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Extreme Phenotypic Variability of ACTG1‐Related Disorders in Hearing Loss

Advanced Genetics(2024)10.1002/ggn2.202400040Source: DataRank Database

Extreme Phenotypic Variability of ACTG1‐Related Disorders in Hearing Loss is a research paper published in Advanced Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 2 times.

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Open Access2 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (6 grants)Impact (FWCI 0.48)OA: goldTopics (15)IDs (PubMed, PMC, OpenAlex)Annotations (2)

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 (17)

Memoona Ramzan ORCID,L.A. Calderón,Franco Salvatore,Maria Agustina De Rosa,Stephanie Bivona ORCID

Live enrichment

PubMed:39734360 PMC:PMC11672310 OpenAlex:https://openalex.org/W4405073205

Agencia Nacional de Promoción Científica y Tecnológica

Grant: PICT‐2021 GRF‐TI‐00422

National Institutes of Health

Grant: R01DC009645

National Institutes of Health

Grant: R01DC012836

National Institutes of Health

Grant: 5R01DC012836-05

Genetic Studies of Inner Ear Anomalies

National Institutes of Health

Grant: 5R01DC009645-08

A Collaborative Search for New Genes for Non-Syndromic Deafness

Consejo Nacional de Investigaciones Científicas y Técnicas

FWCI

0.48

Citation Percentile

0.6%

Citation Trend

2026

goldLicense: cc-by

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ggn2.202400040

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ggn2.202400040

publisherhttps://advanced.onlinelibrary.wiley.com/doi/pdf/10.1002/ggn2.202400040

journalhttps://doi.org/10.1002/ggn2.202400040

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39734360

Fields of Study

Congenital heart defects researchGenomics and Rare DiseasesMuscle Physiology and Disorders0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

Hearing lossAudiologyPhenotypeMedicineGeneticsBiologyActg1QH426-470Research Article

Extreme Phenotypic Variability of ACTG1‐Related Disorders in Hearing Loss

FAIR Checklist

Authors (17)

Funding (6 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)