Genetics variants and expression of the SCARB2 gene in the pathogenesis of Parkinson's disease in Russia

Glucocerebrosidase and its relevance to Parkinson disease

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Autophagy lysosomal pathway dysfunction in Parkinson's disease; evidence from human genetics

(2019) Konstantin Senkevich et al.   PARKINSONISM & RELATED DISORDERS

Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia

(2019) Cornelis Blauwendraat et al.   BRAIN

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

(2019) Mike A Nalls et al.   LANCET NEUROLOGY

Characterization of Brain Lysosomal Activities in GBA-Related and Sporadic Parkinson’s Disease and Dementia with Lewy Bodies

(2018) Tim E. Moors et al.   MOLECULAR NEUROBIOLOGY

Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson’s disease

(2017) S. Pchelina et al.   NEUROSCIENCE LETTERS

Parkinson disease

(2017) Werner Poewe et al.   Nature Reviews Disease Primers

MDS clinical diagnostic criteria for Parkinson's disease

(2015) Ronald B. Postuma et al.   MOVEMENT DISORDERS

Association between rs6812193 polymorphism and sporadic Parkinson’s disease susceptibility

(2015) Qiang Huo et al.   NEUROLOGICAL SCIENCES

A novel SCARB2 mutation in progressive myoclonus epilepsy indicated by reduced β-glucocerebrosidase activity

(2014) Marsha Zeigler et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

(2014) Mike A Nalls et al.   NATURE GENETICS

Is Parkinson disease associated with lysosomal integral membrane protein type-2?: Challenges in interpreting association data

(2013) Emerson Maniwang et al.   MOLECULAR GENETICS AND METABOLISM

The role ofSCARB2as susceptibility factor in Parkinson's disease

(2013) Franziska Hopfner et al.   MOVEMENT DISORDERS

Association study of rs6812193 polymorphism with Parkinson's disease in a Greek population

(2013) Kallirhoe Kalinderi et al.   NEUROSCIENCE LETTERS

Association study of SCARB2 rs6812193 polymorphism with Parkinson's disease in Han Chinese

(2012) Shuai Chen et al.   NEUROSCIENCE LETTERS

A mutation in SCARB2 is a modifier in gaucher disease

(2011) Arash Velayati et al.   HUMAN MUTATION

Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease

(2011) Chuong B. Do et al.   PLoS Genetics