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Modeling rare genetic disease with patient-derived induced pluripotent stem cells: reassessment of the minimum numbers of lines needed

Stem Cells Translational Medicine(2025)10.1093/stcltm/szaf032Source: DataRank Database

Modeling rare genetic disease with patient-derived induced pluripotent stem cells: reassessment of the minimum numbers of lines needed is a research paper published in Stem Cells Translational Medicine (2025). On theSindex it has a DataRank of 0. It has been cited 3 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access3 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 1.27)OA: goldTopics (23)IDs (PubMed, PMC, OpenAlex)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (9)

Diane J. Sutcliffe ORCID,Lauren Grychowski,Erkin Ozel,Anika Thite,Jasper E. Visser ORCID

Live enrichment

PubMed:40751518 PMC:PMC12317316 OpenAlex:https://openalex.org/W4412853291

National Institutes of Health

Grant: NS109242

National Institutes of Health

Grant: NS119758

Lesch-Nyhan Syndrome Children's Research Foundation

FWCI

1.27

Citation Percentile

0.8%

Citation Trend

2025

2026

goldLicense: cc-by-nc

journalhttps://doi.org/10.1093/stcltm/szaf032

publisherhttps://doi.org/10.1093/stcltm/szaf032

publisherhttps://academic.oup.com/stcltm/article-pdf/14/8/szaf032/63923880/szaf032.pdf

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40751518

repositoryhttps://hdl.handle.net/2066/321857

Fields of Study

RNA modifications and cancerBiochemical and Molecular ResearchEpigenetics and DNA Methylation

MeSH Terms

Cell LineHumansLesch-Nyhan SyndromeRare DiseasesInduced Pluripotent Stem Cells

Keywords

Induced pluripotent stem cellStem cellDiseaseBiologyComputational biologyGeneticsMedicinePathologyEmbryonic stem cellGeneHumanTranscriptomeDisease ModelingHprt1Lesch–nyhan Disease