| A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis AL Nishimura, M Mitne-Neto, HCA Silva, A Richieri-Costa, S Middleton, ... The American Journal of Human Genetics 75 (5), 822-831, 2004 | 1163 | 2004 |
| Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene TGA Mack nature neuroscience 4 (12), 1199-1206, 2001 | 683* | 2001 |
| Selective vulnerability of motor neurons and dissociation of pre-and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy LM Murray, LH Comley, D Thomson, N Parkinson, K Talbot, ... Human molecular genetics 17 (7), 949-962, 2008 | 415 | 2008 |
| Total protein analysis as a reliable loading control for quantitative fluorescent Western blotting SL Eaton, SL Roche, M Llavero Hurtado, KJ Oldknow, C Farquharson, ... PloS one 8 (8), e72457, 2013 | 402 | 2013 |
| Spinal muscular atrophy: going beyond the motor neuron G Hamilton, TH Gillingwater Trends in molecular medicine, 2013 | 371 | 2013 |
| Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy D Bäumer, S Lee, G Nicholson, JL Davies, NJ Parkinson, LM Murray, ... PLoS genetics 5 (12), e1000773, 2009 | 271 | 2009 |
| Emerging therapies and challenges in spinal muscular atrophy MA Farrar, SB Park, S Vucic, KA Carey, BJ Turner, TH Gillingwater, ... Annals of neurology 81 (3), 355-368, 2017 | 240 | 2017 |
| Synaptic vulnerability in neurodegenerative disease TM Wishart, SH Parson, TH Gillingwater Journal of Neuropathology & Experimental Neurology 65 (8), 733-739, 2006 | 235 | 2006 |
| Advances in therapy for spinal muscular atrophy: promises and challenges EJN Groen, K Talbot, TH Gillingwater Nature Reviews Neurology 14 (4), 214-224, 2018 | 214 | 2018 |
| Cellular and molecular anatomy of the human neuromuscular junction RA Jones, C Harrison, SL Eaton, ML Hurtado, LC Graham, L Alkhammash, ... Cell reports 21 (9), 2348-2356, 2017 | 192 | 2017 |
| Dysregulation of ubiquitin homeostasis and β-catenin signaling promote spinal muscular atrophy TM Wishart, CA Mutsaers, M Riessland, MM Reimer, G Hunter, ... The Journal of clinical investigation 124 (4), 1821-1834, 2014 | 192 | 2014 |
| Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation RR Ribchester, D Thomson, NI Wood, T Hinks, TH Gillingwater, ... European Journal of Neuroscience 20 (11), 3092-3114, 2004 | 187 | 2004 |
| VAPB interacts with and modulates the activity of ATF6 C Gkogkas, S Middleton, AM Kremer, C Wardrope, M Hannah, ... Human molecular genetics 17 (11), 1517-1526, 2008 | 184 | 2008 |
| WldS prevents axon degeneration through increased mitochondrial flux and enhanced mitochondrial Ca2+ buffering MA Avery, TM Rooney, JD Pandya, TM Wishart, TH Gillingwater, ... Current Biology 22 (7), 596-600, 2012 | 178 | 2012 |
| The role of survival motor neuron protein (SMN) in protein homeostasis H Chaytow, YT Huang, TH Gillingwater, KME Faller Cellular and Molecular Life Sciences 75, 3877-3894, 2018 | 161 | 2018 |
| The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy JN Sleigh, TH Gillingwater, K Talbot Disease models & mechanisms 4 (4), 457-467, 2011 | 144 | 2011 |
| Neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy LM Murray, K Talbot, TH Gillingwater Neuropathology and applied neurobiology 36 (2), 133-156, 2010 | 143 | 2010 |
| Transcriptional regulation of the AP-1 and Nrf2 target gene sulfiredoxin FX Soriano, P Baxter, LM Murray, MB Sporn, TH Gillingwater, ... Molecules and cells 27, 279-282, 2009 | 142 | 2009 |
| Synaptic NMDA receptor activity is coupled to the transcriptional control of the glutathione system PS Baxter, KFS Bell, P Hasel, AM Kaindl, M Fricker, D Thomson, ... Nature communications 6 (1), 6761, 2015 | 135 | 2015 |
| The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy mice W Mi, B Beirowski, TH Gillingwater, R Adalbert, D Wagner, D Grumme, ... Brain 128 (2), 405-416, 2005 | 135 | 2005 |
Simon ParsonVerified email at abdn.ac.uk
