Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth

Reappraisal of Reported Genes for Sudden Arrhythmic Death: An Evidence-Based Evaluation of Gene Validity for Brugada Syndrome

(2018) S. Mohsen Hosseini et al.   CIRCULATION

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples

(2016) Roddy Walsh et al.   GENETICS IN MEDICINE

Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?

(2016) Georgia Sarquella-Brugada et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

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

Assessment of HaloPlex Amplification for Sequence Capture and Massively Parallel Sequencing of Arrhythmogenic Right Ventricular Cardiomyopathy–Associated Genes

(2015) Anna Gréen et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Risk of recurrent stillbirth: systematic review and meta-analysis

(2015) K. Lamont et al.   BMJ-British Medical Journal

Risk of recurrent stillbirth: systematic review and meta-analysis

(2015) K. Lamont et al.   BMJ-British Medical Journal

Molecular and Cytogenetic Analysis in Stillbirth: Results from 481 Consecutive Cases

(2014) Ellika Sahlin et al.   FETAL DIAGNOSIS AND THERAPY

A general framework for estimating the relative pathogenicity of human genetic variants

(2014) Martin Kircher et al.   NATURE 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

Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death

(2013) Lia Crotti et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

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

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

Fetal Presentation of Long QT Syndrome – Evaluation of Prenatal Risk Factors: A Systematic Review

(2012) Satoshi Ishikawa et al.   FETAL DIAGNOSIS AND THERAPY

Sarcomeric gene mutations in sudden infant death syndrome (SIDS)

(2012) Maria Brion et al.   FORENSIC SCIENCE INTERNATIONAL

Karyotype versus Microarray Testing for Genetic Abnormalities after Stillbirth

(2012) Uma M. Reddy et al.   NEW ENGLAND JOURNAL OF MEDICINE

Cardiac Channelopathies and Sudden Infant Death Syndrome

(2011) Jacob Tfelt-Hansen et al.   CARDIOLOGY

Genetics of Stillbirth

(2010) RONALD J. WAPNER   CLINICAL OBSTETRICS AND GYNECOLOGY

Cardiomyopathies—Misdiagnosed as Sudden Infant Death Syndrome (SIDS)

(2009) R.B. Dettmeyer et al.   FORENSIC SCIENCE INTERNATIONAL

The Stockholm classification of stillbirth

(2008) Ingela hulthén Varli et al.   ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA

Sudden infant death syndrome: Do ion channels play a role?

(2008) David W. Van Norstrand et al.   HEART RHYTHM