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| 36289003 | Truncating Variants in <i>RFC1</i> in Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome. | Neurology | 2023 |
| 36289003 | Truncating Variants in <i>RFC1</i> in Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome. | Neurology | 2023 |
| 38021223 | Transcriptional changes in the rat brain induced by repetitive transcranial magnetic stimulation. | Front Hum Neurosci | 2023 |
| 37650884 | Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy. | Genet Med | 2023 |
| 37810464 | Repeat expansions in <i>NOP56</i> are a cause of spinocerebellar ataxia Type 36 in the British population. | Brain Commun | 2023 |
| 37129365 | Age-related telomere attrition in the human putamen. | Aging Cell | 2023 |
| 38021223 | Transcriptional changes in the rat brain induced by repetitive transcranial magnetic stimulation. | Front Hum Neurosci | 2023 |
| 37650884 | Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy. | Genet Med | 2023 |
| 37810464 | Repeat expansions in <i>NOP56</i> are a cause of spinocerebellar ataxia Type 36 in the British population. | Brain Commun | 2023 |
| 37129365 | Age-related telomere attrition in the human putamen. | Aging Cell | 2023 |
| 34622992 | Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism. | Mov Disord | 2022 |
| 35708913 | Longitudinal analysis reveals age-related changes in the T cell receptor repertoire of human T cell subsets. | J Clin Invest | 2022 |
| 35903017 | Neurofilament light levels predict clinical progression and death in multiple system atrophy. | Brain | 2022 |
| 35704994 | DNA methylation signatures reveal that distinct combinations of transcription factors specify human immune cell epigenetic identity. | Immunity | 2022 |
| 35577512 | Combining biomarkers for prognostic modelling of Parkinson's disease. | J Neurol Neurosurg Psychiatry | 2022 |
| 35575213 | The role of body fat in multiple sclerosis susceptibility and severity: A Mendelian randomisation study. | Mult Scler | 2022 |
| 36074904 | Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 loci. | Brain | 2022 |
| 35732412 | Genetics of validated Parkinson's disease subtypes in the Oxford Discovery and Tracking Parkinson's cohorts. | J Neurol Neurosurg Psychiatry | 2022 |
| 36441670 | Aberrant expression and localization of the RAP1 shelterin protein contribute to age-related phenotypes. | PLoS Genet | 2022 |
| 34622992 | Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism. | Mov Disord | 2022 |
| 35080042 | Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia. | Mov Disord | 2022 |
| 35708913 | Longitudinal analysis reveals age-related changes in the T cell receptor repertoire of human T cell subsets. | J Clin Invest | 2022 |
| 35732412 | Genetics of validated Parkinson's disease subtypes in the Oxford Discovery and Tracking Parkinson's cohorts. | J Neurol Neurosurg Psychiatry | 2022 |
| 35704994 | DNA methylation signatures reveal that distinct combinations of transcription factors specify human immune cell epigenetic identity. | Immunity | 2022 |
| 35577512 | Combining biomarkers for prognostic modelling of Parkinson's disease. | J Neurol Neurosurg Psychiatry | 2022 |
| 35575213 | The role of body fat in multiple sclerosis susceptibility and severity: A Mendelian randomisation study. | Mult Scler | 2022 |
| 36441670 | Aberrant expression and localization of the RAP1 shelterin protein contribute to age-related phenotypes. | PLoS Genet | 2022 |
| 36074904 | Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 loci. | Brain | 2022 |
| 35903017 | Neurofilament light levels predict clinical progression and death in multiple system atrophy. | Brain | 2022 |
| 35080042 | Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia. | Mov Disord | 2022 |
| 32873436 | Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease. | Neurobiol Aging | 2021 |
| 33543803 | Expanding the Spectrum of AP5Z1-Related Hereditary Spastic Paraplegia (HSP-SPG48): A Multicenter Study on a Rare Disease. | Mov Disord | 2021 |
| 33970200 | Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. | Brain | 2021 |
| 33969176 | Spastic paraplegia preceding <i>PSEN1</i>-related familial Alzheimer's disease. | Alzheimers Dement (Amst) | 2021 |
| 33539324 | Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia. | J Clin Invest | 2021 |
| 33795677 | Skeletal muscle transcriptome in healthy aging. | Nat Commun | 2021 |
| 34056740 | Mendelian Randomisation Finds No Causal Association between Urate and Parkinson's Disease Progression. | Mov Disord | 2021 |
| 33523105 | Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets. | JAMA Neurol | 2021 |
| 33563805 | RFC1-related ataxia is a mimic of early multiple system atrophy. | J Neurol Neurosurg Psychiatry | 2021 |
| 34145635 | Childhood-Onset Chorea Caused by a Recurrent De Novo DRD2 Variant. | Mov Disord | 2021 |
| 34184781 | Genome-Wide Association Study Identifies Risk Loci for Cluster Headache. | Ann Neurol | 2021 |
| 33377220 | NOTCH2NLC Intermediate-Length Repeat Expansion and Parkinson's Disease in Patients of European Descent. | Ann Neurol | 2021 |
| 32873436 | Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease. | Neurobiol Aging | 2021 |
| 33026126 | Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement Disorders. | Mov Disord | 2021 |
| 33111402 | Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease. | Mov Disord | 2021 |
| 34658065 | Mendelian Randomization Studies: A Path to Better Understand Sex and Gender Differences in Parkinson's Disease? | Mov Disord | 2021 |
| 34706222 | DNA methylation signatures reveal that distinct combinations of transcription factors specify human immune cell epigenetic identity. | Immunity | 2021 |
| 34480796 | Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. | Brain | 2021 |
| 34758253 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. | N Engl J Med | 2021 |
| 34930919 | Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome. | Nat Commun | 2021 |