| Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease D Chan, NC Fox, RI Scahill, WR Crum, JL Whitwell, G Leschziner, ... Annals of neurology 49 (4), 433-442, 2001 | 853 | 2001 |
| Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia A Cortese, R Simone, R Sullivan, J Vandrovcova, H Tariq, WY Yau, ... Nature genetics 51 (4), 649-658, 2019 | 410 | 2019 |
| Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing SM Murphy, M Laura, K Fawcett, A Pandraud, YT Liu, GL Davidson, ... Journal of Neurology, Neurosurgery & Psychiatry 83 (7), 706-710, 2012 | 398 | 2012 |
| Clinical implications of genetic advances in Charcot–Marie–Tooth disease AM Rossor, JM Polke, H Houlden, MM Reilly Nature Reviews Neurology 9 (10), 562-571, 2013 | 375 | 2013 |
| Axonal transport and neurological disease JN Sleigh, AM Rossor, AD Fellows, AP Tosolini, G Schiavo Nature Reviews Neurology 15 (12), 691-703, 2019 | 250 | 2019 |
| The distal hereditary motor neuropathies AM Rossor, B Kalmar, L Greensmith, MM Reilly Journal of Neurology, Neurosurgery & Psychiatry 83 (1), 6-14, 2012 | 250 | 2012 |
| Plasma neurofilament light chain concentration in the inherited peripheral neuropathies Å Sandelius, H Zetterberg, K Blennow, R Adiutori, A Malaspina, M Laura, ... Neurology 90 (6), e518-e524, 2018 | 214 | 2018 |
| Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia EC Oates, AM Rossor, M Hafezparast, M Gonzalez, F Speziani, ... The American Journal of Human Genetics 92 (6), 965-973, 2013 | 186 | 2013 |
| Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion A Cortese, S Tozza, WY Yau, S Rossi, SJ Beecroft, Z Jaunmuktane, ... Brain 143 (2), 480-490, 2020 | 182 | 2020 |
| Next-generation sequencing in Charcot–Marie–Tooth disease: opportunities and challenges M Pipis, AM Rossor, M Laura, MM Reilly Nature Reviews Neurology 15 (11), 644-656, 2019 | 172 | 2019 |
| Intracranial volume and Alzheimer disease: evidence against the cerebral reserve hypothesis R Jenkins, NC Fox, AM Rossor, RJ Harvey, MN Rossor Archives of neurology 57 (2), 220-224, 2000 | 154 | 2000 |
| Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy M Scoto, AM Rossor, MB Harms, S Cirak, M Calissano, S Robb, ... Neurology 84 (7), 668-679, 2015 | 134 | 2015 |
| Recent advances in the genetic neuropathies AM Rossor, PJ Tomaselli, MM Reilly Current opinion in neurology 29 (5), 537-548, 2016 | 121 | 2016 |
| Charcot–Marie–Tooth disease and related disorders: an evolving landscape M Laurá, M Pipis, AM Rossor, MM Reilly Current Opinion in Neurology 32 (5), 641-650, 2019 | 113 | 2019 |
| Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes A Cortese, Y Zhu, AP Rebelo, S Negri, S Courel, L Abreu, CJ Bacon, ... Nature genetics 52 (5), 473-481, 2020 | 112 | 2020 |
| Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2 AM Rossor, EC Oates, HK Salter, Y Liu, SM Murphy, R Schule, ... Brain 138 (2), 293-310, 2015 | 103 | 2015 |
| A practical approach to the genetic neuropathies AM Rossor, MRB Evans, MM Reilly Practical neurology 15 (3), 187-198, 2015 | 95 | 2015 |
| Targeted next-generation sequencing panels in the diagnosis of Charcot-Marie-Tooth disease A Cortese, JE Wilcox, JM Polke, R Poh, M Skorupinska, AM Rossor, ... Neurology 94 (1), e51-e61, 2020 | 92 | 2020 |
| Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies E Burnor, L Yang, H Zhou, KR Patterson, C Quinn, MM Reilly, AM Rossor, ... Neurology 90 (1), e31-e38, 2018 | 86 | 2018 |
| Clinical and genetic characterization of leukoencephalopathies in adults DS Lynch, A Rodrigues Brandão de Paiva, WJ Zhang, E Bugiardini, ... Brain 140 (5), 1204-1211, 2017 | 80 | 2017 |
