| Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019 | 1530 | 2019 |
| Collaborative analysis of α-synuclein gene promoter variability and Parkinson disease DM Maraganore, M De Andrade, A Elbaz, MJ Farrer, JP Ioannidis, ... Jama 296 (6), 661-670, 2006 | 606 | 2006 |
| Prevalence of smell loss in Parkinson's disease–a multicenter study A Haehner, S Boesveldt, HW Berendse, A Mackay-Sim, J Fleischmann, ... Parkinsonism & related disorders 15 (7), 490-494, 2009 | 529 | 2009 |
| Anxiety disorders in Parkinson's disease: prevalence and risk factors NNW Dissanayaka, A Sellbach, S Matheson, JD O'Sullivan, PA Silburn, ... Movement Disorders 25 (7), 838-845, 2010 | 450 | 2010 |
| Parkinson's disease, pesticides, and glutathione transferase polymorphisms A Menegon, PG Board, AC Blackburn, GD Mellick, DG Le Couteur The Lancet 352 (9137), 1344-1346, 1998 | 422 | 1998 |
| 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 | 338 | 2011 |
| UCHL1 is a Parkinson's disease susceptibility gene DM Maraganore, TG Lesnick, A Elbaz, MC Chartier‐Harlin, T Gasser, ... Annals of neurology 55 (4), 512-521, 2004 | 331 | 2004 |
| GSK3B polymorphisms alter transcription and splicing in Parkinson's disease JBJ Kwok, M Hallupp, CT Loy, DKY Chan, J Woo, GD Mellick, ... Annals of Neurology: Official Journal of the American Neurological …, 2005 | 248 | 2005 |
| The Vps35 D620N mutation linked to Parkinson's disease disrupts the cargo sorting function of retromer J Follett, SJ Norwood, NA Hamilton, M Mohan, O Kovtun, S Tay, Y Zhe, ... Traffic 15 (2), 230-244, 2014 | 247 | 2014 |
| Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology GR Wilson, JCH Sim, C McLean, M Giannandrea, CA Galea, JR Riseley, ... The American Journal of Human Genetics 95 (6), 729-735, 2014 | 240 | 2014 |
| Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing Q Zhang, CL Vallerga, RM Walker, T Lin, AK Henders, GW Montgomery, ... Genome medicine 11, 1-11, 2019 | 220 | 2019 |
| Disease-specific, neurosphere-derived cells as models for brain disorders N Matigian, G Abrahamsen, R Sutharsan, AL Cook, AM Vitale, ... Disease models & mechanisms 3 (11-12), 785-798, 2010 | 220 | 2010 |
| Imagining an interdisciplinary doctoral pedagogy C Manathunga, P Lant, G Mellick Teaching in Higher Education 11 (3), 365-379, 2006 | 203 | 2006 |
| Tau haplotypes regulate transcription and are associated with Parkinson's disease JBJ Kwok, ET Teber, C Loy, M Hallupp, G Nicholson, GD Mellick, ... Annals of Neurology: Official Journal of the American Neurological …, 2004 | 201 | 2004 |
| Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population M Saad, S Lesage, A Saint-Pierre, JC Corvol, D Zelenika, JC Lambert, ... Human molecular genetics 20 (3), 615-627, 2011 | 195 | 2011 |
| Factors associated with depression in Parkinson's disease NNW Dissanayaka, A Sellbach, PA Silburn, JD O'Sullivan, R Marsh, ... Journal of affective disorders 132 (1-2), 82-88, 2011 | 178 | 2011 |
| Large-scale replication and heterogeneity in Parkinson disease genetic loci M Sharma, JPA Ioannidis, JO Aasly, G Annesi, A Brice, ... Neurology 79 (7), 659-667, 2012 | 158 | 2012 |
| Variance of gene expression identifies altered network constraints in neurological disease JC Mar, NA Matigian, A Mackay-Sim, GD Mellick, CM Sue, PA Silburn, ... PLoS genetics 7 (8), e1002207, 2011 | 158 | 2011 |
| Heterozygous PINK1 p. G411S increases risk of Parkinson’s disease via a dominant-negative mechanism A Puschmann, FC Fiesel, TR Caulfield, R Hudec, M Ando, D Truban, ... Brain 140 (1), 98-117, 2017 | 137 | 2017 |
| Variations in the monoamine oxidase B lpar; MAOB) gene are associated with Parkinson's disease GD Mellick, DD Buchanan, SJ McCann, KM James, AG Johnson, ... Movement disorders: official journal of the Movement Disorder Society 14 (2 …, 1999 | 123 | 1999 |
