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UnknownIdentification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome.
Not available
S-EPMC2427184 | biostudies-literature
UnknownNonsteroidal Anti-inflammatory Use and LRRK2 Parkinson's Disease Penetrance.
Not available
S-EPMC7572560 | biostudies-literature
UnknownCognitive Function in Young Persons With and Without Perinatal HIV in the AALPHI Cohort in England: Role of Non-HIV-Related Factors.
Not available
S-EPMC5091348 | biostudies-literature
UnknownInvestigation of Autosomal Genetic Sex Differences in Parkinson's Disease.
Not available
S-EPMC8422907 | biostudies-literature
UnknownDiagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study.
Not available
S-EPMC4575273 | biostudies-literature
UnknownThe Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Not available
S-EPMC8393828 | biostudies-literature
UnknownMitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset.
Not available
S-EPMC6531455 | biostudies-literature
UnknownIdentification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
Not available
S-EPMC8422160 | biostudies-literature
UnknownRegulatory sites for splicing in human basal ganglia are enriched for disease-relevant information.
Not available
S-EPMC7042265 | biostudies-literature
UnknownHuman-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage.
Not available
S-EPMC8024253 | biostudies-literature
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