Publications by authors named "Holly Ellard"

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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, Myra Bluebond-Langner, Celine Lewis

J Med Genet· December 2025

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Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation.
Michael P Mackley, Pankaj B Agrawal, Sara S Ali, Alison D Archibald, Belinda Dawson-McClaren, Holly Ellard

Eur J Hum Genet· November 2025

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Characteristics of parents accessing a new postmortem imaging service to diagnose miscarriage in the United Kingdom.
Holly Ellard, Celine Lewis, Ulrika Kreicbergs, Audrey Lamouroux, Owen J Arthurs

AJOG Glob Rep· November 2025

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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, Holly Ellard, Celine Lewis

J Genet Couns· August 2025

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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, Celine Lewis

Eur J Hum Genet· April 2025

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Parental knowledge, attitudes, satisfaction and decisional conflict regarding whole genome sequencing in the Genomic Medicine Service: a multisite survey study in England.
Ria Patel, Bettina Friedrich, Saskia C Sanderson, Holly Ellard, Celine Lewis

J Med Genet· March 2025

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Written communication of whole genome sequencing results in the NHS Genomic Medicine Service: a multi-centre service evaluation.
Holly Ellard, Angus Clarke, Sarah Wynn, Amanda Pichini, Celine Lewis

Eur J Hum Genet· November 2024

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