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Journal of Neurology, Neurosurgery, and Psychiatry|January 7, 2016
Increased functional connectivity common to symptomatic amyotrophic lateral sclerosis and those at genetic riskRicarda A L Menke, Malcolm Proudfoot, Joanne Wuu, et al.Annals of Clinical and Translational Neurology|August 15, 2015
CSF neurofilament light chain reflects corticospinal tract degeneration in ALSRicarda A L Menke, Elizabeth Gray, Ching-Hua Lu, et al.European Journal of Neurology|May 9, 2023
Advantages of routine next-generation sequencing over standard genetic testing in the amyotrophic lateral sclerosis clinicJakub Scaber, Alexander G Thompson, Lucy Farrimond, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 28, 2024
Venous thromboembolism risk in amyotrophic lateral sclerosis: a hospital record-linkage studyRaph Goldacre, Michael Trubshaw, Eva J A Morris, et al.Brain : a Journal of Neurology|July 19, 2025
Neurodegenerative disease in C9orf72 repeat expansion carriers: population risk and effect of UNC13AJiali Gao, Andrew G L Douglas, Christos V Chalitsios, et al.Expert Opinion on Drug Discovery|March 3, 2025
Drug repurposing in amyotrophic lateral sclerosis (ALS)Emily Carroll, Jakub Scaber, Kilian V M Huber, et al.Plos Genetics|December 19, 2009
Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophyDirk Bäumer, Sheena Lee, George Nicholson, et al.Annals of Medicine|October 31, 2022
Profiling non-coding RNA expression in cerebrospinal fluid of amyotrophic lateral sclerosis patientsGreig Joilin, Elizabeth Gray, Alexander G Thompson, et al.Plos One|December 25, 2013
An eye-tracking version of the trail-making testStephen L Hicks, Rakesh Sharma, Amad N Khan, et al.Brain Communications|June 9, 2023
Limited value of serum neurofilament light chain in diagnosing amyotrophic lateral sclerosisJennifer C Davies, Thanuja Dharmadasa, Alexander G Thompson, et al.Pageof 35