Anne van Herwijnen

Anne van Herwijnen

I know how important knowledge of hereditary predisposition to cancer can be. This is why I think it is so important that comprehensive patient reports include precisely that carrier information, if the patient wishes to be informed of it.

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SAGE: New algorithm for analysis of tumor DNA reveals mutations previously not found

SAGE: New algorithm for analysis of tumor DNA reveals mutations previously not found

23-07-2020

At Hartwig we “analyse sequenced tumor DNA”. This is something we try to continuously improve. These analyses are shared with …

Collaboration between Hartwig and CKB makes both parties stronger 

Collaboration between Hartwig and CKB makes both parties stronger 

13-06-2023

Hartwig Medical Foundation has worked with The Jackson Laboratory (JAX) Clinical Knowledgebase (CKB) team since 2020, to the benefit of …

Whole genome sequencing to improve individual cancer treatment in Finland

Whole genome sequencing to improve individual cancer treatment in Finland

10-07-2020

Since August 2019, Docrates, a private cancer center in Finland, uses the whole genome sequencing test from Hartwig Medical Foundation to …

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