| Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome EL Berg, MC Pride, SP Petkova, RD Lee, NA Copping, Y Shen, A Adhikari, ... Translational psychiatry 10 (1), 39, 2020 | 49 | 2020 |
| Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice JL Haigh, A Adhikari, NA Copping, T Stradleigh, AA Wade, R Catta-Preta, ... Genome Medicine 13 (1), 69, 2021 | 22 | 2021 |
| Promoter element arising from the fusion of standard BioBrick parts AI Yao, TA Fenton, K Owsley, P Seitzer, DJ Larsen, H Sit, J Lau, A Nair, ... ACS synthetic biology 2 (2), 111-120, 2013 | 18 | 2013 |
| Excessive laughter-like vocalizations, microcephaly, and translational outcomes in the Ube3a deletion rat model of Angelman syndrome EL Berg, SA Jami, SP Petkova, A Berz, TA Fenton, JP Lerch, DJ Segal, ... Journal of Neuroscience 41 (42), 8801-8814, 2021 | 17 | 2021 |
| Gait as a quantitative translational outcome measure in Angelman syndrome SP Petkova, A Adhikari, EL Berg, TA Fenton, J Duis, JL Silverman Autism Research 15 (5), 821-833, 2022 | 15 | 2022 |
| Transcriptional reprogramming restores UBE3A brain-wide and rescues behavioral phenotypes in an Angelman syndrome mouse model H O’Geen, U Beitnere, MS Garcia, A Adhikari, DL Cameron, TA Fenton, ... Molecular Therapy 31 (4), 1088-1105, 2023 | 14 | 2023 |
| Touchscreen cognitive deficits, hyperexcitability and hyperactivity in males and females using two models of Cdkl5 deficiency A Adhikari, FKB Buchanan, TA Fenton, DL Cameron, JANM Halmai, ... Human molecular genetics 31 (18), 3032-3050, 2022 | 14 | 2022 |
| Cyclin D2-knock-out mice with attenuated dentate gyrus neurogenesis have robust deficits in long-term memory formation SP Petkova, M Pride, C Klocke, TA Fenton, J White, PJ Lein, J Ellegood, ... Scientific reports 10 (1), 8204, 2020 | 8 | 2020 |
| Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy S Quinn, N Zhang, TA Fenton, M Brusel, P Muruganandam, Y Peleg, ... Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1870 (5), 167127, 2024 | 1 | 2024 |
| Hyperexcitability and translational phenotypes in a preclinical model of SYNGAP1 mutations TA Fenton, OY Haouchine, EL Hallam, EM Smith, KC Jackson, ... bioRxiv, 2023.07. 24.550093, 2023 | 1 | 2023 |
| Structural, biophysical, and neurophysiological effects of SCN2A mutations SMA Wafa, G Yazdani, TA Fenton, CH Thompson, R Ben-Shalom, ... Biophysical Journal 123 (3), 12a, 2024 | | 2024 |
| Hyperexcitability and translational phenotypes in a preclinical model of SYNGAP1 mutations JL Silverman, T Fenton, O Haouchine, E Hallam, E Smith, K Jackson, ... Research Square, 2023 | | 2023 |
| The SCN8A p.(Gly1625Arg) variant associated with developmental and epileptic encephalopathy causes complex biophysical changes and reduced neuronal firing S Quinn, N Zhang, TA Fenton, M Brusel, P Muruganandam, Y Peleg, ... bioRxiv, 2023 | | 2023 |
| Translational in vitro and in vivo Neurobiological and Behavioral Outcomes in Preclinical Models of Neurodevelopmental Disorders TA Fenton UC Davis, 2023 | | 2023 |
| Durable and Specific Rescue of UBE3A Expression in the Brain of an Angelman Syndrome Mouse Model Using an Artificial Transcription Factor H O'Geen, U Beitnere, MS Palomares, NA Copping, DL Cameron, ... MOLECULAR THERAPY 30 (4), 223-224, 2022 | | 2022 |
| Cas13d for Ube3a-ATS Targeting in Angelman Syndrome U Beitnere, MS Palomares, H O'Geen, PB Deng, DL Cameron, A Adhikari, ... MOLECULAR THERAPY 29 (4), 269-269, 2021 | | 2021 |
| Correction to Promoter Element Arising from the Fusion of Standard BioBrick Parts AI Yao, TA Fenton, K Owsley, P Seitzer, DJ Larsen, H Sit, J Lau, A Nair, ... ACS Synthetic Biology 2 (6), 351-351, 2013 | | 2013 |
