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

Asymptomatic Infant With Atypical SCID and Novel Hypomorphic RAG Variant Identified by Newborn Screening: A Diagnostic and Treatment Dilemma

Frontiers in Immunology(2020)10.3389/fimmu.2020.01954Source: DataRank Database

Asymptomatic Infant With Atypical SCID and Novel Hypomorphic RAG Variant Identified by Newborn Screening: A Diagnostic and Treatment Dilemma is a research paper published in Frontiers in Immunology (2020). On theSindex it has a DataRank of 0. It has been cited 10 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access10 citations

Download PDF

Cite:

Linked data & code

doi

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 (38)IDs (PubMed, PMC)Annotations (1)SDGs (1)

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 (15)

Emma Westermann-Clark ORCID,Irina Dawson,Boglárka Ujházi,Krisztián Csomós ORCID,Kerry Dobbs ORCID

Live enrichment

PubMed:33117328 PMC:PMC7552884

NIAID NIH HHS

Grant: R01 AI100887

National Institutes of Health

Grant: 5R01AI100887-06

Immune repertoire and function in typical and atypical SCID

goldLicense: cc-by

publisherhttps://www.frontiersin.org/articles/10.3389/fimmu.2020.01954/pdf

publisherhttps://www.frontiersin.org/article/10.3389/fimmu.2020.01954/full

repositoryhttps://doaj.org/article/36d42f20d39f4d0a9fe1c2a88ce9eead

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7552884

Europe_PMChttps://europepmc.org/articles/PMC7552884

Fields of Study

0301 basic medicine03 medical and health sciences0303 health sciences

MeSH Terms

HumansSevere Combined ImmunodeficiencyGenetic Predisposition to DiseaseHomeodomain ProteinsNeonatal ScreeningTreatment OutcomeHematopoietic Stem Cell TransplantationPredictive Value of TestsPhenotypeInfant, NewbornMaleGenetic VariationAsymptomatic Diseases

Keywords

ImmunodeficiencySCIDHSCTNewborn ScreeningAsymptomatic InfantRecombinase Activating Gene (Rag)MaleImmunologyNeonatal ScreeningPredictive Value of TestsHumansGenetic Predisposition to DiseaseHomeodomain ProteinsHematopoietic Stem Cell TransplantationInfant, NewbornGenetic VariationRC581-607PhenotypeTreatment OutcomeAsymptomatic DiseasesSevere Combined ImmunodeficiencyImmunologic diseases. Allergy

Sustainable Development Goals

SDG 3: 3. Good health

Asymptomatic Infant With Atypical SCID and Novel Hypomorphic RAG Variant Identified by Newborn Screening: A Diagnostic and Treatment Dilemma

FAIR Checklist

Authors (15)

Funding (2 grants)

Open Access

Topics

Annotations (Europe PMC)