Elizabeth Fisher
Elizabeth Fisher
University College London, Institute of Neurology
Verified email at ucl.ac.uk
Cited by
Cited by
Genealogies of mouse inbred strains
JA Beck, S Lloyd, M Hafezparast, M Lennon-Pierce, JT Eppig, ...
Nature genetics 24 (1), 23-25, 2000
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
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
Genetic meta-analysis of diagnosed Alzheimerís 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
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
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
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
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
Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease
M Filimonenko, S Stuffers, C Raiborg, A Yamamoto, L Malerød, ...
The Journal of cell biology 179 (3), 485-500, 2007
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
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
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
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
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
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
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
The origins and uses of mouse outbred stocks
R Chia, F Achilli, MFW Festing, EMC Fisher
Nature genetics 37 (11), 1181-1186, 2005
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
Down syndromeórecent progress and future prospects
FK Wiseman, KA Alford, VLJ Tybulewicz, EMC Fisher
Human molecular genetics 18 (R1), R75-R83, 2009
Species-specific transcription in mice carrying human chromosome 21
MD Wilson, NL Barbosa-Morais, D Schmidt, CM Conboy, L Vanes, ...
Science 322 (5900), 434-438, 2008
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