Author

Paul G.A. Volders

Maastricht University Medical CentreORCID 0000-0002-2652-1598Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Organism:human· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Assay:electrophysiology· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Arthur A.M. WildeiD· 2 shared Ahmad S. AminiD· 1 shared Alex LipoviD· 1 shared Ammar Al‐ChalabiiD· 1 shared Andrew A. GraceiD· 1 shared Andrew Michael GlazeriD· 1 shared Anneline S.J.M. te RieleiD· 1 shared Antoine LeenhardtiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Arthur A.M. WildeORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 10, 2026

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

Alex Lipov, Manon Baudic, Pierre Lindenbaum…·Connie R. Bezzina

This study identifies rare and low-frequency non-coding variants at the SCN5A locus associated with Brugada syndrome using whole-genome sequencing and functional assays.

DOI 10.64898/2026.07.07.26356386

humanwhole-genome sequencing

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Cell BiologyThe Journal of General PhysiologyPeer-reviewedJul 16, 2025

Variability in reported midpoints of (in)activationof cardiac INa

Michael Clerx, Paul G.A. Volders, Gary R. Mirams

This paper reviews and visualizes variability in reported midpoints of activation and inactivation of cardiac INa, finding large between-experiment variation and classifying contributing factors.

3 citations

electrophysiologystatistical model

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Genetic & Genomic MedicineJournal of Cardiovascular Translational ResearchPeer-reviewedJan 9, 2023

Phenotypic and genetic factors are associated with absence of cardiomyopathy symptoms in PLN c.40_42delAGA carriers

Esteban A. Lopera-Maya, Shuang� Li, Remco de Brouwer…·Rudolf A. de Boer

The paper identifies shorter QRS duration in asymptomatic PLN c.40_42delAGA carriers and links it to genetic sensitivity in symptomatic carriers.

6 citations

humanstatistical model

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