| A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ... Neuron 72 (2), 257-268, 2011 | 5015 | 2011 |
| Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 M Baker, IR Mackenzie, SM Pickering-Brown, J Gass, R Rademakers, ... Nature 442 (7105), 916-919, 2006 | 2315 | 2006 |
| Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ... The Lancet Neurology 11 (4), 323-330, 2012 | 1405 | 2012 |
| Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults CF Skibola, MT Smith, E Kane, E Roman, S Rollinson, RA Cartwright, ... Proceedings of the National Academy of Sciences 96 (22), 12810-12815, 1999 | 710 | 1999 |
| Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1267-1288, 2018 | 666 | 2018 |
| Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations JS Snowden, S Rollinson, JC Thompson, JM Harris, CL Stopford, ... Brain 135 (3), 693-708, 2012 | 614 | 2012 |
| Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium N Rothman, CF Skibola, SS Wang, G Morgan, Q Lan, MT Smith, ... The lancet oncology 7 (1), 27-38, 2006 | 445 | 2006 |
| Frontotemporal dementia and its subtypes: a genome-wide association study R Ferrari, DG Hernandez, MA Nalls, JD Rohrer, A Ramasamy, JBJ Kwok, ... The Lancet Neurology 13 (7), 686-699, 2014 | 436 | 2014 |
| Polymorphism in glutathione S-transferase P1 is associated with susceptibility to chemotherapy-induced leukemia JM Allan, CP Wild, S Rollinson, EV Willett, AV Moorman, GJ Dovey, ... Proceedings of the National Academy of Sciences 98 (20), 11592-11597, 2001 | 345 | 2001 |
| Polymorphisms in the thymidylate synthase and serine hydroxymethyltransferase genes and risk of adult acute lymphocytic leukemia CF Skibola, MT Smith, A Hubbard, B Shane, AC Roberts, GR Law, ... Blood, The Journal of the American Society of Hematology 99 (10), 3786-3791, 2002 | 313 | 2002 |
| Functional FAS promoter polymorphisms are associated with increased risk of acute myeloid leukemia K Sibley, S Rollinson, JM Allan, AG Smith, GR Law, PL Roddam, ... Cancer research 63 (15), 4327-4330, 2003 | 248 | 2003 |
| Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no … SM Pickering-Brown, S Rollinson, D Du Plessis, KE Morrison, A Varma, ... Brain 131 (3), 721-731, 2008 | 238 | 2008 |
| Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in … DMA Mann, S Rollinson, A Robinson, J Bennion Callister, JC Thompson, ... Acta neuropathologica communications 1, 1-13, 2013 | 231 | 2013 |
| Low NAD (P) H: quinone oxidoreductase 1 activity is associated with increased risk of acute leukemia in adults MT Smith, Y Wang, E Kane, S Rollinson, JL Wiemels, E Roman, ... Blood, The Journal of the American Society of Hematology 97 (5), 1422-1426, 2001 | 209 | 2001 |
| A complex population of RNAs exists in human ejaculate spermatozoa: implications for understanding molecular aspects of spermiogenesis D Miller, D Briggs, H Snowden, J Hamlington, S Rollinson, R Lilford, ... Gene 237 (2), 385-392, 1999 | 200 | 1999 |
| Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis S Bandres‐Ciga, AJ Noyce, G Hemani, A Nicolas, A Calvo, G Mora, ... Annals of neurology 85 (4), 470-481, 2019 | 181 | 2019 |
| Colonic dendritic cells, intestinal inflammation, and T cell-mediated bone destruction are modulated by recombinant osteoprotegerin AJ Ashcroft, SM Cruickshank, PI Croucher, MJ Perry, S Rollinson, ... Immunity 19 (6), 849-861, 2003 | 178 | 2003 |
| Polymorphic variation within the glutathione S-transferase genes and risk of adult acute leukaemia S Rollinson, P Roddam, E Kane, E Roman, R Cartwright, A Jack, ... Carcinogenesis 21 (1), 43-47, 2000 | 159 | 2000 |
| UBAP1 is a component of an endosome-specific ESCRT-I complex that is essential for MVB sorting F Stefani, L Zhang, S Taylor, J Donovan, S Rollinson, A Doyotte, ... Current Biology 21 (14), 1245-1250, 2011 | 158 | 2011 |
| The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene JS Snowden, Q Hu, S Rollinson, N Halliwell, A Robinson, YS Davidson, ... Acta neuropathologica 122, 99-110, 2011 | 151 | 2011 |
