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Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

Molecular Case Studies(2021)10.1101/mcs.a005991Source: DataRank Database

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay is a research paper published in Molecular Case Studies (2021). On theSindex it has a DataRank of 0.241. It has been cited 4 times.

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0.241DataRank · unranked

Scored on demand from live citation data

Open Access4 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (2 grants)OA: goldTopics (52)IDs (PubMed, PMC)Annotations (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)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.241

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (15)

Ana S.A. Cohen ORCID,Cathryn Poulton ORCID,Tina Duelund Hjortshøj ORCID,Moe Akahira‐Azuma ORCID,Geetu Mendiratta

Live enrichment

PubMed:34117072 PMC:PMC8208047

NICHD NIH HHS

Grant: P01 HD078233

National Institutes of Health

Grant: 1P01HD078233-01A1

Project III: Systems Biology of Bone in Coronal Nonsyndromic Craniosynostosis

goldLicense: cc-by-nc

publisherhttp://molecularcasestudies.cshlp.org/content/7/3/a005991.full.pdf

repositoryhttps://research-repository.uwa.edu.au/en/publications/e31facc2-bda5-4971-80b6-63519e3c3d78

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8208047

Europe_PMChttps://europepmc.org/articles/PMC8208047

Europe_PMChttps://europepmc.org/articles/PMC8208047?pdf=render

Fields of Study

03 medical and health sciences0303 health sciences

MeSH Terms

SkullHumansGenetic Predisposition to DiseaseMembrane ProteinsTranscription FactorsRepressor ProteinsDevelopmental DisabilitiesGene DeletionHeterozygotePhenotypeAdolescentChildChild, PreschoolFemaleMaleProto-Oncogene Protein c-ets-2Sodium-Potassium-Exchanging ATPaseGenetic TestingGenetic Association StudiesDNA Copy Number VariationsIntellectual DisabilityNeurodevelopmental Disorders

Keywords

Intellectual DisabilityCraniosynostosisGlobal Developmental DelayMacrocephaly At BirthCongenital StrabismusWidely Patent Coronal SutureResearch ReportMaleHeterozygote572AdolescentDNA Copy Number VariationsDevelopmental DisabilitiesProto-Oncogene Protein c-ets-2Medicine and Health SciencesHumansGenetic Predisposition to DiseaseGenetic TestingChildGenetic Association StudiesSkullMembrane ProteinsRepressor ProteinsPhenotypeNeurodevelopmental DisordersChild, PreschoolFemaleGene Deletion

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

FAIR Checklist

DataRank Breakdown

Authors (15)

Funding (2 grants)

Open Access

Topics

Annotations (Europe PMC)