I was appointed to the position of Scientist at the Children’s Hospital of Eastern Ontario Research Institute (CHEO RI) and Assistant Professor in the Department of Biochemistry, Microbiology and Immunology (BMI) at the University of Ottawa in January 2014. My training is in virology, innate immune responses, cell biology, and oncology. I received my B.Sc. (2000) in Biochemistry from Université Laval and my Ph.D.
(2007) in Medical Science from the University of Calgary. During my Ph.D., I studied the virology and the oncolytic potencies of reovirus, vesicular stomatitis virus, herpes simplex virus and myxoma virus against brain cancers. From 2007 to 2013, I pursued post-doctoral work at McGill University studying mRNA translational control and the mammalian target of rapamycin (mTOR) signaling pathway, linking both viral immunity and oncology research.
My current research in Ottawa focuses on exploiting translation initiation factors and downstream effectors of mTOR complex 1 (mTORC1) to modulate innate immune responses to oncolytic viruses, and to augment the anti-proliferative efficacies of cancer therapeutics.
Identification of pannexin 1-regulated genes, interactome, and pathways in rhabdomyosarcoma and its tumor inhibitory interaction with AHNAK.
Using this unbiased genome-wide approach, our transcriptomic analysis identified the genes that are regulated in PANX1-expressing RMS cells together with the key cellular processes in which they may be involved.
Catching a resurgence: Increase in SARS-CoV-2 viral RNA identified in wastewater 48 hours before COVID-19 clinical tests and 96 hours before hospitalizations
Wastewater-based COVID-19 epidemiology programs have been initiated in many countries to provide public health agencies with a complementary disease tracking metric and non-discriminating surveillance tool.
Quantitative analysis of SARS-CoV-2 RNA from wastewater solids in communities with low COVID-19 incidence and prevalence
Can we find COVID-19 markers in the wastewater that will help predict outbreaks?
Induction of an Alternative mRNA 5′ Leader Enhances Translation of the Ciliopathy Gene Inpp5e and Resistance to Oncolytic Virus Infection
Oncolytic virus infection decouples transcription and translation in cancer cells
Active-site mTOR inhibitors augment HSV1-dICP0 infection in cancer cells via dysregulated eIF4E/4E-BP axis