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

Variable expression of MECP2, CDKL5, and FMR1 in the human brain: Implications for gene restorative therapies

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2312757121Source: DataRank Database

Variable expression of MECP2, CDKL5, and FMR1 in the human brain: Implications for gene restorative therapies is a research paper published in Proceedings of the National Academy of Sciences (2024). 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:

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 (3 grants)Impact (FWCI 3.77)OA: hybridTopics (37)IDs (PubMed, PMC, OpenAlex)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 (2)

Jeannie T. Lee ORCID,Antonino Zito ORCID

Live enrichment

PubMed:38386709 PMC:PMC10907246 OpenAlex:https://openalex.org/W4392028291

U.S. Department of Defense

Grant: W81XWH-19-1-0022

HHS | NIH | Office of Extramural Research, National Institutes of Health

Grant: R01-MH118351

NIMH NIH HHS

Grant: R01 MH118351

FWCI

3.77

Citation Percentile

0.9%

Citation Trend

2024

2025

2026

hybridLicense: cc-by-nc-nd

journalhttps://www.pnas.org/doi/pdf/10.1073/pnas.2312757121

publisherhttps://www.pnas.org/doi/pdf/10.1073/pnas.2312757121

publisherhttps://pnas.org/doi/pdf/10.1073/pnas.2312757121

journalhttps://doi.org/10.1073/pnas.2312757121

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38386709

Fields of Study

Genetics and Neurodevelopmental DisordersAdvanced biosensing and bioanalysis techniquesRNA modifications and cancerHumansBrainEpileptic SyndromesFragile X Messenger Ribonucleoprotein 1Genes, X-LinkedGenetic TherapyProtein Serine-Threonine KinasesSpasms, InfantileCDKL5 deficiency disorder

MeSH Terms

Epileptic SyndromesBrainHumansSpasms, InfantileGenetic TherapyProtein Serine-Threonine KinasesGenes, X-LinkedFragile X Mental Retardation ProteinFragile X Messenger Ribonucleoprotein 1

Keywords

Rett syndromeNeuroscienceMECP2BiologyHuman brainGene expressionCell typeGeneComputational biologyBioinformaticsPhenotypeGeneticsCellFMR1Fragile X SyndromeCdkl5

Sustainable Development Goals

SDG 0: Life in Land