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Abnormal synaptic architecture in iPSC-derived neurons from a multi-generational family with genetic Creutzfeldt-Jakob disease

Stem Cell Reports(2024)10.1016/j.stemcr.2024.08.010Source: DataRank Database

Abnormal synaptic architecture in iPSC-derived neurons from a multi-generational family with genetic Creutzfeldt-Jakob disease is a research paper published in Stem Cell Reports (2024). On theSindex it has a DataRank of 0. It has been cited 11 times.

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Scored on demand from live citation data

Open Access11 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (9 grants)Impact (FWCI 1.78)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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Authors (9)

Nhat T. T. Le ORCID,Robert C.C. Mercer ORCID,Seonmi Park,Bei Wu ORCID,Alice Anane

Live enrichment

PubMed:39332406 PMC:PMC11561462 OpenAlex:https://openalex.org/W4402859794

National Institutes of Health

Grant: R01 NS065244

NINDS NIH HHS

Grant: R21 NS107755

Creutzfeldt-Jakob Disease Foundation

Grant: 1R21NS111499-01

Modeling prion diseases using human iPSC-derived neurons

NINDS NIH HHS

Grant: R21 NS111499

National Institutes of Health

Grant: N0175N92020C00005

National Institutes of Health

Grant: 1R01DA051889-01

Synergistic Mechanisms of chronic Innate Immune Activation in Microglia by Opiates and HIV Infection

NIAID NIH HHS

Grant: P01 AI077774

NIDA NIH HHS

Grant: R01 DA051889

Warren Alpert Foundation

FWCI

1.78

Citation Percentile

0.9%

Citation Trend

2025

2026

goldLicense: cc-by-nc-nd

journalhttps://doi.org/10.1016/j.stemcr.2024.08.010

publisherhttps://doi.org/10.1016/j.stemcr.2024.08.010

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39332406

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/11561462

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11561462/pdf/main.pdf

Fields of Study

Prion Diseases and Protein MisfoldingNeurological diseases and metabolismAmino Acid Enzymes and Metabolism03 medical and health sciences0302 clinical medicine

MeSH Terms

Prion ProteinsAdultCell DifferentiationFemaleHumansCreutzfeldt-Jakob SyndromeMaleMiddle AgedMutationNeuronsPedigreeSynapsesReceptors, N-Methyl-D-AspartatePrPSc ProteinsInduced Pluripotent Stem Cells

Keywords

BiologyDiseaseGenetic architectureNeuroscienceArchitectureGeneticsGeneInternal medicinePhenotypeSynapsePrionNeurodegenerationPrPscPrPPrion DiseaseIpscGenetic Prion DiseaseE200kNeuronsMaleAdultPrPSc ProteinsInduced Pluripotent Stem CellsCell DifferentiationMiddle AgedReceptors, N-Methyl-D-AspartateCreutzfeldt-Jakob SyndromePrion ProteinsPedigreeSynapsesMutationHumansFemale

Abnormal synaptic architecture in iPSC-derived neurons from a multi-generational family with genetic Creutzfeldt-Jakob disease

FAIR Checklist

Authors (9)

Funding (9 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)