Publications
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
Nalls M, et al.
Lancet Neurol . 2019 Dec;18(12):1091-1102.
PMID:31701892
Phenotypes
- Parkinson's disease
Experiment summary
This study is a meta-analysis of 17 Parkinson's disease genome-wide association studies, including 37,688 cases, 18,618 UK Biobank proxy-cases (individuals with a first degree relative who has Parkinson's disease), and 1.4 million controls, all of European ancestry. The results integrated into the Portal, for over 482,000 individuals, do not include the 23andMe participants.
Dataset ID
Nalls2019_Parkinsons_eu