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Introduction to Genetic Association Studies

Cold Spring Harbor Protocols(2012)10.1101/pdb.top068163Source: DataRank Database

Introduction to Genetic Association Studies is a research paper published in Cold Spring Harbor Protocols (2012). On theSindex it has a DataRank of 8.1. It has been cited 209 times, with 200 citing works in its 1-hop citation network.

N/A
8.1DataRank · unranked

Scored on demand from live citation data

209 citations · 200 citing works in its network
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›Methodology & internals
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring
Enrichment:OA: bronzeTopics (20)IDs (PubMed, OpenAlex)

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 10%Citation Network 90%

        Base Score Contribution

        0.802

        From this paper's citation signal

        Citation Network Contribution

        7.3

        From 153 citing papers with measurable signal

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        Authors (2)

        Jo KnightORCID,Cathryn M. Lewis
        Live enrichment
        PubMed:22383645OpenAlex:https://openalex.org/W2152579567

        bronze
        journalhttp://cshprotocols.cshlp.org/content/2012/3/pdb.top068163.full.pdf
        publisherhttp://cshprotocols.cshlp.org/content/2012/3/pdb.top068163.full.pdf
        publisherhttps://syndication.highwire.org/content/doi/10.1101/pdb.top068163
        journalhttps://doi.org/10.1101/pdb.top068163
        repositoryhttps://pubmed.ncbi.nlm.nih.gov/22383645

        Fields of Study

        Genetic Associations and EpidemiologyGenomics and Rare DiseasesGenomic variations and chromosomal abnormalities

        MeSH Terms

        HumansCase-Control StudiesGenetic Predisposition to DiseaseGenetic Association Studies

        Keywords

        Candidate geneGenetic associationBiologyGenetic variationGenome-wide association studyGeneticsGeneComputational biologyEvolutionary biologyDiseaseGenotypeSingle-nucleotide polymorphismMedicine