Phenotype-driven molecular autopsy for sudden cardiac death

Sudden cardiac death associated with physical exertion in the US military, 2005–2010

(2015) Darlene P Smallman et al.   BRITISH JOURNAL OF SPORTS MEDICINE

Incidence, Cause, and Comparative Frequency of Sudden Cardiac Death in National Collegiate Athletic Association AthletesCLINICAL PERSPECTIVE

(2015) Kimberly G. Harmon et al.   CIRCULATION

Genetic purgatory and the cardiac channelopathies: Exposing the variants of uncertain/unknown significance issue

(2015) Michael J. Ackerman   HEART RHYTHM

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

(2013) Catherine McGorrian 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

Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC)

(2013) Wouter P te Rijdt et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

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

Molecular Autopsy for Sudden Unexplained Death? Time to Discuss Pros and Cons

(2012) ANDREA MAZZANTI et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

Uptake of Cardiac Screening and Genetic Testing Among Hypertrophic and Dilated Cardiomyopathy Families

(2012) Erin M. Miller et al.   Journal of Genetic Counseling

Hypertrophic cardiomyopathy

(2012) Barry J Maron et al.   LANCET

Truncations of Titin Causing Dilated Cardiomyopathy

(2012) Daniel S. Herman et al.   NEW ENGLAND JOURNAL OF MEDICINE

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

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

In the Thick of It

(2011) Samantha P. Harris et al.   CIRCULATION RESEARCH

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

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

Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy

(2011) Ray E. Hershberger et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Sudden Cardiac Death Prediction and Prevention

(2010) Glenn I. Fishman et al.   CIRCULATION

A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death

(2010) Eyal Nof et al.   Circulation-Cardiovascular Genetics

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

Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin

(2010) A. La Gerche et al.   HEART

A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy

(2009) G Frisso et al.   CLINICAL GENETICS

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

Extreme phenotypic diversity and nonpenetrance in families with theLMNA gene mutation R644C

(2008) Julia Rankin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

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