Peter Kind

University of Edinburgh, Edinburgh, Scotland, United Kingdom 
Developmental Neuroscience
"Peter Kind"
Mean distance: 13.38 (cluster 6)


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Colin Blakemore grad student 1993 Oxford
Susan J. Hockfield post-doc 1993-1997 Yale
Colin Blakemore post-doc 1997-2000 Oxford


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Daniel Giffney research assistant Edinburgh
Tommas J. Ellender research assistant 2003-2004 Edinburgh
Chih-Yuan Chiang grad student 2011- Edinburgh
Sally Till post-doc 2006- Edinburgh
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Zoupi L, Booker SA, Eigel D, et al. (2021) Selective vulnerability of inhibitory networks in multiple sclerosis. Acta Neuropathologica
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
Booker SA, Simões de Oliveira L, Anstey NJ, et al. (2020) Input-Output Relationship of CA1 Pyramidal Neurons Reveals Intact Homeostatic Mechanisms in a Mouse Model of Fragile X Syndrome. Cell Reports. 32: 107988
Das Sharma S, Pal R, Reddy BK, et al. (2020) Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patterns. Molecular Autism. 11: 52
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
Booker SA, Domanski APF, Dando OR, et al. (2019) Altered dendritic spine function and integration in a mouse model of fragile X syndrome. Nature Communications. 10: 4813
Domanski APF, Booker SA, Wyllie DJA, et al. (2019) Cellular and synaptic phenotypes lead to disrupted information processing in Fmr1-KO mouse layer 4 barrel cortex. Nature Communications. 10: 4814
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
Strehlow V, Heyne HO, Vlaskamp DRM, et al. (2018) GRIN2A-related disorders: genotype and functional consequence predict phenotype. Brain : a Journal of Neurology
McKay S, Ryan TJ, McQueen J, et al. (2018) The Developmental Shift of NMDA Receptor Composition Proceeds Independently of GluN2 Subunit-Specific GluN2 C-Terminal Sequences. Cell Reports. 25: 841-851.e4
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