Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders is a research paper published in European Journal of Human Genetics (2013). On theSindex it has a DataRank of 0.668. It has been cited 85 times.
Scored on demand from live citation data
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DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
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Base Score Contribution
0.668
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 →NINDS NIH HHS
Grant: R13 NS040925
Telethon
Grant: GGP08045
Telethon
Grant: GGP08145
NHGRI NIH HHS
Grant: U54HG003067
NINDS NIH HHS
Grant: R01 NS048453
European Research Council
Grant: 260888
Understanding the basis of cerebellar and brainstem congenital defects: from clinical and molecular characterisation to the development of a novel neuroembryonic in vitro model
National Institutes of Health
Grant: 3U54HG003067-07S1
Large Scale Sequencing and Analysis of Genomes
National Institutes of Health
Grant: 5R01NS048453-13
Molecular Characterization of Joubert Syndrome
Wellcome Trust
Grant: unidentified
unidentified
FWCI
4.23
Citation Percentile
0.9%
Influential Citations
5
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 1 of Expression patterns of ciliopathy genes ARL3 and CEP120 reveal roles in multisystem development
Additional file 1 of Expression patterns of ciliopathy genes ARL3 and CEP120 reveal roles in multisystem development