J. Saenen

发表

Molecular aspects of the congenital and acquired Long QT Syndrome: clinical implications.

J. Saenen, C. Vrints, 2008, Journal of molecular and cellular cardiology.

Diagnostic yield of genetic testing in heart transplant recipients with prior cardiomyopathy

H. Heidbuchel, P. Pauwels, B. Loeys, 2022, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.

Two novel MYLK nonsense mutations causing thoracic aortic aneurysms/dissections in patients without apparent family history

W. Wuyts, J. Hendriks, B. Loeys, 2017, Clinical Genetics.

A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes.

A. Paulussen, J. Aerssens, D. Snyders, 2007, Journal of molecular and cellular cardiology.

iPSC-Cardiomyocyte Models of Brugada Syndrome—Achievements, Challenges and Future Perspectives

B. Loeys, A. Labro, M. Alaerts, 2021, International journal of molecular sciences.

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

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

A new prediction model for left ventricular systolic function recovery after catheter ablation of atrial fibrillation in patients with heart failure.

C. Tondo, W. Huybrechts, M. Casella, 2022, International journal of cardiology.

Vulnerability to cardiac arrest in patients with ST elevation myocardial infarction: Is it time or patient dependent? Results from a nationwide observational study

P. Sinnaeve, M. Claeys, C. Beauloye, 2020, European heart journal. Acute cardiovascular care.

Differential presentation of atrioventricular nodal re-entrant tachycardia in athletes and non-athletes.

H. Heidbuchel, J. Ector, C. Garweg, 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.

Clinical characterization of the first Belgian SCN5A founder mutation cohort.

H. Heidbuchel, G. Mortier, C. Vrints, 2020, Europace.

Life-threatening ventricular arrhythmias during ajmaline challenge in patients with Brugada syndrome: incidence, clinical features, and prognosis.

P. Brugada, Y. Saitoh, G. Pappaert, 2013, Heart rhythm.

Out-of-hospital cardiac arrest due to idiopathic ventricular fibrillation in patients with normal electrocardiograms: results from a multicentre long-term registry

H. Heidbuchel, P. Lambiase, C. Rinaldi, 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.

Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation.

B. Suys, A. Corveleyn, B. Loeys, 2018, European Journal of Medical Genetics.

Diagnostic yield of genetic testing in heart transplant recipients with prior cardiomyopathy

H. Heidbuchel, B. Loeys, I. Rodrigus, 2018, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.

Long-term effect of atrial fibrillation on the evolution of mitral and tricuspid valve regurgitation

H. Heidbuchel, M. Claeys, H. Heuten, 2020, Acta cardiologica.

Electrocardiographic phenotype of exercise-induced arrhythmogenic cardiomyopathy: A retrospective observational study

W. Huybrechts, A. Sarkozy, G. Claessen, 2022, Frontiers in Cardiovascular Medicine.

Less Pulmonary Vein Reconnection at Redo Procedures Following Radiofrequency Point-by-Point Antral Pulmonary Vein Isolation With the Use of Contemporary Catheter Ablation Technologies.

H. Heidbuchel, W. Huybrechts, A. Sarkozy, 2018, JACC. Clinical electrophysiology.

Indications and utility of cardiac genetic testing in athletes.

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

Screening for Fabry Disease in Male Patients With Arrhythmia Requiring a Pacemaker or an Implantable Cardioverter-Defibrillator.

B. Poppe, D. Hemelsoet, A. Bondue, 2021, Circulation.

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.

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

R. Redon, P. Lambiase, P. Ellinor, 2020, Genetics in medicine : official journal of the American College of Medical Genetics.

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

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

Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections

M. Goumans, K. Devriendt, J. Timmermans, 2015, Journal of the American College of Cardiology.

Reproducibility and predictive value of a simple novel method to measure atrial fibrillation cycle length in persistent atrial fibrillation – FARS‐AF study

M. Claeys, W. Huybrechts, A. Sarkozy, 2022, Journal of cardiovascular electrophysiology.

Etiology and Outcome of Catheter Ablation in Patients With Onset of Atrial Fibrillation <45 Years of Age.

C. Tondo, W. Huybrechts, S. Riva, 2021, The American journal of cardiology.

Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population

B. Loeys, A. Labro, D. Snyders, 2023, Orphanet Journal of Rare Diseases.

Contact Force in Atrial Fibrillation: Role of Atrial Rhythm and Ventricular Contractions: Co-Force Atrial Fibrillation Study.

D. Shah, C. Vrints, J. Sieira, 2015, Circulation. Arrhythmia and electrophysiology.

Prospective study of tricuspid valve regurgitation associated with permanent leads in patients undergoing cardiac rhythm device implantation: Background, rationale, and design

A. Capucci, J. Healey, S. Connolly, 2015, Global cardiology science & practice.

Anterior mitral line in patients with persistent AF and anterior scar: a multicenter matched comparison. The MiLine Study

W. Huybrechts, M. Valderrábano, A. Sarkozy, 2023, Heart rhythm.

Characterization of Atrial Substrate to Predict the Success of Pulmonary Vein Isolation: The Prospective, Multicenter MASH‐AF II (Multipolar Atrial Substrate High Density Mapping in Atrial Fibrillation) Study

J. González-Juanatey, W. Huybrechts, M. Valderrábano, 2022, Journal of the American Heart Association.

Performant Mutation Identification Using Targeted Next‐Generation Sequencing of 14 Thoracic Aortic Aneurysm Genes

D. Roden, G. Mortier, H. Dietz, 2015, Human mutation.

Genetics of sudden cardiac death in the young

B. Loeys, F. Marchau, E. V. Van Craenenbroeck, 2015, Clinical genetics.

Recommendations for participation in leisure-time physical activity and competitive sports of patients with arrhythmias and potentially arrhythmogenic conditions. Part 2: ventricular arrhythmias, channelopathies, and implantable defibrillators.

H. Heidbuchel, P. Schwartz, D. Corrado, 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.

Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical Disease.

G. Mortier, C. Vrints, W. Wuyts, 2017, The Journal of molecular diagnostics : JMD.

Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport Restriction

T. Mazza, S. Castellana, M. Carella, 2021, Frontiers in Cardiovascular Medicine.

Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes

H. Heidbuchel, W. D. De Vos, E. Fransen, 2022, Biology open.

Monomorphic ventricular tachycardia in patients with Brugada syndrome: A multicenter retrospective study.

P. Lambiase, J. Brugada, P. Brugada, 2016, Heart rhythm.

Prospective Study of Tricuspid Regurgitation Associated With Permanent Leads After Cardiac Rhythm Device Implantation.

A. Capucci, J. Healey, S. Connolly, 2019, The Canadian journal of cardiology.

Chapter 2 . 3 Mutations in a TGFß ligand , TGFB 3 , cause syndromic aortic aneurysms and dissections Mutations in TGFB 3 cause syndromic aortic aneurysms and dissections

M. Goumans, K. Devriendt, J. Timmermans, 2019 .