Follow
Mathias Toft
Mathias Toft
Department of Neurology, Oslo University Hospital and University of Oslo
Verified email at medisin.uio.no - Homepage
Title
Cited by
Cited by
Year
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
14962019
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
6272005
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
2842019
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
2812006
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
2302005
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
1902004
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
1742015
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
1732020
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
1582010
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
1352019
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
1342014
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
1162015
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
1162013
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
1122021
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
1122019
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
1072006
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
982008
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
972013
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
932019
Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
BioRxiv, 388165, 2019
922019
The system can't perform the operation now. Try again later.
Articles 1–20