Author

Harriet E. Nilsson

Karolinska InstitutetORCID 0000-0001-7739-4405Unclaimed 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· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anca DragomiriD· 1 shared Andrea BiederiD· 1 shared Anna LindstrandiD· 1 shared Elísabet EinarsdóttiriD· 1 shared Hans MatssoniD· 1 shared Isabel Tapia‐PáeziD· 1 shared Jesper EisfeldtiD· 1 shared Juha KereiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Anca DragomirORCID

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1 paper

Recent·Most cited

GeneticsBMC Medical GeneticsPeer-reviewedMay 1, 2020

Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia

Andrea Bieder, Elísabet Einarsdóttir, Hans Matsson…·Isabel Tapia‐Páez

The paper identifies rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia, suggesting a potential link between dynein dysfunction and these conditions.

5 citations

humanwhole-genome sequencing

𝕏 PostBluesky