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Psychosocial aspects of “routine” germline sequencing in children with cancer
Phone 06 50006690

Genetic sequencing is playing an increasingly important role in scientific research and care for children with cancer. This means that an increasing number of parents and children are asked to make a choice on participation in genetic research, and more families are receiving the results of such research. Previous studies have shown that these choices can be challenging for families, and that genetic research and its outcomes can be complex. In my research, we use interviews and questionnaires to explore the experiences of parents and adolescents. Additionally, we inquire about the ideas that families have regarding how future genetic counselling should be conducted. Through our research, we aim to contribute to better information provision and support for families involved in genetic sequencing. We will also collaborate in designing the associated policies at the Princess Máxima Center. Lastly, we will develop educational materials with the involvement of parents and patients. Ultimately, we hope to support families in making choices that suit them best.

Prof. dr. Martha Grootenhuis, prof. dr. Marry van den Heuvel-Eibrink, dr. Marjolijn Jongmans, and dr. Roel Wouters are directly involved in this research project. Close collaboration is maintained with researchers in the field of genetic predisposition, primarily with prof. dr. Roland Kuiper, prof. dr. Hans Merks, dr. Janna Hol en drs. Jette Bakhuizen.

  • Exploring germline variants in genes associated with inborn errors of immunity and inherited bone marrow failure syndromes in pediatric hematological malignancies

    • aug. 2025
    • Jette J., Bakhuizen, et al
    • European Journal of Cancer
  • Parents' experiences with sequencing of all known pediatric cancer predisposition genes in children with cancer

    • jan. 2025
    • S. B.B., Bon, et al
    • Genetics in Medicine
  • Feasibility, Barriers, and Facilitators of Long-Term Physical Activity Tracking During Treatment

    • jan. 2025
    • Emma, den Hartog, et al
    • JMIR Pediatrics and Parenting
  • Comparison of clinical selection-based genetic testing with phenotype-agnostic extensive germline sequencing to diagnose genetic predisposition in children with cancer

    • okt. 2024
    • Jette J., Bakhuizen, et al
    • The Lancet Child and Adolescent Health
  • Experiences of pediatric cancer patients (age 12–18 years) with extensive germline sequencing for cancer predisposition

    • mei 2024
    • Sebastian B.B., Bon, et al
    • European Journal of Human Genetics
View all publications