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

DOCK8 deficiency due to a deep intronic variant in two kindreds with hyper-IgE syndrome

Clinical Immunology(2024)10.1016/j.clim.2024.110384Source: DataRank Database

DOCK8 deficiency due to a deep intronic variant in two kindreds with hyper-IgE syndrome is a research paper published in Clinical Immunology (2024). On theSindex it has a DataRank of 0.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access0 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 (4 grants)Impact (FWCI 0.15)OA: greenTopics (37)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)

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 (11)

Muyun Wang ORCID,Sevgi Keleş ORCID,Hatice Güngör ORCID,Murat Cansever ORCID,Salim Can ORCID

Live enrichment

PubMed:39437980 PMC:PMC11531991 OpenAlex:https://openalex.org/W4403583277

NIAID NIH HHS

Grant: R01 AI128976

National Institute of Allergy and Infectious Diseases

Istanbul University Scientific Research Projects Unit

Scientific and Technological Research Council of Turkey

FWCI

0.15

Citation Percentile

0.5%

Citation Trend

2026

greenLicense: http://www.elsevier.com/open-access/userlicense/1.0/

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11531991/pdf/nihms-2031028.pdf

publisherhttps://api.elsevier.com/content/article/PII:S1521661624004935?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1521661624004935?httpAccept=text/plain

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11531991/

Fields of Study

Immunodeficiency and Autoimmune DisordersChronic Lymphocytic Leukemia ResearchBlood disorders and treatmentsHumansGuanine Nucleotide Exchange FactorsJob SyndromeFemaleMaleIntronsPedigreeExome SequencingChildMutationSTAT3 Transcription FactorChild, Preschool

MeSH Terms

Exome SequencingChildChild, PreschoolFemaleHumansIntronsJob SyndromeMaleMutationPedigreeGuanine Nucleotide Exchange FactorsSTAT3 Transcription Factor

Keywords

Immunoglobulin EGeneticsBiologyMedicineAntibodyDock8Intronic MutationWhole Exome Sequencing (Wes)Hyper-immunoglobulin E Syndrome (Hies)Inborn Errors Of Immunity