John Collinge, BSc, MB, ChB, MD, FRCP, FRS

Affiliations: 
Neurodegenerative Diseases University College London, London, United Kingdom 
Area:
http://www.biomedexperts.com/Profile.bme/255990/John_Collinge
Website:
http://www.ion.ucl.ac.uk/departments/neurodegeneration
Google:
"John Collinge"
Bio:

http://www.ucl.ac.uk/neuroscience/Page.php?ID=12&ResearcherID=35

Cross-listing: Neurotree - Neuropathology Tree

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Publications

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Rostgaard N, Roos P, Budtz-Jørgensen E, et al. (2017) TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3). Neurobiology of Aging
Wadsworth JDF, Adamson G, Joiner S, et al. (2017) Methods for Molecular Diagnosis of Human Prion Disease. Methods in Molecular Biology (Clifton, N.J.). 1658: 311-346
Sims R, van der Lee SJ, Naj AC, et al. (2017) Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics
Kenny J, Woollacott I, Koriath C, et al. (2017) A novel prion protein variant in a patient with semantic dementia. Journal of Neurology, Neurosurgery, and Psychiatry
Mok T, Jaunmuktane Z, Joiner S, et al. (2017) Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129. The New England Journal of Medicine. 376: 292-294
Luk C, Jones S, Thomas C, et al. (2016) Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine. Jama Neurology
Collinge J, Jaunmuktane Z, Mead S, et al. (2016) Collinge et al. reply. Nature. 537: E7-9
Franko E, Wehner T, Joly O, et al. (2016) Quantitative EEG parameters correlate with the progression of human prion diseases. Journal of Neurology, Neurosurgery, and Psychiatry
Collinge J, Jaunmuktane Z, Mead S, et al. (2016) Collinge et al. reply. Nature. 535: E2-3
Properzi F, Badhan A, Klier S, et al. (2016) Physical, chemical and kinetic factors affecting prion infectivity. Prion. 0
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