Evaluating the Implementation of the Rapid Prenatal Exome Sequencing Service in England
We have identified multiple barriers and facilitators that are associated with implementing a major change to genomic services in a complex national healthcare system. This study highlights which models of pES may work in practice and why. Findings will inform future development of the pES service.
Authors
- Holly Walton (ORCID: https://orcid.org/0000-0002-8746-059X)
- Naomi Fulop (ORCID: https://orcid.org/0000-0001-5306-6140)
- Stephanie K. Allen (ORCID: https://orcid.org/0000-0003-1511-613X)
- Lyn S. Chitty (ORCID: https://orcid.org/0000-0002-4857-7138)
- Melissa K. Hill (ORCID: https://orcid.org/0000-0003-3900-1425)
- Hannah McInnes‐Dean (ORCID: https://orcid.org/0000-0002-5204-0069)
- Rhiannon Mellis (ORCID: https://orcid.org/0000-0001-9905-0654)
- Michelle Peter (ORCID: https://orcid.org/0000-0002-4977-8708)
- Morgan Daniel (ORCID: https://orcid.org/0000-0002-4455-5521)
Institutions
- Great Ormond Street Hospital (GB)
- Great Ormond Street Hospital for Children NHS Foundation Trust (GB)
- Wessex Regional Genetics Laboratory (GB)
- University College London (GB)
Publication Details
- Journal
- Public Health Genomics
- Published
- 2024-12-12
- DOI
- https://doi.org/10.1159/000543104
- Citations
- 7
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 7.76
Funders
- National Institute for Health and Care Research
- Great Ormond Street Institute of Child Health
- Health Services and Delivery Research Programme