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Elizabeth Fisher
Elizabeth Fisher
University College London, Institute of Neurology
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
13135*2021
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
22802019
Genealogies of mouse inbred strains
JA Beck, S Lloyd, M Hafezparast, M Lennon-Pierce, JT Eppig, ...
Nature genetics 24 (1), 23-25, 2000
15262000
The sex-determining region of the human Y chromosome encodes a finger protein
DC Page, R Mosher, EM Simpson, EMC Fisher, G Mardon, J Pollack, ...
cell 51 (6), 1091-1104, 1987
10771987
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
G Skibinski, NJ Parkinson, JM Brown, L Chakrabarti, SL Lloyd, ...
Nature genetics 37 (8), 806-808, 2005
9992005
Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment
DC Rogers, EMC Fisher, SDM Brown, J Peters, AJ Hunter, JE Martin
Mammalian Genome 8 (10), 711-713, 1997
8841997
Mutations in dynein link motor neuron degeneration to defects in retrograde transport
M Hafezparast, R Klocke, C Ruhrberg, A Marquardt, A Ahmad-Annuar, ...
Science 300 (5620), 808-812, 2003
8332003
C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins
S Mizielinska, S Grönke, T Niccoli, CE Ridler, EL Clayton, A Devoy, ...
Science 345 (6201), 1192-1194, 2014
7742014
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse
PM Nolan, J Peters, M Strivens, D Rogers, J Hagan, N Spurr, IC Gray, ...
Nature genetics 25 (4), 440-443, 2000
7632000
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
7482021
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse
JA Curtin, E Quint, V Tsipouri, RM Arkell, B Cattanach, AJ Copp, ...
Current Biology 13 (13), 1129-1133, 2003
7122003
Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease
M Filimonenko, S Stuffers, C Raiborg, A Yamamoto, L Malerřd, ...
The Journal of cell biology 179 (3), 485-500, 2007
7022007
A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome
FK Wiseman, T Al-Janabi, J Hardy, A Karmiloff-Smith, D Nizetic, ...
Nature Reviews Neuroscience 16 (9), 564-574, 2015
5752015
A genome-wide investigation of SNPs and CNVs in schizophrenia
AC Need, D Ge, ME Weale, J Maia, S Feng, EL Heinzen, KV Shianna, ...
PLoS genetics 5 (2), e1000373, 2009
5662009
Molecular mapping of Alzheimer‐type dementia in Down's syndrome
VP Prasher, MJ Farrer, AM Kessling, EMC Fisher, RJ West, PC Barber, ...
Annals of neurology 43 (3), 380-383, 1998
5211998
An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes
A O'Doherty, S Ruf, C Mulligan, V Hildreth, ML Errington, S Cooke, ...
Science 309 (5743), 2033-2037, 2005
5192005
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
N Parkinson, PG Ince, MO Smith, R Highley, G Skibinski, PM Andersen, ...
Neurology 67 (6), 1074-1077, 2006
5182006
Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome
EMC Fisher, P Beer-Romero, LG Brown, A Ridley, JA McNeil, ...
Cell 63 (6), 1205-1218, 1990
4891990
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics
S Mead, MPH Stumpf, J Whitfield, JA Beck, M Poulter, T Campbell, ...
Science 300 (5619), 640-643, 2003
4832003
The origins and uses of mouse outbred stocks
R Chia, F Achilli, MFW Festing, EMC Fisher
Nature genetics 37 (11), 1181-1186, 2005
4812005
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