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

Recessive Loss of PI4K2A Function Causes a Developmental and Epileptic Dyskinetic Encephalopathy with Prominent Orolingual Dyskinesia

Movement Disorders(2025)10.1002/mds.30286Source: DataRank Database

Recessive Loss of PI4K2A Function Causes a Developmental and Epileptic Dyskinetic Encephalopathy with Prominent Orolingual Dyskinesia is a research paper published in Movement Disorders (2025). On theSindex it has a DataRank of 0. It has been cited 1 time.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access1 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 (1 grants)OA: hybridTopics (17)IDs (PubMed, PMC)

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 (10)

Juan Darío Ortigoza‐Escobar ORCID,Pooja Rohilla ORCID,Javeria Raza Alvi ORCID,Aziza Mushiba ORCID,Naif A. M. Almontashiri ORCID

Live enrichment

PubMed:40879273 PMC:PMC13001697

Development and Innovation Authority (RDIA), Kingdom of Saudi Arabia

Grant: Award # 12996-iau-2023-TAU-R-3-1-HW

hybridLicense: cc-by

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.30286

publisherhttps://movementdisorders.onlinelibrary.wiley.com/doi/pdf/10.1002/mds.30286

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC13001697/

Europe_PMChttps://europepmc.org/articles/PMC13001697

Europe_PMChttps://europepmc.org/articles/PMC13001697?pdf=render

MeSH Terms

HumansMovement DisordersDyskinesiasPhosphotransferases (Alcohol Group Acceptor)Minor Histocompatibility AntigensDevelopmental DisabilitiesChildChild, PreschoolFemaleMaleNeurodevelopmental Disorders

Keywords

Genetic VariantsNeurodevelopmental DisordersPi4k2aPediatric Movement DisordersDevelopmental And Epileptic EncephalopathiesOrolingual Dyskinesia