Author

Christine Rootwelt‐Norberg

Oslo University HospitalORCID 0000-0002-4312-9969Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anna Isotta CastriniiD· 1 shared Bjørn Olav ÅsvoldiD· 1 shared Brooke N. WolfordiD· 1 shared Cecilie BuggeiD· 1 shared Christian K FiveiD· 1 shared Eivind CowardiD· 1 shared John‐Peder Escobar KvittingiD· 1 shared Julie Van Den BerghiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anna Isotta CastriniORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 7, 2026

Whole-genome sequencing in mitral valve prolapse: an exploratory study on genes associated with mitral valve prolapse and cardiac arrhythmias

Nikhil Arora, Julie Van Den Bergh, Christine Rootwelt‐Norberg…·Kristina Hermann Haugaa

This study uses whole-genome sequencing to identify genetic variants associated with mitral valve prolapse and arrhythmias in a Norwegian cohort, finding enriched variants in genes related to extracellular matrix and electrophysiological pathways.

DOI 10.64898/2026.09.03.26362147

humanwhole-genome sequencing