Prince J. Kannankeril

Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy.

Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family.

Andersen-Tawil syndrome.

Polymorphic ventricular tachycardia and abnormal Ca2+ handling in very-long-chain acyl-CoA dehydrogenase null mice.

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation.

ACE I/D polymorphism associated with abnormal atrial and atrioventricular conduction in lone atrial fibrillation and structural heart disease: implications for electrical remodeling.

Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.

Arrhythmia pharmacogenomics: methodological considerations.

Entrainment to distinguish orthodromic reciprocating tachycardia from atrioventricular nodal reentry tachycardia in children.

Factors affecting the degree of QT prolongation with drug challenge in a large cohort of normal volunteers.

Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia.

A genetic contribution to risk for postoperative junctional ectopic tachycardia in children undergoing surgery for congenital heart disease.

Relation of milrinone after surgery for congenital heart disease to significant postoperative tachyarrhythmias.

A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.

Antitachycardia pacing reduces appropriate and inappropriate shocks in children and congenital heart disease patients.

Diagnosis and management of sudden death in children.

Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardia.

Accelerated sinus rhythm prevents catecholaminergic polymorphic ventricular tachycardia in mice and in patients.

Opioid Use After Cardiac Surgery in Children With Down Syndrome.

Emergency response planning and sudden cardiac arrests in high schools after automated external defibrillator legislation.

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes.

A common angiotensin-converting enzyme polymorphism and preoperative angiotensin-converting enzyme inhibition modify risk of tachyarrhythmias after congenital heart surgery.

Suppression of spontaneous ca elevations prevents atrial fibrillation in calsequestrin 2-null hearts.

Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.

Predictors of myocardial recovery in pediatric tachycardia-induced cardiomyopathy.

The safety of modern anesthesia for children with long QT syndrome.

Association between perioperative dexmedetomidine and arrhythmias after surgery for congenital heart disease.

Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.

Serial assessment of accessory pathway antegrade conduction in children.

A Clinical Risk Score to Improve the Diagnosis of Tachycardia-Induced Cardiomyopathy in Childhood.

Association of Shunt Type With Arrhythmias After Norwood Procedure.

Association Between Early Postoperative Acetaminophen Exposure and Acute Kidney Injury in Pediatric Patients Undergoing Cardiac Surgery.

Chronotropic incompetence as a risk predictor in children and young adults with catecholaminergic polymorphic ventricular tachycardia.

is associated with indomethacin treatment failure for patent ductus arteriosus.

Higher risk at the lower end of the age spectrum in Brugada syndrome.

Molecular and tissue mechanisms of catecholaminergic polymorphic ventricular tachycardia.

Highly Reactive Isolevuglandins Promote Atrial Fibrillation Caused by Hypertension.

Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT Syndrome.

Research consent rates before and during a COVID-19 one-visitor policy in a children's hospital.

Optimizing transesophageal atrial pacing in mice to detect atrial fibrillation.

Developmental changes in cardiac expression of KCNQ1 and SCN5A spliceoforms: Implications for sudden unexpected infant death.

Sotalol vs amiodarone for postoperative junctional ectopic tachycardia: Citius, Altius, Fortius?