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Evan Reid
Evan Reid
Professor of Neurogenetics and Molecular Neurobiology, University of Cambridge
Verified email at cam.ac.uk
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Cited by
Year
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)
E Reid, M Kloos, A Ashley-Koch, L Hughes, S Bevan, IK Svenson, ...
The American Journal of Human Genetics 71 (5), 1189-1194, 2002
6042002
Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease
KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ...
The American Journal of Human Genetics 100 (1), 75-90, 2017
3602017
Hereditary spastic paraplegias: membrane traffic and the motor pathway
C Blackstone, CJ O'kane, E Reid
Nature Reviews Neuroscience 12 (1), 31-42, 2011
3272011
Spastin couples microtubule severing to membrane traffic in completion of cytokinesis and secretion
JW Connell, C Lindon, JP Luzio, E Reid
Traffic 10 (1), 42-56, 2009
2632009
Spastin couples microtubule severing to membrane traffic in completion of cytokinesis and secretion
JW Connell, C Lindon, JP Luzio, E Reid
Traffic 10 (1), 42-56, 2009
2632009
The cargo-selective retromer complex is a recruiting hub for protein complexes that regulate endosomal tubule dynamics
ME Harbour, SYA Breusegem, R Antrobus, C Freeman, E Reid, ...
Journal of cell science 123 (21), 3703-3717, 2010
2472010
Idiopathic Epilepsies with Seizures Precipitated by Fever and SCN1A Abnormalities
C Marini, D Mei, T Temudo, AR Ferrari, D Buti, C Dravet, AI Dias, ...
Epilepsia 48 (9), 1678-1685, 2007
2242007
Idiopathic Epilepsies with Seizures Precipitated by Fever and SCN1A Abnormalities
C Marini, D Mei, T Temudo, AR Ferrari, D Buti, C Dravet, AI Dias, ...
Epilepsia 48 (9), 1678-1685, 2007
2242007
The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B
E Reid, J Connell, TL Edwards, S Duley, SE Brown, CM Sanderson
Human molecular genetics 14 (1), 19-38, 2005
2192005
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia
PN Valdmanis, IA Meijer, A Reynolds, A Lei, P MacLeod, D Schlesinger, ...
The American Journal of Human Genetics 80 (1), 152-161, 2007
2042007
Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners
CM Sanderson, JW Connell, TL Edwards, NA Bright, S Duley, ...
Human molecular genetics 15 (2), 307-318, 2006
1922006
A systematic analysis of human CHMP protein interactions: additional MIT domain-containing proteins bind to multiple components of the human ESCRT III complex
HTH Tsang, JW Connell, SE Brown, A Thompson, E Reid, CM Sanderson
Genomics 88 (3), 333-346, 2006
1892006
Drosophila spichthyin inhibits BMP signaling and regulates synaptic growth and axonal microtubules
X Wang, WR Shaw, HTH Tsang, E Reid, CJ O'Kane
Nature neuroscience 10 (2), 177-185, 2007
1882007
Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias
E Reid
Journal of medical genetics 40 (2), 81-86, 2003
1802003
Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches
S Shribman, E Reid, AH Crosby, H Houlden, TT Warner
The Lancet Neurology 18 (12), 1136-1146, 2019
1662019
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12
G Montenegro, AP Rebelo, J Connell, R Allison, C Babalini, M D’Aloia, ...
The Journal of clinical investigation 122 (2), 538-544, 2012
1662012
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis
JC Lindsey, ME Lusher, CJ McDermott, KD White, E Reid, ...
Journal of medical genetics 37 (10), 759-765, 2000
1512000
The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling
HTH Tsang, TL Edwards, X Wang, JW Connell, RJ Davies, HJ Durrington, ...
Human molecular genetics 18 (20), 3805-3821, 2009
1472009
An ESCRT–spastin interaction promotes fission of recycling tubules from the endosome
R Allison, JH Lumb, C Fassier, JW Connell, D Ten Martin, MNJ Seaman, ...
Journal of Cell Biology 202 (3), 527-543, 2013
1462013
Defects in ER–endosome contacts impact lysosome function in hereditary spastic paraplegia
R Allison, JR Edgar, G Pearson, T Rizo, T Newton, S GŁnther, F Berner, ...
Journal of Cell Biology 216 (5), 1337-1355, 2017
1372017
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