Genetics of sudden death: focus on inherited channelopathies

Identification of a Kir3.4 Mutation in Congenital Long QT Syndrome

(2010) Yanzong Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome

(2010) V. Probst et al.   CIRCULATION

The Fifteen Years of Discoveries That Shaped Molecular Electrophysiology

(2010) Silvia G. Priori   CIRCULATION RESEARCH

Purkinje Cells From RyR2 Mutant Mice Are Highly Arrhythmogenic But Responsive to Targeted Therapy

(2010) Guoxin Kang et al.   CIRCULATION RESEARCH

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

Defining a New Paradigm for Human Arrhythmia Syndromes

(2010) Michael J. Ackerman et al.   CIRCULATION RESEARCH

Common Variants in Cardiac Ion Channel Genes Are Associated With Sudden Cardiac Death

(2010) Christine M. Albert et al.   Circulation-Arrhythmia and Electrophysiology

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

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

NOS1AP Is a Genetic Modifier of the Long-QT Syndrome

(2009) Lia Crotti et al.   CIRCULATION

α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current

(2009) Jianding Cheng et al.   Circulation-Arrhythmia and Electrophysiology

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

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

Catecholaminergic polymorphic ventricular tachycardia: A paradigm to understand mechanisms of arrhythmias associated to impaired Ca2+ regulation

(2009) Marina Cerrone et al.   HEART RHYTHM

Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study

(2009) M. Eijgelsheim et al.   HUMAN MOLECULAR GENETICS

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

(2009) Arne Pfeufer et al.   NATURE GENETICS

Common variants at ten loci influence QT interval duration in the QTGEN Study

(2009) Christopher Newton-Cheh et al.   NATURE GENETICS

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

(2009) Hiroshi Watanabe et al.   NATURE MEDICINE

Fragmented QRS as a Marker of Conduction Abnormality and a Predictor of Prognosis of Brugada Syndrome

(2008) Hiroshi Morita et al.   CIRCULATION

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

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

Atrial Fibrillation in Patients With Brugada Syndrome

(2008) Kengo F. Kusano et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Long QT Syndrome

(2008) Ilan Goldenberg et al.   JOURNAL OF THE AMERICAN COLLEGE OF 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