Steven J. Clapcote, Ph.D.

University of Leeds, Leeds, England, United Kingdom 
Genetics, Mouse models, Behaviour, Psychiatric disorders
"Steven Clapcote"

Ph.D. supervisor: Prof. Steve Kemp, University of Liverpool.
Postdoctoral supervisors: Prof. Chris Graham FRS, University of Oxford; Dr John Roder, Mount Sinai Hospital, Toronto.

Mean distance: 17.59 (cluster 29)
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B Hughes R, Whittingham-Dowd J, Simmons RE, et al. (2019) Ketamine Restores Thalamic-Prefrontal Cortex Functional Connectivity in a Mouse Model of Neurodevelopmental Disorder-Associated 2p16.3 Deletion. Cerebral Cortex (New York, N.Y. : 1991)
Pervolaraki E, Tyson AL, Pibiri F, et al. (2019) The within-subject application of diffusion tensor MRI and CLARITY reveals brain structural changes in deletion mice. Molecular Autism. 10: 8
Al-Amri AH, Al Saegh A, Al-Mamari W, et al. (2018) LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics
Cheung SY, Henrot M, Al-Saad M, et al. (2018) TRPC4/TRPC5 channels mediate adverse reaction to the cancer cell cytotoxic agent (-)-Englerin A. Oncotarget. 9: 29634-29643
Timothy JWS, Klas N, Sanghani HR, et al. (2017) Circadian Disruptions in the Myshkin Mouse Model of Mania Are Independent of Deficits in Suprachiasmatic Molecular Clock Function. Biological Psychiatry
McGirr A, Lipina TV, Mun HS, et al. (2017) Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 42: 1178
Kirshenbaum GS, Idris NF, Dachtler J, et al. (2016) Deficits in social behavioral tests in a mouse model of alternating hemiplegia of childhood. Journal of Neurogenetics. 30: 42-9
Al-Amri A, Saegh AA, Al-Mamari W, et al. (2016) Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. American Journal of Medical Genetics. Part A
Dachtler J, Elliott C, Rodgers RJ, et al. (2016) Missense mutation in DISC1 C-terminal coiled-coil has GSK3β signaling and sex-dependent behavioral effects in mice. Scientific Reports. 6: 18748
Dachtler J, Ivorra JL, Rowland TE, et al. (2015) Heterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia. Behavioral Neuroscience. 129: 765-76
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