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UnknownLoss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
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S-EPMC4800038 | biostudies-literature
UnknownUse of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities.
Not available
S-EPMC5968822 | biostudies-literature
UnknownGenetic comorbidities in Parkinson's disease.
Not available
S-EPMC3888265 | biostudies-literature
UnknownA pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.
Not available
S-EPMC3561909 | biostudies-literature
UnknownDiscovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.
Not available
S-EPMC5282828 | biostudies-literature
UnknownGWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19.
Not available
S-EPMC10208981 | biostudies-literature
UnknownStratified analyses refine association between TLR7 rare variants and severe COVID-19.
Not available
S-EPMC11320601 | biostudies-literature
UnknownA two-stage meta-analysis identifies several new loci for Parkinson's disease.
Not available
S-EPMC3128098 | biostudies-literature
UnknownSusceptibility loci for pigmentation and melanoma in relation to Parkinson's disease.
Not available
S-EPMC3961492 | biostudies-literature
UnknownExcessive burden of lysosomal storage disorder gene variants in Parkinson's disease.
Not available
S-EPMC5841393 | biostudies-literature
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