Author

S Meyer

Friedrich-Alexander-Universität Erlangen-Nürnberg

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:long-read sequencing· 1 Organism:non-human primate· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Beat M. FreyiD· 1 shared Berit RoshaniiD· 1 shared Charlotte EngströmiD· 1 shared Christiane Stahl‐HennigiD· 1 shared Christoph GassneriD· 1 shared Dennis LapuenteiD· 1 shared Edmond J. RemarqueiD· 1 shared Gerrit KoopmaniD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Beat M. FreyORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

A confirmatory, dual-centric non-human primate study on the efficacy of novel oropharyngeal spray immunization with an adenoviral vector vaccine against RSV -- Important lessons learned

Matthias Tenbusch, Gerrit Koopman, Petra Mooij, Berit Roshani, Pascal Irrgang, Dennis Lapuente, Ivanela I. Kondova, Willy M J M Bogers, Edmond J. Remarque, Ramona Vestweber, Samuel Alberto Mérida Ruíz, Nadine Krüger, S Meyer, Olaf Gefeller, Christiane Stahl‐Hennig, Klaus Überla

This study evaluates a DNA-adenoviral prime-boost vaccine for RSV in non-human primates, showing reduced viral replication but challenges in multi-centre trials.

bioRxiv · Apr 20, 2026 · PreprintImmunology

Resolving genotype-phenotype discrepancies of the Kidd blood group using nanopore sequencing

Morgan Gueuning, Gian Andri Thun, Nadine Trost, Linda H. Schneider, Sonja Sigurdardottir, Charlotte Engström, Naemi Larbes, Yvonne Merki, Beat M. Frey, Christoph Gassner, S Meyer, Maja P. Mattle‐Greminger

This study uses nanopore sequencing to resolve genotype-phenotype discrepancies in the Kidd blood group system by detecting structural variants and novel alleles.

Biomedicines · Jan 19, 2024Peer-reviewedGenetics