Author

Stefan Meyer

Swiss Red CrossPrimary ORCID profile (0000-0002-2283-3690 · 2 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Stefan MeyeriD2 papers · University of Manchester

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Beat M. FreyiD· 1 shared Charlotte EngströmiD· 1 shared Eduardo Meyer· 1 shared Elise GourriiD· 1 shared Gian Andri ThuniD· 1 shared Kathrin Neuenschwander· 1 shared Linda H. SchneideriD· 1 shared Maja P. Mattle‐Greminger· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Beat M. FreyORCID

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1 paper

Recent·Most cited

Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype

Gian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, Eduardo Meyer, Elise Gourri, Linda H. Schneider, Yvonne Merki, Nadine Trost, Kathrin Neuenschwander, Charlotte Engström, Beat M. Frey, Stefan Meyer, Maja P. Mattle‐Greminger

The paper identifies a novel regulatory variant in the ABO gene's RUNX1 binding site associated with an A3 blood phenotype using long-read sequencing.

Vox Sanguinis · Jan 16, 2024Peer-reviewedGenetics