| Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium IG McKeith, BF Boeve, DW Dickson, G Halliday, JP Taylor, D Weintraub, ... Neurology 89 (1), 88-100, 2017 | 4034 | 2017 |
| Age and age-related diseases: role of inflammation triggers and cytokines IM Rea, DS Gibson, V McGilligan, SE McNerlan, HD Alexander, OA Ross Frontiers in immunology 9, 586, 2018 | 1196 | 2018 |
| VPS35 mutations in Parkinson disease C Vilariño-Güell, C Wider, OA Ross, JC Dachsel, JM Kachergus, ... The American Journal of Human Genetics 89 (1), 162-167, 2011 | 1097 | 2011 |
| Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study ME Murray, NR Graff-Radford, OA Ross, RC Petersen, R Duara, ... The Lancet Neurology 10 (9), 785-796, 2011 | 1057 | 2011 |
| Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data MV Holmes, CE Dale, L Zuccolo, RJ Silverwood, Y Guo, Z Ye, ... Bmj 349, g4164, 2014 | 869 | 2014 |
| Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ... Nature genetics 43 (7), 699-705, 2011 | 655 | 2011 |
| Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations J Kachergus, IF Mata, M Hulihan, JP Taylor, S Lincoln, J Aasly, JM Gibson, ... The American Journal of Human Genetics 76 (4), 672-680, 2005 | 649 | 2005 |
| Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids R Rademakers, M Baker, AM Nicholson, NJ Rutherford, NC Finch, ... Nature genetics 44 (2), 200-205, 2012 | 574 | 2012 |
| Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson’s disease O Cooper, H Seo, S Andrabi, C Guardia-Laguarta, J Graziotto, ... Science translational medicine 4 (141), 141ra90-141ra90, 2012 | 567 | 2012 |
| Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication J Fuchs, C Nilsson, J Kachergus, M Munz, EM Larsson, B Schule, ... Neurology 68 (12), 916-922, 2007 | 507 | 2007 |
| TREM2 in neurodegeneration: evidence for association of the p. R47H variant with frontotemporal dementia and Parkinson’s disease S Rayaprolu, B Mullen, M Baker, T Lynch, E Finger, WW Seeley, ... Molecular neurodegeneration 8, 1-5, 2013 | 431 | 2013 |
| Translation initiator EIF4G1 mutations in familial Parkinson disease MC Chartier-Harlin, JC Dachsel, C Vilariño-Güell, SJ Lincoln, F Leprêtre, ... The American Journal of Human Genetics 89 (3), 398-406, 2011 | 413 | 2011 |
| Genomic investigation of α‐synuclein multiplication and parkinsonism OA Ross, AT Braithwaite, LM Skipper, J Kachergus, MM Hulihan, ... Annals of Neurology: Official Journal of the American Neurological …, 2008 | 413 | 2008 |
| Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease LV Kalia, AE Lang, LN Hazrati, S Fujioka, ZK Wszolek, DW Dickson, ... JAMA neurology 72 (1), 100-105, 2015 | 388 | 2015 |
| DNAJC13 mutations in Parkinson disease C Vilariño-Güell, A Rajput, AJ Milnerwood, B Shah, C Szu-Tu, J Trinh, I Yu, ... Human molecular genetics 23 (7), 1794-1801, 2014 | 371 | 2014 |
| Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank KF Bieniek, OA Ross, KA Cormier, RL Walton, A Soto-Ortolaza, ... Acta neuropathologica 130, 877-889, 2015 | 364 | 2015 |
| DCTN1 mutations in Perry syndrome MJ Farrer, MM Hulihan, JM Kachergus, JC Dächsel, AJ Stoessl, ... Nature genetics 41 (2), 163-165, 2009 | 362 | 2009 |
| Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study OA Ross, AI Soto-Ortolaza, MG Heckman, JO Aasly, N Abahuni, G Annesi, ... The Lancet Neurology 10 (10), 898-908, 2011 | 357 | 2011 |
| Clinicopathologic and 11C-Pittsburgh compound B implications of Thal amyloid phase across the Alzheimer’s disease spectrum ME Murray, VJ Lowe, NR Graff-Radford, AM Liesinger, A Cannon, ... Brain 138 (5), 1370-1381, 2015 | 354 | 2015 |
| Meta‐analysis of Parkinson's Disease: Identification of a novel locus, RIT2 N Pankratz, GW Beecham, AL DeStefano, TM Dawson, KF Doheny, ... Annals of neurology 71 (3), 370-384, 2012 | 354 | 2012 |