Common X-chromosome variants are associated with Parkinson’s disease risk is a research paper published in medRxiv (2020). On theSindex it has a DataRank of 0. It has been cited 5 times.
Scored on demand from live citation data
Linked data & code
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full — never from an abstract alone.
National Institutes of Health
Grant: 5P50AG047366-03
Stanford Alzheimer's Disease Research Center
Wellcome Trust
Grant: unidentified
unidentified
Wellcome Trust
Grant: 076113
The genetics of weight, BMI, adiposity and obesity
Wellcome Trust
Grant: 085475
WTCCC2 core activities
Wellcome Trust
Grant: 090355
WTCCC3 core activities.
National Institutes of Health
Grant: 1P50NS071674-01
Discovery of Rare Variants and Mutations in Parkinson Disease
National Institutes of Health
Grant: 5P50NS072187-04
Identification of novel Parkinsonian genes by wholegenome
National Institutes of Health
Grant: 1P50NS062684-01A1
Pacific Northwest Udall Center
National Institutes of Health
Grant: 5R01AG060747-03
The Stanford Extreme Phenotypes in Alzheimer's Disease (StEP AD) Cohort
National Institutes of Health
Grant: 7R01NS036960-05
Genetic Analysis of Onset Age of Parkinsons Disease
National Institutes of Health
Grant: 7U01HG008657-04
The Electronic Medical Records and Genomics (eMERGE) Network, Phase III
Fields of Study
Keywords
Sustainable Development Goals