Genomic characterization of patients with colorectal cancer
These findings highlight the utility of NGS in identifying germline variants linked to hereditary CRC syndromes and emphasize the need for functional studies to assess the pathogenicity of VUS.
Authors
- Hakan Gürkan (ORCID: https://orcid.org/0000-0002-8967-6124)
- Drenushe Zhuri̇ (ORCID: https://orcid.org/0000-0002-8370-1990)
- Sinem Yalçıntepe (ORCID: https://orcid.org/0000-0002-8557-8885)
- Marwa Mahdouani (ORCID: https://orcid.org/0000-0001-7709-498X)
- Fulya Dusenkalkan
Institutions
- Trakya University (TR)
- Hôpital Farhat Hached (TN)
Publication Details
- Journal
- Hereditary Cancer in Clinical Practice
- Published
- 2025-09-26
- DOI
- https://doi.org/10.1186/s13053-025-00322-x
- Primary Topic
- Genetic factors in colorectal cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Trakya Üniversitesi