| Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis BN Smith, SD Topp, C Fallini, H Shibata, HJ Chen, C Troakes, A King, ... Science translational medicine 9 (388), eaad9157, 2017 | 151 | 2017 |
| Novel mutations support a role for Profilin 1 in the pathogenesis of ALS BN Smith, C Vance, EL Scotter, C Troakes, CH Wong, S Topp, ... Neurobiology of aging 36 (3), 1602. e17-1602. e27, 2015 | 117 | 2015 |
| Non-nuclear pool of splicing factor SFPQ regulates axonal transcripts required for normal motor development S Thomas-Jinu, PM Gordon, T Fielding, R Taylor, BN Smith, V Snowden, ... Neuron 94 (2), 322-336. e5, 2017 | 83 | 2017 |
| ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function M de Majo, SD Topp, BN Smith, AL Nishimura, HJ Chen, AS Gkazi, ... Neurobiology of aging 71, 266. e1-266. e10, 2018 | 76 | 2018 |
| The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients CH Wong, S Topp, AS Gkazi, C Troakes, JW Miller, M de Majo, J Kirby, ... Neurobiology of Aging 36 (10), 2908. e17-2908. e18, 2015 | 24 | 2015 |
| C9ORF72 and UBQLN2 mutations are causes of amyotrophic lateral sclerosis in New Zealand: a genetic and pathologic study using banked human brain tissue EL Scotter, L Smyth, CH Wong, M de Majo, CA Vance, BJ Synek, C Turner, ... Neurobiology of aging 49, 214. e1-214. e5, 2017 | 23 | 2017 |
| A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay M Gotkine, M de Majo, CH Wong, SD Topp, R Michaelson-Cohen, ... Neurobiology of Aging 106, 1-6, 2021 | 3 | 2021 |
| Genome-scale requirements for dynein-based transport revealed by a high-content arrayed CRISPR screen CH Wong, SW Wingett, C Qian, MR Hunter, JM Taliaferro, ... Journal of Cell Biology 223 (5), e202306048, 2024 | 1 | 2024 |
| Genome-scale requirements for dynein-based trafficking revealed by a high-content arrayed CRISPR screen CH Wong, SW Wingett, C Qian, JM Taliaferro, D Ross-Thriepland, ... bioRxiv, 2023 | 1 | 2023 |
| Characterisation of ARPP21 as a novel causative gene for amyotrophic lateral sclerosis CH Wong King's College London, 2018 | | 2018 |
