
Paul G. Volders
Maastricht, LI, Netherlands
Last Updated: 09/26/2026
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Found 7 publications
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
Anatomical Determinants of Papillary Muscle Arrhythmias in Apparently Normal Hearts.
Journal: Arrhythmia & electrophysiology review
Published: February 28, 2025
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Journal: Nature genetics
Published: April 27, 2022
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Journal: Nature genetics
Published: September 25, 2020
Lamin A/C-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation.
Journal: Circulation. Cardiovascular genetics
Published: February 20, 2016
Improving survival after out-of-hospital cardiac arrest requires new tools.
Journal: European heart journal
Published: May 20, 2015
Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members.
Journal: Circulation. Cardiovascular genetics
Published: August 29, 2014
Showing 1-7 of 7
Last Updated: 09/26/2026