Code and summary stats release. Common X‐Chromosome Variants Are Associated with Parkinson Disease Risk. Annals of Neurology 2021. http://doi.org/10.1002/ana.26051
Scripts release: WIP
Discovery summary stats are stored with Git Large File Storage. Please refer to each of dataset in the discovery for appropriate License usage.
Data Availability:
IPDGC NeuroX data available at: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000918.v1.p1
NINDS data available at: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001172.v1.p2
APDGC data available at: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/dataset.cgi?study_id=phs000394.v1.p1
NGRC data available at: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000196.v3.p1
EBI MERGE data available at: https://www.ebi.ac.uk/ega/studies/EGAS00000000034
UK Biobank data available at: http://biobank.ctsu.ox.ac.uk/crystal/
PDCGC data available at: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001664.v1.p1
ACT data available at: https://www.niagads.org/datasets/ng00034
For McGill please contact the Quebec Parkinson Network: http://rpq-qpn.ca/en/