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Paper Details

Single-cell multi-omics reveals dyssynchrony of the innate and adaptive immune system in progressive COVID-19.
Nat Commun
104
2022
/, CD8, COVID-19, HLA-DR, IGHG, LAG-3, MHC-II, S100A, S100A/, SARS-CoV, SARS-CoV-2 virus, T cell receptor, V(D)J repertoires, activated LAG-3 T cells, expanded effector CD8 clones, mutated B cell clones, myeloid, myeloid and T cells, patients, tocilizumab, unmutated IGHG B cell clones
Author NameAffiliation
Hiromitsu AsashimaYale University
Hiromitsu AsashimaYale University
Neal G RavindraYale University
Neal G RavindraCardiovascular Research Center, Yale School of Medicine
Christopher CastaldiYale Center for Genome Analysis, Yale School of Medicine
Patrick WongYale University
John FournierYale University
Santos BermejoYale University
Arnau Casanovas-MassanaYale School of Public Health
Chantal B F VogelsYale School of Public Health
Anne L WyllieYale School of Public Health
Nathan D GrubaughYale School of Public Health
Subhasis MohantyYale School of Medicine, Yale University
Albert I KoYale School of Public Health
Shelli F FarhadianYale University
Shelli F FarhadianYale School of Medicine, Yale University
Akiko IwasakiYale University
Akiko IwasakiHoward Hughes Medical Institute
Albert C ShawYale School of Medicine, Yale University
David van DijkYale University
David van DijkCardiovascular Research Center, Yale School of Medicine
David A HaflerYale University
David A HaflerYale University
David A HaflerYale University
David A HaflerYale University
Charles S Dela CruzYale University
Charles S Dela CruzWest Haven Veterans Affair Medical Center
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