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Genome-Wide Association Study and Subsequent Exclusion of ATCAY as a Candidate Gene Involved in Equine Neuroaxonal Dystrophy Using Two Animal Models

Genes(2020)10.3390/genes11010082Source: DataRank Database

Genome-Wide Association Study and Subsequent Exclusion of ATCAY as a Candidate Gene Involved in Equine Neuroaxonal Dystrophy Using Two Animal Models is a research paper published in Genes (2020). On theSindex it has a DataRank of 0. It has been cited 6 times.

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Open Access6 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (5 grants)Impact (FWCI 0.25)OA: goldTopics (84)IDs (PubMed, OpenAlex)SDGs (4)

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 (7)

Christina Esparza,Sichong Peng ORCID,Anna R. Dahlgren ORCID,Janel Peterson ORCID,Andrew D. Miller ORCID

Live enrichment

PubMed:31936863 OpenAlex:https://openalex.org/W2999669948

National Institutes of Health

Grant: 5K01OD015134

National Institutes of Health

Grant: L40 TR001136

U.S. Department of Agriculture

Grant: 20143842021796

Center for Equine Health, University of California, Davis

Grant: N/A

National Institutes of Health

Grant: 3K01OD015134-04S1

Molecular pathogenesis of alpha-tocopherol associated neuroaxonal dystrophy in an

FWCI

0.25

Citation Percentile

0.5%

Citation Trend

2020

2022

2024

2025

goldLicense: cc-by

journalhttps://www.mdpi.com/2073-4425/11/1/82/pdf?version=1578669069

GOLDhttps://www.mdpi.com/2073-4425/11/1/82/pdf?version=1578669069

publisherhttps://www.mdpi.com/2073-4425/11/1/82/pdf?version=1578669069

publisherhttps://www.mdpi.com/2073-4425/11/1/82/pdf

journalhttps://doi.org/10.3390/genes11010082

Fields of Study

Neurological diseases and metabolismPlant and fungal interactionsPeroxisome Proliferator-Activated ReceptorsMedicineBiology0301 basic medicine03 medical and health sciences0303 health sciencesAnimalsDisease Models, AnimalFemaleGenome-Wide Association StudyHomozygoteHorse DiseasesHorsesMaleMiceMice, Inbred C3HMice, KnockoutNerve Tissue ProteinsNeuroaxonal DystrophiesPhenotypeVitamin EVitamin E Deficiency

MeSH Terms

AnimalsDisease Models, AnimalFemaleHomozygoteHorse DiseasesHorsesMaleMice, Inbred C3HNerve Tissue ProteinsPhenotypeVitamin EVitamin E DeficiencyMice, KnockoutNeuroaxonal DystrophiesMiceGenome-Wide Association Study

Keywords

Candidate geneGenome-wide association studyBiologyAtaxiaGeneticsPhenotypePopulationGenetic associationSingle-nucleotide polymorphismGenotypingGeneGenotypeMedicineNeuroscienceMaleKnockoutNeuroaxonal Dystrophies610Nerve Tissue Proteinsvitamin E630ArticleMiceRare DiseasesCayman Ataxiaalpha-tocopherol2.1 Biological and endogenous factorsAnimalsVitamin E DeficiencyHorsesMice, KnockoutMice, Inbred C3HAnimalHuman GenomeHomozygoteNeurosciencesBiological Sciencesequine degenerative myeloencephalopathyInbred C3HhorseDisease Models, AnimalDisease ModelsFemaleHorse Diseases

Sustainable Development Goals

SDG 2: 2. Zero hungerSDG 3: 3. Good healthSDG 10: 10. No inequalitySDG 0: Good health and well-being