Targeted genetic screening for identifying carrier status and early-onset disease risks in Chinese newborns
This large-scale study highlights the utility of targeted genetic screening for identifying carrier status and early-onset disease risks in newborns. The findings provide a critical foundation for integrating genetic screening into routine newborn care and for optimizing public health strategies.
Authors
- Feng Jin (ORCID: https://orcid.org/0000-0002-5141-3986)
- Xuyun Hu (ORCID: https://orcid.org/0000-0003-4345-5024)
- Xin Ni (ORCID: https://orcid.org/0000-0002-7781-2600)
- Ruolan Guo (ORCID: https://orcid.org/0000-0002-3378-2008)
- Chanjuan Hao (ORCID: https://orcid.org/0000-0002-9220-8356)
- Wei Li (ORCID: https://orcid.org/0000-0002-0248-5510)
- Huimin Li (ORCID: https://orcid.org/0000-0001-9105-1070)
- Limin Xie
- Zhan Qi (ORCID: https://orcid.org/0000-0002-2239-4333)
Institutions
- Capital Medical University (CN)
- Henan Provincial Institute of Occupational Health (CN)
- Henan Academy of Sciences (CN)
- Center for Children (US)
- Zhengzhou Children's Hospital (CN)
- National Center for Women and Children’s Health, China CDC (CN)
- Beijing Children’s Hospital (CN)
Publication Details
- Journal
- Communications Medicine
- Published
- 2025-11-14
- DOI
- https://doi.org/10.1038/s43856-025-01208-8
- Primary Topic
- Cystic Fibrosis Research Advances
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Beijing Municipal Health Commission
- Beijing Municipal Science and Technology Commission