Author

Rebecca R. J. Collins

Indiana University BloomingtonORCID 0000-0003-0936-2270Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Cancer Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:proteomics· 1 Assay:spatial transcriptomics· 1

Frequent Co-Authors

Adrian Mejia-SantanaiD· 1 shared Anna K. LeeiD· 1 shared Barbara BreznikiD· 1 shared Cristina LandetaiD· 1 shared Dinesh RakhejaiD· 1 shared Emma H. DoudiD· 1 shared Heather S. Tillman· 1 shared Jon P. ConnellyiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 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

1 shared paperMicrobiology

Adrian Mejia-SantanaORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

MicrobiologymBioPeer-reviewedJul 31, 2025

Disulfide bonds are required for cell division, cell envelope biogenesis and antibiotic resistance proteins in mycobacteria

Adrian Mejia-Santana, Rebecca R. J. Collins, Emma H. Doud, Cristina Landeta

The paper identifies cell envelope proteins in mycobacteria that require disulfide bonds for stability and shows that inhibiting the DsbA-VKOR pathway affects cell division and antibiotic resistance.

7 citationstop 4%

proteomicsexperimental assay

𝕏 PostBluesky

Cancer BiologyActa Neuropathologica CommunicationsPeer-reviewedJul 28, 2025

Melanoma antigens in pediatric medulloblastoma contribute to tumor heterogeneity and species-specificity of group 3 tumors

Rebecca R. J. Collins, Rebecca R. Florke Gee, Sima Tozandehjani…·Klementina Fon Tacer

This study identifies MAGE antigens as markers of tumor heterogeneity and species-specificity in group 3 medulloblastoma, showing their role in cell survival and potential as therapeutic targets.

3 citations

humanbulk RNA-seq

𝕏 PostBluesky