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Association analyses of rare variants identify two genes associated with refractive error

PLOS ONE(2022)10.1371/journal.pone.0272379Source: DataRank Database

Association analyses of rare variants identify two genes associated with refractive error is a research paper published in PLOS ONE (2022). On theSindex it has a DataRank of 0.208. It has been cited 3 times.

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0.208DataRank · unranked

Scored on demand from live citation data

3 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (5 grants)Impact (FWCI 0.44)OA: goldTopics (36)IDs (PubMed, PMC, OpenAlex)Annotations (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (0/2)

Interoperable (0/2)

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.208

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (14)

Annechien E. G. Haarman ORCID,Anthony M. Musolf,Omar A. Mahroo ORCID,Jugnoo S. Rahi ORCID,Mario Falchi

Live enrichment

PubMed:36137074 PMC:PMC9499304 OpenAlex:https://openalex.org/W4296794555

Wellcome Trust

Grant: 206619/Z/17/Z

Medical Research Council

Grant: MC_PC_17228

Fight for Sight

Grant: 5038

Medical Research Council

Grant: MC_QA137853

National Institute for Health Research (NIHR)

Grant: NF-SI-0617-10031

FWCI

0.44

Citation Percentile

0.6%

Citation Trend

2023

2025

goldLicense: cc-by

journalhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0272379&type=printable

publisherhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0272379&type=printable

journalhttps://doi.org/10.1371/journal.pone.0272379

repositoryhttps://pubmed.ncbi.nlm.nih.gov/36137074

repositoryhttps://kclpure.kcl.ac.uk/portal/en/publications/8c9f696e-ecbf-4a04-b07b-2a8993033e97

Fields of Study

Ophthalmology and Visual Impairment StudiesGlaucoma and retinal disordersRetinal Development and DisordersGene FrequencyGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPolymorphism, Single NucleotideRefractive ErrorsTranscription Factors

MeSH Terms

Gene FrequencyHumansRefractive ErrorsTranscription FactorsGenetic Predisposition to DiseasePolymorphism, Single NucleotideGenome-Wide Association Study

Keywords

Minor allele frequencyBonferroni correctionGenome-wide association studyGeneticsGenetic associationMultiple comparisons problemBiology1000 Genomes ProjectLocus (genetics)PopulationAlleleAllele frequencySingle-nucleotide polymorphismGeneCandidate geneGenotypeMedicineMathematicsStatistics

Association analyses of rare variants identify two genes associated with refractive error

FAIR Checklist

DataRank Breakdown

Authors (14)

Funding (5 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)