Author

Kjell‐Morten Myhr

Haukeland University HospitalORCID 0000-0002-0980-510XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Assay:flow cytometry· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Adam SantanielloiD· 1 shared An GorisiD· 1 shared Anne Haney CrossiD· 1 shared Anne Kristine LehmanniD· 1 shared Anne SpurklandiD· 1 shared Antonios BayasiD· 1 shared Ashley Harris BeechamiD· 1 shared Astrid Marta OlsnesiD· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Adam SantanielloORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

ImmunologybioRxivPreprintJul 1, 2025

Lineage-Specific Immune Remodeling Following Autologous Hematopoietic Stem Cell Transplantation in Relapsing-Remitting Multiple Sclerosis

Sonia Gavasso, Jonas Bull Haugsøen, Dimitrios Kleftogiannis…·Anne Kristine Lehmann

This study examines immune remodeling after aHSCT in RRMS patients, finding lineage-specific changes in T and B cells rather than full immune restoration.

1 citation

humanflow cytometry

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GeneticsCellPeer-reviewedOct 18, 2018

Low frequency and rare coding variation contributes to multiple sclerosis risk

Mitja Mitrovič, Nikolaos A. Patsopoulos, Ashley Harris Beecham…·Hakon H. Hakonarson

The paper identifies low-frequency coding variants contributing to multiple sclerosis risk using a large case-control study.

173 citationstop 1%

humanGWAS summary statistics

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