Rare pathogenic variants in WNK3 cause X-linked intellectual disability is a research paper published in Genetics in Medicine (2022). On theSindex it has a DataRank of 0.416. It has been cited 15 times.
Scored on demand from live citation data
DataRank reads this dataset's downstream impact straight off the citation graph â 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 â never from an abstract alone.
Base Score Contribution
0.416
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
Learn more about DataRank methodology âNHGRI NIH HHS
Grant: UM1 HG008900
NINDS NIH HHS
Grant: R01 NS073854
NHGRI NIH HHS
Grant: U01 HG009599
National Institutes of Health
Grant: 5R01NS073854-03
Identification of Novel X-linked Intellectual Disability Genes
National Institutes of Health
Grant: 5UM1HG008900-04
Joint Center for Mendelian Genomics
National Institutes of Health
Grant: 5U01HG009599-02
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
FWCI
1.25
Citation Percentile
0.8%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals