Author

Mark P. van Opijnen

Leiden University Medical CenterORCID 0000-0002-2400-4626Unclaimed 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 Filip De VosiD· 1 shared Joep de LigtiD· 1 shared Marike L. D. BroekmaniD· 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

Devin R. van Valkengoed

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1 paper

Recent·Most cited

Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedOct 30, 2025

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

Mark P. van Opijnen, Devin R. van Valkengoed, Joep de Ligt…·Roelof Koster

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

5 citations

humanwhole-genome sequencing

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