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Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias
Mitochondrial haplogroups and cognitive progression in Parkinson's disease
Investigation of autosomal genetic sex differences in Parkinson's disease
Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (vol 22, pg 1851, 2020)
Differences in the presentation and progression of Parkinson's disease by sex
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease
Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and alpha-synuclein mechanisms
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Prediction of cognition in Parkinson's disease with a clinical-genetic score: a longitudinal analysis of nine cohorts
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's
Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies