Anny Devoy

King's College London — United Kingdom

Medicine · Health Sciences

18h-index2.2kcitations37works15.52yr avg
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Research Topics

Amyotrophic Lateral Sclerosis Research(22), Neurogenetic and Muscular Disorders Research(13), Prion Diseases and Protein Misfolding(7), RNA Research and Splicing(6), Genetic Neurodegenerative Diseases(4)

Publications37 total

<i>C9orf72</i> polyGA knock-in mice exhibit mild motor and proteomic changes consistent with ALS/FTD
2025Open Access
PolyGR and polyPR knock-in mice reveal a conserved neuroprotective extracellular matrix signature in C9orf72 ALS/FTD neurons
Nature Neuroscience·2024· 31 citedOpen Access
PolyGR and polyPR knock-in mice reveal a conserved neuroprotective extracellular matrix signature in <i>C9orf72</i> ALS/FTD neurons
2023Open Access
Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models
iScience·2022Open Access
Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models
iScience·2021· 15 citedOpen Access
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation
Science Advances·2021· 63 citedOpen Access
Generation, quality control, and analysis of the first genomically humanised knock-in mice for the ALS/FTD genes <i>SOD1, TARDBP</i> (TDP-43), and <i>FUS</i>
2021Open Access
The phase separation-dependent FUS interactome reveals nuclear and cytoplasmic function of liquid–liquid phase separation
Nucleic Acids Research·2021· 121 citedOpen Access
Aberrant interaction of FUS with the U1 snRNA provides a molecular mechanism of FUS induced amyotrophic lateral sclerosis
Nature Communications·2020· 79 citedOpen Access
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation
2020· 7 citedOpen Access
FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retention
Nucleic Acids Research·2020· 110 citedOpen Access
Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes
Cell Reports·2020· 89 citedOpen Access
The phase separation-dependent FUS interactome reveals nuclear and cytoplasmic function of liquid-liquid phase separation
2019· 6 citedOpen Access
<i>FUS</i> ALS-causative mutations impact <i>FUS</i> autoregulation and the processing of RNA-binding proteins through intron retention
2019· 5 citedOpen Access
ALS Mice Carrying Pathological Mutant TDP-43, But Not Mutant FUS, Display Axonal Transport Defects &lt;i&gt;in vivo&lt;/i&gt;
SSRN Electronic Journal·2019· 2 citedOpen Access
ALS mice carrying pathological mutant TDP-43, but not mutant FUS, display axonal transport defects <i>in vivo</i>
2018· 6 citedOpen Access
Knock in mouse models to understand ALS pathomechanisms
Faculty of 1000 Research Ltd·2018Open Access
Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’ knockin mice
Brain·2017· 122 citedOpen Access
Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin–proteasome system
Acta Neuropathologica·2015· 66 citedOpen Access
Regulation of Postsynaptic Function by the Dementia-Related ESCRT-III Subunit CHMP2B
Journal of Neuroscience·2015· 60 citedOpen Access
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Frequent Co-authors

Elizabeth Fisher(26), Pietro Fratta(14), Adrian M. Isaacs(10), Rosie Bunton-Stasyshyn(8), Giampietro Schiavo(7), Jack Humphrey(5), Linda Greensmith(5), Abraham Acevedo‐Arozena(5), Marc‐David Ruepp(5), Carmelo Milioto(5), Vincent Plagnol(4), Benjamin Davies(4), Oliver Mühlemann(4), Nicol Birsa(4), Agnieszka M Ule(4), Seth Jarvis(4), Cristian Bodo(4), Maria Giovanna Garone(4), Alessandro Rosa(4), Thomas J. Cunningham(4)