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Paper Details

Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19.
Nat Genet
57
2022
12q24, COVID-19, OAS1, OAS1/2/3 cluster, chromosomal region, effector gene, people, risk locus, splice variant
Author NameAffiliation
Jennifer E HuffmanVA Boston Healthcare System
Guillaume Butler-LaporteMcGill University, Lady Davis Institute, Jewish General Hospital
Theodore G DrivasPerelman School of Medicine, University of Pennsylvania,
Theodore G DrivasChildren's Hospital of Philadelphia
Theodore G DrivasPerelman School of Medicine, University of Pennsylvania
Gina M PelosoVA Boston Healthcare System
Gina M PelosoBoston University School of Public Health
Andrea GannaInstitute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki
Andrea GannaMassachusetts General Hospital, Harvard Medical School
Andrea GannaInstitute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki
Andrea GannaMassachusetts General Hospital, Harvard Medical School
Anurag VermaPerelman School of Medicine, University of Pennsylvania,
Anurag VermaPerelman School of Medicine, University of Pennsylvania
Anurag VermaCorporal Michael Crescenz VA Medical Center
John Kenneth BaillieRoslin Institute, University of Edinburgh
John Kenneth BaillieMedical Research Council Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Western General Hospital
Krzysztof KirylukVagelos College of Physicians & Surgeons, Columbia University
Krzysztof KirylukInstitute for Genomic Medicine, Columbia University
Krzysztof KirylukVagelos College of Physicians & Surgeons, Columbia University
Krzysztof KirylukInstitute for Genomic Medicine, Columbia University
John Brent RichardsMcGill University, Lady Davis Institute, Jewish General Hospital
John Brent RichardsKing's College London
John Brent RichardsMcGill University, Lady Davis Institute, Jewish General Hospital
John Brent RichardsKing's College London
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