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Functional analysis of human EED variants using Drosophila

Genetics(2025)10.1093/genetics/iyaf120Source: DataRank Database

Functional analysis of human EED variants using Drosophila is a research paper published in Genetics (2025). On theSindex it has a DataRank of 0.

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (13 grants)Impact (FWCI 0.00)OA: greenTopics (43)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)

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Authors (5)

Sònia Medina Giró,Tianshun Lian ORCID,Douglas W. Allan ORCID,William T Gibson ORCID,Sharri Cyrus ORCID

Live enrichment

PubMed:40539649 PMC:PMC12405997 OpenAlex:https://openalex.org/W4411492788

Canadian Institutes of Health Research

Grant: AWD-013471

Canadian Institutes of Health Research

Grant: PJT-168982

Simons Foundation Autism Research Initiative

Grant: 886158

NIH HHS

Grant: P40 OD010949

NIH HHS

Grant: P40 OD018537

Canadian Institutes of Health Research

Grant: unidentified

unidentified

CRCEF

BC Children's Hospital Research Institute

IGAP

BC Children's Hospital Research Institute

IGAP

BC Children's Hospital Research Institute

CRCEF

FWCI

0.00

Citation Percentile

0.1%

greenLicense: other-oa

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC12405997/

publisherhttps://academic.oup.com/genetics/advance-article-pdf/doi/10.1093/genetics/iyaf120/63535933/iyaf120.pdf

publisherhttps://academic.oup.com/genetics/article-pdf/231/1/iyaf120/63535933/iyaf120.pdf

journalhttps://doi.org/10.1093/genetics/iyaf120

Fields of Study

Epigenetics and DNA MethylationGenetics and Neurodevelopmental DisordersCancer Genomics and Diagnostics0303 health sciences03 medical and health sciencesAnimalsPolycomb Repressive Complex 2HumansMutation, MissenseDrosophila ProteinsDrosophilaLoss of Function MutationDrosophila melanogaster

MeSH Terms

Loss of Function MutationAnimalsDrosophilaDrosophila melanogasterHumansMutation, MissenseDrosophila ProteinsPolycomb Repressive Complex 2

Keywords

BiologyGeneticsMissense mutationGermlineEpigeneticsLoss functionDrosophila melanogasterGeneMutationPhenotypePolycomb Repressive Complex 2Variants Of Unknown SignificanceEedFunctional StudiesCohen–gibson SyndromeInvestigationLoss of Function MutationMutation, MissenseAnimalsHumansDrosophila ProteinsDrosophila

Sustainable Development Goals

SDG 0: Quality Education