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Spontaneous allelic variant in deafness–blindness gene Ush1g resulting in an expanded phenotype

Genes Brain & Behavior(2023)10.1111/gbb.12849Source: DataRank Database

Spontaneous allelic variant in deafness–blindness gene Ush1g resulting in an expanded phenotype is a research paper published in Genes Brain & Behavior (2023). On theSindex it has a DataRank of 0. It has been cited 3 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access3 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (3 grants)Impact (FWCI 0.49)OA: hybridTopics (39)IDs (PubMed, 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 (12)

Jocelyn F. Krey ORCID,Paroma Chatterjee,Allison Curtis ORCID,Makayla Six,Sean P. M. Rice ORCID

Live enrichment

PubMed:37328946 OpenAlex:https://openalex.org/W4381046889

National Eye Institute

Grant: P30EY010572

National Institute of Environmental Health Sciences

Grant: R01ES031086

National Institute on Deafness and Other Communication Disorders

Grant: R01DC002368

FWCI

0.49

Citation Percentile

0.6%

Citation Trend

2023

2024

2025

hybridLicense: cc-by-nc

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/gbb.12849

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/gbb.12849

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/gbb.12849

journalhttps://doi.org/10.1111/gbb.12849

repositoryhttps://pubmed.ncbi.nlm.nih.gov/37328946

Fields of Study

Hearing, Cochlea, Tinnitus, Geneticsbioluminescence and chemiluminescence researchRNA and protein synthesis mechanismsMiceAnimalsAllelesUsher SyndromesMutationPhenotypeDNA GlycosylasesUsher Syndrome, Type IG

MeSH Terms

AllelesAnimalsMutationPhenotypeDNA GlycosylasesMiceUsher Syndromes

Keywords

Stereocilia (inner ear)BiologyGeneticsRetinal degenerationHair cellAlleleUsher syndromePhenotypeNull alleleMutationMutagenesisGeneInner earRetinitis pigmentosaNeuroscienceRetinaCochleaDNA repairHyperactivityStereociliaBackward Walking Mouse

Sustainable Development Goals

SDG 0: Life below water