Karel Van Duijvenboden

Amsterdam, NH 1105AZ, Netherlands

Last Updated: 09/26/2026

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Found 30 publications

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026

AAV6-based ZEB2 delivery promotes cardiomyocyte dedifferentiation in adult human myocardium.

AAV6-based ZEB2 delivery promotes cardiomyocyte dedifferentiation in adult human myocardium.

Journal: Cardiovascular research
Published: June 13, 2025

PITX2 dosage-dependent changes in pacemaker cell state underlie sinus node dysfunction and atrial arrhythmias.

PITX2 dosage-dependent changes in pacemaker cell state underlie sinus node dysfunction and atrial arrhythmias.

Journal: Nature communications
Published: April 22, 2025

AAV-mediated long-term TBX18 expression causes cardiac fibrosis and fails to induce pacemaker activity in rodents.

AAV-mediated long-term TBX18 expression causes cardiac fibrosis and fails to induce pacemaker activity in rodents.

Journal: The Journal of clinical investigation
Published: December 26, 2024

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.

Journal: Circulation
Published: October 11, 2024

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Journal: American journal of human genetics
Published: August 18, 2024

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.

Journal: medRxiv : the preprint server for health sciences
Published: July 15, 2024

An atrial fibrillation-associated regulatory region modulates cardiac Tbx5 levels and arrhythmia susceptibility.

An atrial fibrillation-associated regulatory region modulates cardiac Tbx5 levels and arrhythmia susceptibility.

Journal: eLife
Published: May 27, 2022

Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction.

Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction.

Journal: Circulation
Published: February 03, 2022

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.

Journal: Circulation research
Published: December 10, 2021

Epigenetic State Changes Underlie Metabolic Switch in Mouse Post-Infarction Border Zone Cardiomyocytes.

Epigenetic State Changes Underlie Metabolic Switch in Mouse Post-Infarction Border Zone Cardiomyocytes.

Journal: Journal of cardiovascular development and disease
Published: September 14, 2021

A Variant Noncoding Region Regulates Prrx1 and Predisposes to Atrial Arrhythmias.

A Variant Noncoding Region Regulates Prrx1 and Predisposes to Atrial Arrhythmias.

Journal: Circulation research
Published: June 07, 2021
Showing 1-12 of 30

Last Updated: 09/26/2026