Author

Menachem Viktor Sarusie

University of CopenhagenORCID 0000-0003-4341-9787Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Developmental Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 3 Approach:statistical model· 3 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Organism:zebrafish· 2 Research Focus:cell type annotation· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Lars Allan LarseniD· 3 shared Karen GrønskoviD· 2 shared Line KesseliD· 2 shared Søren T. ChristenseniD· 2 shared Yeasmeen AliiD· 2 shared Brage Storstein AndreseniD· 1 shared Canan DoğanlıiD· 1 shared Cathrine Jespersgaard· 1 shared

Activity by Year

2022-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Lars Allan LarsenORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Developmental BiologyPLoS BiologyPeer-reviewedAug 4, 2026

TAK1 operates at the primary cilium in non-canonical TGFB/BMP signaling to control heart development

Canan Doğanlı, Oskar Kaaber Thomsen, Daniel A. Baird…·Lars Allan Larsen

The paper identifies TAK1's role in heart development through genetic analysis and shows its activation at the primary cilium via TGFB/BMP signaling.

9 citationstop 2%

zebrafishstatistical model

𝕏 PostBluesky

Genetic & Genomic MedicineEuropean Journal of Human GeneticsPeer-reviewedMar 11, 2026

Oculocutaneous albinism variants in 28 consanguineous families and functional classification of a pathogenic deep intron variant in TYR

Muhammad Farooq, Gitte Hoffmann Bruun, Menachem Viktor Sarusie…·Karen Grønskov

The paper reports molecular genetic diagnoses for 28 consanguineous OCA families and identifies a pathogenic deep intron variant in TYR that causes OCA through pseudoexon inclusion.

3 citationstop 2%

humanstatistical model

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintNov 9, 2022

Loss of GFAP causes retinal dysplasia and vision impairment

Menachem Viktor Sarusie, Cecilia Rönnbäck, Cathrine Jespersgaard…·Karen Grønskov

The paper identifies a loss-of-function GFAP variant causing retinal dysplasia and vision impairment in a family, revealing a novel role for GFAP in eye development.

DOI 10.1101/2022.11.09.22282105

𝕏 PostBluesky