researcher · Stuart Pickering-Brown · YYNN

Stuart Pickering-Brown

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researcher

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Works
8

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

scientific article

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

scientific article

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

scientific article

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

scientific article

Extracellular Vesicles Isolated from Human Induced Pluripotent Stem Cell-Derived Neurons Contain a Transcriptional Network

scientific article published on 02 May 2020

Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

scientific article published on 02 February 2017

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

scientific article published on 11 January 2008

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)

scientific article

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Websitepureprojects.ppad.man.ac.uk

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