Steven J. Clapcote, Ph.D.
Affiliations: | University of Leeds, Leeds, England, United Kingdom |
Area:
Genetics, Mouse models, Behaviour, Psychiatric disordersWebsite:
http://www.fbs.leeds.ac.uk/staff/profile.php?tag=Clapcote_SGoogle:
"Steven Clapcote"Bio:
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)
Parents
Sign in to add mentor| John Carling Roder | grad student | 2002-2007 | Mount Sinai Hospital (University of Toronto). |
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Publications
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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 |