Vis enkel innførsel

dc.contributor.authorHaftorn, Kristine Løkås
dc.contributor.authorDenault, William Robert Paul
dc.contributor.authorLee, Yunsung
dc.contributor.authorPage, Christian Magnus
dc.contributor.authorRomanowska, Julia
dc.contributor.authorLyle, Robert
dc.contributor.authorNæss, Øyvind Erik
dc.contributor.authorKristjansson, Dana
dc.contributor.authorMagnus, Per Minor
dc.contributor.authorHåberg, Siri Eldevik
dc.contributor.authorBohlin, Jon
dc.contributor.authorJugessur, Astanand
dc.date.accessioned2024-01-02T07:20:43Z
dc.date.available2024-01-02T07:20:43Z
dc.date.created2023-03-02T14:01:43Z
dc.date.issued2023
dc.identifier.citationCommunications Biology. 2023, 6:224 1-11.
dc.identifier.issn2399-3642
dc.identifier.urihttps://hdl.handle.net/11250/3109213
dc.description.abstractDetermining if specific cell type(s) are responsible for an association between DNA methylation (DNAm) and a given phenotype is important for understanding the biological mechanisms underlying the association. Our EWAS of gestational age (GA) in 953 newborns from the Norwegian MoBa study identified 13,660 CpGs significantly associated with GA (pBonferroni
dc.description.abstractNucleated red blood cells explain most of the association between DNA methylation and gestational age
dc.language.isoeng
dc.titleNucleated red blood cells explain most of the association between DNA methylation and gestational age
dc.title.alternativeNucleated red blood cells explain most of the association between DNA methylation and gestational age
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber1-11
dc.source.volume6:224
dc.source.journalCommunications Biology
dc.identifier.doi10.1038/s42003-023-04584-w
dc.identifier.cristin2130785
dc.relation.projectNorges forskningsråd: 262700
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel