Chantal Bogaard Stoepker

Chantal Bogaard-Stoepker

Postdoctoral fellow

+31 20 512 7978 Hein Te Riele

I completed a MSc in Oncology, followed by a PhD at the VU University Medical Center, where I worked on the cancer predisposition syndrome Fanconi anemia (FA). We identified mutations in SLX4 as causative for a subtype of FA and I investigated the FA DNA repair pathway in sporadic head and neck cancer. As a postdoctoral fellow at the Leiden University Medical Center, I continued working in the field of DNA repair.

Now at the NKI, my project aims to improve and help implement a diagnostic test to classify disease-causing mutations in Lynch syndrome, a form of hereditary colorectal cancer.

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