Sarah Dyack

3PUBLICATIONS
29CO-AUTHORS
Gene mappingRecommender systemsInfant and child health
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Publications (3)

|Aug 26, 2026
Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.

|Oct 21, 2024
Barriers and facilitators to designing, maintaining, and utilizing rare disease patient registries: a scoping review protocol.

Catherine Stratton, Andrew Taylor, Menelaos Konstantinidis

|Aug 27, 2021
Detection of Early Onset Carnitine Palmitoyltransferase II Deficiency by Newborn Screening: Should CPT II Deficiency Be a Primary Disease Target?

Rachel Mador-House, Zaiping Liu, Sarah Dyack

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Frequent Collaborators

1 joint publications

Rachel Mador-House

1 joint publications

Catherine Stratton

1 joint publications

Menelaos Konstantinidis

1 joint publications

Ian Stedman