Sally Till
Affiliations: | Columbia University, New York, NY |
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"Sally Till"Mean distance: 12.6 (cluster 6) | S | N | B | C | P |
Parents
Sign in to add mentorEric R. Kandel | grad student | 2006 | Columbia | |
(Genetic approaches to fragile X syndrome.) | ||||
Peter Kind | post-doc | 2006- | Edinburgh |
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Publications
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Couto-Ovejero S, Ye J, Kind PC, et al. (2023) Cerebellar contributions to fear-based emotional processing: relevance to understanding the neural circuits involved in autism. Frontiers in Systems Neuroscience. 17: 1229627 |
Grandjean J, Desrosiers-Gregoire G, Anckaerts C, et al. (2023) Author Correction: A consensus protocol for functional connectivity analysis in the rat brain. Nature Neuroscience |
Grandjean J, Desrosiers-Gregoire G, Anckaerts C, et al. (2023) A consensus protocol for functional connectivity analysis in the rat brain. Nature Neuroscience |
Buller-Peralta I, Maicas-Royo J, Lu Z, et al. (2022) Abnormal brain state distribution and network connectivity in a rat model. Brain Communications. 4: fcac263 |
Till SM, Hickson RDL, Kind PC. (2022) Cross-species considerations in models of neurodevelopmental disorders. Trends in Neurosciences |
Wong H, Hooper AWM, Niibori Y, et al. (2020) Sexually dimorphic patterns in electroencephalography power spectrum and autism-related behaviors in a rat model of fragile X syndrome. Neurobiology of Disease. 105118 |
Mastro TL, Preza A, Basu S, et al. (2020) A sex difference in the response of the rodent postsynaptic density to synGAP haploinsufficiency. Elife. 9 |
Asiminas A, Jackson AD, Louros SR, et al. (2019) Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X Syndrome. Science Translational Medicine. 11 |
Till SM, Asiminas A, Jackson AD, et al. (2015) Conserved hippocampal cellular pathophysiology but distinct behavioural deficits in a new rat model of FXS. Human Molecular Genetics |
Till SM, Wijetunge LS, Seidel VG, et al. (2012) Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome. Human Molecular Genetics. 21: 2143-56 |