RNA-Seq Reveals Spliceosome and Proteasome Genes as Most Consistent Transcripts in Human Cancer Cells

por MacRae, Tara, Sargeant, Tobias, Lemieux, Sébastien, Hébert, Josée, Deneault, Éric, Sauvageau, Guy
Publicado 2013

A role for GPx3 in activity of normal and leukemia stem cells

por Herault, Olivier, Hope, Kristin J., Deneault, Eric, Mayotte, Nadine, Chagraoui, Jalila, Wilhelm, Brian T., Cellot, Sonia, Sauvageau, Martin, Andrade-Navarro, Miguel A., Hébert, Josée, Sauvageau, Guy
Publicado 2012

Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly

por Woodbury-Smith, Marc, Deneault, Eric, Yuen, Ryan K. C., Walker, Susan, Zarrei, Mehdi, Pellecchia, Giovanna, Howe, Jennifer L., Hoang, Ny, Uddin, Mohammed, Marshall, Christian R., Chrysler, Christina, Thompson, Ann, Szatmari, Peter, Scherer, Stephen W.
Publicado 2017

Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neurons

por Faheem, Muhammad, Deneault, Eric, Alexandrova, Roumiana, Rodrigues, Deivid C., Pellecchia, Giovanna, Shum, Carole, Zarrei, Mehdi, Piekna, Alina, Wei, Wei, Howe, Jennifer L., Thiruvahindrapuram, Bhooma, Lamoureux, Sylvia, Ross, P. Joel, Bradley, Clarrisa A., Ellis, James, Scherer, Stephen W.
Publicado 2023

CNTN5(-)(/+)or EHMT2(-)(/+)human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networks

por Deneault, Eric, Faheem, Muhammad, White, Sean H, Rodrigues, Deivid C, Sun, Song, Wei, Wei, Piekna, Alina, Thompson, Tadeo, Howe, Jennifer L, Chalil, Leon, Kwan, Vickie, Walker, Susan, Pasceri, Peter, Roth, Frederick P, Yuen, Ryan KC, Singh, Karun K, Ellis, James, Scherer, Stephen W
Publicado 2019

Transcriptional Dysregulation and Impaired Neuronal Activity in FMR1 Knock-Out and Fragile X Patients’ iPSC-Derived Models

por Maussion, Gilles, Rocha, Cecilia, Abdian, Narges, Yang, Dimitri, Turk, Julien, Carrillo Valenzuela, Dulce, Pimentel, Luisa, You, Zhipeng, Morquette, Barbara, Nicouleau, Michael, Deneault, Eric, Higgins, Samuel, Chen, Carol X.-Q., Reintsch, Wolfgang E., Ho, Stanley, Soubannier, Vincent, Lépine, Sarah, Modrusan, Zora, Lund, Jessica, Stephenson, William, Schubert, Rajib, Durcan, Thomas M.
Publicado 2023

SHANK2 mutations associated with Autism Spectrum Disorder cause hyperconnectivity of human neurons

por Zaslavsky, Kirill, Zhang, Wen-Bo, McCready, Fraser P., Rodrigues, Deivid C., Deneault, Eric, Loo, Caitlin, Zhao, Melody, Ross, P. Joel, Hajjar, Joelle El, Romm, Asli, Thompson, Tadeo, Piekna, Alina, Wei, Wei, Wang, Zhuozhi, Khattak, Shahryar, Mufteev, Marat, Pasceri, Peter, Scherer, Stephen W., Salter, Michael W., Ellis, James
Publicado 2019

Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons

por Deneault, Eric, White, Sean H., Rodrigues, Deivid C., Ross, P. Joel, Faheem, Muhammad, Zaslavsky, Kirill, Wang, Zhuozhi, Alexandrova, Roumiana, Pellecchia, Giovanna, Wei, Wei, Piekna, Alina, Kaur, Gaganjot, Howe, Jennifer L., Kwan, Vickie, Thiruvahindrapuram, Bhooma, Walker, Susan, Lionel, Anath C., Pasceri, Peter, Merico, Daniele, Yuen, Ryan K.C., Singh, Karun K., Ellis, James, Scherer, Stephen W.
Publicado 2018

Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons

por Deneault, Eric, White, Sean H., Rodrigues, Deivid C., Ross, P. Joel, Faheem, Muhammad, Zaslavsky, Kirill, Wang, Zhuozhi, Alexandrova, Roumiana, Pellecchia, Giovanna, Wei, Wei, Piekna, Alina, Kaur, Gaganjot, Howe, Jennifer L., Kwan, Vickie, Thiruvahindrapuram, Bhooma, Walker, Susan, Lionel, Anath C., Pasceri, Peter, Merico, Daniele, Yuen, Ryan K.C., Singh, Karun K., Ellis, James, Scherer, Stephen W.
Publicado 2019

Midbrain organoids with an SNCA gene triplication model key features of synucleinopathy

por Mohamed, Nguyen-Vi, Sirois, Julien, Ramamurthy, Janani, Mathur, Meghna, Lépine, Paula, Deneault, Eric, Maussion, Gilles, Nicouleau, Michael, Chen, Carol X -Q, Abdian, Narges, Soubannier, Vincent, Cai, Eddie, Nami, Harris, Thomas, Rhalena A, Wen, Dingke, Tabatabaei, Mahdieh, Beitel, Lenore K, Singh Dolt, Karamjit, Karamchandani, Jason, Stratton, Jo Anne, Kunath, Tilo, Fon, Edward A, Durcan, Thomas M
Publicado 2021

Genome-wide characteristics of de novo mutations in autism

por Yuen, Ryan KC, Merico, Daniele, Cao, Hongzhi, Pellecchia, Giovanna, Alipanahi, Babak, Thiruvahindrapuram, Bhooma, Tong, Xin, Sun, Yuhui, Cao, Dandan, Zhang, Tao, Wu, Xueli, Jin, Xin, Zhou, Ze, Liu, Xiaomin, Nalpathamkalam, Thomas, Walker, Susan, Howe, Jennifer L, Wang, Zhuozhi, MacDonald, Jeffrey R, Chan, Ada JS, D’Abate, Lia, Deneault, Eric, Siu, Michelle T, Tammimies, Kristiina, Uddin, Mohammed, Zarrei, Mehdi, Wang, Mingbang, Li, Yingrui, Wang, Jun, Wang, Jian, Yang, Huanming, Bookman, Matt, Bingham, Jonathan, Gross, Samuel S, Loy, Dion, Pletcher, Mathew, Marshall, Christian R, Anagnostou, Evdokia, Zwaigenbaum, Lonnie, Weksberg, Rosanna, Fernandez, Bridget A, Roberts, Wendy, Szatmari, Peter, Glazer, David, Frey, Brendan J, Ring, Robert H, Xu, Xun, Scherer, Stephen W
Publicado 2016