Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting

Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases

(2015) Christin Loeth Hertz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart

(2015) C. L. Hertz et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

Cardiac and Autonomic Mechanisms Contributing to SUDEP

(2015) Adriana C. Bermeo-Ovalle et al.   JOURNAL OF CLINICAL NEUROPHYSIOLOGY

Sudden unexpected death in epilepsy: some approaches for its prevention and medico-legal consideration

(2014) Archana Verma et al.   ACTA NEUROLOGICA BELGICA

PDZ Domain–Binding Motif Regulates Cardiomyocyte Compartment-Specific Na V 1.5 Channel Expression and Function

(2014) Diana Shy et al.   CIRCULATION

Burden of Sudden Cardiac Death in Persons Aged 1 to 49 Years

(2014) Bjarke Risgaard et al.   Circulation-Arrhythmia and Electrophysiology

Risk of arrhythmia induced by psychotropic medications: a proposal for clinical management

(2014) S. Fanoe et al.   EUROPEAN HEART JOURNAL

Exome analysis–based molecular autopsy in cases of sudden unexplained death in the young

(2014) Richard D. Bagnall et al.   HEART RHYTHM

Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series

(2014) Sara Partemi et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

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

(2014) C. L. Hertz et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

Post-mortem Whole Exome Sequencing with Gene-Specific Analysis for Autopsy-Negative Sudden Unexplained Death in the Young: A Case Series

(2014) Nupoor Narula et al.   PEDIATRIC CARDIOLOGY

Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes

(2013) Kirk E. Lohmueller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes

(2013) Michael O. Dorschner et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Excess Early Mortality in Schizophrenia

(2013) Thomas Munk Laursen et al.   Annual Review of Clinical Psychology

Confirmation of Cause and Manner of Death Via a Comprehensive Cardiac Autopsy Including Whole Exome Next-Generation Sequencing

(2013) Christina G. Loporcaro et al.   ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE

Missense Mutations in Plakophilin-2 Cause Sodium Current Deficit and Associate With a Brugada Syndrome Phenotype

(2013) Marina Cerrone et al.   CIRCULATION

Interpreting Secondary Cardiac Disease Variants in an Exome Cohort

(2013) David Ng et al.   Circulation-Cardiovascular Genetics

Epilepsy and risk of death and sudden unexpected death in the young: A nationwide study

(2013) Anders Gaarsdal Holst et al.   EPILEPSIA

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

(2013) Charlotte Andreasen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic analysis of sudden unexplained death: A multidisciplinary approach

(2013) Silke Kauferstein et al.   FORENSIC SCIENCE INTERNATIONAL

Postmortem analysis of cardiovascular deaths in schizophrenia: A 10-year review

(2013) Joanna Sweeting et al.   SCHIZOPHRENIA RESEARCH

Intercalated disc abnormalities, reduced Na+ current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes

(2012) Stefania Rizzo et al.   CARDIOVASCULAR RESEARCH

Antidepressant Use and Risk of Out-of-Hospital Cardiac Arrest: A Nationwide Case–Time–Control Study

(2012) P Weeke et al.   CLINICAL PHARMACOLOGY & THERAPEUTICS

Sarcomeric gene mutations in sudden infant death syndrome (SIDS)

(2012) Maria Brion et al.   FORENSIC SCIENCE INTERNATIONAL

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

Differential confounding of rare and common variants in spatially structured populations

(2012) Iain Mathieson et al.   NATURE GENETICS

PKP2 Mutations in Sudden Death From Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) and Sudden Unexpected Death With Negative Autopsy (SUDNA)

(2011) Mingchang Zhang et al.   CIRCULATION JOURNAL

Post-Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases

(2010) Emily Tu et al.   BRAIN PATHOLOGY

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

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

A novel custom resequencing array for dilated cardiomyopathy

(2010) Rebekah S Zimmerman et al.   GENETICS IN MEDICINE

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

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

Missense Variants in Plakophilin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy Patients – Disease-Causing or Innocent Bystanders?

(2009) Alex Hørby Christensen et al.   CARDIOLOGY

Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy

(2009) Jason D. Roberts et al.   CARDIOVASCULAR PATHOLOGY

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test

(2009) Jamie D. Kapplinger et al.   HEART RHYTHM

Atypical Antipsychotic Drugs and the Risk of Sudden Cardiac Death

(2009) Wayne A. Ray et al.   NEW ENGLAND JOURNAL OF MEDICINE

Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

(2008) Hiroyuki Morita et al.   NEW ENGLAND JOURNAL OF MEDICINE