Genetic Testing of Inherited Arrhythmias

Trafficking Defects and Gating Abnormalities of a Novel SCN5A Mutation Question Gene-Specific Therapy in Long QT Syndrome Type 3

(2010) Yanfei Ruan et al.   CIRCULATION RESEARCH

Mutation-Specific Effects of Polymorphism H558R inSCN5A-Related Sick Sinus Syndrome

(2010) JUNHONG GUI et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

Polymorphisms in the NOS1APGene Modulate QT Interval Duration and Risk of Arrhythmias in the Long QT Syndrome

(2010) Marta Tomás et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Genetic Testing for Long-QT Syndrome

(2009) Suraj Kapa et al.   CIRCULATION

NOS1AP Is a Genetic Modifier of the Long-QT Syndrome

(2009) Lia Crotti et al.   CIRCULATION

A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype

(2009) Dan Hu et al.   Circulation-Cardiovascular Genetics

A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations

(2009) Fabio Marroni et al.   Circulation-Cardiovascular Genetics

Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae

(2009) J. Gustav Smith et al.   HEART RHYTHM

Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia

(2009) Barbara Bauce et al.   HEART RHYTHM

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

(2009) Arne Pfeufer et al.   NATURE GENETICS

Sodium channel mutations and arrhythmias

(2009) Yanfei Ruan et al.   Nature Reviews Cardiology

The largest prospective warfarin-treated cohort supports genetic forecasting

(2008) M. Wadelius et al.   BLOOD

Unexpected Structural and Functional Consequences of the R33Q Homozygous Mutation in Cardiac Calsequestrin

(2008) Nicoletta Rizzi et al.   CIRCULATION RESEARCH

Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome

(2008) Eva Delpón et al.   Circulation-Arrhythmia and Electrophysiology

Polymorphisms in multiple genes are associated with resting heart rate in a stepwise allele-dependent manner

(2008) Stephen B. Wilton et al.   HEART RHYTHM

Ryanodine receptor and calsequestrin in arrhythmogenesis: What we have learnt from genetic diseases and transgenic mice

(2008) Nian Liu et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart

(2008) K.-C. Chang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

(2008) K. Ueda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Erratum: Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression

(2008) Andre Keren et al.   Nature clinical practice. Cardiovascular medicine