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A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels

Genes & Development(2023)10.1101/gad.350733.123Source: DataRank Database

A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels is a research paper published in Genes & Development (2023). On theSindex it has a DataRank of 0.425. It has been cited 16 times.

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0.425DataRank · unranked

Scored on demand from live citation data

Open Access16 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (22 grants)OA: goldTopics (53)IDs (PubMed, PMC, OpenAlex)Annotations (3)

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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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.425

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (24)

Claudia Cattoglio ORCID,Yingyao Shao ORCID,Harini P Tirumala ORCID,Carlo Vetralla ORCID,Sameer S. Bajikar ORCID

Live enrichment

PubMed:37890975 PMC:PMC10691473 OpenAlex:https://openalex.org/W4387971282

National Institutes of Health

Grant: 5R01NS057819

National Institutes of Health

Grant: R01NS100738

National Institutes of Health

Grant: 1F32HD100048-01

Investigating the role of Growth-differentiation factor 11 in neurodevelopmental and MECP2-related disorders

National Institutes of Health

Grant: P30 CA125123

National Institutes of Health

Grant: S10 OD028591

National Institutes of Health

Grant: P50HD103555

NINDS NIH HHS

Grant: K99 NS129963

NINDS NIH HHS

Grant: R01 NS057819

NINDS NIH HHS

Grant: R56 NS100738

NICHD NIH HHS

Grant: F32 HD100048

National Institutes of Health

Grant: 5R01NS100738-02

Deep brain stimulation in Rett syndrome mice: cognitive effects and their mechanisms

National Institutes of Health

Grant: 1S10OD028591-01

NanoCellect WOLF Cell Sorter and N1 Single-Cell Dispenser System

National Institutes of Health

Grant: 5R01NS057819-15

Molecular Pathogenesis Studies of Rett Syndrome

National Institutes of Health

Grant: 3P30CA125123-09S3

Baylor College of Medicine Cancer Center

National Institutes of Health

Grant: 1P50HD103555-01

Baylor College of Medicine Intellectual and Developmental Disabilities Research Center

Centro Europeo Università e Ricerca

Foundation

Henry Engel Fund

Erasmus Exchange Extra UE Program

Howard Hughes Medical Institute

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Howard Hughes Medical Institute

goldLicense: cc-by

journalhttp://genesdev.cshlp.org/content/early/2023/10/27/gad.350733.123.full.pdf

publisherhttp://genesdev.cshlp.org/content/early/2023/10/27/gad.350733.123.full.pdf

publisherhttps://syndication.highwire.org/content/doi/10.1101/gad.350733.123

journalhttps://doi.org/10.1101/gad.350733.123

repositoryhttps://pubmed.ncbi.nlm.nih.gov/37890975

Fields of Study

Genetics and Neurodevelopmental DisordersUbiquitin and proteasome pathwaysChromatin Remodeling and Cancer0303 health sciences03 medical and health sciencesFemaleHumansMaleMiceAnimalsChromatinBrainMethyl-CpG-Binding Protein 2Rett SyndromeMutationNeurons

MeSH Terms

AnimalsBrainChromatinFemaleHumansMaleMutationNeuronsRett SyndromeMiceMethyl-CpG-Binding Protein 2

Keywords

MECP2Rett syndromeBiologyMissense mutationMutationChromatinGeneticsCell biologyNeurosciencePhenotypeDNAGeneNeurological DisordersChromatin DynamicsSingle-molecular ImagingMaleNeurons570Methyl-CpG-Binding Protein 2610BrainResearch PapersMiceHumansAnimalsFemale