| 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 | 636 | 2002 |
| 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 | 409 | 2017 |
| Hereditary spastic paraplegias: membrane traffic and the motor pathway C Blackstone, CJ O'kane, E Reid Nature Reviews Neuroscience 12 (1), 31-42, 2011 | 349 | 2011 |
| 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 | 272 | 2009 |
| 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 | 264 | 2010 |
| 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 | 232 | 2007 |
| 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 | 228 | 2007 |
| 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 | 226 | 2005 |
| Thrombotic variables and risk of idiopathic venous thromboembolism in women aged 45-64 years G Lowe, M Woodward, M Vessey, A Rumley, P Gough, E Daly Thrombosis and haemostasis 83 (04), 530-535, 2000 | 224 | 2000 |
| 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 | 217 | 2019 |
| Different effects of oral and transdermal hormone replacement therapies on factor IX, APC resistance, t-PA, PAI and C-reactive protein GDO Lowe, MN Upton, A Rumley, A McConnachie, DSJ O’Reilly, ... Thrombosis and haemostasis 86 (08), 550-556, 2001 | 209 | 2001 |
| 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 | 197 | 2006 |
| 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 | 196 | 2006 |
| 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 | 195 | 2007 |
| 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 | 186 | 2012 |
| Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias E Reid Journal of medical genetics 40 (2), 81-86, 2003 | 176 | 2003 |
| 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 | 161 | 2013 |
| 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 | 157 | 2009 |
| Defects in ER–endosome contacts impact lysosome function in hereditary spastic paraplegia R Allison, JR Edgar, G Pearson, T Rizo, T Newton, S Günther, F Berner, ... Journal of Cell Biology 216 (5), 1337-1355, 2017 | 156 | 2017 |
| 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 | 154 | 2000 |
David RubinszteinUniversity of CambridgeAdresse e-mail validée de cam.ac.uk
