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High-content synaptic phenotyping in human cellular models reveals a role for BET proteins in synapse assembly Berryer, Martin H.; Rizki, Gizem; Nathanson, Anna; Klein, Jenny A.; Trendafilova, Darina; Susco, Sara G.; Lam, Daisy; Messana, Angelica; Holton, Kristina M.; Karhohs, Kyle W.; Cimini, Beth A.; Pfaff, Kathleen; Carpenter, Anne E.; Rubin, Lee L.; Barrett, Lindy E.; Goda, Yukiko Share Save
Molecular convergence between Down syndrome and fragile X syndrome identified using human pluripotent stem cell models Susco, Sara G.; Ghosh, Sulagna; Mazzucato, Patrizia; Angelini, Gabriella; Beccard, Amanda; Barrera, Victor; Berryer, Martin H.; Messana, Angelica; Lam, Daisy; Hazelbaker, Dane Z.; Barrett, Lindy E. Share Save
Sensitive period for rescuing parvalbumin interneurons connectivity and social behavior deficits caused by TSC1 loss Amegandjin, Clara A.; Choudhury, Mayukh; Jadhav, Vidya; Carrico, Josianne Nunes; Quintal, Ariane; Berryer, Martin; Snapyan, Marina; Chattopadhyaya, Bidisha; Saghatelyan, Armen; Di Cristo, Graziella Share Save
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Antenatal Suppression of IL-1 Protects against Inflammation-Induced Fetal Injury and Improves Neonatal and Developmental Outcomes in Mice Nadeau-Vallee, Mathieu; Chin, Peck-Yin; Belarbi, Lydia; Brien, Marie-Eve; Pundir, Sheetal; Berryer, Martin H.; Beaudry-Richard, Alexandra; Madaan, Ankush; Sharkey, David J.; Lupien-Meilleur, Alexis; Hou, Xin; Quiniou, Christiane; Beaulac, Alexandre; Boufaied, Ines; Boudreault, Amarilys; Carbonaro, Adriana; Ngoc-Duc Doan; Joyal, Jean-Sebastien; Lubell, William D.; Olson, David M.; Robertson, Sarah A.; Girard, Sylvie; Chemtob, Sylvain Share Save
Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function Berryer, Martin H.; Chattopadhyaya, Bidisha; Xing, Paul; Riebe, Ilse; Bosoi, Ciprian; Sanon, Nathalie; Antoine-Bertrand, Judith; Levesque, Maxime; Avoli, Massimo; Hamdan, Fadi F.; Carmant, Lionel; Lamarche-Vane, Nathalie; Lacaille, Jean-Claude; Michaud, Jacques L.; Di Cristo, Graziella Share Save
Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency Berryer, Martin H.; Hamdan, Fadi F.; Klitten, Laura L.; Moller, Rikke S.; Carmant, Lionel; Schwartzentruber, Jeremy; Patry, Lysanne; Dobrzeniecka, Sylvia; Rochefort, Daniel; Neugnot-Cerioli, Mathilde; Lacaille, Jean-Claude; Niu, Zhiyv; Eng, Christine M.; Yang, Yaping; Palardy, Sylvain; Belhumeur, Celine; Rouleau, Guy A.; Tommerup, Niels; Immken, LaDonna; Beauchamp, Miriam H.; Patel, Gayle Simpson; Majewski, Jacek; Tarnopolsky, Mark A.; Scheffzek, Klaus; Hjalgrim, Helle; Michaud, Jacques L.; Di Cristo, Graziella Share Save
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