Holly Ellard

5PUBLICATIONS
13CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Pacific Peoples youth and familyLatin and classical Greek languages
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Publications (5)

|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

|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

|Nov 26, 2024
What does a consent conversation for whole genome sequencing look like in the NHS Genomic Medicine Service? An observational study.

Holly Ellard, Huda Alfardus, Saskia Sanderson

|May 28, 2024
Written communication of whole genome sequencing results in the NHS Genomic Medicine Service: a multi-centre service evaluation.

Holly Ellard, Angus Clarke, Sarah Wynn

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Frequent Collaborators

5 joint publications

Celine Lewis

2 joint publications

Saskia Sanderson

1 joint publications

Angus Clarke

1 joint publications

Amanda Pichini