Author

Elena Glick

University of MichiganORCID 0009-0007-0949-9812Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:deep learning· 2 Assay:DNA methylation· 2 Organism:human· 2 Research Focus:variant effect prediction· 2 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Jacob Otto KitzmaniD· 2 shared Shelby L. HemkeriD· 2 shared Alyssa Bashir· 1 shared Arjun Kumar· 1 shared Ashley P.L. MarshiD· 1 shared Caleb M. StrattoniD· 1 shared Ella Roberts· 1 shared Felicia Hernandez· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 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

2 shared papersCancer Biology

Jacob Otto KitzmanORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Cancer BiologybioRxivPreprintJan 11, 2026

High-throughput mapping of 6,888 RAD51D variants identifies distinct biochemical functions needed for homologous recombination and olaparib response

Kristie E. Darrah, Shelby L. Hemker, Yashpal Rawal…·Kara Anne Bernstein

This paper maps 6,888 RAD51D variants to identify biochemical functions critical for homologous recombination and olaparib response, revealing key regions and mechanisms of variant impact.

1 citation

humanDNA methylation

𝕏 PostBluesky

GenomicsThe American Journal of Human GeneticsPeer-reviewedJul 29, 2025

Saturation mapping of MUTYH variant effects using DNA repair reporters

Shelby L. Hemker, Ashley P.L. Marsh, Felicia Hernandez…·Jacob Otto Kitzman

The paper maps the functional effects of MUTYH variants using deep mutational scanning and DNA repair reporters, resolving variants of uncertain significance and identifying risk-associated mutations.

11 citationstop 2%

humanDNA methylation

𝕏 PostBluesky