Author

Sabina Trebinjac

Sunnybrook Health Science Centre

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:statistical model· 2 Research Focus:batch correction / integration· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Eliseos J. MucakiiD· 2 shared Michael T. HallettiD· 2 shared Sharon Nofech‐MozesiD· 2 shared Vanessa DumeauxiD· 2 shared A Saha· 1 shared E RakovitchiD· 1 shared Eileen Rakovitch· 1 shared Emily L Salmini· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 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 papersBioinformatics

Eliseos J. MucakiORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Generative and integrative modeling for transcriptomics with formalin fixed paraffin embedded material

Eliseos J. Mucaki, Wenhan Zhang, A Saha, Sabina Trebinjac, Sharon Nofech‐Mozes, E Rakovitch, Vanessa Dumeaux, Michael T. Hallett

The paper introduces PREFFECT, a probabilistic framework to improve analysis of FFPE-derived RNA-seq data by addressing transcript dropout and variance through generative models and graph attention mechanisms.

Journal of Translational Medicine · Sep 30, 2025Peer-reviewedBioinformatics

Mutational landscape of pure ductal carcinoma in situ and associations with disease prognosis and response to radiotherapy

Noor Rizvi, Eliseos J. Mucaki, Emily L Salmini, Monica Zhang, Sabina Trebinjac, Ezra Hahn, Lawrence Paszat, Sharon Nofech‐Mozes, Michael T. Hallett, Eileen Rakovitch, Vanessa Dumeaux

This study identifies genetic alterations associated with recurrence and radiotherapy response in ductal carcinoma in situ using whole-exome sequencing and copy number analysis.

Breast Cancer Research · Jul 8, 2025Peer-reviewedGenetic & Genomic Medicine