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

Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms

(2023)10.7554/elife.87147.2Source: DataRank Database

Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms is a research paper (2023). On theSindex it has a DataRank of 0. It has been cited 2 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access2 citations

Download PDF

Cite:

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 (2 grants)OA: goldTopics (29)IDs (PubMed)

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 (5)

Chi Sun ORCID,Xiaodong Zhang ORCID,Philip A. Ruzycki ORCID,Shiming Chen ORCID,Yiqiao Zheng ORCID

Live enrichment

PubMed:23304386

National Institutes of Health

Grant: 5R01EY032136-04

Understanding and treating CRX-linked retinopathies

National Institutes of Health

Grant: 5R01EY012543-10

CRX AND ITS REGULATORY NETWORK IN RETINAL DEGENERATIONS

goldLicense: cc-by

https://github.com/elifesciences/enhanced-preprints-data/raw/master/data/87147/v2/87147-v2.pdf

publisherhttps://elifesciences.org/reviewed-preprints/87147v2/pdf

https://doi.org/10.7554/elife.87147.4

https://doi.org/10.7554/elife.87147.1

https://doi.org/10.7554/elife.87147

Fields of Study

0301 basic medicine03 medical and health sciences

Keywords

inherited retinal diseasesQH301-705.5ScienceMutation, MissenseArticleRetinaMiceRetinal DiseasesMedicine and Health SciencesAnimalsHumansphotoreceptor developmentBiology (General)transcription factorDNA-binding specificityHomeodomain ProteinsCRX disease mutationsQICTS (Institute of Clinical and Translational Sciences)RGenetics and GenomicshomeodomainMutationTrans-ActivatorsMedicineMissenseTranscription Factors