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Evidence for common mechanisms of pathology between SHANK3 and other genes of Phelan‐McDermid syndrome

Clinical Genetics(2024)10.1111/cge.14503Source: DataRank Database

Evidence for common mechanisms of pathology between SHANK3 and other genes of Phelan‐McDermid syndrome is a research paper published in Clinical Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 14 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access14 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (2 grants)Impact (FWCI 5.53)OA: hybridTopics (31)IDs (PubMed, PMC, OpenAlex)Annotations (1)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 (3)

Luigi Boccuto ORCID,Audrey Thurm ORCID,Andrew R. Mitz

Live enrichment

PubMed:38414139 PMC:PMC11025605 OpenAlex:https://openalex.org/W4392236350

Intramural NIH HHS

Grant: ZIC MH002961

Intramural NIH HHS

Grant: ZIA MH002886

FWCI

5.53

Citation Percentile

1.0%

Citation Trend

2024

2025

2026

hybridLicense: cc-by-nc

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.14503

HYBRIDhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.14503

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.14503

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14503

journalhttps://doi.org/10.1111/cge.14503

Fields of Study

Genomic variations and chromosomal abnormalitiesCongenital heart defects researchGenetics and Neurodevelopmental DisordersMedicineBiologyHumansNerve Tissue ProteinsChromosome DisordersChromosome DeletionPhenotypeChromosomes, Human, Pair 22Transcription FactorsTelomeric 22q13 Monosomy Syndrome

MeSH Terms

Chromosome DeletionChromosomes, Human, Pair 22HumansNerve Tissue ProteinsPhenotypeTranscription FactorsChromosome Disorders

Keywords

PhenotypeGeneticsGeneBiologyChromosomeBioinformaticsNeurodevelopmentInflammationGene ExpressionSynaptic FunctionPhelan‐mcdermid Syndrome

Sustainable Development Goals

SDG 0: Good health and well-being