Author

Maggie M. Balas

University of Colorado AnschutzORCID 0000-0002-0701-1787Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:experimental assay· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:perturbation response prediction· 1 Assay:proteomics· 1

Frequent Co-Authors

Galen T SquiersiD· 2 shared Jason C. KleiniD· 2 shared Joshua J. LingoiD· 2 shared Aaron M. JohnsoniD· 1 shared April M. GriffiniD· 1 shared Arjun M. BashyamiD· 1 shared Attila KumánovicsiD· 1 shared Benjamin A. NanesiD· 1 shared

Activity by Year

2026-2026 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersGenomics

Galen T SquiersORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Perturb-seq resolves physiologic programs and bidirectional regulation of non-canonical NF-κB signaling in epidermal organoids

Galen T Squiers, Benjamin A. Nanes, Maggie M. Balas, Joshua J. Lingo, L H Wang, Huan Zhao, Sabahat Munawar, Mpathi Nzima, Gary C. Hon, Jason C. Klein

The paper uses Perturb-seq in epidermal organoids to study non-canonical NF-κB signaling's role in keratinocyte differentiation.

bioRxiv · Jul 23, 2026 · PreprintGenomics

Proteomics and single-cell transcriptomics identify LRP1 as a diagnostic biomarker for atypical fibroxanthoma and pleomorphic dermal sarcoma.

Joshua J. Lingo, Maggie M. Balas, Arjun M. Bashyam, Gregory A. Hosler, Galen T Squiers, Jason C. Klein

The paper identifies LRP1 as a more accurate biomarker for diagnosing atypical fibroxanthoma and pleomorphic dermal sarcoma compared to existing markers.

bioRxiv · Feb 9, 2026 · PreprintCancer Biology

Characterization of an immunodeficiency-associated EZH2 variant

Francisco Perez de los Santos, Lily Beck, Emily DeCurtis, April M. Griffin, Maggie M. Balas, Charlotte Marchioni, Attila Kumánovics, Matthew R.G. Taylor, Kimberly Rae Jordan, Charles H. Kirkpatrick, Aaron M. Johnson

This study identifies an EZH2 variant associated with immunodeficiency and shows it impairs PRC2 function by disrupting H3K27me3 methylation at specific genomic regions.

bioRxiv · Jan 21, 2026 · PreprintMolecular Biology