Eline A. Nannenberg

Amsterdam, NH 1105AZ, Netherlands

Last Updated: 09/26/2026

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Found 20 publications

Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death.

Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death.

Journal: European heart journal

Published: June 21, 2021

SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families.

SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families.

Journal: Circulation. Genomic and precision medicine

Published: November 09, 2020

Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case.

Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case.

Journal: American journal of medical genetics. Part A

Published: November 09, 2020

Cardiogenetics, 25 years a growing subspecialism.

Cardiogenetics, 25 years a growing subspecialism.

Journal: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation

Published: August 12, 2020

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 01, 2020

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.

Journal: Circulation

Published: May 21, 2020

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome.

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome.

Journal: Circulation

Published: January 28, 2020

Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases.

Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases.

Journal: Circulation. Genomic and precision medicine

Published: October 26, 2018

Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia.

Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia.

Journal: JACC. Clinical electrophysiology

Published: September 10, 2018

A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy.

A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy.

Journal: European heart journal

Published: November 10, 2017

Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death: Single-Center Experience With 482 Families.

Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death: Single-Center Experience With 482 Families.

Journal: JACC. Clinical electrophysiology

Published: February 13, 2017

GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.

GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.

Journal: American journal of human genetics

Published: September 03, 2016

Showing 1-12 of 20

Last Updated: 09/26/2026