Negative autopsy and sudden cardiac death

Genetic analysis of sudden unexplained death: A multidisciplinary approach

(2013) Silke Kauferstein et al.   FORENSIC SCIENCE INTERNATIONAL

A Missense Mutation in the Sodium Channel β2 Subunit RevealsSCN2Bas a New Candidate Gene for Brugada Syndrome

(2013) Helena Riuró et al.   HUMAN MUTATION

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

(2012) Mette Nyegaard et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Sudden Cardiac Death and Genetic Ion Channelopathies

(2012) Carlo Napolitano et al.   CIRCULATION

Brugada Syndrome 2012

(2012) Paola Berne et al.   CIRCULATION JOURNAL

Long-QT Syndrome

(2012) Peter J. Schwartz et al.   Circulation-Arrhythmia and Electrophysiology

Cardiac channelopathies: Genetic and molecular mechanisms

(2012) Hugues Abriel et al.   GENE

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human

(2012) Nathalie Roux-Buisson et al.   HUMAN MOLECULAR GENETICS

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

The Molecular Autopsy: Should the Evaluation Continue After the Funeral?

(2012) David J. Tester et al.   PEDIATRIC CARDIOLOGY

Increase in sudden death from coronary artery disease in young adults

(2011) Dabit Arzamendi et al.   AMERICAN HEART JOURNAL

Next generation sequencing--implications for clinical practice

(2011) E. Raffan et al.   BRITISH MEDICAL BULLETIN

Cardiac Channelopathies and Sudden Infant Death Syndrome

(2011) Jacob Tfelt-Hansen et al.   CARDIOLOGY

Cardiogenetic screening of first-degree relatives after sudden cardiac death in the young: a population-based approach

(2011) A. Hendrix et al.   EUROPACE

Genetics of inherited cardiomyopathy

(2011) D. Jacoby et al.   EUROPEAN HEART JOURNAL

Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)

(2011) C. Templin et al.   EUROPEAN HEART JOURNAL

Sudden death: managing the patient who survives

(2011) M. Pachon et al.   HEART

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

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

Cardiac ion channel mutations in the sudden infant death syndrome

(2011) Eva C. Klaver et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Sudden, Unexpected Death in Epilepsy

(2011) Orrin Devinsky   NEW ENGLAND JOURNAL OF MEDICINE

Prevalence and Spectrum of Large Deletions or Duplications in the Major Long QT Syndrome-Susceptibility Genes and Implications for Long QT Syndrome Genetic Testing

(2010) David J. Tester et al.   AMERICAN JOURNAL OF CARDIOLOGY

Sudden cardiac death with normal heart:

(2010) Cristina Basso et al.   CARDIOVASCULAR PATHOLOGY

Biophysical and Molecular Characterization of a Novel De Novo KCNJ2 Mutation Associated With Andersen-Tawil Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia Mimicry

(2010) Hector Barajas-Martinez et al.   Circulation-Cardiovascular Genetics

Catecholaminergic polymorphic ventricular tachycardia

(2010) Kaisa Ylänen et al.   EUROPEAN JOURNAL OF PEDIATRICS

Analysis of mRNA from human heart tissue and putative applications in forensic molecular pathology

(2010) Sara Partemi et al.   FORENSIC SCIENCE INTERNATIONAL

New technologies in the genetic approach to sudden cardiac death in the young

(2010) M. Brion et al.   FORENSIC SCIENCE INTERNATIONAL

Genetics and cardiac channelopathies

(2010) Oscar Campuzano et al.   GENETICS IN MEDICINE

Genetic analysis of sudden cardiac death victims: a survey of current forensic autopsy practices

(2010) Katarzyna Michaud et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

Sudden cardiac death: epidemiology and risk factors

(2010) A. Selcuk Adabag et al.   Nature Reviews Cardiology

Short QT Syndrome

(2009) Umang Patel et al.   Cardiology in Review

Sudden death: ethical and legal problems of post-mortem forensic genetic testing for hereditary cardiac diseases

(2009) BS Elger et al.   CLINICAL GENETICS

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

Postmortem Genetic Testing for Conventional Autopsy–Negative Sudden Unexplained Death

(2008) Elisa Carturan et al.   AMERICAN JOURNAL OF CLINICAL PATHOLOGY

Long-QT Syndrome

(2008) Dan M. Roden   NEW ENGLAND JOURNAL OF MEDICINE