Roy Hanna

Deregulation of Neuro-Developmental Genes and Primary Cilium Cytoskeleton Anomalies in iPSC Retinal Sheets from Human Syndromic Ciliopathies

Benjamin S. Freedman, E. Héon, G. Bernier, 2020, Stem cell reports.

Loss of Bmi1 causes anomalies in retinal development and degeneration of cone photoreceptors

N. Motoyama, M. Hébert, G. Bernier, 2016, Development.

Retinal development anomalies and cone photoreceptors degeneration upon Bmi 1 deficiency

N. Motoyama, M. Hébert, G. Bernier, 2016 .

Off-target effect of the BMI1 inhibitor PTC596 drives epithelial-mesenchymal transition in glioblastoma multiforme

G. Bernier, M. Abdouh, A. Barabino, 2020, npj Precision Oncology.

The Polycomb Repressive Complex 1 Protein BMI1 Is Required for Constitutive Heterochromatin Formation and Silencing in Mammalian Somatic Cells*

G. Bernier, M. Abdouh, A. Flamier, 2015, The Journal of Biological Chemistry.

G-quadruplexes originating from evolutionary conserved L1 elements interfere with neuronal gene expression in Alzheimer’s disease

G. Bernier, A. Barabino, A. Flamier, 2021, Nature Communications.

Heterochromatic genome instability and neurodegeneration sharing similarities with Alzheimer’s disease in old Bmi1+/− mice

Y. Tse, N. Tétreault, T. Wong, 2019, Scientific Reports.

Epigenomic anomalies in induced pluripotent stem cells from Alzheimer’s disease cases

E. Tavares, A. Flamier, Roy Hanna, 2024, bioRxiv.