Author

Éric A. Cohen

Montreal Clinical Research InstituteORCID 0000-0003-1269-3791Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Immunology· 1 Microbiology· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:cell-cell communication· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

Tram N. Q. PhamiD· 2 shared Amélie CattiniD· 1 shared Christopher PoweriD· 1 shared Élie HaddadiD· 1 shared Éric LécuyeriD· 1 shared Eunjeong Kwon· 1 shared Frank KirchhoffiD· 1 shared Gabrielle Deschamps-FrancoeuriD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersMolecular Biology

Tram N. Q. PhamORCID

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3 papers

Recent·Most cited

MicrobiologybioRxivPreprintOct 29, 2026

Impact of HIV-1 infection on the microglia transcriptome: induction of microRNA-23b leads to G3BP2-mediated stress granules assembly disruption

Robert Lodge, William G. Branton, Frank Kirchhoff…·Éric A. Cohen

This study shows HIV-1 infection alters microglia transcriptome by upregulating microRNA-23b, which disrupts G3BP2 and stress granule assembly, promoting HIV-1 replication.

DOI 10.64898/2026.10.28.762254

humanbulk RNA-seq

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Molecular BiologybioRxivPreprintJan 23, 2026

Comparative profiling of SARS-CoV-2 variant infections reveals diverse impacts on host cell RNA and RNA binding protein distribution and regulation

Grégoire De Bisschop, Tram N. Q. Pham, Nicolas Jacques-De Vries…·Éric Lécuyer

This study compares the impact of SARS-CoV-2 variants on host cell RNA and RNA binding protein distribution, finding Omicron causes less disruption and maintains higher expression of translation factors.

DOI 10.64898/2026.01.22.701202

humanbulk RNA-seq

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ImmunologybioRxivPreprintJan 31, 2025

Humanized Bone Marrow-Liver-Thymus Mice for Studying HIV-1 Persistence in Liver and Lung CD4+ T and Myeloid Cell Subsets during Antiretroviral Therapy

Amélie Cattin, Tram N. Q. Pham, Jonathan Dias…·Petronela Ancuța

This study uses humanized mice to compare HIV-1 persistence in liver/lung macrophages and CD4+ T-cells during ART, finding macrophages contribute less to viral reservoirs than T-cells.

1 citation

humanexperimental assay

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