Author: Ugur Sahin

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Preprints

Improved Neutralization of Omicron BA.4/5, BA.4.6, BA.2.75.2, BQ.1.1, and XBB.1 with Bivalent BA.4/5 Vaccine

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Peptide-MHC Structure Prediction With Mixed Residue and Atom Graph Neural Network

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A prefusion SARS-CoV-2 spike RNA vaccine is highly immunogenic and prevents lung infection in non-human primates

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Phase 1/2 Study to Describe the Safety and Immunogenicity of a COVID-19 RNA Vaccine Candidate (BNT162b1) in Adults 18 to 55 Years of Age: Interim Report

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Neutralization of SARS-CoV-2 lineage B.1.1.7 pseudovirus by BNT162b2 vaccine-elicited human sera

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Concurrent human antibody andTH1 type T-cell responses elicited by a COVID-19 RNA vaccine

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BNT162b2 induces SARS-CoV-2-neutralising antibodies and T cells in humans

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Omicron breakthrough infection drives cross-variant neutralization and memory B cell formation

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D614G Spike Mutation Increases SARS CoV-2 Susceptibility to Neutralization.

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Early Computational Detection of Potential High Risk SARS-CoV-2 Variants

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BNT162b vaccines are immunogenic and protect non-human primates against SARS-CoV-2

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Exposure to BA.4/BA.5 Spike glycoprotein drives pan-Omicron neutralization in vaccine-experienced humans and mice

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Large-scale analysis of SARS-CoV-2 spike-glycoprotein mutants demonstrates the need for continuous screening of virus isolates

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BNT162b2-Elicited Neutralization of Delta Plus, Lambda, and Other Variants

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Neutralization of SARS-CoV-2 Omicron pseudovirus by BNT162b2 vaccine-elicited human sera

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Omicron BA.2 breakthrough infection enhances cross-neutralization of BA.2.12.1 and BA.4/BA.5

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Neutralization of Omicron sublineages and Deltacron SARS-CoV-2 by 3 doses of BNT162b2 vaccine or BA.1 infection

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Multiple instance learning to predict immune checkpoint blockade efficacy using neoantigen candidates

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