Celine Lewis

39PUBLICATIONS
56CO-AUTHORS
Pacific Peoples youth and familyGene expression (incl. microarray and other genome-wide approaches)NeonatologyPsychosocial aspects of childbirth and perinatal mental healthLatin and classical Greek languages
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Publications (39)

|Jun 10, 2026
"If I go down, if I crumble, then everybody does" - identity crisis and emotional strain in parents of children with rare and undiagnosed conditions: a qualitative study.

|Dec 11, 2025
Challenges associated with disclosing results from whole genome sequencing to diagnose paediatric rare diseases: analysis of parent-clinician interactions.

Holly Ellard, Jhumana Ali, Phoebe Buxton

|Nov 29, 2025
"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.

Tara Maria Hoffmann, Bettina Friedrich, Celine Lewis

|Aug 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation.

Michael P Mackley, Pankaj B Agrawal, Sara S Ali

|Aug 06, 2025
Anxiety and quality-of-life for parents of children with undiagnosed rare conditions: A multi-site quantitative survey study.

Ria Patel, Bettina Friedrich, Saskia C Sanderson

|Apr 11, 2025
Mainstreaming genomics in the National Health Service in England: a survey to understand preparedness and confidence among paediatricians.

Rachel Griffiths, Celine Lewis

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Frequent Collaborators

16 joint publications

Melissa Hill

7 joint publications

Lyn S Chitty

5 joint publications

Kelly E Ormond

5 joint publications

Holly Ellard