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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.
Acta Neuropathologica|July 3, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementiaPietro Fratta, Mark Poulter, Tammaryn Lashley, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Neurology|September 2, 2016
Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementiaJonathan D Rohrer, Ione O C Woollacott, Katrina M Dick, et al.
Neurobiology of Aging|September 28, 2015
Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's diseaseNatalie S Ryan, Geert-Jan Biessels, Lois Kim, et al.
Acta Neuropathologica|November 4, 2025
Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivoElizabeth Hill, Mitali Patel, Juan M Ribes, et al.
Brain : a Journal of Neurology|April 23, 2021
Plasma amyloid-β ratios in autosomal dominant Alzheimer's disease: the influence of genotypeAntoinette O'Connor, Josef Pannee, Teresa Poole, et al.
Molecular Psychiatry|July 16, 2020
Plasma phospho-tau181 in presymptomatic and symptomatic familial Alzheimer's disease: a longitudinal cohort studyAntoinette O'Connor, Thomas K Karikari, Teresa Poole, 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.
The New England Journal of Medicine|November 15, 2013
A novel prion disease associated with diarrhea and autonomic neuropathySimon Mead, Sonia Gandhi, Jon Beck, et al.
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