Author

Linda H. Schneider

Swiss Red CrossORCID 0000-0002-9866-4723Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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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 Maja P. Mattle‐Greminger· 2 shared Morgan GueuningiD· 2 shared Nadine Trost· 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

GeneticsBiomedicinesPeer-reviewedJan 19, 2024

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

Morgan Gueuning, Gian Andri Thun, Nadine Trost…·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.

12 citations

humanlong-read sequencing

GeneticsVox SanguinisPeer-reviewedJan 16, 2024

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

Gian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir…·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.

13 citations

humanwhole-genome sequencing