| The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study J Phukan, M Elamin, P Bede, N Jordan, L Gallagher, S Byrne, C Lynch, ... Journal of Neurology, Neurosurgery & Psychiatry 83 (1), 102-108, 2012 | 802 | 2012 |
| Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study S Byrne, M Elamin, P Bede, A Shatunov, C Walsh, B Corr, M Heverin, ... The Lancet Neurology 11 (3), 232-240, 2012 | 582 | 2012 |
| Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis S Byrne, C Walsh, C Lynch, P Bede, M Elamin, K Kenna, R McLaughlin, ... Journal of Neurology, Neurosurgery & Psychiatry 82 (6), 623-627, 2011 | 488 | 2011 |
| Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia M Elamin, J Phukan, P Bede, N Jordan, S Byrne, N Pender, O Hardiman Neurology 76 (14), 1263-1269, 2011 | 366 | 2011 |
| Cognitive changes predict functional decline in ALS: a population-based longitudinal study M Elamin, P Bede, S Byrne, N Jordan, L Gallagher, B Wynne, C O’Brien, ... Neurology 80 (17), 1590-1597, 2013 | 339 | 2013 |
| A multidisciplinary clinic approach improves survival in ALS: a comparative study of ALS in Ireland and Northern Ireland J Rooney, S Byrne, M Heverin, K Tobin, A Dick, C Donaghy, O Hardiman Journal of Neurology, Neurosurgery & Psychiatry 86 (5), 496-501, 2015 | 253 | 2015 |
| Anti-N-methyl-d-aspartate receptor encephalitis: review of clinical presentation, diagnosis and treatment H Barry, S Byrne, E Barrett, KC Murphy, DR Cotter BJPsych Bulletin 39 (1), 19-23, 2015 | 236 | 2015 |
| Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing KP Kenna, RL McLaughlin, S Byrne, M Elamin, M Heverin, EM Kenny, ... Journal of medical genetics 50 (11), 776-783, 2013 | 205 | 2013 |
| Multiparametric MRI study of ALS stratified for the C9orf72 genotype P Bede, ALW Bokde, S Byrne, M Elamin, RL McLaughlin, K Kenna, ... Neurology 81 (4), 361-369, 2013 | 192 | 2013 |
| Basal ganglia involvement in amyotrophic lateral sclerosis P Bede, M Elamin, S Byrne, RL McLaughlin, K Kenna, A Vajda, N Pender, ... Neurology 81 (24), 2107-2115, 2013 | 188 | 2013 |
| Proposed criteria for familial amyotrophic lateral sclerosis S Byrne, P Bede, M Elamin, K Kenna, C Lynch, R McLaughlin, ... Amyotrophic Lateral Sclerosis 12 (3), 157-159, 2011 | 171 | 2011 |
| Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism D Ebrahimi-Fakhari, A Saffari, L Wahlster, J Lu, S Byrne, GF Hoffmann, ... Brain 139 (2), 317-337, 2016 | 167 | 2016 |
| Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality P Bede, A Bokde, M Elamin, S Byrne, RL McLaughlin, N Jordan, ... Journal of Neurology, Neurosurgery & Psychiatry 84 (7), 766-773, 2013 | 167 | 2013 |
| Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: A population‐based case–control cohort study of familial and sporadic … S Byrne, M Heverin, M Elamin, P Bede, C Lynch, K Kenna, ... Annals of neurology 74 (5), 699-708, 2013 | 151 | 2013 |
| Earlier treatment of NMDAR antibody encephalitis in children results in a better outcome S Byrne, C Walsh, Y Hacohen, E Muscal, J Jankovic, A Stocco, RC Dale, ... Neuroimmunology & Neuroinflammation 2 (4), e130, 2015 | 139 | 2015 |
| EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy S Byrne, L Jansen, JM U-King-Im, A Siddiqui, HGW Lidov, I Bodi, L Smith, ... Brain 139 (3), 765-781, 2016 | 133 | 2016 |
| Pediatric ischemic stroke: an infrequent complication of SARS‐CoV‐2 LA Beslow, AB Linds, CK Fox, M Kossorotoff, YC Zuniga Zambrano, ... Annals of neurology 89 (4), 657-665, 2021 | 105 | 2021 |
| Survival analysis of Irish amyotrophic lateral sclerosis patients diagnosed from 1995–2010 J Rooney, S Byrne, M Heverin, B Corr, M Elamin, A Staines, B Goldacre, ... PloS one 8 (9), e74733, 2013 | 99 | 2013 |
| Absence of consensus in diagnostic criteria for familial neurodegenerative diseases S Byrne, M Elamin, P Bede, O Hardiman Journal of Neurology, Neurosurgery & Psychiatry 83 (4), 365-367, 2012 | 86 | 2012 |
| Vici syndrome: a review S Byrne, C Dionisi-Vici, L Smith, M Gautel, H Jungbluth Orphanet Journal of Rare Diseases 11, 1-9, 2016 | 79 | 2016 |