Author

Patrick Frosk

Children's Hospital Research Institute of ManitobaORCID 0000-0002-9673-795XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Alexandria Martin· 1 shared Alondra Griffiths· 1 shared Bradley W. DobleiD· 1 shared Britt I. DrögemölleriD· 1 shared Danielle M. PascualiD· 1 shared Galen E.B. WrightiD· 1 shared Harsimran Kaur· 1 shared Jessica N. HartleyiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetics

Alexandria Martin

Mutual co-authors in cluster

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2 papers

Recent·Most cited

CK2 variant function and disease modelling in Drosophila reveal allelic heterogeneity and Wnt/β-catenin-mediated phenotypes

Yina Her, Danielle M. Pascual, Ying Lao, Harsimran Kaur, Alondra Griffiths, Robert Beattie, Bradley W. Doble, Patrick Frosk, René Peiman Zahedi, Paul C. Marcogliese

The paper uses Drosophila to model CK2 variants causing neurodevelopmental disorders, finding loss- and gain-of-function effects and Wnt/β-catenin-mediated phenotypes.

bioRxiv · Aug 21, 2026 · PreprintGenetics

Identifying fundamental properties of neuromuscular disorder genes through genomic feature analysis

Alexandria Martin, M. Alejandra Llanes-Cuesta, Jessica N. Hartley, Patrick Frosk, Britt I. Drögemöller, Galen E.B. Wright

The paper identifies genomic features distinguishing neuromuscular disorder genes from other genes using machine learning and statistical analysis.

Human Molecular Genetics · Jan 1, 2026Peer-reviewedGenetics