Emily Woods

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 8

Top Topics

Cross Sectional

Intellectual Disability

Autism Spectrum Disorder

Top Venues

Clinical genetics

American journal of medical genetics. Part A

BMJ case reports

This page only lists publications with an associated author ORCID identifier.

Publications

Emily Woods, Nicola Holmes, Shadi Albaba, Iwan Robert Evans, Meena Balasubramanian
ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism. Clinical genetics (2024)
Emily Woods, Nicola Holmes, Shadi Albaba, Iwan Robert Evans, Meena Balasubramanian
ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism. Clinical genetics 105 (5) (2024)
Emily Woods, Nicola Holmes, Shadi Albaba, Iwan Robert Evans, Meena Balasubramanian
ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism. Clinical genetics 105 (5) (2024)
Emily Woods, Nicola Holmes, Shadi Albaba, Iwan Robert Evans, Meena Balasubramanian
ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism. Clinical genetics 105 (5) (2024)
Emily Woods, Imogen Marson, Emanuele Coci, Michael Spiller, Ajith Kumar, Angela Brady, Tessa Homfray, Richard Fisher, Peter Turnpenny, Julia Rankin, Farah Kanani, Konrad Platzer, Athina Ververi, Eleftheria Emmanouilidou, Nourxan Bourboun, George Giannakoulas, Meena Balasubramanian
Expanding the phenotype of TAB2 variants and literature review. American journal of medical genetics. Part A 188 (11) (2022)
Schaida Schirwani, Emily Woods, David A Koolen, Charlotte W Ockeloen, Sally Ann Lynch, Karl Kavanagh, John M Graham, Katheryn Grand, Tyler Mark Pierson, Jeffrey M Chung, Meena Balasubramanian
Familial Bainbridge-Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotype. American journal of medical genetics. Part A (2022)
Emily Woods, Michael Spiller, Meena Balasubramanian
Report of two children with global developmental delay in association with de novo TLK2 variant and literature review. American journal of medical genetics. Part A (2021)
Emily Woods, Charlotte Dawson, Latha Senthil, Tarekegn Geberhiwot
Cerebral venous thrombosis as the first presentation of classical homocystinuria in an adult patient. BMJ case reports 2017 (2017)