Author

Filip De Vos

University Medical Center UtrechtORCID 0000-0002-9082-5991Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Devin R. van Valkengoed· 1 shared Edwin P. J. G. CuppeniD· 1 shared Joep de LigtiD· 1 shared Marike L. D. BroekmaniD· 1 shared Mark P. van OpijneniD· 1 shared Roelof KosteriD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 15 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Devin R. van Valkengoed

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1 paper

Recent·Most cited

Whole genome sequencing-based analysis of genetic predisposition to adult glioblastoma

Mark P. van Opijnen, Devin R. van Valkengoed, Joep de Ligt, Filip De Vos, Marike L. D. Broekman, Edwin P. J. G. Cuppen, Roelof Koster

This study identifies pathogenic germline variants in 11% of adult glioblastoma patients, with mismatch repair deficiency as the main predisposition mechanism.

npj Genomic Medicine · Oct 30, 2025Peer-reviewedGenetic & Genomic Medicine