Author

Viktor Henmyr

Skåne University Hospital

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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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

Anders JemtiD· 2 shared Esmee ten Berk de BoeriD· 2 shared Karl Nyrén· 2 shared Valtteri WirtaiD· 2 shared Aashish SrivastavaiD· 1 shared Adam AmeuriD· 1 shared Agnes Söderberg· 1 shared Alexander KociD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Anders JemtORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

A national ecosystem for long-read genome sequencing: Integrating population genomics and rare disease diagnostics in Sweden

Adam Ameur, Fulya Taylan, Marlene Ek, Jesper Eisfeldt, Susana Häggqvist, Maria Pettersson, Ignas Bunikis, Joakim Klar, Ida Höijer, Maria Strandh, Rebecca Josefson, Michela Barbaro, Anna Beskow, Anders Blomberg, Marie-Louise Bondeson, , Hans Ehrencrona

This paper evaluates the clinical use of long-read genome sequencing in Sweden, showing it provides molecular diagnoses and reduces diagnostic costs.

medRxiv · Oct 13, 2026 · PreprintGenetic & Genomic Medicine

Recommendations for Bioinformatics in Clinical Practice

Ksenia Lavrichenko, Emilie Sofie Engdal, Rasmus L. Marvig, Anders Jemt, Jone Marius Vignes, Henrikki Almusa, Kristine Bilgrav Sæther, Eiríkur Briem, Eva Caceres, Edda María Elvarsdóttir, Magnús Halldór Gíslason, Maria K. Haanpää, Viktor Henmyr, Ronja Hotakainen, Eevi Kaasinen, , Frederik Otzen Bagger

This paper provides consensus recommendations for standardizing bioinformatics practices in clinical whole genome sequencing to ensure accuracy, reproducibility, and comparability of results.

Genome Medicine · Oct 17, 2025Peer-reviewedBioinformatics