Author

Serhiy Havrylov

University of AlbertaORCID 0000-0001-8952-2523Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Research Focus:differential expression· 3 Research Focus:gene regulatory network inference· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:mouse· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1

Frequent Co-Authors

Ordan J. LehmanniD· 3 shared Andrew Jan WaskiewicziD· 2 shared Curtis R. FrenchiD· 2 shared Paul W. ChrystaliD· 2 shared Suey van Baarle· 2 shared Ann-Marie PetursoniD· 1 shared Armin M. GamperiD· 1 shared David B. PilgrimiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 34 mutual co-author links

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3 shared papersGenetics

Ordan J. LehmannORCID

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3 papers

Recent·Most cited

Molecular BiologyeLifePeer-reviewedMay 22, 2026

Mechanistic insights into transcriptional regulation of ARHGAP36 expression identify a factor predictive of neuroblastoma survival

Serhiy Havrylov, Armin M. Gamper, Ordan J. Lehmann

The paper identifies FOXC1 as a transcription factor that enhances ARHGAP36 expression, increasing Hedgehog pathway activity and predicting improved neuroblastoma survival.

DOI 10.7554/elife.108827.3

mousebulk RNA-seq

𝕏 PostBluesky

GeneticsGenesPeer-reviewedJan 26, 2021

The Axenfeld-Rieger syndrome gene FOXC1 contributes to left-right patterning

Paul W. Chrystal, Curtis R. French, Francesca Jean…·Andrew Jan Waskiewicz

This paper shows that FOXC1 mutations in zebrafish cause left-right axis defects and congenital heart defects, similar to human Axenfeld-Rieger syndrome.

8 citations

zebrafishexperimental assay

𝕏 PostBluesky

GeneticsbioRxivPreprintAug 13, 2020

Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling

Serhiy Havrylov, Paul W. Chrystal, Suey van Baarle…·Ordan J. Lehmann

The paper shows that FOXC1 affects ciliation and cilia-dependent signaling, contributing to pleiotropic phenotypes in Axenfeld-Rieger Syndrome.

DOI 10.1101/2020.08.13.249334

mousestatistical model

𝕏 PostBluesky