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Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63578Source: DataRank Database

Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype is a research paper published in American Journal of Medical Genetics Part A (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 (9 grants)Impact (FWCI 0.79)OA: greenTopics (45)IDs (PubMed, PMC, OpenAlex)

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)

Lisa Weingarten ORCID,Nicolas J. Abreu ORCID,Houda Zghal Elloumi,Tobias B. Haack ORCID,Clara Hildebrant

Live enrichment

PubMed:38425142 PMC:PMC11161304 OpenAlex:https://openalex.org/W4392354091

National Institutes of Health

Grant: KL2TR001446

National Institute on Aging

Grant: T35AG044303

Wellcome Trust

Grant: WT223718/Z/21/Z

NICHD NIH HHS

Grant: P50 HD105351

National Center for Advancing Translational Sciences

Wellcome Trust

Ministerio de Ciencia e Innovación

Wellcome Trust

FWCI

0.79

Citation Percentile

0.7%

Citation Trend

2025

2026

greenLicense: http://onlinelibrary.wiley.com/termsAndConditions#vor

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11161304/pdf/nihms-1972182.pdf

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.63578

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/11161304

journalhttp://dx.doi.org/10.1002/ajmg.a.63578

Fields of Study

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchEpigenetics and DNA MethylationAdolescentChildChild, PreschoolFemaleHumansMaleDevelopmental DisabilitiesGenetic Association StudiesGenetic Predisposition to DiseaseIntellectual DisabilityNerve Tissue ProteinsNeurodevelopmental DisordersPhenotypeTranscription Factors

MeSH Terms

AdolescentChildDevelopmental DisabilitiesChild, PreschoolFemaleHumansMaleIntellectual DisabilityNerve Tissue ProteinsPhenotypeTranscription FactorsGenetic Predisposition to DiseaseGenetic Association StudiesNeurodevelopmental Disorders

Keywords

PhenotypeAutismIntellectual disabilityGeneticsMissense mutationNeurodevelopmental disorderBiologyGeneNonsenseNonsense-mediated decayMedicinePsychiatryExome SequencingFezf2