SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores

(2019) Rafik Tadros et al.   EUROPEAN HEART JOURNAL

OUP accepted manuscript

(2018)   EUROPEAN HEART JOURNAL

The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy

(2018) Michael Papadakis et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Can genetics predict risk for sudden cardiac death? The relentless search for the Holy Grail

(2018) Peter J Schwartz et al.   EUROPEAN HEART JOURNAL

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

(2016) Charles Antzelevitch et al.   HEART RHYTHM

Further Insights in the Most CommonSCN5AMutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

(2016) Christian Veltmann et al.   Journal of the American Heart Association

High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia

(2015) Can Hasdemir et al.   HEART RHYTHM

HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

(2013) Silvia G. Priori et al.   HEART RHYTHM

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

(2013) Connie R Bezzina et al.   NATURE GENETICS

SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome

(2009) Vincent Probst et al.   Circulation-Cardiovascular Genetics

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

(2009) Jamie D. Kapplinger et al.   HEART RHYTHM