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

Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants

Clinical Genetics(2024)10.1111/cge.14614Source: DataRank Database

Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants is a research paper published in Clinical Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 11 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access11 citations

Free full text

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 (5 grants)OA: hybridTopics (40)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 (25)

Vincent De Man,Isabelle Audo ORCID,Irina Balikova ORCID,Wadih M. Zein ORCID,Vasily Smirnov ORCID

Live enrichment

PubMed:39199020

Universiteit Gent

Grant: BOF20/GOA/023

Retina France

Grant: ANR‐18‐IAHU‐0001

Retina France

Grant: ANR‐18‐IAHU‐01

French National Research Agency (ANR)

Grant: ANR-11-IDEX-0004

French National Research Agency (ANR)

Grant: ANR-18-IAHU-0001

hybridLicense: CC BY

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14614

https://doi.org/10.1111/cge.14614

https://pubmed.ncbi.nlm.nih.gov/39199020

http://dx.doi.org/10.1111/cge.14614

https://lirias.kuleuven.be/handle/20.500.12942/749786

Fields of Study

0301 basic medicine03 medical and health sciences0303 health sciences

Keywords

MaleAdultlysosomal sulfataseMUCOPOLYSACCHARIDOSISDISEASE3105 GeneticsDEFICIENTRETINITIS-PIGMENTOSAMedicine and Health SciencesHumansGenetic Predisposition to Diseaserod-cone dystrophy (RCD)rod‐cone dystrophy (RCD)ArylsulfatasesAgedGenetics & Heredity0604 GeneticsScience & TechnologyIDENTIFICATIONCLN33202 Clinical sciencesBiology and Life Sciences1103 Clinical SciencesMiddle Agedretinitis pigmentosa (RP)PedigreePhenotypeMutationsensorineural hearing loss (SNHL)Usher syndrome (USH)Original ArticleFemaleLife Sciences & BiomedicineUsher SyndromesARSGcanine variant p.(Arg99His)Retinitis Pigmentosa