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Paper Details

Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries.
Nat Genet
59
2022
COVID-19, OAS1, OAS1 exonic variants, OAS1 haplotype, OAS1 protein, OAS3, SARS, SARS-CoV, SARS-CoV-2, chr12q24, coronavirus disease 2019, human, human-specific alleles, patients, pegIFN-, rs10774671, rs1131454, severe acute respiratory syndrome coronavirus
Author NameAffiliation
Lisa MirabelloClinical Genetics Branch, National Cancer Institute
Lisa MirabelloClinical Genetics Branch, National Cancer Institute
Evgeny AronsCenter for Cancer Research, National Cancer Institute
Evgeny AronsCenter for Cancer Research, National Cancer Institute
Gregory S BarshHudsonAlpha Institute for Biotechnology
Leslie G BieseckerCenter for Precision Health Research, National Human Genome Research Institute
Leslie G BieseckerCenter for Precision Health Research, National Human Genome Research Institute
David L BoyleAltman Clinical & Translational Research Institute, university of california san diego Health Sciences
Mary CarringtonFrederick National Laboratory for Cancer Research, National Cancer Institute
Mary CarringtonRagon Institute of MGH
Mary CarringtonCenter for Cancer Research, National Cancer Institute
Mary CarringtonFrederick National Laboratory for Cancer Research, National Cancer Institute
Mary CarringtonCenter for Cancer Research, National Cancer Institute
Mary CarringtonRagon Institute of MGH
Rex L ChisholmCenter for Genetic Medicine, Northwestern University Feinberg School of Medicine
Clifton L DalgardUniformed Services University of the Health Sciences
Heather Spencer FeigelsonInstitute for Health Research, Kaiser Permanente Colorado
Gary S FiresteinAltman Clinical & Translational Research Institute, university of california san diego Health Sciences
Hogune ImInc.
Robert J KreitmanCenter for Cancer Research, National Cancer Institute
Robert J KreitmanCenter for Cancer Research, National Cancer Institute
Jennifer A PachecoCenter for Genetic Medicine, Northwestern University Feinberg School of Medicine
Daniel J RaderPerelman School of Medicine, University of Pennsylvania
Marylyn D RitchiePerelman School of Medicine, University of Pennsylvania
Marylyn D RitchiePerelman School of Medicine, University of Pennsylvania
Sharon A SavageClinical Genetics Branch, National Cancer Institute
Sharon A SavageClinical Genetics Branch, National Cancer Institute
Anurag VermaPerelman School of Medicine, University of Pennsylvania
Meredith YeagerFrederick National Laboratory for Cancer Research
Meredith YeagerFrederick National Laboratory for Cancer Research
Stephen J ChanockNational Cancer Institute
Stephen J ChanockNational Cancer Institute
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