Elizabeth Fisher - Concepedia

Author

Elizabeth Fisher

Also Known As

Atahualpa Castillo Morales, David Miller, E Fisher, E M C Fisher, E M Fisher, E. Fisher, E. M. C. Fisher, E. M. Fisher, E. M.C. Fisher, E.M. Fisher

606

Publications

32.6K

Citations

H-Index

254

Concepts

All Affiliations

University College London National Hospital for Neurology and Neurosurgery Imperial College London The Francis Crick Institute Queen Mary University of London

About

Elizabeth Fisher is an author at University College London specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	48	96	12.6K
2	Natural Sciences	10	10	786
3	Engineering	6	6	333
4	Health Sciences	5	6	563
5	Education	2	2	144

Elizabeth Fisher

190

Publications

21.6K

Citations

H-Index

Page 1

	Year	Citations
The sex-determining region of the human Y chromosome encodes a finger protein David C. Page, Rebecca A. Mosher, Elizabeth M. Simpson, Cell Human Y ChromosomeChromatinCytogeneticsGenetic DisorderGenetics	1987	843
Genealogies of mouse inbred strains J. Beck, Sarah E. Lloyd, Majid Hafezparast, Nature Genetics Knockout MouseQuantitative GeneticsMolecular EcologyMedicineGenetics	2000	830
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia Gaia Skibinski, Jeremy Brown, Lisa Chakrabarti, Nature Genetics Neurodegenerative DiseasesMolecular NeuroscienceGenetic DisorderGeneticsDementia	2005	804
Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment Derek C. Rogers, Elizabeth Fisher, Steve D. M. Brown, Mammalian Genome Knockout MouseGenotype-phenotype AssociationBehavioral NeuroscienceComprehensive Phenotype AssessmentGenetics	1997	796
<i>C9orf72</i> repeat expansions cause neurodegeneration in <i>Drosophila</i> through arginine-rich proteins Sarah Mizielinska, Sebastian Grönke, Teresa Niccoli, Science	2014	735
Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport Majid Hafezparast, Rainer Klocke, Christiana Ruhrberg, Science GeneticsRetrograde TransportCytoskeletonSocial SciencesDegenerative Disorders	2003	681
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse Patrick M. Nolan, Jo Peters, Mark Strivens, Nature Genetics Knockout MouseTransgenic Mouse ModelsGeneticsPhenotype-driven Mutagenesis ProgrammeGene Characterization	2000	655
Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease Maria Filimonenko, Susanne Stuffers, Camilla Raiborg, The Journal of Cell Biology MitophagyProtein AggregatesFunctional Multivesicular BodiesNeuroinflammationCell Autophagy	2007	623
Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse John A. Curtin, Elizabeth Quint, Vicky Tsipouri, Current Biology Molecular NeuroscienceDevelopmental BiologyGeneticsMorphogenesisNeurogenetics	2003	617
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A Anna‐Leigh Brown, Oscar G. Wilkins, Matthew J. Keuss, Nature	2022	471

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