Author

Ann Wallblom

Karolinska Institutet

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

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Genetics· 1

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

Frequent Co-Authors

Aleksandra Krstic· 1 shared Anna LindstrandiD· 1 shared Charlotte GraniD· 1 shared Charlotte GustafssoniD· 1 shared Fanny Taborsak-LinesiD· 1 shared Jesper EisfeldtiD· 1 shared Julia HauensteiniD· 1 shared Lucía Peña‐PéreziD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Aleksandra Krstic

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1 paper

Recent·Most cited

GeneticsBlood AdvancesPeer-reviewedJun 8, 2022

Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma

Lucía Peña‐Pérez, Nicolai Sebastian Frengen, Julia Hauenstein…·Robert Månsson

This study uses linked-read whole-genome sequencing to detect structural variants and copy number variations in multiple myeloma, identifying both common and private variants that affect gene regulation and molecular classification.

3 citations

humanwhole-genome sequencing

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