Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow

Life Science Alliance(2024)10.26508/lsa.202402708Source: DataRank Database

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow is a research paper published in Life Science Alliance (2024). On theSindex it has a DataRank of 0. It has been cited 6 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access6 citations

Download PDF

Cite:

Linked data & code

gen omim refseq

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)OA: goldTopics (34)IDs (PubMed, PMC)Annotations (3)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (20)

Irmak Sakin ORCID,Stephen Viviano ORCID,Gülten Tuncel ORCID,Stephanie Marie Aguilera ORCID,Gizem Goles ORCID

Live enrichment

PubMed:39168639 PMC:PMC11339347

HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

Grant: R01NS127879

NCATS NIH HHS

Grant: UL1 TR001863

National Institutes of Health

Grant: 1R01NS127879-01

Analysis of Congenital Hydrocephalus Genes in Xenopus

goldLicense: cc-by

publisherhttps://doi.org/10.26508/lsa.202402708

publisherhttps://syndication.highwire.org/content/doi/10.26508/lsa.202402708

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11339347/pdf/LSA-2024-02708.pdf

repositoryhttps://doaj.org/article/60cee08444d34ae9881cfb727a1a7bf9

Europe_PMChttps://europepmc.org/articles/PMC11339347

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciences

MeSH Terms

KidneyBrainCiliaFibroblastsCerebrospinal FluidAnimalsXenopusHumansDNA-Binding ProteinsPedigreeMutationFemaleMaleIntellectual DisabilityCiliopathies

Keywords

MaleXenopusBrainFibroblastsKidneyCiliopathiesPedigreeDNA-Binding ProteinsIntellectual DisabilityMutationAnimalsHumansFemaleCiliaResearch ArticlesCerebrospinal Fluid

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow

FAIR Checklist

Authors (20)

Funding (3 grants)

Open Access

Topics

Annotations (Europe PMC)