Arjen Mensenkamp
0000-0003-3805-877X
7 papers found
Refreshing results…
Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases
Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors
Functional categorization of BRCA1 variants of uncertain clinical significance in homologous recombination repair complementation assays
Clinical, Pathology, Genetic, and Molecular Features of Colorectal Tumors in Adolescents and Adults 25 Years or Younger
Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines
Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
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