

Multifocal Ectopic Purkinje Premature Contractions : a new SCN 5 A-related cardiac channelopathy

C. Dina, A. Wilde, F. Charpentier, 2012 .

SUBSTITUTIONN OF A CONSERVED ALANINE IN THE DOMAINN IIIS 4S 5 LINKER OF THE HUMAN CARDIAC SODIUMM CHANNEL CAUSES LONG QT SYNDROME

A. Wilde, Z. Bhuiyan, '. J..P.P.Smits, 2007 .

Channel Mutation Causing Both Long-qt and Brugada Syndromes + a Single Na

A. Wilde, M. P. van den Berg, C. Bezzina, 2022 .

Post-Pacing Abnormal Repolarization in Catecholaminergic Polymorphic Ventricular Tachycardia Associated with a Mutation in the Cardiac Ryanodine Receptor Gene (RyR2)

S. Viskin, C. Antzelevitch, A. Wilde, 2011 .

A single sodium channel mutation causing both long QT- and Brugada syndrome

A. Wilde, M. Mannens, I. M. Langen, 1999 .

Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia

A. Wilde, P. Guicheney, M. Mannens, 2002, Circulation research.

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).

H. Calkins, P. Ellinor, S. Priori, 2011, Heart rhythm.

Syncope in hypertrophic cardiomyopathy (part II): An expert consensus statement on the diagnosis and management.

G. Parati, A. Wilde, S. Ommen, 2022, International journal of cardiology.

A Gain-of-Function TBX 5 Mutation Is Associated With Atypical Holt – Oram Syndrome and Paroxysmal Atrial Fibrillation

A. Moorman, A. Wilde, I. B. Mathijssen, 2008 .

Long-term prognosis of individuals with right predordial ST-elevation - Brugada syndrome

G. Breithardt, L. Eckardt, M. Borggrefe, 2005 .

Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Diagnostic Task Force Criteria: Impact of New Task Force Criteria

L. Jordaens, R. Hauer, D. Atsma, 2010, Circulation. Arrhythmia and electrophysiology.

A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation

A. Moorman, A. Wilde, I. B. Mathijssen, 2008, Circulation research.

ECGscreening of nevvborns to avoi sudden infant death syndrome?

A. Wilde, M. I., V. Langen, 2008 .

Clinical characteristics and electrophysiologic properties of SCN5A variants in fever-induced Brugada syndrome

C. Antzelevitch, A. Wilde, C. Pappone, 2021, EBioMedicine.

Indications and utility of cardiac genetic testing in athletes.

E. Behr, A. Wilde, C. Basso, 2022, European journal of preventive cardiology.

COVID-19 vaccination in patients with long QT syndrome

P. Schwartz, A. Wilde, M. Ackerman, 2022, Heart Rhythm O2.

Genotype–phenotype analysis of Jervell and Lange‐Nielsen syndrome in six families from Saudi Arabia

A. Wilde, Z. Bhuiyan, S. Al-ghamdi, 2015, Clinical genetics.

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

Yan V. Sun, P. Deloukas, T. Lehtimäki, 2019, Circulation. Genomic and precision medicine.

ESC guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 2—care pathways, treatment, and follow-up

G. Hindricks, D. Andreini, T. Potpara, 2021, Cardiovascular research.

ESC guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 2—care pathways, treatment, and follow-up

G. Hindricks, D. Andreini, T. Potpara, 2021, European heart journal.

An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia

J. Skinner, E. Behr, P. Schwartz, 2021, Circulation.

2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families

C. Morillo, E. Kaufman, C. Albert, 2020, Heart rhythm.

A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding.

A. Moorman, A. Wilde, R. L. Lekanne Deprez, 2013, Biochimica et biophysica acta.

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

R. Redon, K. Strauch, P. Lambiase, 2022, Nature Genetics.

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

Kevin Knight, D. O’Regan, Y. Pinto, 2023, medRxiv.

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.

R. Redon, E. Behr, D. Roden, 2015, Cardiovascular research.

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

Dan M Roden, Beverley Balkau, Pierre Lindenbaum, 2013, Nature Genetics.

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

J. Towbin, J. Brugada, R. Brugada, 2010, Heart rhythm.

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

S. Tezenas du Montcel, W. Shimizu, E. Schulze-Bahr, 2015, European Journal of Human Genetics.

Female predominance and transmission distortion in the long-QT syndrome.

S. Priori, M. Imboden, C. Napolitano, 2006, The New England journal of medicine.

European Society of Cardiology guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 1—epidemiology, pathophysiology, and diagnosis

G. Hindricks, D. Andreini, T. Potpara, 2021, European heart journal.

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 frame mutational analysis.

Michael J Ackerman, J Peter van Tintelen, Hennie Bikker, 2009, Journal of the American College of Cardiology.

2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families

C. Morillo, E. Kaufman, C. Albert, 2020, Journal of arrhythmia.

Clinical Aspects and Prognosis of Brugada Syndrome in Children

A. Wilde, M. Haissaguerre, F. Sacher, 2007, Circulation.

Proposed diagnostic criteria for the Brugada syndrome: consensus report.

R. Hauer, S. Priori, J. Towbin, 2002, Circulation.

UvA-DARE ( Digital Academic Repository ) Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period

A. Wilde, A. Wilde, G. van Ommen, 1997 .

Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.

R. Hauer, H. Calkins, T. Callis, 2011, Journal of the American College of Cardiology.

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

S. Priori, D. Roden, J. Brugada, 2009, Heart rhythm.

G. Hindricks, E. Kaufman, T. Chao, 2020, Journal of arrhythmia.

A. Wilde, A. Wilde, E. Smets, 2008, American journal of medical genetics. Part A.

Diagnosis, management and therapeutic strategies for congenital long QT syndrome

P. Postema, A. Wilde, A. Amin, 2021, Heart.

Brugada syndrome and reduced right ventricular outflow tract conduction reserve: a final common pathway?

E. Behr, A. Wilde, A. Krahn, 2021, European heart journal.

Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.

E. Behr, P. Schwartz, A. Wilde, 2016, Heart rhythm.

Long-Term Prognosis of Individuals With Right Precordial ST-Segment–Elevation Brugada Syndrome

G. Breithardt, L. Eckardt, M. Borggrefe, 2005, Circulation.

Inherited Arrhythmias: Brugada Syndrome and Early Repolarisation Syndrome

P. Postema, A. Wilde, K. Lieve, 2018 .

Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation

T. Callis, A. Wilde, N. Larson, 2018, Circulation. Genomic and precision medicine.

Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?

J. Healey, E. Behr, A. Moss, 2017, Circulation. Arrhythmia and electrophysiology.

Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-QT Syndrome

Michael J Ackerman, Marielle Alders, A. Wilde, 2012, Circulation. Cardiovascular genetics.

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

M. Perez, H. Feilotter, V. Novelli, 2020, Circulation.

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

T. Meitinger, D. Roden, A. Pfeufer, 2015, Circulation. Cardiovascular genetics.

Impact of Genetics on the ClinicalManagementof Channelopathies

P. Schwartz, A. Wilde, M. Ackerman, 2019 .

The Common Long-QT Syndrome Mutation KCNQ1/A341V Causes Unusually Severe Clinical Manifestations in Patients With Different Ethnic Backgrounds: Toward a Mutation-Specific Risk Stratification

A. Moss, P. Schwartz, W. Shimizu, 2007, Circulation.

Yield of Molecular and Clinical Testing for Arrhythmia Syndromes: Report of 15 Years’ Experience

Hanno L. Tan, H. Tan, A. Wilde, 2013, Circulation.

European Society of Cardiology guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 1—epidemiology, pathophysiology, and diagnosis

G. Hindricks, D. Andreini, T. Potpara, 2021, Cardiovascular research.

Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome

P. Postema, A. Wilde, N. Hofman, 2010, Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation.

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

A. Wilde, M. Alders, R. Jongbloed, 2003, Journal of medical genetics.

G. Hindricks, E. Kaufman, T. Chao, 2020, Heart rhythm.

Determination and Interpretation of the QT Interval: Comprehensive Analysis of a Large Cohort of Long QT Syndrome Patients and Controls

P. Postema, A. Wilde, N. Blom, 2018, Circulation.

Mutation Location Effect on Severity of Phenotype During Exercise Testing in Type 1 Long‐QT Syndrome: Impact of Transmembrane and C‐Loop Location

A. Wilde, A. Wilde, A. Krahn, 2013, Journal of cardiovascular electrophysiology.

Clinical utility gene card for: Long-QT Syndrome (types 1–13)

Stefan Kääb, A. Wilde, S. Kääb, 2013, European Journal of Human Genetics.

Combined assessment of sex- and mutation-specific information for risk stratification in type 1 long QT syndrome.

E. Kaufman, A. Moss, J. Towbin, 2012, Heart rhythm.

Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation.

A. Wilde, D. Tester, B. Salisbury, 2010, Heart rhythm.

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

H. Tan, A. Wilde, N. Hofman, 2010, Journal of the American College of Cardiology.

Genetic Testing for Long-QT Syndrome: Distinguishing Pathogenic Mutations From Benign Variants

Michael J Ackerman, Suraj Kapa, Marielle Alders, 2009, Circulation.

Value of history-taking in syncope patients: in whom to suspect long QT syndrome?

A. Wilde, A. Wilde, J. Reitsma, 2009, Europace.

Who Are the Long-QT Syndrome Patients Who Receive an Implantable Cardioverter-Defibrillator and What Happens to Them?: Data From the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry

L. Jordaens, S. Hohnloser, S. Priori, 2010, Circulation.

Channelopathies in Children and Adults

A. Wilde, A. Wilde, 2008, Pacing and clinical electrophysiology : PACE.

Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands

A. Wilde, B. Engelen, G. Drost, 2018, Neuromuscular Disorders.

Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events: Implications for Mutation-Specific Response to &bgr;-Blocker Therapy in Type 1 Long-QT Syndrome

E. Kaufman, A. Moss, J. Towbin, 2012, Circulation.

Clinical and Genetic Analysis of Long QT Syndrome in Children from Six Families in Saudi Arabia: Are They Different?

A. Wilde, Z. Bhuiyan, T. Momenah, 2009, Pediatric Cardiology.

The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene

A. Wilde, H. Wellens, J. Geraedts, 1997, Human Genetics.

The long QT syndrome: a novel missense mutation in the S6 region of KVLQT1 gene Berg,

A. Wilde, H. Wellens, R. Jongbloed, 1997 .

Effect of Age and Sex on the QTc Interval in Children and Adolescents With Type 1 and 2 Long-QT Syndrome

A. Wilde, R. Geskus, N. Blom, 2017, Circulation. Arrhythmia and electrophysiology.

The genetic architecture of long QT syndrome: A critical reappraisal.

A. Wilde, M. Ackerman, J. Giudicessi, 2018, Trends in cardiovascular medicine.

Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause?

A. Wilde, A. Wilde, H. Franssen, 2014, Muscle & nerve.

Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy

G. Cascino, A. Wilde, M. Ackerman, 2009, Neurology.

TGFβ‐inducible early gene‐1 (TIEG1) mutations in hypertrophic cardiomyopathy

W. Edwards, A. Wilde, M. Ackerman, 2012, Journal of cellular biochemistry.

Quality of life and psychological distress in hypertrophic cardiomyopathy mutation carriers: A cross‐sectional cohort study

G. Bonsel, A. Wilde, E. Smets, 2009, American journal of medical genetics. Part A.

Syncope in Brugada syndrome: prevalence, clinical significance, and clues from history taking to distinguish arrhythmic from nonarrhythmic causes.

H. Tan, A. Wilde, N. van Dijk, 2015, Heart rhythm.

Quinidine Induced Electrocardiographic Normalization in Two Patients with Brugada Syndrome

A. Wilde, M. Alings, M Alings, 2001, Pacing and clinical electrophysiology : PACE.

Genetic Arrhythmias Complicating Patients with Dilated Cardiomyopathy.

M. Link, A. Wilde, Dao-wu Wang, 2020, Heart rhythm.

Risk stratification for sudden cardiac death: current status and challenges for the future

Maarten L. Simoons, Marek Malik, Karl Swedberg, 2014, European heart journal.

The Brugada ECG Pattern: A Marker of Channelopathy, Structural Heart Disease, or Neither? Toward a Unifying Mechanism of the Brugada Syndrome

Ruben Coronel, Arthur A M Wilde, Pieter G Postema, 2010, Circulation. Arrhythmia and electrophysiology.

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

I. V. Van Gelder, A. Wilde, M. Rook, 1999, Cardiovascular research.

Drug‐Induced J Point Elevation

D. Roden, A. Wilde, A. Wilde, 1999, Journal of cardiovascular electrophysiology.

Risk stratification for sudden cardiac death: current status and challenges for the future†

S. Hohnloser, K. Swedberg, M. Malik, 2014, European heart journal.

Expanding Spectrum of Human RYR2-Related Disease: New Electrocardiographic, Structural, and Genetic Features

A. Wilde, M. P. van den Berg, A. Wilde, 2007, Circulation.

A Novel Early Onset Lethal Form of Catecholaminergic Polymorphic Ventricular Tachycardia Maps to Chromosome 7p14‐p22

A. Wilde, L. Al-Gazali, Z. Bhuiyan, 2007, Journal of cardiovascular electrophysiology.

Clinical and Functional Characterization of Ryanodine Receptor 2 Variants Implicated in Calcium-Release Deficiency Syndrome.

Jeffrey M. Vinocur, A. Wilde, A. Krahn, 2021, JAMA cardiology.

Role of Genetic Testing in Patients with Ventricular Arrhythmias in Apparently Normal Hearts.

A. Wilde, N. Hofman, 2016, Cardiac electrophysiology clinics.

Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.

A. Wilde, N. Hofman, L. T. van Lochem, 2010, Future cardiology.

Exploring Coronavirus Disease 2019 and Brugada Syndrome

A. Baranchuk, P. Brugada, A. Wilde, 2022, The Journal of innovations in cardiac rhythm management.

Effect of age and gender on the QTc-interval in healthy individuals and patients with long-QT syndrome.

A. Wilde, N. Blom, S. Clur, 2018, Trends in cardiovascular medicine.

Diagnostic Performance of Various QTc Interval Formulas in a Large Family with Long QT Syndrome Type 3: Bazett's Formula Not So Bad After All …

D. Grobbee, A. Wilde, M. P. van den Berg, 2003, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

Cardiac ryanodine receptor calcium release deficiency syndrome

S. Priori, C. Napolitano, A. Wilde, 2021, Science Translational Medicine.

An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia

Rahul C. Deo, J. Healey, C. January, 2020, Circulation.

The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handling.

E. Schulze-Bahr, A. Wilde, F. Müller, 2010, Journal of molecular and cellular cardiology.

Life-threatening arrhythmias with autosomal recessive TECRL variants.

J. Rioux, A. Wilde, L. Al-Gazali, 2020, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Family History of Sudden Cardiac Death in the Young and Inherited Arrhythmia Syndromes: Awareness and Attitudes of General Practitioners and Private Practice Cardiologists

E. Behr, A. Wilde, A. Auricchio, 2023, Circulation. Genomic and precision medicine.

Repeatability of ventricular arrhythmia characteristics on the exercise-stress test in RYR2-mediated catecholaminergic polymorphic ventricular tachycardia

A. Wilde, M. Ackerman, N. Blom, 2022, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

An Evaluation of Age at Symptom-Onset, Proband Status and Sex as Predictors of Disease Severity in Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia.

A. Wilde, A. Krahn, P. Kannankeril, 2021, Heart rhythm.

An International Multicenter Evaluation of Type 5 Long QT Syndrome

M. Perez, E. Kaufman, E. Vittinghoff, 2020, Circulation.

An International Multicenter Evaluation of Type 5 Long QT Syndrome

M. Perez, E. Kaufman, E. Vittinghoff, 2020, Circulation.

S. Priori, E. Behr, C. Napolitano, 2018, Heart rhythm.

SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups

J. Skinner, E. Behr, P. Schwartz, 2018, European heart journal.

Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants.

E. Behr, M. Sheppard, A. Wilde, 2018, Heart rhythm.

Prevalence and Clinical Characteristics of Brugada Syndrome

P. Postema, A. Wilde, 2016 .

Genetic counseling and cardiac care in predictively tested hypertrophic cardiomyopathy mutation carriers: The patients' perspective

G. Bonsel, A. Wilde, E. Smets, 2009, American journal of medical genetics. Part A.

Common Sodium Channel Promoter Haplotype in Asian Subjects Underlies Variability in Cardiac Conduction

D. Roden, W. Shimizu, A. Wilde, 2006, Circulation.

The β-angle can help guide clinical decisions in the diagnostic work-up of patients suspected of Brugada syndrome: a validation study of the β-angle in determining the outcome of a sodium channel provocation test.

P. Postema, H. Tan, A. Wilde, 2021, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Brugada Phenocopy: New Terminology and Proposed Classification

A. Wilde, A. Baranchuk, Timothy Nguyen, 2012, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

Characterization of SEMA3A-Encoded Semaphorin as a Naturally Occurring Kv4.3 Protein Inhibitor and its Contribution to Brugada Syndrome

J. Nerbonne, P. Schwartz, A. Wilde, 2014, Circulation research.

Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey.

É. Marijon, E. Behr, E. Schulze-Bahr, 2021, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study.

Jørgen K. Kanters, E. Kaufman, A. Moss, 2016, Circulation.

Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants

L. Mestroni, E. Ashley, H. Calkins, 2021, Circulation.

A Potential Diagnostic Approach for Foetal Long-QT Syndrome, Developed and Validated in Children

A. Wilde, N. Blom, S. Clur, 2018, Pediatric Cardiology.

Left Ventricular Isovolumetric Relaxation Time Is Prolonged in Fetal Long-QT Syndrome

M. Donofrio, A. Wilde, M. Ackerman, 2018, Circulation. Arrhythmia and electrophysiology.

Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy

Y. Pinto, A. Wilde, R. D. de Boer, 2017, European journal of heart failure.

Cardiac abnormalities in athletes after SARS-CoV-2 infection: a systematic review

Y. Pinto, A. Wilde, M. Groenink, 2021, BMJ Open Sport & Exercise Medicine.

A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression.

S. Brunak, A. Wilde, H. Wellens, 2018, The New England journal of medicine.

Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2

P. Schwartz, P. Sager, A. Wilde, 2023, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Mothers with long QT syndrome are at increased risk for fetal death: Findings from a multicenter international study.

P. Schwartz, A. Wilde, M. Ackerman, 2020, American Journal of Obstetrics and Gynecology.

Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3

A. Moorman, A. Wilde, C. Bezzina, 2000, Human Genetics.

Suppression of torsades de pointes by atropine

H. Tan, A. Wilde, R. Peters, 1998, Heart.

Fever-Induced Life-Threatening Arrhythmias in Children Harboring an SCN5A Mutation

P. Postema, A. Wilde, N. Blom, 2011, Pediatrics.

Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death

M. Perez, H. Feilotter, V. Novelli, 2021, European heart journal.

Sex- and age specific association of new-onset atrial fibrillation with in-hospital mortality in hospitalised COVID-19 patients

F. Rutten, R. Tieleman, A. Wilde, 2022, International Journal of Cardiology. Heart & Vasculature.

Human RyR2 (Ryanodine Receptor 2) Loss-of-Function Mutations

A. Wilde, M. Gollob, Jason D. Roberts, 2021, Circulation. Arrhythmia and electrophysiology.

Subepicardial Cardiomyopathy: A Disease Underlying J-Wave Syndromes and Idiopathic Ventricular Fibrillation

E. Behr, K. Nademanee, A. Wilde, 2023, Circulation.

Diagnosis and Treatment of the Congenital Long Qt Syndrome

A. Wilde, X. Wehrens, M. Vos, 2001 .

Implantable cardioverter defibrillator as a bridge to recovery in an infant with cardiac rhabdomyoma

A. Wilde, N. Blom, P. Chockalingam, 2009, European Journal of Pediatrics.

Use, misuse, and pitfalls of the drug challenge test in the diagnosis of the Brugada syndrome.

H. Morita, A. Wilde, R. Tadros, 2023, European heart journal.

Learning From Mistakes: The Case of Clinical Electrophysiology: A Perspective on Evidence-Based Rhythmology

P. Coumel, A. Wilde, A. Wilde, 2001, Circulation.

Provocation Testing in Congenital Long QT Syndrome: A Practical Guide.

P. Postema, A. Wilde, A. Krahn, 2023, Heart rhythm.

Quality of athlete screening for high-risk cardiovascular conditions-A systematic review.

A. Wilde, R. Goedkoop, A. Malekzadeh, 2023, Scandinavian journal of medicine & science in sports.

Proposed diagnostic criteria for the Brugada syndrome.

R. Hauer, S. Priori, J. Towbin, 2002, European heart journal.

Diagnostic Accuracy of the Standing Test in Adults Suspected for Congenital Long‐QT Syndrome

T. Delhaas, P. Postema, A. Wilde, 2023, Journal of the American Heart Association.

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

Ashutosh Kumar Singh, Jeffrey M. Vinocur, E. Behr, 2023, European heart journal.

MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset

A. Wilde, R. L. Lekanne Deprez, S. Mercier, 2023, Netherlands Heart Journal.

Multifocal Ectopic Purkinje-Related Premature Contractions A New SCN5A -Related Cardiac Channelopathy

C. Dina, A. Wilde, F. Charpentier, 2012 .

Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

M Borggrefe, F Gaita, A A M Wilde, 2010, Circulation.

Long QT Syndrome, a Diagnosis That Warrants Expert Opinion and Expert Centers.

P. Schwartz, A. Wilde, 2023, Journal of the American College of Cardiology.

Left cardiac sympathetic denervation in the Netherlands for the treatment of inherited arrhythmia syndromes

P. Schwartz, A. Wilde, A. Wilde, 2014, Netherlands Heart Journal.

UvA-DARE ( Digital Academic Repository ) Variable Na ( v ) 1 . 5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn 5 a ( + /-) Mouse Model

A. Wilde, Céline Marionneau, D. Escande, 2010 .

Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update

P. Postema, A. Wilde, P. Volders, 2023, Netherlands Heart Journal.

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

H. Tan, A. Wilde, N. Hofman, 2010, Journal of the American College of Cardiology.

Familial disease with a risk of sudden death: a longitudinal study of the psychological consequences of predictive testing for long QT syndrome.

M. Hendriks, A. Wilde, A. Wilde, 2008, Heart rhythm.

Association Between Syncope Trigger Type and Risk of Subsequent Life-Threatening Events in Patients With Long QT Syndrome.

W. Zareba, A. Wilde, I. Goldenberg, 2023, JAMA cardiology.

In silico cardiac risk assessment in patients with long QT syndrome: type 1: clinical predictability of cardiac models.

Jørgen K. Kanters, A. Moss, W. Zareba, 2012, Journal of the American College of Cardiology.

Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).

R. Hauer, H. Smeets, A. Wilde, 1999, Journal of the American College of Cardiology.

Genetic and Molecular Basis of Cardiac Arrhythmias: Impact on Clinical Management

R. Hauer, S. Priori, D. Roden, 2022 .

Quality of life and psychological distress in hypertrophic cardiomyopathy mutation carriers: A cross‐sectional cohort study

G. Bonsel, A. Wilde, E. Smets, 2009, American journal of medical genetics. Part A.

Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a +/− Mouse Model

A. Wilde, Céline Marionneau, D. Escande, 2010, PloS one.

Clinical characteristics and electrophysiologic properties of SCN5A variants in fever-induced Brugada syndrome

C. Antzelevitch, A. Wilde, C. Pappone, 2022, EBioMedicine.

In Children and Adolescents From Brugada Syndrome-Families, Only SCN5A Mutation Carriers Develop a Type-1 ECG Pattern Induced By Fever.

A. Wilde, N. Blom, S. Clur, 2020, Circulation.

Congenital Long QT Syndrome.

P. Postema, A. Wilde, A. Krahn, 2022, JACC. Clinical electrophysiology.

Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events: Implications for Mutation-Specific Response to &bgr;-Blocker Therapy in Type 1 Long-QT Syndrome

Derick R. Peterson, E. Kaufman, A. Moss, 2012, Circulation.

Familial disease with a risk of sudden death: a longitudinal study of the psychological consequences of predictive testing for long QT syndrome.

M. Hendriks, A. Wilde, J. van den Bout, 2008, Heart rhythm.

Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Voltage – Dependent L-Type Calcium Channel

S. Priori, R. Brugada, A. Wilde, 2011 .

Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study.

Derick R. Peterson, Jørgen K. Kanters, E. Kaufman, 2016, Circulation.

Sodium Channelopathies: Do We Really Understand What's Going On?

A. Wilde, P. Postema, A. Wilde, 2011, Journal of cardiovascular electrophysiology.

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II.

R. Hauer, S. Priori, D. Roden, 1999, Circulation.

Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome?

R. Hennekam, A. Wilde, A. van Haeringen, 2021, European Journal of Medical Genetics.

Genotype-phenotype aspects of type 2 long QT syndrome.

E. Kaufman, C. January, A. Moss, 2009, Journal of the American College of Cardiology.

Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest.

J. Skinner, E. Behr, P. Schwartz, 2019, European heart journal.

From a Polish 3 year old boy who visited Maastricht, to automatic detection using deep learning: Brugada syndrome is being revolutionized.

A. Wilde, H. Bleijendaal, 2021, The Canadian journal of cardiology.

Clinical ResearchHeart Rhythm DisordersIn Silico Cardiac Risk Assessment in Patients With Long QT Syndrome: Type 1: Clinical Predictability of Cardiac Models

Jørgen K. Kanters, A. Moss, W. Zareba, 2012 .

Relation Between Basic and Clinical Electrophysiologic Characteristics in Brugada Syndrome: Facts or Fiction?

A. Wilde, H. Tan, A. Wilde, 2003, Cardiovascular Electrophysiology.

Clinical ResearchHeart Rhythm DisorderActive Cascade Screening in Primary Inherited Arrhythmia Syndromes: Does It Lead to Prophylactic Treatment?

H. Tan, A. Wilde, N. Hofman, 2010 .