Defined neuronal populations drive fatal phenotype in a mouse model of Leigh syndrome I Bolea, A Gella, E Sanz, P Prada-Dacasa, F Menardy, AM Bard, ... Elife 8, e47163, 2019 | 46 | 2019 |
Disordered autonomic function during exposure to moderate heat or exercise in a mouse model of Dravet syndrome N Sahai, AM Bard, O Devinsky, F Kalume Neurobiology of disease 147, 105154, 2021 | 16 | 2021 |
Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability AD Wei, P Wakenight, TA Zwingman, AM Bard, N Sahai, MH Willemsen, ... Journal of neurophysiology 128 (1), 40-61, 2022 | 12 | 2022 |
Differential effects of mTOR inhibition and dietary ketosis in a mouse model of subacute necrotizing encephalomyelopathy R Bornstein, K James, J Stokes, KY Park, EB Kayser, J Snell, A Bard, ... Neurobiology of disease 163, 105594, 2022 | 10 | 2022 |
Non-synaptic Cell-Autonomous Mechanisms Underlie Neuronal Hyperactivity in a Genetic Model of PIK3CA-Driven Intractable Epilepsy A Roy, VZ Han, AM Bard, DT Wehle, SEP Smith, JM Ramirez, F Kalume, ... Frontiers in Molecular Neuroscience 14, 772847, 2021 | 6 | 2021 |
AAV-mediated interneuron-specific gene replacement for Dravet syndrome JK Mich, J Ryu, AD Wei, BB Gore, R Guo, AM Bard, RA Martinez, ... bioRxiv, 2023.12. 15.571820, 2023 | 3 | 2023 |
Suppression of PIK3CA-driven epileptiform activity by acute pathway control A Roy, VZ Han, AM Bard, DT Wehle, SEP Smith, JM Ramirez, F Kalume, ... bioRxiv, 2021.03. 03.433821, 2021 | 3 | 2021 |
Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing AM Bard, LV Clark, E Cosgun, KA Aldinger, A Timms, LA Quina, ... American Journal of Medical Genetics Part A, e63596, 2024 | | 2024 |
Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death (SUID) using Whole Genome Sequencing (WGS) JM Ramirez, AM Bard, LV Clark, E Cosgun, KA Aldinger, A Timms, ... medRxiv, 2023.09. 11.23295207, 2023 | | 2023 |
Defined neuronal populations drive fatal phenotype in Leigh Syndrome I Bolea, A Gella, E Sanz, P Prada-Dacasa, F Menardy, ... bioRxiv, 556019, 2019 | | 2019 |