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Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson’s disease

Cell Reports(2025)10.1016/j.celrep.2025.115355Source: DataRank Database

Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson’s disease is a research paper published in Cell Reports (2025). On theSindex it has a DataRank of 0. It has been cited 12 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access12 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (7 grants)Impact (FWCI 5.37)OA: goldTopics (36)IDs (PubMed, PMC, OpenAlex)Annotations (2)

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 (27)

Chloe F. Sands,Isabella R. Juan,Jonathan Mitchell ORCID,Vida Ravanmehr ORCID,Jessica C. Butts ORCID

Live enrichment

PubMed:40056900 PMC:PMC12124131 OpenAlex:https://openalex.org/W4408225632

Intramural NIH HHS

Grant: ZIA AG000935

NIH HHS

Grant: DP5 OD036131

Intramural NIH HHS

Grant: ZIA NS003154

Wellcome Trust

National Institutes of Health Office of the Director

Huffington Foundation

Howard Hughes Medical Institute

FWCI

5.37

Citation Percentile

1.0%

Citation Trend

2025

2026

goldLicense: cc-by

journalhttps://www.cell.com/action/showPdf?pii=S2211124725001263

publisherhttps://www.cell.com/action/showPdf?pii=S2211124725001263

publisherhttps://api.elsevier.com/content/article/PII:S2211124725001263?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2211124725001263?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.celrep.2025.115355

Fields of Study

RNA regulation and diseaseGenomic variations and chromosomal abnormalitiesGenomics and Rare Diseases

MeSH Terms

AgedAnimalsDrosophilaDrosophila melanogasterFemaleHumansMaleParkinson DiseaseRisk FactorsCase-Control StudiesGenetic Predisposition to DiseaseDrosophila Proteinsalpha-SynucleinHaploinsufficiency

Keywords

HaploinsufficiencyDiseaseParkinson's diseaseMedicineGeneticsInternal medicineBiologyGenePhenotypeEndocytosisSynucleinNeurodegenerationsynaptic transmissionAutismRare VariantsSncaItsn1Cp: GenomicsIntersectin 1