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Author Correction: The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data
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Genome-wide Analysis of Motor Progression in Parkinson Disease
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Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease
medRxiv
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Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers
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Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease
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Combining biomarkers for prognostic modelling of Parkinson's disease
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Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes
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Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk
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Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease
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Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome
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Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
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SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease
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The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy
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Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study
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Jabbari E, Woodside J, Tan MMX, Shoai M, Pittman A, Ferrari R, Mok KY, Zhang D, Reynolds RH, de Silva R, Grimm MJ, Respondek G, Müller U, Al-Sarraj S, Gentleman SM, Lees AJ, Warner TT, Hardy J, Revesz T, Höglinger GU, Holton JL, Ryten M, Morris HR (2018)
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J Neurol Neurosurg Psychiatry, 89 (7), 702-709
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Johnston IN, Tan M, Cao J, Matsos A, Forrest DRL, Si E, Fardell JE, Hutchinson MR (2017)
Ibudilast reduces oxaliplatin-induced tactile allodynia and cognitive impairments in rats
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Norman BP, Lubbe SJ, Tan M, Warren N, Morris HR (2017)
Early Onset Parkinson's Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report
BMC Neurol, 17 (1), 153
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