Corinna Clark

7PUBLICATIONS
28CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Development cooperationEpigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|Apr 09, 2026
Acceptability of newborn screening for spinal muscular atrophy: views of the UK public, screened families, health professionals and the SMA community.

Felicity Boardman, Rebecca Howitt, Philip Young

|Dec 08, 2025
Evaluating whole genome sequencing for rare diseases in newborn screening: evidence synthesis from a series of systematic reviews.

Karoline Freeman, Jacqueline Dinnes, Bethany Shinkins

|Dec 01, 2025
Challenges in evaluating whole genome sequencing for newborn screening: series of systematic reviews and roadmap for evidence generation for policy advisers.

Karoline Freeman, Dylan Taylor, Jacqueline Dinnes

|Mar 07, 2025
Development of an Online Scenario-Based Tool to Enable Research Participation and Public Engagement in Cystic Fibrosis Newborn Screening: Mixed Methods Study.

Louise Moody, Samantha Clarke, Matt Compton

|Apr 23, 2024
International Perspectives of Extended Genetic Sequencing When Used as Part of Newborn Screening to Identify Cystic Fibrosis.

Corinna C A Clark, Pru Holder, Felicity K Boardman

|Feb 23, 2024
Stakeholder Views of the Proposed Introduction of Next Generation Sequencing into the Cystic Fibrosis Screening Protocol in England.

Pru Holder, Corinna C Clark, Louise Moody

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Frequent Collaborators

7 joint publications

Felicity Kate Boardman

3 joint publications

Pru Holder

3 joint publications

Louise Moody

3 joint publications

James R Bonham