Homologous recombination deficiency gene panel analysis results in synchronous endometrial and ovarian cancers
Pathogenic variations confirming the diagnosis of synchronous endometrial ovarian cancer with genetic alterations were identified in all but one case. ATM gene mutation emerged as the most common alteration and has a potential association with a favorable prognosis.
Authors
- Mehmet Anıl Onan (ORCID: https://orcid.org/0000-0001-7643-1585)
- Zerrin Yılmaz (ORCID: https://orcid.org/0000-0001-9158-220X)
- Feride İffet Şahin (ORCID: https://orcid.org/0000-0001-7308-9673)
- Mert Polat (ORCID: https://orcid.org/0000-0002-9555-4932)
- Ferah Kazancı (ORCID: https://orcid.org/0000-0002-3910-0821)
- Ferhat Karademir (ORCID: https://orcid.org/0009-0001-6477-0982)
- Ozlem Erdem (ORCID: https://orcid.org/0000-0002-8396-458X)
Institutions
- Başkent University (TR)
- Acıbadem University (TR)
- Gazi University (TR)
Publication Details
- Journal
- Revista da Associação Médica Brasileira
- Published
- 2024-09-30
- DOI
- https://doi.org/10.1590/1806-9282.20240534
- Citations
- 2
- Primary Topic
- PARP inhibition in cancer therapy
- Type
- article
- Field-Weighted Citation Impact
- 0.57
Funders
- Baskent Üniversitesi