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dc.contributor.authorHernández Cordero, Ana I.en_AU
dc.contributor.authorLi, Xuanen_AU
dc.contributor.authorMilne, Stephenen_AU
dc.contributor.authorYang, Chen Xien_AU
dc.contributor.authorBossé, Yohanen_AU
dc.contributor.authorJoubert, Philippeen_AU
dc.contributor.authorTimens, Wimen_AU
dc.contributor.authorvan den Berge, Maartenen_AU
dc.contributor.authorNickle, Daviden_AU
dc.contributor.authorHao, Keen_AU
dc.contributor.authorSin, Don D.en_AU
dc.date.accessioned2021-06-02T04:55:02Z
dc.date.available2021-06-02T04:55:02Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/2123/25226
dc.description.abstractSARS-CoV-2 is responsible for the coronavirus disease 2019 (COVID-19) and the current health crisis. Despite intensive research efforts, the genes and pathways that contribute to COVID-19 remain poorly understood. We, therefore, used an integrative genomics (IG) approach to identify candidate genes responsible for COVID-19 and its severity. We used Bayesian colocalization (COLOC) and summary-based Mendelian randomization to combine gene expression quantitative trait loci (eQTLs) from the Lung eQTL (n = 1,038) and eQTLGen (n = 31,784) studies with published COVID-19 genome-wide association study (GWAS) data from the COVID-19 Host Genetics Initiative. Additionally, we used COLOC to integrate plasma protein quantitative trait loci (pQTL) from the INTERVAL study (n = 3,301) with COVID-19 loci. Finally, we determined any causal associations between plasma proteins and COVID-19 using multi-variable two-sample Mendelian randomization (MR). The expression of 18 genes in lung and/or blood co-localized with COVID-19 loci. Of these, 12 genes were in suggestive loci (PGWASen_AU
dc.language.isoenen_AU
dc.subjectCOVID-19en_AU
dc.subjectCoronavirusen_AU
dc.titleMulti-omics highlights ABO plasma protein as a causal risk factor for COVID-19en_AU
dc.typeArticleen_AU
dc.identifier.doi10.1007/s00439-021-02264-5
dc.relation.otherMitacsen_AU
dc.relation.otherCanada Research Chairsen_AU


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