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Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Classification of GBA Variants and Their Effects in Synucleinopathies
Age at Onset of Parkinson's Disease Among Ashkenazi Jewish Patients: Contribution of Environmental Factors, LRRK2 p.G2019S and GBA p.N370S Mutations
Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson's disease
Sequencing of the GBA coactivator, Saposin C, in Parkinson disease
Genetic and epidemiological characterization of restless legs syndrome in Québec
Common and rare GCH1 variants are associated with Parkinson's disease
Triple A syndrome presenting as complicated hereditary spastic paraplegia
