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Nature Communications|June 10, 2011
Interaction between prion protein and toxic amyloid β assemblies can be therapeutically targeted at multiple sitesDarragh B Freir, Andrew J Nicoll, Igor Klyubin, et al.BMJ (Clinical Research Ed.)|October 17, 2013
Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale surveyO Noel Gill, Yvonne Spencer, Angela Richard-Loendt, et al.Brain : a Journal of Neurology|January 27, 2025
Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genesFahri Küçükali, Elizabeth Hill, Tijs Watzeels, et al.Plos One|July 30, 2024
Genome wide association study of clinical duration and age at onset of sporadic CJDHolger Hummerich, Helen Speedy, Tracy Campbell, et al.Journal of Alzheimer'S Disease : JAD|February 6, 2013
Genetic influences on atrophy patterns in familial Alzheimer's disease: a comparison of APP and PSEN1 mutationsRachael I Scahill, Gerard R Ridgway, Jonathan W Bartlett, et al.The Lancet. Neurology|October 26, 2016
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case seriesNatalie S Ryan, Jennifer M Nicholas, Philip S J Weston, et al.Human Brain Mapping|February 11, 2014
Profiles of white matter tract pathology in frontotemporal dementiaColin J Mahoney, Gerard R Ridgway, Ian B Malone, et al.Nature Genetics|October 16, 2012
A common single-nucleotide variant in T is strongly associated with chordomaNischalan Pillay, Vincent Plagnol, Patrick S Tarpey, et al.The Lancet. Neurology|February 20, 2021
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob diseasePeter Hermann, Brian Appleby, Jean-Philippe Brandel, et al.The Journal of Infectious Diseases|January 27, 2021
Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and MooseJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.Pageof 36