Author

Ronald Wilders

Amsterdam University Medical CentersORCID 0000-0002-1340-0869Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:electrophysiology· 1 Approach:experimental assay· 1

Frequent Co-Authors

Arie O. VerkerkiD· 2 shared Alex Vincent PostmaiD· 1 shared Alexa M.C. VermeeriD· 1 shared Andrea Ulrike SteinbickeriD· 1 shared Antonio M. A. MirandaiD· 1 shared Arthur A.M. WildeiD· 1 shared Ástrós SkúladóttiriD· 1 shared Bitten AagaardiD· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersPhysiology

Arie O. VerkerkORCID

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2 papers

Recent·Most cited

PhysiologybioRxivPreprintSep 4, 2024

TMPRSS6 cleaves KCNE1 and causes arrhythmias in iron overload disease

Stefan Peischard, Philipp Kastl, Gunnar Goerges…·Guiscard Seebohm

This study identifies TMPRSS6 cleavage of KCNE1 as a mechanism causing arrhythmias in iron overload disease using human iPSC-derived cardiomyocytes and computational models.

1 citation

humanelectrophysiology

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJul 4, 2024

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

Michele Nicastro, Alexa M.C. Vermeer, Pieter Gerard Postema…·Najim Lahrouchi

DOI 10.1101/2024.07.04.24309755

humanbulk RNA-seq

𝕏 PostBluesky