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Genome-wide association scan in Parkinson's disease

Genome-wide association scan was performed in 1,705 cases of parkinson's genotyped on the Illumina Human 660W SNP array, and 5,175 controls genotyped on the Illumina1.2M-Duo. Analysis was carried out on the overlaps set of SNPs.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00000000021 3000
EGAD00000000022 3000
EGAD00000000023 1
EGAD00000000024 1
EGAD00000000057 Illumina 610K Quad 1705
Publications Citations
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
Hum Mol Genet 20: 2011 345-353
Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression.
Nature 533: 2016 95-99
Imputation of DNA Methylation Levels in the Brain Implicates a Risk Factor for Parkinson's Disease.
Genetics 204: 2016 771-781
SumHer better estimates the SNP heritability of complex traits from summary statistics.
Nat Genet 51: 2019 277-284
Midnolin is a confirmed genetic risk factor for Parkinson's disease.
Ann Clin Transl Neurol 6: 2019 2205-2211
Common X-Chromosome Variants Are Associated with Parkinson Disease Risk.
Ann Neurol 90: 2021 22-34
Automated machine learning for genome wide association studies.
Bioinformatics 39: 2023 btad545