Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases

A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification

(2014) Christin L Hertz et al.   EUROPACE

Mutations in Genes Encoding Cardiac Ion Channels Previously Associated With Sudden Infant Death Syndrome (SIDS) Are Present With High Frequency in New Exome Data

(2013) Charlotte Andreasen et al.   CANADIAN JOURNAL OF CARDIOLOGY

Sudden Cardiac Death With Autopsy Findings of Uncertain Significance

(2013) Michael Papadakis et al.   Circulation-Arrhythmia and Electrophysiology

Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience

(2013) Karin Y. van Spaendonck-Zwarts et al.   EUROPEAN JOURNAL OF HEART FAILURE

The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases

(2012) BO GREGERS WINKEL et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

Cardiac Channel Molecular Autopsy: Insights From 173 Consecutive Cases of Autopsy-Negative Sudden Unexplained Death Referred for Postmortem Genetic Testing

(2012) David J. Tester et al.   MAYO CLINIC PROCEEDINGS

Identification of Six Novel SCN5A Mutations in Japanese Patients With Brugada Syndrome

(2011) Tadashi Nakajima et al.   International Heart Journal

Nationwide study of sudden cardiac death in persons aged 1–35 years

(2010) Bo Gregers Winkel et al.   EUROPEAN HEART JOURNAL

Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds

(2010) Jonathan R. Skinner et al.   HEART RHYTHM

Epigenetics and cardiovascular disease

(2010) José M. Ordovás et al.   Nature Reviews Cardiology

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS

The genetic basis of Brugada syndrome: A mutation update

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

The genetic basis of long QT and short QT syndromes: A mutation update

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

Cardiomyopathic and Channelopathic Causes of Sudden Unexplained Death in Infants and Children

(2008) David J. Tester et al.   Annual Review of Medicine

Molecular genetics of sudden cardiac death

(2008) María Sol Rodríguez-Calvo et al.   FORENSIC SCIENCE INTERNATIONAL

Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers

(2008) K. E. Berge et al.   SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION