Alisdair McNeill (A McNeill, Alisdair McNeil)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 12

Top Topics

Systematic Review

Intellectual Disability

Gene Expression

Cross Sectional

Top Venues

American journal of medical genetics. Part A

Journal of medical genetics

Multiple sclerosis international

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

Publications

Jade Howard, Hilary L Bekker, Christopher J McDermott, Alisdair McNeill
Survey of service needs to embed genome sequencing for motor neuron disease in neurology in the English National Health Service. Journal of medical genetics (2024)
Jade Howard, Hilary L Bekker, Christopher J McDermott, Alisdair McNeill
Survey of service needs to embed genome sequencing for motor neuron disease in neurology in the English National Health Service. Journal of medical genetics 61 (7) (2024)
Jade Howard, Hilary L Bekker, Christopher J McDermott, Alisdair McNeill
Survey of service needs to embed genome sequencing for motor neuron disease in neurology in the English National Health Service. Journal of medical genetics 61 (7) (2024)
Jade Howard, Hilary L Bekker, Christopher J McDermott, Alisdair McNeill
Survey of service needs to embed genome sequencing for motor neuron disease in neurology in the English National Health Service. Journal of medical genetics 61 (7) (2024)
H Smith, R Al-Jawahiri, L Stokes, M Freeth, S Fricke, D Matthews, Alisdair McNeill
Impaired communication ability in SOX11 syndrome. Journal of intellectual disability research : JIDR (2023)
Katharine Edgerley, Lisa Bryson, Lucy Hanington, Rachel Irving, Shelagh Joss, Anne Lampe, Isabelle Maystadt, Deborah Osio, Ruth Richardson, Miranda Split, Francis H Sansbury, Ingrid Scurr, Helen Stewart, Alisdair McNeill, Karen Jaqueline Low
SOX5: Lamb-Shaffer syndrome-A case series further expanding the phenotypic spectrum. American journal of medical genetics. Part A (2023)
Tarub Binshalan, Krishnan Padmakumari Sivaraman Nair, Alisdair McNeill
The Effectiveness of Physiotherapy Interventions for Mobility in Severe Multiple Sclerosis: A Systematic Review and Meta-Analysis. Multiple sclerosis international 2022 (2022)
Alisdair McNeill, Paul Aurora, Kaukab Rajput, Robert Nash, Karen Stals, Hannah Robinson, Emma Wakeling
Dominant and recessive SLC12A2-syndrome. American journal of medical genetics. Part A (2021)
Alisdair McNeill, Ruth Lewis, Megan Freeth
Views of adults with 22q11 deletion syndrome on reproductive choices. American journal of medical genetics. Part A 182 (5) (2020)
Oanh Kieu Vo, Alisdair McNeill, Katharina Sophie Vogt
The psychosocial impact of 22q11 deletion syndrome on patients and families: A systematic review. American journal of medical genetics. Part A 176 (10) (2018)
Patricia Blanchet, E Martina Bebin, Shaam Bruet, Gregory M Cooper, Michelle L Thompson, Benedicte Duban-Bedu, Benedicte Gerard, Amelie Piton, Sylvie Suckno, Charu Deshpande, Virginia Clowes, Julie Vogt, Peter Turnpenny, Michael P Williamson, Yves Alembik, null null, null null, Eric Glasgow, Alisdair McNeill
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus. PLoS genetics 13 (8) (2017)
Azeem Siddique, Josh Willoughby, null null, Alisdair McNeill
A 7q21.11 microdeletion presenting with apparent intellectual disability without epilepsy. American journal of medical genetics. Part A 173 (4) (2017)