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Cascading epigenomic analysis for identifying disease genes from the regulatory landscape of GWAS variants

PLoS Genetics(2021)10.1371/journal.pgen.1009918Source: DataRank Database

Cascading epigenomic analysis for identifying disease genes from the regulatory landscape of GWAS variants is a research paper published in PLoS Genetics (2021). On theSindex it has a DataRank of 0.

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Enrichment:Funding (15 grants)Impact (FWCI 0.00)OA: goldTopics (39)IDs (PubMed, PMC, OpenAlex)Annotations (1)

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Context only (not used in score)

Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (10)

William Casazza ORCID,Nam Hee Kim ORCID,Chendi Wang ORCID,Farnush Farhadi ORCID,Shinya Tasaki ORCID

Live enrichment

PubMed:34807913 PMC:PMC8648125 OpenAlex:https://openalex.org/W3203288170

National Institute on Aging

Grant: P30AG10161

National Institute on Aging

Grant: U01 AG046152

National Institute on Aging

Grant: U01AG61356

National Institute on Aging

Grant: AG057911

National Institute on Aging

Grant: AG061798

National Institute on Aging

Grant: P30AG72975

National Institute on Aging

Grant: R01AG15819

NIA NIH HHS

Grant: R01 AG015819

NIA NIH HHS

Grant: P30 AG010161

NIA NIH HHS

Grant: RF1 AG036042

NIA NIH HHS

Grant: U01 AG061356

NIA NIH HHS

Grant: R01 AG057911

NIA NIH HHS

Grant: R01 AG061798

NIA NIH HHS

Grant: P30 AG072975

NIA NIH HHS

Grant: R01 AG017917

FWCI

0.00

Citation Percentile

0.1%

goldLicense: cc-by

journalhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009918&type=printable

publisherhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009918&type=printable

publisherhttps://dx.plos.org/10.1371/journal.pgen.1009918

journalhttps://doi.org/10.1371/journal.pgen.1009918

repositoryhttps://pubmed.ncbi.nlm.nih.gov/34807913

Fields of Study

Genetic Associations and EpidemiologyEpigenetics and DNA MethylationGenomics and Chromatin DynamicsAllelesEpigenomeGenetic Diseases, InbornGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPhenotypePolymorphism, Single NucleotideQuantitative Trait LociTranscriptome

MeSH Terms

EpigenomeAllelesHumansPhenotypeGenetic Predisposition to DiseasePolymorphism, Single NucleotideGenetic Diseases, InbornQuantitative Trait LociGenome-Wide Association StudyTranscriptome

Keywords

EpigenomicsGenome-wide association studyEpigenomeBiologyPhenomeComputational biologyGenetic associationGeneticsGenomicsGeneExpression quantitative trait lociGenomeDNA methylationGene expressionSingle-nucleotide polymorphismGenotype

Cascading epigenomic analysis for identifying disease genes from the regulatory landscape of GWAS variants

FAIR Checklist

Authors (10)

Funding (15 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)