Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval

The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the European Society of Human Genetics

(2015) J. Mogensen et al.   EUROPEAN HEART JOURNAL

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

The Role of CAV3 in Long–QT Syndrome

(2013) Paula L. Hedley et al.   Circulation-Cardiovascular Genetics

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

HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

(2013) Silvia G. Priori et al.   HEART RHYTHM

Accuracy of the ICD-10 discharge diagnosis for syncope

(2012) M. H. Ruwald et al.   EUROPACE

High prevalence of genetic variants previously associated with LQT syndrome in new exome data

(2012) Lena Refsgaard et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Prevention of Torsade de Pointes in Hospital Settings

(2010) Barbara J. Drew et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Prevalence of the Congenital Long-QT Syndrome

(2009) Peter J. Schwartz et al.   CIRCULATION

Long-QT Syndrome After Age 40

(2008) Ilan Goldenberg et al.   CIRCULATION