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

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

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

Diagnosis and management of patients with inherited arrhythmia syndromes in Europe: results of the European Heart Rhythm Association Survey

(2014) M. Hocini et al.   EUROPACE

Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions

(2014) L. C. H. Wong et al.   EUROPACE

Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy

(2013) Julia Daher Carneiro Marsiglia et al.   AMERICAN HEART JOURNAL

Mutation Spectrum in a Large Cohort of Unrelated Chinese Patients With Hypertrophic Cardiomyopathy

(2013) Wen Liu et al.   AMERICAN JOURNAL OF CARDIOLOGY

Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan

(2013) Mihoko Kawamura et al.   CIRCULATION JOURNAL

Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

(2013) Seiko Ohno et al.   CIRCULATION JOURNAL

Sudden Cardiac Death With Autopsy Findings of Uncertain Significance

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

Screening and risk evaluation for sudden cardiac death in ischaemic and non-ischaemic cardiomyopathy: results of the European Heart Rhythm Association survey

(2013) A. Proclemer et al.   EUROPACE

Family-based cardiac screening in relatives of victims of sudden arrhythmic death syndrome

(2013) Catherine McGorrian et al.   EUROPACE

The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths

(2013) Sofia V. de Noronha et al.   EUROPACE

Familial cardiological evaluation in sudden arrhythmic death syndrome: essential but challenging

(2013) L. C. H. Wong et al.   EUROPACE

Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes

(2013) Silvia G. Priori et al.   EUROPACE

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

Results of Genetic Testing in 855 Consecutive Unrelated Patients Referred for Long QT Syndrome in a Clinical Laboratory

(2013) Krystien V. Lieve et al.   Genetic Testing and Molecular Biomarkers

Familial cardiological and targeted genetic evaluation: Low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes

(2013) Saurabh Kumar et al.   HEART RHYTHM

Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing

(2013) Luis R Lopes et al.   JOURNAL OF MEDICAL GENETICS

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

(2012) Eva-Lena Stattin et al.   BMC Cardiovascular Disorders

Sodium Current and Potassium Transient Outward Current Genes in Brugada Syndrome: Screening and Bioinformatics

(2012) Anders G. Holst et al.   CANADIAN JOURNAL OF CARDIOLOGY

Postmortem genetic testing of the ryanodine receptor 2 (RYR2) gene in a cohort of sudden unexplained death cases

(2012) M. K. Larsen et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

(2012) Neal K. Lakdawala et al.   JOURNAL OF CARDIAC 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

Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing

(2012) Lia Crotti et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

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

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

Compound and Digenic Heterozygosity in Desmosome Genes as a Cause of Arrhythmogenic Right Ventricular Cardiomyopathy in Japanese Patients

(2011) Tadashi Nakajima et al.   CIRCULATION JOURNAL

Therapeutic approach for patients with catecholaminergic polymorphic ventricular tachycardia: state of the art and future developments

(2011) C. van der Werf et al.   EUROPACE

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)

(2011) M. J. Ackerman et al.   EUROPACE

Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy

(2011) Giovanni Quarta et al.   EUROPEAN HEART JOURNAL

Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy

(2011) Gilles Millat et al.   European Journal of Medical Genetics

Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy

(2011) M.K. Larsen et al.   FORENSIC SCIENCE INTERNATIONAL

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

(2011) Tadashi Nakajima et al.   International Heart Journal

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases

(2011) Catarina Allegue et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

Sudden Death in Young Adults

(2011) Robert E. Eckart et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

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

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

(2010) Perry Elliott et al.   Circulation-Cardiovascular Genetics

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice

(2010) Veronique Fressart et al.   EUROPACE

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

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

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: Proposed Modification of the Task Force Criteria

(2010) F. I. Marcus et al.   EUROPEAN HEART JOURNAL

Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy

(2010) Gilles Millat et al.   European Journal of Medical Genetics

Strategy for clinical evaluation and screening of sudden cardiac death relatives

(2010) Laura Ferrero-Miliani et al.   FUNDAMENTAL & CLINICAL PHARMACOLOGY

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

Sodium Channelopathies: Do We Really Understand What's Going On?

(2010) PIETER G. POSTEMA et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy

(2010) A. H. Christensen et al.   JOURNAL OF MEDICAL GENETICS

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

(2010) Francesca Girolami et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

(2009) Annukka Marjamaa et al.   BMC Medical Genetics

Genetic Testing for Long-QT Syndrome

(2009) Suraj Kapa et al.   CIRCULATION

Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients

(2009) Zahurul A. Bhuiyan et al.   Circulation-Cardiovascular Genetics

The magnitude of sudden cardiac death in the young: a death certificate-based review in England and Wales

(2009) M. Papadakis et al.   EUROPACE

Sudden death in persons younger than 40 years of age: incidence and causes

(2009) Ilonca Vaartjes et al.   EUROPEAN JOURNAL OF CARDIOVASCULAR PREVENTION & REHABILITATION

The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy

(2009) Daniel Vega Møller et al.   EUROPEAN JOURNAL OF HEART FAILURE

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

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

(2009) Barbara Bauce et al.   HEART RHYTHM

Postmortem Genetic Testing for Conventional Autopsy–Negative Sudden Unexplained Death

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

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

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

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families

(2008) Elijah R. Behr et al.   EUROPEAN HEART JOURNAL

Molecular genetics of sudden cardiac death

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

Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome

(2008) Carey-Anne Eddy et al.   HEART RHYTHM

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

(2008) Paal Skytt Andersen et al.   HUMAN MUTATION

The Brugada Syndrome⁎⁎Editorials published in the Journal of the American College of Cardiology reflect the views of the authors and do not necessarily represent the views of JACC or the American College of Cardiology.

(2008) Peng-Sheng Chen et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

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