Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

World-leading ALS/MND research group

Overview

Motor neurons are cells which initiate and control voluntary movement. Amyotrophic lateral sclerosis (ALS), the commonest form of motor neuron disease (MND) and the third commonest form of neurodegenerative disease after Alzheimer’s and Parkinson’s, is currently incurable. We now know that it arises for a complex set of reasons, including harmful genetic variants and environmental factors.

Research

The MND research programme in Oxford uniquely spans molecular to network function of the motor system and its degeneration, led by three neurologists. Cellular work led by Professor Talbot has created novel models of ALS, investigating the effect of human genetic mutations in mice and in motor neurons derived from stem cells grown from the skin of patients with ALS. Professor Turner’s human biomarker development programme involves deep clinical phenotyping with biofluid analysis and advanced brain imaging, aimed at developing improved trial outcome measures and stratification. Associate Professor Thompson has expertise in advanced proteomics and epidemiology focused on understanding risk factors and modifiers in ALS.

Having established promising approaches for therapy development and testing in those with established disease, we are leading in the application of these techniques to people who carry genetic risk factors for ALS, but who may be some years from developing disease symptoms. This includes the ACORN and FaTHoM initiatives. Our ultimate aim is to identify the earliest changes which occur in the disease and apply protective therapies before the onset of significant disability in those at risk and those already living with ALS.

Anyone who either knows someone or works with patients with MND can understand the urgency of finding out more about the disease. The study is very organised and well explained with friendly, professional staff who were very thorough and patient. It was a pleasure to take part.An Oxford research volunteer

The foundation of our approach is that excellence in research comes from excellence in care. We are one of the major centres for international as well as UK ALS therapeutic trials. All patients attending the Oxford Motor Neuron Disease Clinic are also given the opportunity to engage in other vital research, through participation in genetic and biomarker studies. 

Selected publications

Progression and life expectancy in primary lateral sclerosis

Journal article

Lester DG. et al, (2025), Journal of Neurology, Neurosurgery & Psychiatry, 96, 1008 - 1011

Gamma activation spread reflects disease activity in amyotrophic lateral sclerosis

Journal article

Trubshaw M. et al, (2025), Clinical Neurophysiology, 177, 2110823 - 2110823

Personalised penetrance estimation for C9orf72-related amyotrophic lateral sclerosis and frontotemporal dementia

Journal article

Douglas AGL. et al, (2024), BMJ Neurology Open, 6, e000792 - e000792

Cellular and axonal transport phenotypes due to the C9ORF72 HRE in iPSC motor and sensory neurons

Journal article

Scaber J. et al, (2024), Stem Cell Reports, 19, 957 - 972

Premorbid brain structure influences risk of amyotrophic lateral sclerosis

Journal article

Thompson AG. et al, (2024), Journal of Neurology, Neurosurgery & Psychiatry, 95, 360 - 365

C9orf72-ALS human iPSC microglia are pro-inflammatory and toxic to co-cultured motor neurons via MMP9

Journal article

Vahsen BF. et al, (2023), Nature Communications, 14