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USP27Xvariants underlying X-linked intellectual disability disrupt protein function via distinct mechanisms

Life Science Alliance(2024)10.26508/lsa.202302258Source: DataRank Database

USP27Xvariants underlying X-linked intellectual disability disrupt protein function via distinct mechanisms is a research paper published in Life Science Alliance (2024). On theSindex it has a DataRank of 0. It has been cited 7 times.

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Scored on demand from live citation data

Open Access7 citations

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Linked data & code

omim refseq uniprot

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)Impact (FWCI 1.13)OA: goldTopics (29)IDs (PubMed, PMC, OpenAlex)Annotations (3)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 (29)

Maya Slovik ORCID,Yuling Zhang ORCID,Bingyu Liu ORCID,Martin L. Rennie ORCID,Emily Konz ORCID

Live enrichment

PubMed:38182161 PMC:PMC10770416 OpenAlex:https://openalex.org/W4390645748

National Institute of Health

Grant: R01CA272771

National Institute of Health

Grant: P30GM145398

ZonMw Vidi

Grant: 09150172110002

NHGRI NIH HHS

Grant: K08 HG012811

FWCI

1.13

Citation Percentile

0.8%

Citation Trend

2024

2025

goldLicense: cc-by

journalhttps://www.life-science-alliance.org/content/lsa/7/3/e202302258.full.pdf

publisherhttps://www.life-science-alliance.org/content/lsa/7/3/e202302258.full.pdf

publisherhttps://syndication.highwire.org/content/doi/10.26508/lsa.202302258

journalhttps://doi.org/10.26508/lsa.202302258

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38182161

Fields of Study

Ubiquitin and proteasome pathwaysGenetics and Neurodevelopmental DisordersPeptidase Inhibition and AnalysisHumansCell ProliferationComputational BiologyIntellectual DisabilityNeurogenesisX-Linked Intellectual DisabilityUbiquitin-Specific Proteases

MeSH Terms

HumansIntellectual DisabilityComputational BiologyMental Retardation, X-LinkedX-Linked Intellectual DisabilityCell ProliferationNeurogenesisUbiquitin-Specific Proteases

Keywords

Intellectual disabilityBiologyPhenotypeGeneGeneticsFunction (biology)Loss functionProtein functionComputational biologyNeuroscienceBioinformatics

Sustainable Development Goals

SDG 0: Quality Education

USP27Xvariants underlying X-linked intellectual disability disrupt protein function via distinct mechanisms

FAIR Checklist

Authors (29)

Funding (4 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)