Arjen R Mensenkamp

23PUBLICATIONS
125CO-AUTHORS
Cancer geneticsGene expression (incl. microarray and other genome-wide approaches)Haematological tumoursCancer diagnosisBehavioural epidemiology
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Publications (23)

|May 14, 2026
Updated ENIGMA recommendations for reporting germline variants in cancer susceptibility genes and their translation into twenty languages.

|Apr 16, 2026
Genome Sequencing of Undiagnosed European Patients Suspected of Hereditary Cancer: Diagnostic Yield and Identification of Candidate Causative Variants.

|Dec 18, 2025
Evidence for pathogenicity of BRCA2 c.8351G>A p.(Arg2784Gln) and the challenges in classification of pathogenic variants with reduced penetrance.

Setareh Moghadasi, Maria Zanti, Fonnet Bleeker

|May 14, 2025
Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with constitutional mismatch repair deficiency.

Dilys D Weijers, Snežana Hinić, Emma Kroeze

|Apr 28, 2025
Deep Phenotyping of Pathology-Confirmed Benign Lesions in PTEN Hamartoma Tumor Syndrome Patients.

Ane J Schei-Andersen, Janneke H M Schuurs-Hoeijmakers, Rachel van der Post

|Feb 20, 2025
Exome-based cancer predisposition gene testing can provide a genetic diagnosis for individuals with heterogeneous tumor phenotypes.

Snežana Hinić, Arjen R Mensenkamp, Janneke H M Schuurs-Hoeijmakers

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Frequent Collaborators

9 joint publications

Nicoline Hoogerbrugge

6 joint publications

Janet R Vos

4 joint publications

Richarda M de Voer

4 joint publications

Rachel van der Post