Items where authors include "Clapcote, SJ"
Article
Clapcote, SJ orcid.org/0000-0002-6662-5690 (2022) How can we obtain truly translational mouse models to improve clinical outcomes in schizophrenia? Disease Models & Mechanisms, 15 (11). dmm049970. ISSN 1754-8403
Al-Amri, AH, Armstrong, P orcid.org/0000-0001-8735-3762, Amici, M et al. (22 more authors) (2022) PDZD8 Disruption Causes Cognitive Impairment in Humans, Mice and Fruit Flies. Biological Psychiatry, 92 (4). pp. 323-334. ISSN 0006-3223
Hughes, RB, Whittingham-Dowd, J, Clapcote, SJ orcid.org/0000-0002-6662-5690 et al. (2 more authors) (2022) Altered medial prefrontal cortex and dorsal raphé activity predict genotype and correlate with abnormal learning behavior in a mouse model of autism-associated 2p16.3 deletion. Autism research : official journal of the International Society for Autism Research, 15 (4). pp. 614-627. ISSN 1939-3792
Wilkinson, ID, Mahmood, T, Yasmin, SF et al. (11 more authors) (2022) In memory of Professor Iain Wilkinson: cognitive and neuroimaging endophenotypes in a consanguineous schizophrenia multiplex family. Psychological Medicine. PII S0033291721005250. ISSN 0033-2917
Ng, HWY, Ogbeta, JA and Clapcote, SJ orcid.org/0000-0002-6662-5690 (2021) Genetically altered animal models for ATP1A3-related disorders. Disease Models and Mechanisms, 14 (10). dmm048938. ISSN 1754-8403
Hosalli, P, Cardno, A orcid.org/0000-0002-6136-5965, Brewin, A et al. (4 more authors) (2021) Risk of psychosis in Yorkshire African, Caribbean and Mixed Ethnic communities. Journal of Psychiatric Intensive Care, 17 (2). pp. 107-111. ISSN 1742-6464
Cole, BA, Clapcote, SJ, Muench, SP et al. (1 more author) (2021) Targeting KNa1.1 channels in KCNT1-associated epilepsy. Trends in Pharmacological Sciences. ISSN 0165-6147
Mahmood, T, El-Asrag, ME, Poulter, JA orcid.org/0000-0003-2048-5693 et al. (19 more authors) (2020) A recessively inherited risk locus on chromosome 13q22-31 conferring susceptibility to schizophrenia. Schizophrenia Bulletin. ISSN 0586-7614
Hughes, RB, Whittingham-Dowd, J, Simmons, RE et al. (3 more authors) (2020) Ketamine Restores Thalamic-Prefrontal Cortex Functional Connectivity in a Mouse Model of Neurodevelopmental Disorder-Associated 2p16.3 Deletion. Cerebral Cortex, 30 (4). pp. 2358-2371. ISSN 1047-3211
Al-Amri, AH, Al Saegh, A, Al-Mamari, W et al. (10 more authors) (2019) LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics, 62 (12). 103592. ISSN 1769-7212
Pervolaraki, E, Tyson, AL, Pibiri, F et al. (7 more authors) (2019) The within-subject application of diffusion tensor MRI and CLARITY reveals brain structural changes in Nrxn2 deletion mice. Molecular Autism, 10 (1). ARTN 8. ISSN 2040-2392
Alsaady, I, Tedford, E, Alsaad, M et al. (8 more authors) (2019) Downregulation of the central noradrenergic system by Toxoplasma gondii infection. Infection and Immunity, 87 (2). e00789-18. ISSN 0019-9567
Timothy, JWS, Klas, N, Sanghani, HR et al. (8 more authors) (2018) Circadian Disruptions in the Myshkin Mouse Model of Mania Are Independent of Deficits in Suprachiasmatic Molecular Clock Function. Biological Psychiatry, 84 (11). pp. 827-837. ISSN 0006-3223
Cheung, SY, Henrot, M, Al-Saad, M et al. (17 more authors) (2018) TRPC4/TRPC5 channels mediate adverse reaction to the cancer cell cytotoxic agent (-)-Englerin A. Oncotarget, 9 (51). pp. 29634-29643. ISSN 1949-2553
Al-Amri, A, Saegh, AA, Al-Mamari, W et al. (6 more authors) (2016) Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. American Journal of Medical Genetics Part A, 170 (7). pp. 1826-1831. ISSN 1552-4825
Kirshenbaum, GS, Idris, NF, Dachtler, J et al. (2 more authors) (2016) Deficits in social behavioral tests in a mouse model of alternating hemiplegia of childhood. Journal of Neurogenetics, 30 (1). pp. 42-49. ISSN 0167-7063
McGirr, A, Lipina, TV, Mun, HS et al. (11 more authors) (2016) Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition. Neuropsychopharmacology, 41. pp. 1080-1092. ISSN 0893-133X
Dachtler, J, Elliott, C, Rodgers, RJ et al. (2 more authors) (2016) Missense mutation in DISC1 C-terminal coiled-coil has GSK3β signaling and sex-dependent behavioral effects in mice. Scientific Reports, 6. 18748. ISSN 2045-2322
Kirshenbaum, GS, Dachtler, JD, Roder, JC et al. (1 more author) (2016) Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood. Neurogenetics, 17 (1). pp. 57-63. ISSN 1364-6745
Kirshenbaum, GS, Dachtler, J, Roder, JC et al. (1 more author) (2015) Characterization of Cognitive Deficits in Mice with an Alternating Hemiplegia-Linked Mutation. Behavioral Neuroscience, 129 (6). pp. 822-831. ISSN 0735-7044
Dachtler, J, Ivorra, JL, Rowland, TE et al. (3 more authors) (2015) Heterozygous Deletion of α-Neurexin I or α-Neurexin II Results in Behaviors Relevant to Autism and Schizophrenia. Behavioral Neuroscience, 129 (6). 765 - 776. ISSN 0735-7044
Dachtler, J, Glasper, J, Cohen, RN et al. (6 more authors) (2014) Deletion of α-neurexin II results in autism-related behaviors in mice. Translational Psychiatry, 4 (11). e484. e484 - ?. ISSN 2158-3188
Chandran, JS, Kazanis, I, Clapcote, SJ et al. (4 more authors) (2014) Disc1 variation leads to specific alterations in adult neurogenesis. PLoS ONE, 9 (10). ARTN e108088. ISSN 1932-6203
Ritchie, DJ and Clapcote, SJ (2013) Disc1 deletion is present in Swiss-derived inbred mouse strains: implications for transgenic studies of learning and memory. Laboratory Animals, 47 (3). 162 - 167. ISSN 0023-6772
Edwards, IJ, Bruce, G, Lawrenson, C et al. (4 more authors) (2013) Na+/K+ ATPase α1 and α3 Isoforms Are Differentially Expressed in α- and γ-Motoneurons. Journal of Neuroscience, 33 (24). 9913 - 9919. ISSN 0270-6474