Prenatal diagnostic value of medium-coverage WGS and clinical Exome sequencing in fetal congenital heart disease
Integrating CMA-seq and CES enhances prenatal CHD diagnosis by uncovering genetic etiologies, improving accuracy, and supporting personalized management strategies.
Authors
- Yuanhang Zhu (ORCID: https://orcid.org/0000-0002-0996-7926)
- Wei Victor Zhang
- Yuan Tian (ORCID: https://orcid.org/0000-0003-1419-4806)
- Xuewen Yang (ORCID: https://orcid.org/0000-0002-9420-1625)
- Xuezhe Ouyang
- Lei Xu (ORCID: https://orcid.org/0000-0002-6585-829X)
- Ling Liu (ORCID: https://orcid.org/0000-0003-0426-2414)
- Yunxiao Zhi
- Ying Li (ORCID: https://orcid.org/0000-0003-0166-6528)
- Jinghua Li (ORCID: https://orcid.org/0000-0003-0533-9890)
- Qian Zhang (ORCID: https://orcid.org/0000-0001-5975-9781)
Institutions
- ID Genomics (United States) (US)
- Third Affiliated Hospital of Zhengzhou University (CN)
Publication Details
- Journal
- Future Science OA
- Published
- 2025-11-07
- DOI
- https://doi.org/10.1080/20565623.2025.2570035
- Primary Topic
- Congenital heart defects research
- Type
- article
- Field-Weighted Citation Impact
- 0.00