Infantile‐onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotype is a research paper published in Epilepsia Open (2021). On theSindex it has a DataRank of 0.680. It has been cited 12 times, with 9 citing works in its 1-hop citation network.
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.
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Base Score Contribution
0.385
From this paper's citation signal
Citation Network Contribution
0.295
From 6 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 9 citers.
National Human Genome Research Institute
Grant: UM1 HG008895
National Human Genome Research Institute
Grant: 5U01HG009088‐02
NHGRI NIH HHS
Grant: U01 HG009088
FWCI
3.33
Citation Percentile
0.9%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 1 of A non-coding variant in the Kozak sequence of RARS2 strongly decreases protein levels and causes pontocerebellar hypoplasia
Additional file 1 of A non-coding variant in the Kozak sequence of RARS2 strongly decreases protein levels and causes pontocerebellar hypoplasia
Additional file 2 of A non-coding variant in the Kozak sequence of RARS2 strongly decreases protein levels and causes pontocerebellar hypoplasia
Additional file 2 of A non-coding variant in the Kozak sequence of RARS2 strongly decreases protein levels and causes pontocerebellar hypoplasia