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Molecular Consequences of a Missense PHF21A Variant, c.1285G > A, Associated With Syndromic Neurodevelopmental Disorder

Cellular and Molecular Neurobiology(2025)10.1007/s10571-025-01584-8Source: DataRank Database

Molecular Consequences of a Missense PHF21A Variant, c.1285G > A, Associated With Syndromic Neurodevelopmental Disorder is a research paper published in Cellular and Molecular Neurobiology (2025). On theSindex it has a DataRank of 0.

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (9 grants)Impact (FWCI 0.89)OA: hybridTopics (29)IDs (PubMed, PMC, OpenAlex)Annotations (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 (7)

Yumie Murata-Nakamura,Robert S. Porter ORCID,Bradley Cutler,Sehj Rai,Hyung‐Goo Kim ORCID

Live enrichment

PubMed:40622422 PMC:PMC12234916 OpenAlex:https://openalex.org/W4412068810

NIH Awards

Grant: R01MH133632

NINDS NIH HHS

Grant: R21 NS104774

NINDS NIH HHS

Grant: R01 NS116008

NICHD NIH HHS

Grant: T32 HD079342

National Institutes of Health

Grant: 2T32HD079342-11

Career Training in Reproductive Biology

National Institutes of Health

Grant: 1R01MH133632-01A1

Dissecting Histone H3K4 Methylation Enzymes in Neuroplasticity

National Institutes of Health

Grant: 5R01NS116008-05

A Neuron-specific Methyl-histone Regulatory Complex

Rackham Graduate School Pre-doctoral Research Grant

the University of Michigan Predoctoral Career Training in the Reproductive Sciences Program

FWCI

0.89

Citation Percentile

0.8%

Citation Trend

2026

hybridLicense: cc-by-nc-nd

journalhttps://link.springer.com/content/pdf/10.1007/s10571-025-01584-8.pdf

publisherhttps://link.springer.com/content/pdf/10.1007/s10571-025-01584-8.pdf

publisherhttps://link.springer.com/article/10.1007/s10571-025-01584-8/fulltext.html

journalhttps://doi.org/10.1007/s10571-025-01584-8

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40622422

Fields of Study

Genetics and Neurodevelopmental DisordersGenomics and Rare DiseasesEpigenetics and DNA Methylation0303 health sciences03 medical and health sciencesHumansMutation, MissenseNeurodevelopmental DisordersAlternative SplicingDNA

MeSH Terms

DNAHumansAlternative SplicingMutation, MissenseNeurodevelopmental Disorders

Keywords

Missense mutationNeurodevelopmental disorderMedicineGeneticsNeuroscienceBiologyMutationGeneAlternative SplicingNeurodevelopmental DisordersBrief ReportMutation, MissenseHumansDNA

Molecular Consequences of a Missense PHF21A Variant, c.1285G > A, Associated With Syndromic Neurodevelopmental Disorder

FAIR Checklist

Authors (7)

Funding (9 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)