Elizabeth Mary Claire Fisher, PhD, FMedSci, FRSB
Affiliations: | 1990- | Neurodegenerative Disease | UCL Institute of Neurology, Queen Square, London, England, United Kingdom |
Area:
Neuromuscular disorders, Neurodegenerative disorders, Neurogenetics, Down syndromeWebsite:
https://iris.ucl.ac.uk/iris/browse/profile?upi=EMCFI97Google:
"Elizabeth Fisher"Bio:
https://en.m.wikipedia.org/wiki/Elizabeth_Fisher_(neuroscientist)
Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Stephen D. M. Brown | grad student | MRC - Harwell | ||
| (Source:) | ||||
| Mary F. Lyon | grad student | 1983-1986 | MRC Harwell | |
| (Source: https://iris.ucl.ac.uk/iris/browse/profile?upi=EMCFI97) | ||||
| David C. Page | post-doc | 1987-1990 | Whitehead Institute (MIT) (Cell Biology Tree) | |
| (Source: https://iris.ucl.ac.uk/iris/browse/profile?upi=EMCFI97) | ||||
Collaborators
Sign in to add collaborator| Victor Tybulewicz | collaborator | 1991- | UCL Institute of Neurology, Queen Square |
BETA: Related publications
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Publications
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| Prudencio M, Humphrey J, Pickles S, et al. (2020) Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia. The Journal of Clinical Investigation |
| Lana-Elola E, Watson-Scales S, Slender A, et al. (2020) Correction: Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel. Elife. 9 |
| Wiseman FK, Pulford LJ, Barkus C, et al. (2019) Trisomy of human chromosome 21 enhances amyloid-beta 3 deposition independently of an extra copy of APP (vol 141, pg 2457, 2018) Brain. 142 |
| Naert G, Ferré V, Keller E, et al. (2017) In vivo and ex vivo analyses of amyloid toxicity in the Tc1 mouse model of Down syndrome. Journal of Psychopharmacology (Oxford, England). 269881117743484 |
| Holmes HE, Powell NM, Ma D, et al. (2017) Comparison of In Vivo and Ex Vivo MRI for the Detection of Structural Abnormalities in a Mouse Model of Tauopathy. Frontiers in Neuroinformatics. 11: 20 |
| Wiseman FK, Pulford LJ, Barkus C, et al. (2017) TRISOMY 21 CAUSES A DEFICIT IN LYSOSOMAL CATHEPSINS AND ALTERS APP/Aβ PROCESSING, INDEPENDENTLY OF AN EXTRA COPY OF APP Alzheimers & Dementia. 13 |
| Qiu J, McQueen J, Bilican B, et al. (2016) Evidence for evolutionary divergence of activity-dependent gene expression in developing neurons. Elife. 5 |
| Powell NM, Modat M, Cardoso MJ, et al. (2016) Fully-Automated μMRI Morphometric Phenotyping of the Tc1 Mouse Model of Down Syndrome. Plos One. 11: e0162974 |
| Buss L, Fisher E, Hardy J, et al. (2016) Intracerebral haemorrhage in Down syndrome: protected or predisposed? F1000research. 5 |
| Peiris H, Duffield MD, Fadista J, et al. (2016) A Syntenic Cross Species Aneuploidy Genetic Screen Links RCAN1 Expression to β-Cell Mitochondrial Dysfunction in Type 2 Diabetes. Plos Genetics. 12: e1006033 |