Author

Sjoerd Ruizenaar

Erasmus MC

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:metagenomics· 1

Frequent Co-Authors

Alexander HirschiD· 1 shared Andrei HrynevichiD· 1 shared Claudine W.B. RuijmbeekiD· 1 shared Daniela Peneda PachecoiD· 1 shared Edgar E. NolletiD· 1 shared Federico FerraroiD· 1 shared Henk S. SchipperiD· 1 shared Herma C. van der LindeiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexander HirschORCID

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2 papers

Recent·Most cited

Mucus-associated microbiota consortia: Insights from the advanced TIM-2muc model

Sjoerd Ruizenaar, Katja Lange, Olaf Heckert, Jan Lelieveld, Andrei Hrynevich, Daniela Peneda Pacheco, Lars Verdurmen, Maitrayee Chatterjee

The paper introduces TIM-2muc, a novel in vitro model that mimics the mucus-associated microbiome, showing it closely resembles the in vivo MAM and enables non-invasive study of both MAM and luminal microbiome.

bioRxiv · Jul 16, 2025 · PreprintMicrobiology

Bi-allelic variants in the aminopeptidase XPNPEP3 cause mitochondrial disease with pediatric cardiomyopathy

Claudine W.B. Ruijmbeek, Sjoerd Ruizenaar, Herma C. van der Linde, Edgar E. Nollet, Wouter A. S. Doff, Victoria C.S. Bogaard, Marlene de Pee, Federico Ferraro, Richard J. Rodenburg, Henk S. Schipper, Alexander Hirsch, Marjon A. van Slegtenhorst, Jan H. von der Thüsen, Jeroen Demmers, Wilfred F. J. van IJcken, , Judith M. A. Verhagen

This study identifies bi-allelic XPNPEP3 variants causing mitochondrial disease with pediatric cardiomyopathy, revealing impaired mitochondrial protein processing as the underlying mechanism.

medRxiv · Jan 11, 2025 · PreprintGenetic & Genomic Medicine