Author

Devin R. van Valkengoed

Hartwig Medical Foundation

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

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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

Edwin P. J. G. CuppeniD· 1 shared Filip De VosiD· 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

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6 top collaborators · 15 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Edwin P. J. G. CuppenORCID

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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