Author

Nadine Trost

Swiss Red Cross

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· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:long-read sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Beat M. FreyiD· 2 shared Charlotte EngströmiD· 2 shared Gian Andri ThuniD· 2 shared Linda H. SchneideriD· 2 shared Maja P. Mattle‐Greminger· 2 shared Morgan GueuningiD· 2 shared Sonja Sigurdardottir· 2 shared Yvonne Merki· 2 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenetics

Beat M. FreyORCID

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2 papers

Recent·Most cited

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

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