Numerous Brugada syndrome–associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

(2015) Elijah R. Behr et al.   CARDIOVASCULAR RESEARCH

Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval

(2015) Jonas Ghouse et al.   EUROPEAN HEART JOURNAL

2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death

(2015) Silvia G. Priori et al.   EUROPEAN HEART JOURNAL

Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome

(2015) Solena Le Scouarnec et al.   HUMAN MOLECULAR GENETICS

Genetics of Brugada syndrome

(2015) Hiroshi Watanabe et al.   JOURNAL OF HUMAN GENETICS

Mutations in SCN10A Are Responsible for a Large Fraction of Cases of Brugada Syndrome

(2014) Dan Hu et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes

(2013) Kirk E. Lohmueller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

High prevalence of genetic variants previously associated with Brugada syndrome in new exome data

(2013) B Risgaard et al.   CLINICAL GENETICS

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

Low disease prevalence and inappropriate implantable cardioverter defibrillator shock rate in Brugada syndrome: a nationwide study

(2012) A. G. Holst et al.   EUROPACE

High prevalence of genetic variants previously associated with LQT syndrome in new exome data

(2012) Lena Refsgaard et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Current electrocardiographic criteria for diagnosis of Brugada pattern: a consensus report

(2012) Antonio Bayés de Luna et al.   JOURNAL OF ELECTROCARDIOLOGY

Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes

(2012) John R. Giudicessi et al.   Translational Research

The Danish National Patient Register

(2011) Elsebeth Lynge et al.   SCANDINAVIAN JOURNAL OF PUBLIC HEALTH

The Danish Register of Causes of Death

(2011) Karin Helweg-Larsen   SCANDINAVIAN JOURNAL OF PUBLIC HEALTH

The genetic basis of Brugada syndrome: A mutation update

(2009) Paula L. Hedley et al.   HUMAN MUTATION

Prevalence and significance of Brugada-type ECG in 12,012 apparently healthy European subjects

(2007) Mark M. Gallagher et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY