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

Sodium Current and Potassium Transient Outward Current Genes in Brugada Syndrome: Screening and Bioinformatics

(2012) Anders G. Holst et al.   CANADIAN JOURNAL OF CARDIOLOGY

Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years

(2012) Morten S. Olesen et al.   CANADIAN JOURNAL OF CARDIOLOGY

High Prevalence of Long QT Syndrome–Associated SCN5A Variants in Patients With Early-Onset Lone Atrial Fibrillation

(2012) Morten S. Olesen et al.   Circulation-Cardiovascular Genetics

Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-QT Syndrome

(2012) John R. Giudicessi et al.   Circulation-Cardiovascular 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

A Novel Nonsense Variant in Nav1.5 Cofactor MOG1 Eliminates Its Sodium Current Increasing Effect and May Increase the Risk of Arrhythmias

(2011) Morten S. Olesen et al.   CANADIAN JOURNAL OF CARDIOLOGY

A Brugada syndrome mutation (p.S216L) and its modulation by p.H558R polymorphism: standard and dynamic characterization

(2011) Stefano Marangoni et al.   CARDIOVASCULAR RESEARCH

Transient outward current (Ito) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome

(2011) John R. Giudicessi et al.   HEART RHYTHM

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

(2011) Michael J. Ackerman et al.   HEART RHYTHM

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

(2011) Hector Barajas-Martínez et al.   HEART RHYTHM

SCN1Bb R214Q found in 3 patients: 1 with Brugada syndrome and 2 with lone atrial fibrillation

(2011) Morten S. Olesen et al.   HEART RHYTHM

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

(2010) Morten S. Olesen et al.   CARDIOVASCULAR RESEARCH

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death

(2010) Elena Burashnikov et al.   HEART RHYTHM

Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study

(2009) M. F. Sinner et al.   EUROPACE

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

Inherited Cardiac Diseases Caused by Mutations in the Nav1.5 Sodium Channel

(2009) JACOB TFELT-HANSEN et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

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

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