Amanda R. Rendall
Affiliations: | 2011-2016 | Yale University, New Haven, CT |
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| Perrino PA, Talbot L, Kirkland R, et al. (2020) Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes. Communications Biology. 3: 180 |
| Rendall AR, Perrino PA, Buscarello AN, et al. (2018) Shank3B mutant mice display pitch discrimination enhancements and learning deficits. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience |
| Rendall AR, Perrino PA, LoTurco JJ, et al. (2017) Evaluation of visual motion perception ability in mice with knockout of the dyslexia candidate susceptibility gene Dcdc2. Genes, Brain, and Behavior |
| Rendall AR, Ford AL, Perrino PA, et al. (2017) Auditory processing enhancements in the TS2-neo mouse model of Timothy Syndrome, a rare genetic disorder associated with autism spectrum disorders. Advances in Neurodevelopmental Disorders. 1: 176-189 |
| Rendall AR, Truong DT, Fitch RH. (2016) Learning delays in a mouse model of Autism Spectrum Disorder. Behavioural Brain Research. 303: 201-7 |
| Rendall AR, Truong DT, Castelluccio BC, et al. (2015) Language deficits in autism and assessment of the Cntnap2 mouse. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 93 |
| Truong DT, Rendall AR, Castelluccio BC, et al. (2015) Auditory Processing and Morphological Anomalies in Medial Geniculate Nucleus of Cntnap2 Mutant Mice. Behavioral Neuroscience |
| Rendall AR, Tarkar A, Contreras-Mora HM, et al. (2015) Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1. Brain and Language |
| Truong DT, Rendall AR, Rosen GD, et al. (2015) Morphometric changes in subcortical structures of the central auditory pathway in mice with bilateral nodular heterotopia. Behavioural Brain Research. 282: 61-9 |
| Rendall AR, Tarkar A, Contreras-Mora HM, et al. (2015) Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1 Brain and Language |