Emily Woods

9PUBLICATIONS
21CO-AUTHORS
Testing, assessment and psychometricsGene expression (incl. microarray and other genome-wide approaches)Epidemiological methodsNeurology and neuromuscular diseasesAnthropological genetics
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Publications (9)

|Dec 10, 2025
Gene-Specific Growth Charts for ASXL3 -Related Disorder.

E Woods, K J Low, T J Cole

|Oct 12, 2025
The LMSz method - an automatable scalable approach to constructing gene-specific growth charts in rare disorders.

Karen J Low, Julia Foreman, Rachel J Hobson

|Jun 24, 2025
An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical Recommendations.

E Woods, N Holmes, A S Denommé-Pichon

|Apr 21, 2025
NOTCH3 -Related Lateral Meningocele Syndrome Presenting as Radiological Copenhagen Syndrome.

Emily Woods, C Jordaan, Amaka C Offiah

|Feb 29, 2024
ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism.

Emily Woods, Nicola Holmes, Shadi Albaba

|Sep 30, 2022
Familial Bainbridge-Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotype.

Schaida Schirwani, Emily Woods, David A Koolen

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Frequent Collaborators

5 joint publications

Meena Balasubramanian

2 joint publications

Charlotte W Ockeloen

2 joint publications

Karen J Low

2 joint publications

Tim J Cole