Whole exome sequencing in patients with Williams–Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk is a research paper published in Human Molecular Genetics (2020). On theSindex it has a DataRank of 0.477. It has been cited 23 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.
Base Score Contribution
0.477
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 →Children’s Discovery Institute of the Washington University School of Medicine
Grant: CH-FR-2011-169
Children’s Discovery Institute of the Washington University School of Medicine
Grant: MD-II-2013-269
National Institutes of Health
Grant: HL053325
National Institutes of Health
Grant: HL006212
NHLBI NIH HHS
Grant: R37 HL053325
NHLBI NIH HHS
Grant: R01 HL053325
FWCI
1.75
Citation Percentile
0.8%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals