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Alternating hemiplegia of childhood associated mutations in Atp1a3 reveal diverse neurological alterations in mice

Neurobiology of Disease(2025)10.1016/j.nbd.2025.106954Source: DataRank Database

Alternating hemiplegia of childhood associated mutations in Atp1a3 reveal diverse neurological alterations in mice is a research paper published in Neurobiology of Disease (2025). On theSindex it has a DataRank of 0.224. It has been cited 3 times, with 2 citing works in its 1-hop citation network.

N/A

0.224DataRank · unranked

Scored on demand from live citation data

Deposits data Open Access3 citations · 2 citing works in its network

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Data availability

Repositories this paper deposited data in (declared in PubMed).

GEOGSE279074

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)Impact (FWCI 2.93)OA: goldTopics (42)IDs (PubMed, PMC, OpenAlex)

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 93%Citation Network 7%

Base Score Contribution

0.208

From this paper's citation signal

Citation Network Contribution

0.0165

From 2 citing papers with measurable signal

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Top 2 citers driving the network score

Ranked by each citer's contribution to N(p) — log1p(C_q) divided by its reference count — out of 2 citers.

CRISPR and Artificial Intelligence in Neuroregeneration: Closed-Loop Strategies for Precision Medicine, Spinal Cord Repair, and Adaptive Neuro-Oncology
International Journal of Molecular Sciences202520 citations287 referencesContributes 0.011
Caenorhabditis elegans models of alternating hemiplegia of childhood have dominant neuromuscular junction defects
Disease Models & Mechanisms20261 citations79 referencesContributes 0.009

Authors (21)

Georgii Krivoshein ORCID,Scott I. Adamson ORCID,Elena Arystarkhova ORCID,Laura Anderson ORCID,John Szwec

Live enrichment

PubMed:40381892 PMC:PMC12798733 OpenAlex:https://openalex.org/W4410396989

NIH HHS

Grant: U42 OD010921

NIH HHS

Grant: U54 OD030187

National Institutes of Health

Grant: 1U54OD030187-01

The Jackson Laboratory Center for Precision Genetics

National Institutes of Health

Grant: 3U42OD010921-05S1

Establishing a Mutant Mouse Regional Resource Center at The Jackson Laboratory

FWCI

2.93

Citation Percentile

0.9%

Citation Trend

2025

2026

goldLicense: cc-by-nc-nd

journalhttps://doi.org/10.1016/j.nbd.2025.106954

publisherhttps://doi.org/10.1016/j.nbd.2025.106954

publisherhttps://api.elsevier.com/content/article/PII:S0969996125001706?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0969996125001706?httpAccept=text/plain

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40381892

Fields of Study

Genomics and Rare DiseasesGenetics and Neurodevelopmental DisordersMitochondrial Function and PathologyMedicineBiology03 medical and health sciences0302 clinical medicine

MeSH Terms

Sodium-Potassium-Exchanging ATPaseAnimalsDisease Models, AnimalFemaleHemiplegiaMaleMice, Inbred C57BLMutationMice

Keywords

NeuroscienceMedicineMutationPsychologyAudiologyGeneticsBiologyGeneATPase activitySeizureDystoniaSpreading DepolarizationAhcAtp1a3And NeuroinflammationMaleNeurosciences. Biological psychiatry. NeuropsychiatryHemiplegiaArticleMice, Inbred C57BLMiceDisease Models, AnimalAnimalsFemaleSodium-Potassium-Exchanging ATPaseRC321-571