| 36348503 | Association between the LRP1B and APOE loci and the development of Parkinson's disease dementia. | Brain | 2023 |
| 38025272 | Active elite rugby participation is associated with altered precentral cortical thickness. | Brain Commun | 2023 |
| 37560120 | Genome-wide Analysis of Motor Progression in Parkinson Disease. | Neurol Genet | 2023 |
| 37652906 | Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. | NPJ Parkinsons Dis | 2023 |
| 37987016 | Investigation of the genetic aetiology of Lewy body diseases with and without dementia. | medRxiv | 2023 |
| 37986980 | NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations. | medRxiv | 2023 |
| 37425912 | Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease. | medRxiv | 2023 |
| 36975168 | Progression of atypical parkinsonian syndromes: PROSPECT-M-UK study implications for clinical trials. | Brain | 2023 |
| 37269181 | Network connectivity and structural correlates of survival in progressive supranuclear palsy and corticobasal syndrome. | Hum Brain Mapp | 2023 |
| 37070039 | <i>MAPT</i>-Associated Familial Progressive Supranuclear Palsy with Typical Corticobasal Degeneration Neuropathology: A Clinicopathological Report. | Mov Disord Clin Pract | 2023 |
| 37398408 | Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed Populations. | medRxiv | 2023 |
| 37163045 | Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's disease. | medRxiv | 2023 |
| 36869417 | Polygenic Parkinson's Disease Genetic Risk Score as Risk Modifier of Parkinsonism in Gaucher Disease. | Mov Disord | 2023 |
| 36938523 | Uncovering spatiotemporal patterns of atrophy in progressive supranuclear palsy using unsupervised machine learning. | Brain Commun | 2023 |
| 34581500 | Current directions in tau research: Highlights from Tau 2020. | Alzheimers Dement | 2022 |
| 35732412 | Genetics of validated Parkinson's disease subtypes in the Oxford Discovery and Tracking Parkinson's cohorts. | J Neurol Neurosurg Psychiatry | 2022 |
| 35577512 | Combining biomarkers for prognostic modelling of Parkinson's disease. | J Neurol Neurosurg Psychiatry | 2022 |
| 35699244 | The Impact of Type 2 Diabetes in Parkinson's Disease. | Mov Disord | 2022 |
| 35856732 | Diabetes and Neuroaxonal Damage in Parkinson's Disease. | Mov Disord | 2022 |
| 35822248 | A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism. | Neuropathology | 2022 |
| 35365675 | Multi-modality machine learning predicting Parkinson's disease. | NPJ Parkinsons Dis | 2022 |
| 35815712 | The emerging role of LRRK2 in tauopathies. | Clin Sci (Lond) | 2022 |
| 36498882 | Potential of Non-Coding RNA as Biomarkers for Progressive Supranuclear Palsy. | Int J Mol Sci | 2022 |
| 36075979 | Towards a global view of multiple sclerosis genetics. | Nat Rev Neurol | 2022 |
| 36177974 | Severe distinct dysautonomia in RFC1-related disease associated with Parkinsonism. | J Peripher Nerv Syst | 2022 |
| 35903017 | Neurofilament light levels predict clinical progression and death in multiple system atrophy. | Brain | 2022 |
| 36356484 | Reflexive and volitional saccadic eye movements and their changes in age and progressive supranuclear palsy. | J Neurol Sci | 2022 |
| 36156206 | Blood based biomarkers for movement disorders. | Acta Neurol Scand | 2022 |
| 34951131 | Elevated 4R-tau in astrocytes from asymptomatic carriers of the MAPT 10+16 intronic mutation. | J Cell Mol Med | 2022 |
| 32873436 | Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease. | Neurobiol Aging | 2021 |
| 33513292 | A Modified Progressive Supranuclear Palsy Rating Scale. | Mov Disord | 2021 |
| 33589841 | Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. | Nat Genet | 2021 |
| 34762687 | The PINK1-Parkin mitophagy signalling pathway is not functional in peripheral blood mononuclear cells. | PLoS One | 2021 |
| 34435188 | White matter abnormalities in active elite adult rugby players. | Brain Commun | 2021 |
| 34758253 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. | N Engl J Med | 2021 |
| 34492572 | Longitudinal risk factors for developing depressive symptoms in Parkinson's disease. | J Neurol Sci | 2021 |
| 34419788 | Altered network stability in progressive supranuclear palsy. | Neurobiol Aging | 2021 |
| 34385707 | Safety and efficacy of anti-tau monoclonal antibody gosuranemab in progressive supranuclear palsy: a phase 2, randomized, placebo-controlled trial. | Nat Med | 2021 |
| 33987465 | Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes. | Neurol Genet | 2021 |
| 34146514 | Progress towards therapies for disease modification in Parkinson's disease. | Lancet Neurol | 2021 |
| 34049922 | Exenatide once weekly over 2 years as a potential disease-modifying treatment for Parkinson's disease: protocol for a multicentre, randomised, double blind, parallel group, placebo controlled, phase 3 trial: The 'Exenatide-PD3' study. | BMJ Open | 2021 |
| 33972362 | Whole-genome sequencing. | Pract Neurol | 2021 |
| 34190430 | Comparison between four published definitions of hyposmia in Parkinson's disease. | Brain Behav | 2021 |
| 33111402 | Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease. | Mov Disord | 2021 |
| 33448283 | Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk. | Hum Mol Genet | 2021 |
| 31552724 | Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes. | J Mov Disord | 2020 |
| 33543129 | Plasma glial fibrillary acidic protein and neurofilament light chain, but not tau, are biomarkers of sports-related mild traumatic brain injury. | Brain Commun | 2020 |
| 31755958 | Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia. | Brain | 2020 |
| 32078185 | Genome-Wide Association Study of Pain in Parkinson's Disease Implicates TRPM8 as a Risk Factor. | Mov Disord | 2020 |
| 31860007 | Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome. | JAMA Neurol | 2020 |