Sarah Wynn

8PUBLICATIONS
50CO-AUTHORS
Disease surveillanceEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsMolecular targets
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Publications (8)

|Jul 28, 2026
Reducing the diagnostic odyssey in rare disease: why screening is not the only answer.

|Apr 29, 2026
Optimising rapid prenatal exome sequencing in the NHS genomic medicine service: the EXPRESS Synopsis.

|Oct 14, 2025
Parental Use of Social Media and the Internet in the Context of Their Child's Genetic Neurodevelopmental Disorder: Mixed Methods Study Nested in the GenROC Cohort Study.

Karen Jaqueline Low, Georgia Treneman-Evans, Sarah L Wynn

|Jul 05, 2025
The Promise and Challenges of Genomics for Patients and Families Affected by Rare Conditions.

Claire A Andersen, Anna L Pelling, Sarah L Wynn

|Oct 03, 2024
Equity and timeliness as factors in the effectiveness of an ethical prenatal sequencing service: reflections from parents and professionals.

Michelle Peter, Melissa Hill, Jane Fisher

|Jun 19, 2024
Exploring the benefits, harms and costs of genomic newborn screening for rare diseases.

Emma L Baple, Richard H Scott, Siddharth Banka

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Frequent Collaborators

2 joint publications

Irene Y Y Szeto

2 joint publications

Michael Parker

2 joint publications

Melissa Hill

2 joint publications

Tiffany Y K Au