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Neurobiology of Aging|December 16, 2014
Novel mutations support a role for Profilin 1 in the pathogenesis of ALSBradley N Smith, Caroline Vance, Emma L Scotter, et al.Neuromuscular Disorders : NMD|January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) geneHaiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.Neurobiology of Aging|June 2, 2014
Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's diseaseCeleste Sassi, Rita Guerreiro, Raphael Gibbs, et al.Acta Neuropathologica|October 5, 2011
TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotypeYvonne S Davidson, Samantha Raby, Penelope G Foulds, et al.Nature Neuroscience|August 18, 2014
Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's diseaseKatie Lunnon, Rebecca Smith, Eilis Hannon, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 10, 2009
EGFRvIII deletion mutations in pediatric high-grade glioma and response to targeted therapy in pediatric glioma cell linesDorine A Bax, Nathalie Gaspar, Suzanne E Little, et al.Acta Neuropathologica|May 21, 2017
Amyotrophic lateral sclerosis-like superoxide dismutase 1 proteinopathy is associated with neuronal loss in Parkinson's disease brainBenjamin G Trist, Katherine M Davies, Veronica Cottam, et al.Brain : a Journal of Neurology|September 13, 2011
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Jonathan M Schott, et al.Genome Research|December 23, 2016
Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network ResourceMichael J Keogh, Wei Wei, Ian Wilson, et al.Acta Neuropathologica Communications|February 4, 2017
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brainsWei Wei, Michael J Keogh, Ian Wilson, et al.Pageof 16