Yanushi D. Wijeyeratne
St George's University Of London
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 29 publications
Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026
Ventricular conduction is a marker for arrhythmic risk in SCN5A-E1784K overlap sodium channel disease.
Journal: 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
Published: December 30, 2025
Influence of age and sex on the diagnostic yield of inherited cardiac conditions in sudden arrhythmic death syndrome decedents.
Journal: European journal of preventive cardiology
Published: July 04, 2024
Characteristics of Patients with Spontaneous Versus Drug-Induced Brugada Electrocardiogram: Sub-Analysis From the SABRUS.
Journal: Circulation. Arrhythmia and electrophysiology
Published: January 03, 2023
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Journal: Nature genetics
Published: April 27, 2022
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families.
Journal: Circulation. Genomic and precision medicine
Published: November 09, 2020
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Journal: Nature genetics
Published: September 25, 2020
Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome.
Journal: Heart rhythm
Published: June 18, 2019
The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy.
Journal: European journal of human genetics : EJHG
Published: December 31, 2018
Last Updated: 09/26/2026