Clinical utility of exome sequencing in hearing loss: a retrospective cohort study
Exome sequencing facilitates genetic diagnosis and improves the management of patients with HL in clinical practice. Identifying the etiology of HL may improve patient care, refine genetic counseling, and facilitate the estimation of recurrence risk.
Authors
- Fake Li
- Yanlin Huang (ORCID: https://orcid.org/0000-0001-6476-8973)
- Yunan Wang (ORCID: https://orcid.org/0009-0008-6065-7086)
- J. F. Jian
- Aihua Yin (ORCID: https://orcid.org/0000-0002-0324-5260)
- Xin Zhao (ORCID: https://orcid.org/0000-0002-1078-7332)
- Ling Liu
- Lihua Yu (ORCID: https://orcid.org/0000-0003-0586-3780)
- Chang Liu (ORCID: https://orcid.org/0000-0002-9306-2475)
- Yan Zhang (ORCID: https://orcid.org/0000-0003-4168-8852)
- Ying Xiong (ORCID: https://orcid.org/0000-0001-8517-7857)
- Yuan Liu (ORCID: https://orcid.org/0009-0007-0993-4458)
- Jing Wu (ORCID: https://orcid.org/0000-0001-7455-7766)
- Xingwang Wang (ORCID: https://orcid.org/0000-0001-6466-8876)
- Yiming Qi
- Yanqin You (ORCID: https://orcid.org/0000-0003-1281-0732)
- Yuanling Liu
- Li Du
- Liyuan Fang (ORCID: https://orcid.org/0009-0003-9912-1098)
- Yukun Zeng
- Hongke Ding
- Anpeng Fu
Institutions
- Chinese PLA General Hospital (CN)
- Guangdong Province Women and Children Hospital (CN)
Publication Details
- Journal
- Frontiers in Genetics
- Published
- 2025-09-10
- DOI
- https://doi.org/10.3389/fgene.2025.1643537
- Citations
- 1
- Primary Topic
- Hearing, Cochlea, Tinnitus, Genetics
- Type
- article
- Field-Weighted Citation Impact
- 1.46
Funders
- National Key Research and Development Program of China