Sian Morgan
3PUBLICATIONS
22CO-AUTHORS
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Publications (3)
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|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
|Sep 02, 2020
Cytogenomic results following high-chance non-invasive prenatal testing: a UK national audit.Fiona S Togneri, Stephanie K Allen, Kathy Mann
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Frequent Collaborators
2 joint publications
Karoline Freeman
2 joint publications
Jacqueline Dinnes
2 joint publications
Bethany Shinkins
2 joint publications
Corinna Clark
2 joint publications
Katie Scandrett
2 joint publications
Felicity Kate Boardman
2 joint publications
Sian Taylor-Phillips
2 joint publications
Yemisi Takwoingi
2 joint publications
David Elliman
2 joint publications
Cristina Visintin
