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Dilys Weijers

PhD student
The somatic mutational footprints associated with DNA repair syndromes
Telefoon 088 97 27 682

The aim of my project is to identify typical mutational patterns that occur in tumors of children with DNA repair syndromes. We focus specifically on Ataxia Telangiectasia, Bloom Syndrome, Constitutional Mismatch Repair Syndrome, Fanconi Anemia, Li-Fraumeni Syndrome and Nijmegen Breakage Syndrome. Ultimately, we hope that this knowledge will lead to better recognition of children with cancer due to underlying DNA repair syndromes and improved care and surveillance of these children.

  • Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with constitutional mismatch repair deficiency

    • dec. 2025
    • Dilys D., Weijers, et al
    • Nature communications
  • Report of the sixth meeting of the European Consortium ‘Care for CMMRD’ (C<sub>4</sub>CMMRD), Paris, France, November 16th 2022

    • nov. 2024
    • , et al
    • Familial Cancer
  • T-cell lymphoblastic lymphoma in constitutional mismatch repair deficiency (CMMRD)

    • mei 2024
    • Emma, Kroeze, et al
    • HemaSphere
  • Molecular analysis of cancer genomes in children with Lynch syndrome

    • apr. 2024
    • Dilys D., Weijers, et al
    • International journal of cancer
  • Clinical and laboratory diversity of diffuse large B-cell lymphomas in children with Nijmegen breakage syndrome

    • okt. 2023
    • Agata, Pastorczak, et al
    • Haematologica
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