Timothy A. Fenton

发表

Cyclin D2-knock-out mice with attenuated dentate gyrus neurogenesis have robust deficits in long-term memory formation

J. Lerch, J. Ellegood, B. Waldau, 2020, Scientific Reports.

Excessive Laughter-like Vocalizations, Microcephaly, and Translational Outcomes in the Ube3a Deletion Rat Model of Angelman Syndrome

J. Lerch, J. Ellegood, J. A. Gray, 2021, The Journal of Neuroscience.

Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome

J. Lerch, E. Weeber, J. Ellegood, 2020, Translational Psychiatry.

Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice

D. Dickel, A. Visel, L. Pennacchio, 2021, Genome Medicine.

Deletion of a non-canonical promoter regulatory element causes loss of Scn1a expression and epileptic phenotypes in mice

D. Dickel, A. Visel, L. Pennacchio, 2019, bioRxiv.

Deletion of a non-canonical regulatory sequence causes loss of Scn 1 a 1 expression and epileptic phenotypes in mice 2 3

D. Dickel, A. Visel, L. Pennacchio, 2022 .

Touchscreen cognitive deficits, hyperexcitability and hyperactivity in males and females using two models of Cdkl5 deficiency

J. Silverman, N. Copping, J. Halmai, 2022, Human molecular genetics.

Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy

H. Bassan, Y. Haitin, Roy Ben-Shalom, 2023, bioRxiv.

The SCN8A p.(Gly1625Arg) variant associated with developmental and epileptic encephalopathy causes complex biophysical changes and reduced neuronal firing

H. Bassan, Y. Haitin, Roy Ben-Shalom, 2022 .

Hyperexcitability and translational phenotypes in a preclinical model of SYNGAP1 mutations

J. Silverman, Roy Ben-Shalom, A. Adhikari, 2023, Research square.

Hyperexcitability and translational phenotypes in a preclinical model of SYNGAP1 mutations

J. Silverman, Roy Ben-Shalom, A. Adhikari, 2023, bioRxiv.