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.
- Type: Other
- Archiver: European Genome-Phenome Archive (EGA)
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 |
141 |
Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression.
Nature 533: 2016 95-99 |
314 |
Imputation of DNA Methylation Levels in the Brain Implicates a Risk Factor for Parkinson's Disease.
Genetics 204: 2016 771-781 |
11 |
SumHer better estimates the SNP heritability of complex traits from summary statistics.
Nat Genet 51: 2019 277-284 |
100 |
Midnolin is a confirmed genetic risk factor for Parkinson's disease.
Ann Clin Transl Neurol 6: 2019 2205-2211 |
6 |
Common X-Chromosome Variants Are Associated with Parkinson Disease Risk.
Ann Neurol 90: 2021 22-34 |
20 |
Automated machine learning for genome wide association studies.
Bioinformatics 39: 2023 btad545 |
1 |