Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort is a dataset published in Human Mutation (2020). On theSindex it has a DataRank of 1.7, placing it in the top 12.6% of the data-sharing corpus. It has been cited 41 times, with 38 citing works in its 1-hop citation network.
Ranks in the top 13% for downstream scientific impact
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
0.561
From this paper's citation signal
Citation Network Contribution
1.1
From 29 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 38 citers.
National Eye Institute
Grant: HHS‐N‐260‐2007‐00001‐C
Intramural NIH HHS
Grant: ZIA EY000564
Intramural NIH HHS
Grant: ZIC EY000478
NEI NIH HHS
Grant: HHS-N-260-2007-00001-C
FWCI
1.62
Citation Percentile
0.8%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals