Area of research
Cardiology and Cardiovascular Medicine · Epidemiology
Research interest
Research interests include Cardiac Arrhythmias and Treatments, Cardiac electrophysiology and arrhythmias, Cardiac pacing and defibrillation studies, and Congenital Heart Disease Studies.
Sudden cardiac arrest: Limitations in risk-stratification and treatment, and the potential for digital technologies and artificial intelligence to improve prediction and outcomes
The Cardiovascular Care of the Pediatric Athlete
2024 HRS expert consensus statement on arrhythmias in the athlete: Evaluation, treatment, and return to play
Multicenter Study of Survival Benefit of Cardiac Resynchronization Therapy in Pediatric and Congenital Heart Disease
Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS Study
Intracardiac echocardiography in paediatric and congenital cardiac ablation shortens procedure duration and improves success without complications
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
Vigorous Exercise in Patients With Hypertrophic Cardiomyopathy
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
Advancing the science of management of arrhythmic disease in children and adult congenital heart disease patients within the last 25 years
Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome
Sudden Cardiac Death in Adolescents
Smart Wearables for Cardiac Monitoring—Real-World Use beyond Atrial Fibrillation
Evaluation of age at symptom onset, proband status, and sex as predictors of disease severity in pediatric catecholaminergic polymorphic ventricular tachycardia
The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele
Management of Congenital Long-QT Syndrome: Commentary From the Experts
COVID-19 Infection and Corrected QT Interval Prolongation—Collateral Damage From Our Newest Enemy
Toward a Long and Happy Life of a Patient With Genetic Heart Disease
Abstract 9544: Physical Activity in Individuals With Hypertrophic Cardiomyopathy: Baseline Data From the Prospective "Lifestyle and Exercise in Hcm" (live-hcm) Study
COVID-19 and cardiac arrhythmias: a global perspective on arrhythmia characteristics and management strategies
Coronavirus Disease 2019 (COVID‐19) Pandemic Implications in Pediatric and Adult Congenital Heart Disease
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i> -Catecholaminergic Polymorphic Ventricular Tachycardia
Loss of ventricular preexcitation during noninvasive testing does not exclude high-risk accessory pathways: A multicenter study of WPW in children
Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT Syndrome
MRI in pediatric and congenital heart disease patients with CIEDs and epicardial or abandoned leads
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry
Risk factors for lethal arrhythmic events in children and adolescents with hypertrophic cardiomyopathy and an implantable defibrillator: An international multicenter study
Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study
Genetic testing and cascade screening in pediatric long QT syndrome and hypertrophic cardiomyopathy