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

Autism-linked UBE3A gain-of-function mutation causes interneuron and behavioral phenotypes when inherited maternally or paternally in mice

Cell Reports(2023)10.1016/j.celrep.2023.112706Source: DataRank Database

Autism-linked UBE3A gain-of-function mutation causes interneuron and behavioral phenotypes when inherited maternally or paternally in mice is a research paper published in Cell Reports (2023). On theSindex it has a DataRank of 0. It has been cited 29 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access29 citations

Download PDF

Cite:

Linked data & code

geo hpa rrid

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 (14 grants)OA: goldTopics (30)IDs (PubMed, PMC)Annotations (3)

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)

Jeremy M. Simon ORCID,Travis Ptacek ORCID,Jason J. Yi ORCID,Lipin Loo ORCID,Hanqian Mao

Live enrichment

PubMed:37389991 PMC:PMC10530456

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Grant: P50 HD103573

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Grant: U54HD079124

National Institutes of Health

Grant: 5R01MH120229

National Institutes of Health

Grant: P30 NS045892

National Institutes of Health

Grant: P30CA016086

NIEHS NIH HHS

Grant: P30 ES010126

NIMH NIH HHS

Grant: R01 MH120229

National Institutes of Health

Grant: 3P30CA016086-42S2

Cancer Center Support Grant

National Institutes of Health

Grant: 3U54HD079124-05S1

Clinical Translational Research Center for Neurodevelopmental Disorders

National Institutes of Health

Grant: 5P50HD103573-03

Clinical Translational Research Center for Neurodevelopmental Disorders

National Institutes of Health

Grant: 5R01MH120229-05

UBE3A gain-of-function and parent-of-origin influence on neurodevelopmental phenotypes

National Institutes of Health

Grant: 5P30NS045892-18

UNC Neuroscience Center Research Cores

University of North Carolina

National Institute of Neurological Disorders and Stroke

goldLicense: cc-by-nc-nd

publisherhttp://www.cell.com/article/S2211124723007179/pdf

publisherhttps://api.elsevier.com/content/article/PII:S2211124723007179?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2211124723007179?httpAccept=text/plain

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10530456/pdf/nihms-1916065.pdf

repositoryhttps://doaj.org/article/e51c03b71c704840a187f7c84c88daee

Fields of Study

0303 health sciences03 medical and health sciences

MeSH Terms

InterneuronsAnimalsMiceAngelman SyndromeDisease Models, AnimalUbiquitin-Protein LigasesAutistic DisorderPhenotypeMaternal InheritanceGain of Function Mutation

Keywords

AutismNeurodevelopmental DisordersAngelman SyndromeUbe3aSingle-cell Rna-seqCp: NeuroscienceQH301-705.5Ubiquitin-Protein LigasesArticleMiceDisease Models, AnimalPhenotypeInterneuronsGain of Function MutationAnimalsMaternal InheritanceBiology (General)Autistic Disorder