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Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

PLoS Genetics(2021)10.1371/journal.pgen.1009413Source: DataRank Database

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach is a research paper published in PLoS Genetics (2021). On theSindex it has a DataRank of 0. It has been cited 4 times.

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Open Access4 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)OA: goldTopics (24)IDs (PubMed)SDGs (1)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (16)

Emine Bircan ORCID,Xinyu Tang ORCID,Mohammed S. Orloff ORCID,Charlotte A. Hobbs ORCID,Marilyn L. Browne ORCID

Live enrichment

PubMed:33684136

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Grant: 5R01HD039054-12

Genomic/Epigenomic Factors and Non-Syndromic Congenital Heart Defect Risk

Centers for Disease Control and Prevention (CDC) cooperative agreements under Program Announcement

Grant: 96043, 02081

Centers for Disease Control and Prevention (CDC) cooperative agreements under Funding Opporunity Annoucement

Grant: FOA #DD09-001, FOA #DD13-003

Centers for Disease Control and Prevention (CDC) cooperative agreements under Notice of Funding Opportunity

Grant: NOFO #DD18-001

Arkansas Biosciences Institute

Grant: 037062

Translational Research Institute

Grant: 1U54TR001629-01A1

Expanding Translational Research in Arkansas

goldLicense: cc-by

publisherhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009413&type=printable

publisherhttps://dx.plos.org/10.1371/journal.pgen.1009413

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7971842

repositoryhttps://doaj.org/article/9282ffc322c144a89147d812f1821ee8

https://doi.org/10.1371/journal.pgen.1009413

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

AdultHeart Defects, CongenitalMaleGenotypeInheritance PatternsChromosome MappingGenetic VariationQH426-470Middle AgedPolymorphism, Single NucleotideRisk AssessmentYoung AdultPhenotypeGeneticsCardiomyopathy, Hypertrophic, FamilialOdds RatioHumansFemaleGenetic Predisposition to DiseaseAllelesResearch Article

Sustainable Development Goals

SDG 3: 3. Good health