Exploring and Expanding Secondary Findings Through Exome Sequencing in the Turkish Population
In this study, we focused on known SFs and identified additional variants that could be considered as new recommendations. While expanding the list of SFs can pose challenges during analyses and genetic counseling, a thoughtfully curated SF list has the potential to enhance patient care and improve clinical outcomes.
Authors
- Mehmet Berkay Akcan (ORCID: https://orcid.org/0000-0003-0160-0377)
- Fatma Sılan (ORCID: https://orcid.org/0000-0001-7191-2240)
- Canan Ceylan Köse (ORCID: https://orcid.org/0000-0003-3789-2607)
- Derya Kaya (ORCID: https://orcid.org/0000-0002-0948-7201)
- Kübra Müge Çelik (ORCID: https://orcid.org/0000-0002-7784-8136)
- Koray Tekin (ORCID: https://orcid.org/0009-0003-4465-2027)
Institutions
- Çanakkale Onsekiz Mart Üniversitesi (TR)
- Izmir University (TR)
Publication Details
- Journal
- Annals of Human Genetics
- Published
- 2025-02-26
- DOI
- https://doi.org/10.1111/ahg.12592
- Citations
- 1
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 1.82