Lewis, Celine
National Health Service · Great Ormond Street Hospital · Great Ormond Street Hospital for Children NHS Foundation Trust · University College London
7 papers on CoChatORCID 0000-0001-7169-1521
Most cited papers
- Verified
Genetic education and the challenge of genomic medicine: development of core competences to support preparation of health professionals in Europe
the members of Eurogentest Unit 6 and ESHG Education Committee, Skirton, H., Lewis, C., Kent, A., & Coviello, D. A. (2010) · European Journal of Human Genetics
Innovations in Medical EducationGenetics, Bioinformatics, and Biomedical Research
Cited by 176
- Verified
Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units
Chitty, L. S., Wright, D., Hill, M., Verhoef, T. I., Daley, R., Lewis, C., Mason, S., McKay, F., Jenkins, L., Howarth, A., et al. (2016) · BMJ
Prenatal Screening and DiagnosticsDown syndrome and intellectual disability research
Cited by 149
- Verified
Women’s Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods Study
Lewis, C., Hill, M., & Chitty, L. S. (2016) · PLOS ONE
Prenatal Screening and DiagnosticsMaternal and Perinatal Health Interventions
Cited by 85
- Verified
Living Without a Diagnosis: The Parental Experience
Lewis, C., Skirton, H., & Jones, R. (2010) · Genetic Testing and Molecular Biomarkers
Family and Disability Support ResearchGenomics and Rare Diseases
Cited by 73
- Verified
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
Peter, M., Hammond, J., Sanderson, S. C., Gurasashvili, J., Hunter, A., Searle, B., Patch, C., Chitty, L. S., Hill, M., & Lewis, C. (2022) · European Journal of Human Genetics
Genomics and Rare DiseasesEthics and Legal Issues in Pediatric Healthcare
Cited by 37
- Verified
The disequilibrium of hope: A grounded theory analysis of parents' experiences of receiving a “no primary finding” result from genome sequencing
Gurasashvili, J., Silverio, S. A., Hill, M., Peter, M., Stafford‐Smith, B., & Lewis, C. (2024) · Journal of Genetic Counseling
Genomics and Rare DiseasesEthics and Legal Issues in Pediatric Healthcare
Cited by 13
- Verified
"I don't grieve as much as I used to": A qualitative study on parents of children with rare and undiagnosed conditions navigating grief in the context of uncertainty.
Hoffmann, T. M., Friedrich, B., & Lewis, C. (2025) · Journal of Genetic Counseling
Grief, Bereavement, and Mental HealthFamily and Disability Support Research
Cited by 3
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