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Journal of Neurology, Neurosurgery, and Psychiatry|January 15, 2018
Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brainsMichael J Keogh, Wei Wei, Juvid Aryaman, et al.Lung|August 8, 2025
Unnerving Cough in CANVAS: Cough Hypersensitivity Despite Airway Nerve DepletionBarnaby Hirons, Katherine Rhatigan, William McNulty, et al.The Lancet. Microbe|August 27, 2020
Histopathological findings and viral tropism in UK patients with severe fatal COVID-19: a post-mortem studyBrian Hanley, Kikkeri N Naresh, Candice Roufosse, et al.Acta Neuropathologica Communications|January 15, 2025
An exceptionally rare case of a diffuse midline glioma with concomitant H3.1 K27M and G34R mutations in the HIST1H3C (H3C3) geneZita Reisz, Rita Pereira, Smitha Nevis, et al.Neurobiology of Aging|September 8, 2015
The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patientsChun Hao Wong, Simon Topp, Athina Soragia Gkazi, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2014
The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite casesGesine Respondek, Maria Stamelou, Carolin Kurz, et al.Journal of Neurogenetics|January 10, 2025
The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.Neurobiology of Aging|August 9, 2014
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's diseaseCeleste Sassi, Rita Guerreiro, Raphael Gibbs, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Frequency and signature of somatic variants in 1461 human brain exomesWei Wei, Michael J Keogh, Juvid Aryaman, et al.Brain : a Journal of Neurology|February 1, 2008
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesJonathan Beck, Jonathan D Rohrer, Tracy Campbell, et al.Pageof 16