| 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 | 1529 | 2019 |
| 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 | 630 | 2005 |
| Parkinson's disease age at onset genome‐wide association study: defining heritability, genetic loci, and α‐synuclein mechanisms C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R Von Coelln, ... Movement Disorders 34 (6), 866-875, 2019 | 288 | 2019 |
| Lrrk2 and Lewy body disease OA Ross, M Toft, AJ Whittle, JL Johnson, S Papapetropoulos, DC Mash, ... Annals of Neurology: Official Journal of the American Neurological …, 2006 | 281 | 2006 |
| Clinical features of LRRK2‐associated Parkinson's disease in central Norway JO Aasly, M Toft, I Fernandez‐Mata, J Kachergus, M Hulihan, LR White, ... Annals of Neurology: Official Journal of the American Neurological …, 2005 | 231 | 2005 |
| Linkage disequilibrium and association of MAPT H1 in Parkinson disease L Skipper, K Wilkes, M Toft, M Baker, S Lincoln, M Hulihan, OA Ross, ... The American Journal of Human Genetics 75 (4), 669-677, 2004 | 190 | 2004 |
| Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia C Blauwendraat, X Reed, L Krohn, K Heilbron, S Bandres-Ciga, M Tan, ... Brain 143 (1), 234-248, 2020 | 178 | 2020 |
| The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease CM Lill, A Rengmark, L Pihlstrøm, I Fogh, A Shatunov, PM Sleiman, ... Alzheimer's & Dementia 11 (12), 1407-1416, 2015 | 175 | 2015 |
| Novel pathogenic LRRK2 p. Asn1437His substitution in familial Parkinson's disease JO Aasly, C Vilariño‐Güell, JC Dachsel, PJ Webber, AB West, ... Movement disorders 25 (13), 2156-2163, 2010 | 158 | 2010 |
| Genetic risk of Parkinson disease and progression: an analysis of 13 longitudinal cohorts H Iwaki, C Blauwendraat, HL Leonard, G Liu, J Maple-Grødem, JC Corvol, ... Neurology: Genetics 5 (4), e348, 2019 | 136 | 2019 |
| Surgical site infections after deep brain stimulation surgery: frequency, characteristics and management in a 10-year period S Bjerknes, IM Skogseid, T Sæhle, E Dietrichs, M Toft PloS one 9 (8), e105288, 2014 | 134 | 2014 |
| Parkinson's disease correlates with promoter methylation in the α‐synuclein gene L Pihlstrøm, V Berge, A Rengmark, M Toft Movement disorders 30 (4), 577-580, 2015 | 117 | 2015 |
| Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease L Pihlstrøm, G Axelsson, KA Bjørnarå, N Dizdar, C Fardell, L Forsgren, ... Neurobiology of aging 34 (6), 1708. e7-1708. e13, 2013 | 116 | 2013 |
| Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ... JAMA neurology 78 (4), 464-472, 2021 | 115 | 2021 |
| Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts H Iwaki, C Blauwendraat, HL Leonard, JJ Kim, G Liu, J Maple‐Grødem, ... Movement Disorders 34 (12), 1839-1850, 2019 | 113 | 2019 |
| Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population M Toft, L Pielsticker, OA Ross, JO Aasly, MJ Farrer Neurology 66 (3), 415-417, 2006 | 107 | 2006 |
| REM sleep behavior disorder in Parkinson's disease–is there a gender difference? KA Bjørnarå, E Dietrichs, M Toft Parkinsonism & related disorders 19 (1), 120-122, 2013 | 98 | 2013 |
| Multiple alpha‐synuclein gene polymorphisms are associated with Parkinson’s disease in a Norwegian population R Myhre, M Toft, J Kachergus, MM Hulihan, JO Aasly, H Klungland, ... Acta Neurologica Scandinavica 118 (5), 320-327, 2008 | 98 | 2008 |
| System Genomics of Parkinson’s Disease Consortium; International Parkinson’s Disease Genomics Consortium. Identification of novel risk loci, causal insights, and heritable risk … MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... Lancet Neurol 18 (12), 1091-1102, 2019 | 94 | 2019 |
| MAPK‐pathway activity, Lrrk2 G2019S, and Parkinson's disease LR White, M Toft, SN Kvam, MJ Farrer, JO Aasly Journal of neuroscience research 85 (6), 1288-1294, 2007 | 93 | 2007 |
