Related references
Note: Only part of the references are listed.Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource
Hirotaka Iwaki et al.
MOVEMENT DISORDERS (2021)
Exploring the Genotype-Phenotype Correlation in GBA-Parkinson Disease: Clinical Aspects, Biomarkers, and Potential Modifiers
Elisa Menozzi et al.
FRONTIERS IN NEUROLOGY (2021)
The genetic architecture of Parkinson's disease
Cornelis Blauwendraat et al.
LANCET NEUROLOGY (2020)
Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies
Lynne Krohn et al.
ANNALS OF NEUROLOGY (2020)
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Cornelis Blauwendraat et al.
BRAIN (2020)
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease
Franziska Hopfner et al.
MOVEMENT DISORDERS (2020)
Genetics of Parkinson's disease: An introspection of its journey towards precision medicine
Sara Bandres-Ciga et al.
NEUROBIOLOGY OF DISEASE (2020)
β-Glucocerebrosidase activity in GBA-linked Parkinson disease The type of mutation matters
Young Eun Huh et al.
NEUROLOGY (2020)
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD
Letizia Straniero et al.
NEUROLOGY-GENETICS (2020)
A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variants
Letizia Straniero et al.
PARKINSONISM & RELATED DISORDERS (2020)
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A. Nalls et al.
LANCET NEUROLOGY (2019)
Revisiting the non-Gaucher-GBA-E326K carrier state: Is it sufficient to increase Parkinson's disease risk?
Orly Goldstein et al.
MOLECULAR GENETICS AND METABOLISM (2019)
Features of GBA-associated Parkinson's disease at presentation in the UK Tracking Parkinson's study
Naveed Malek et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2018)
Integrated Genetic Analysis of Racial Differences of Common GBA Variants in Parkinson's Disease: A Meta-Analysis
Yuan Zhang et al.
FRONTIERS IN MOLECULAR NEUROSCIENCE (2018)
Lysosomal storage diseases
Frances M. Platt et al.
NATURE REVIEWS DISEASE PRIMERS (2018)
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Diana Chang et al.
NATURE GENETICS (2017)
Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease
Laurie A. Robak et al.
BRAIN (2017)
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters
Roberto Cilia et al.
ANNALS OF NEUROLOGY (2016)
The relationship between glucocerebrosidase mutations and Parkinson disease
Anna Migdalska-Richards et al.
JOURNAL OF NEUROCHEMISTRY (2016)
Lysosomal trafficking defects link Parkinson's disease with Gaucher's disease
Yvette C. Wong et al.
MOVEMENT DISORDERS (2016)
Lysosomal Dysfunction and α-Synuclein Aggregation in Parkinson's Disease: Diagnostic Links
Tim Moors et al.
MOVEMENT DISORDERS (2016)
Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression
Albert A. Davis et al.
NEUROBIOLOGY OF AGING (2016)
Differential effects of severe vs mild GBA mutations on Parkinson disease
Ziv Gan-Or et al.
NEUROLOGY (2015)
GBA-Associated Parkinson's Disease: Reduced Survival and More Rapid Progression in a Prospective Longitudinal Study
Kathrin Brockmann et al.
MOVEMENT DISORDERS (2015)
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do et al.
NATURE (2015)
Significant Study of Population Stratification, Sensitivity Analysis and Trim and Fill Analyses on GBA Mutation and Parkinson's Disease
Jie Liu et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2014)
Glucocerebrosidase mutations in primary parkinsonism
Rosanna Asselta et al.
PARKINSONISM & RELATED DISORDERS (2014)
Comparison of Parkinson Risk in Ashkenazi Jewish Patients With Gaucher Disease and GBA Heterozygotes
Roy N. Alcalay et al.
JAMA NEUROLOGY (2014)
Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort
Sophie E. Winder-Rhodes et al.
BRAIN (2013)
The Association Between β-Glucocerebrosidase Mutations and Parkinsonism
Matthew Swan et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2013)
Age-specific Parkinson disease risk in GBA mutation carriers: information for genetic counseling
Huma Q. Rana et al.
GENETICS IN MEDICINE (2013)
Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome
Sophie E. Winder-Rhodes et al.
MOVEMENT DISORDERS (2012)
Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers
M. Anheim et al.
NEUROLOGY (2012)
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
Chuong B. Do et al.
PLOS GENETICS (2011)
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset
W. C. Nichols et al.
NEUROLOGY (2009)
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
E. Sidransky et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Mechanisms of neurodegeneration in mucopolysaccharidoses II and IIIB: analysis of human brain tissue
Kimiko Hamano et al.
ACTA NEUROPATHOLOGICA (2008)
Macular microcirculation characteristics in Parkinson's disease evaluated by OCT-Angiography: a literature review
Evita Evangelia Christou et al.
SEMINARS IN OPHTHALMOLOGY