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Steven J. Clapcote, Ph.D. - Publications

Affiliations: 
University of Leeds, Leeds, England, United Kingdom 
Area:
Genetics, Mouse models, Behaviour, Psychiatric disorders
Website:
http://www.fbs.leeds.ac.uk/staff/profile.php?tag=Clapcote_S
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51 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 B Hughes R, Whittingham-Dowd J, Simmons RE, Clapcote SJ, Broughton SJ, Dawson N. 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). PMID 31812984 DOI: 10.1093/Cercor/Bhz244  0.364
2019 Pervolaraki E, Tyson AL, Pibiri F, Poulter SL, Reichelt AC, Rodgers RJ, Clapcote SJ, Lever C, Andreae LC, Dachtler J. The within-subject application of diffusion tensor MRI and CLARITY reveals brain structural changes in deletion mice. Molecular Autism. 10: 8. PMID 30858964 DOI: 10.1186/S13229-019-0261-9  0.374
2018 Al-Amri AH, Al Saegh A, Al-Mamari W, El-Asrag ME, Al-Kindi MN, Al Khabouri M, Al Wardy N, Al Lamki K, Gabr A, Idris A, Inglehearn CF, Clapcote SJ, Ali M. LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics. PMID 30476627 DOI: 10.1016/J.Ejmg.2018.11.026  0.315
2018 Cheung SY, Henrot M, Al-Saad M, Baumann M, Muller H, Unger A, Rubaiy HN, Mathar I, Dinkel K, Nussbaumer P, Klebl B, Freichel M, Rode B, Trainor S, Clapcote SJ, et al. TRPC4/TRPC5 channels mediate adverse reaction to the cancer cell cytotoxic agent (-)-Englerin A. Oncotarget. 9: 29634-29643. PMID 30038709 DOI: 10.18632/Oncotarget.25659  0.311
2017 Timothy JWS, Klas N, Sanghani HR, Al-Mansouri T, Hughes ATL, Kirshenbaum GS, Brienza V, Belle MDC, Ralph MR, Clapcote SJ, Piggins HD. Circadian Disruptions in the Myshkin Mouse Model of Mania Are Independent of Deficits in Suprachiasmatic Molecular Clock Function. Biological Psychiatry. PMID 28689605 DOI: 10.1016/J.Biopsych.2017.04.018  0.371
2017 McGirr A, Lipina TV, Mun HS, Georgiou J, Al-Amri AH, Ng E, Zhai D, Elliott C, Cameron RT, Mullins JG, Liu F, Baillie GS, Clapcote SJ, Roder JC. Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 42: 1178. PMID 28294143 DOI: 10.1038/npp.2016.263  0.673
2016 Kirshenbaum GS, Idris NF, Dachtler J, Roder JC, Clapcote SJ. Deficits in social behavioral tests in a mouse model of alternating hemiplegia of childhood. Journal of Neurogenetics. 30: 42-9. PMID 27276195 DOI: 10.1080/01677063.2016.1182525  0.564
2016 Al-Amri A, Saegh AA, Al-Mamari W, El-Asrag ME, Ivorra JL, Cardno AG, Inglehearn CF, Clapcote SJ, Ali M. Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. American Journal of Medical Genetics. Part A. PMID 27148795 DOI: 10.1002/Ajmg.A.37690  0.347
2016 Dachtler J, Elliott C, Rodgers RJ, Baillie GS, Clapcote SJ. Missense mutation in DISC1 C-terminal coiled-coil has GSK3β signaling and sex-dependent behavioral effects in mice. Scientific Reports. 6: 18748. PMID 26728762 DOI: 10.1038/Srep18748  0.456
2015 Dachtler J, Ivorra JL, Rowland TE, Lever C, Rodgers RJ, Clapcote SJ. Heterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia. Behavioral Neuroscience. 129: 765-76. PMID 26595880 DOI: 10.1037/Bne0000108  0.474
2015 Kirshenbaum GS, Dachtler J, Roder JC, Clapcote SJ. Characterization of Cognitive Deficits in Mice With an Alternating Hemiplegia-Linked Mutation. Behavioral Neuroscience. PMID 26501181 DOI: 10.1037/Bne0000097  0.596
2015 Kirshenbaum GS, Dachtler J, Roder JC, Clapcote SJ. Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood. Neurogenetics. PMID 26463346 DOI: 10.1007/S10048-015-0461-1  0.567
2015 McGirr A, Lipina TV, Mun HS, Georgiou J, Al-Amri AH, Ng E, Zhai D, Elliott C, Cameron RT, Mullins JG, Liu F, Baillie GS, Clapcote SJ, Roder JC. Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 26272049 DOI: 10.1038/Npp.2015.240  0.744
2014 Dachtler J, Glasper J, Cohen RN, Ivorra JL, Swiffen DJ, Jackson AJ, Harte MK, Rodgers RJ, Clapcote SJ. Deletion of α-neurexin II results in autism-related behaviors in mice. Translational Psychiatry. 4: e484. PMID 25423136 DOI: 10.1038/Tp.2014.123  0.469
2014 Chandran JS, Kazanis I, Clapcote SJ, Ogawa F, Millar JK, Porteous DJ, Ffrench-Constant C. Disc1 variation leads to specific alterations in adult neurogenesis. Plos One. 9: e108088. PMID 25272038 DOI: 10.1371/Journal.Pone.0108088  0.43
2014 Heinzen EL, Arzimanoglou A, Brashear A, Clapcote SJ, Gurrieri F, Goldstein DB, Jóhannesson SH, Mikati MA, Neville B, Nicole S, Ozelius LJ, Poulsen H, Schyns T, Sweadner KJ, van den Maagdenberg A, et al. Distinct neurological disorders with ATP1A3 mutations. The Lancet. Neurology. 13: 503-14. PMID 24739246 DOI: 10.1016/S1474-4422(14)70011-0  0.357
2014 Porteous DJ, Thomson PA, Millar JK, Evans KL, Hennah W, Soares DC, McCarthy S, McCombie WR, Clapcote SJ, Korth C, Brandon NJ, Sawa A, Kamiya A, Roder JC, Lawrie SM, et al. DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan. Molecular Psychiatry. 19: 141-3. PMID 24457522 DOI: 10.1038/Mp.2013.160  0.494
2013 Ritchie DJ, Clapcote SJ. Disc1 deletion is present in Swiss-derived inbred mouse strains: implications for transgenic studies of learning and memory. Laboratory Animals. 47: 162-7. PMID 23563120 DOI: 10.1177/0023677213478299  0.378
2013 Kirshenbaum GS, Dawson N, Mullins JG, Johnston TH, Drinkhill MJ, Edwards IJ, Fox SH, Pratt JA, Brotchie JM, Roder JC, Clapcote SJ. Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice. Plos One. 8: e60141. PMID 23527305 DOI: 10.1371/Journal.Pone.0060141  0.583
2012 Kirshenbaum GS, Clapcote SJ, Petersen J, Vilsen B, Ralph MR, Roder JC. Genetic suppression of agrin reduces mania-like behavior in Na+ , K+ -ATPase α3 mutant mice. Genes, Brain, and Behavior. 11: 436-43. PMID 22520507 DOI: 10.1111/J.1601-183X.2012.00800.X  0.582
2012 Zhang L, Fu D, Belichenko PV, Liu C, Kleschevnikov AM, Pao A, Liang P, Clapcote SJ, Mobley WC, Yu YE. Genetic analysis of Down syndrome facilitated by mouse chromosome engineering. Bioengineered Bugs. 3: 8-12. PMID 22126738 DOI: 10.4161/Bbug.3.1.17696  0.336
2012 Sha L, MacIntyre L, Machell JA, Kelly MP, Porteous DJ, Brandon NJ, Muir WJ, Blackwood DH, Watson DG, Clapcote SJ, Pickard BS. Transcriptional regulation of neurodevelopmental and metabolic pathways by NPAS3. Molecular Psychiatry. 17: 267-79. PMID 21709683 DOI: 10.1038/Mp.2011.73  0.334
2012 Reichelt AC, Rodgers RJ, Clapcote SJ. The role of neurexins in schizophrenia and autistic spectrum disorder. Neuropharmacology. 62: 1519-26. PMID 21262241 DOI: 10.1016/J.Neuropharm.2011.01.024  0.379
2012 Kirshenbaum GS, Clapcote SJ, Duffy S, Burgess CR, Petersen J, Jarowek KJ, Yücel YH, Cortez MA, Snead OC, Vilsen B, Peever JH, Ralph MR, Roder JC. Mania-like behavior induced by genetic dysfunction of the neuron-specific Na +,K +-ATPase α3 sodium pump (Proceedings of the National Academy of Sciences of the United States of America (2011) 108, 44, (18144-18149) DOI: 10.1073/pnas.1108416108) Proceedings of the National Academy of Sciences of the United States of America. 109: 2174. DOI: 10.1073/pnas.1121504109  0.442
2012 Brown SM, Clapcote SJ, Millar JK, Torrance HS, Anderson SM, Walker R, Rampino A, Roder JC, Thomson PA, Porteous DJ, Evans KL. Synaptic modulators Nrxn1 and Nrxn3 are disregulated in a Disc1 mouse model of schizophrenia (Molecular Psychiatry (2011) 16, (585-587) DOI: 10.1038/mp.2010.134) Molecular Psychiatry. 17: 469. DOI: 10.1038/mp.2011.27  0.46
2011 d'Isa R, Clapcote SJ, Voikar V, Wolfer DP, Giese KP, Brambilla R, Fasano S. Mice Lacking Ras-GRF1 Show Contextual Fear Conditioning but not Spatial Memory Impairments: Convergent Evidence from Two Independently Generated Mouse Mutant Lines. Frontiers in Behavioral Neuroscience. 5: 78. PMID 22164138 DOI: 10.3389/Fnbeh.2011.00078  0.345
2011 Kirshenbaum GS, Clapcote SJ, Duffy S, Burgess CR, Petersen J, Jarowek KJ, Yücel YH, Cortez MA, Snead OC, Vilsen B, Peever JH, Ralph MR, Roder JC. Mania-like behavior induced by genetic dysfunction of the neuron-specific Na+,K+-ATPase α3 sodium pump. Proceedings of the National Academy of Sciences of the United States of America. 108: 18144-9. PMID 22025725 DOI: 10.1073/Pnas.1108416108  0.572
2011 Lazar NL, Singh S, Paton T, Clapcote SJ, Gondo Y, Fukumura R, Roder JC, Cain DP. Missense mutation of the reticulon-4 receptor alters spatial memory and social interaction in mice. Behavioural Brain Research. 224: 73-9. PMID 21645550 DOI: 10.1016/J.Bbr.2011.05.020  0.582
2011 Lee FH, Fadel MP, Preston-Maher K, Cordes SP, Clapcote SJ, Price DJ, Roder JC, Wong AH. Disc1 point mutations in mice affect development of the cerebral cortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 3197-206. PMID 21368031 DOI: 10.1523/Jneurosci.4219-10.2011  0.552
2011 Brown SM, Clapcote SJ, Millar JK, Torrance HS, Anderson SM, Walker R, Rampino A, Roder JC, Thomson PA, Porteous DJ, Evans KL. Synaptic modulators Nrxn1 and Nrxn3 are disregulated in a Disc1 mouse model of schizophrenia. Molecular Psychiatry. 16: 585-7. PMID 21321563 DOI: 10.1038/Mp.2010.134  0.512
2011 Lipina TV, Kaidanovich-Beilin O, Patel S, Wang M, Clapcote SJ, Liu F, Woodgett JR, Roder JC. Genetic and pharmacological evidence for schizophrenia-related Disc1 interaction with GSK-3. Synapse (New York, N.Y.). 65: 234-48. PMID 20687111 DOI: 10.1002/Syn.20839  0.57
2010 Yu T, Liu C, Belichenko P, Clapcote SJ, Li S, Pao A, Kleschevnikov A, Bechard AR, Asrar S, Chen R, Fan N, Zhou Z, Jia Z, Chen C, Roder JC, et al. Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice. Brain Research. 1366: 162-71. PMID 20932954 DOI: 10.1016/J.Brainres.2010.09.107  0.555
2010 Xie G, Harrison J, Clapcote SJ, Huang Y, Zhang JY, Wang LY, Roder JC. A new Kv1.2 channelopathy underlying cerebellar ataxia. The Journal of Biological Chemistry. 285: 32160-73. PMID 20696761 DOI: 10.1074/Jbc.M110.153676  0.546
2010 Yu T, Clapcote SJ, Li Z, Liu C, Pao A, Bechard AR, Carattini-Rivera S, Matsui S, Roder JC, Baldini A, Mobley WC, Bradley A, Yu YE. Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 258-67. PMID 20512340 DOI: 10.1007/S00335-010-9262-X  0.582
2010 Yu T, Li Z, Jia Z, Clapcote SJ, Liu C, Li S, Asrar S, Pao A, Chen R, Fan N, Carattini-Rivera S, Bechard AR, Spring S, Henkelman RM, Stoica G, et al. A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions. Human Molecular Genetics. 19: 2780-91. PMID 20442137 DOI: 10.1093/Hmg/Ddq179  0.545
2009 Clapcote SJ, Duffy S, Xie G, Kirshenbaum G, Bechard AR, Rodacker Schack V, Petersen J, Sinai L, Saab BJ, Lerch JP, Minassian BA, Ackerley CA, Sled JG, Cortez MA, Henderson JT, et al. Mutation I810N in the alpha3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS. Proceedings of the National Academy of Sciences of the United States of America. 106: 14085-90. PMID 19666602 DOI: 10.1073/Pnas.0904817106  0.533
2009 Ng D, Pitcher GM, Szilard RK, Sertié A, Kanisek M, Clapcote SJ, Lipina T, Kalia LV, Joo D, McKerlie C, Cortez M, Roder JC, Salter MW, McInnes RR. Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning. Plos Biology. 7: e41. PMID 19243221 DOI: 10.1371/Journal.Pbio.1000041  0.476
2009 Labrie V, Clapcote SJ, Roder JC. Mutant mice with reduced NMDA-NR1 glycine affinity or lack of D-amino acid oxidase function exhibit altered anxiety-like behaviors. Pharmacology, Biochemistry, and Behavior. 91: 610-20. PMID 18940194 DOI: 10.1016/J.Pbb.2008.09.016  0.517
2008 Young EJ, Lipina T, Tam E, Mandel A, Clapcote SJ, Bechard AR, Chambers J, Mount HT, Fletcher PJ, Roder JC, Osborne LR. Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice. Genes, Brain, and Behavior. 7: 224-34. PMID 17680805 DOI: 10.1111/J.1601-183X.2007.00343.X  0.509
2007 Ishizuka K, Chen J, Taya S, Li W, Millar JK, Xu Y, Clapcote SJ, Hookway C, Morita M, Kamiya A, Tomoda T, Lipska BK, Roder JC, Pletnikov M, Porteous D, et al. Evidence that many of the DISC1 isoforms in C57BL/6J mice are also expressed in 129S6/SvEv mice. Molecular Psychiatry. 12: 897-9. PMID 17895924 DOI: 10.1038/Sj.Mp.4002024  0.55
2007 Millar JK, Mackie S, Clapcote SJ, Murdoch H, Pickard BS, Christie S, Muir WJ, Blackwood DH, Roder JC, Houslay MD, Porteous DJ. Disrupted in schizophrenia 1 and phosphodiesterase 4B: towards an understanding of psychiatric illness. The Journal of Physiology. 584: 401-5. PMID 17823207 DOI: 10.1113/Jphysiol.2007.140210  0.557
2007 Clapcote SJ, Lipina TV, Millar JK, Mackie S, Christie S, Ogawa F, Lerch JP, Trimble K, Uchiyama M, Sakuraba Y, Kaneda H, Shiroishi T, Houslay MD, Henkelman RM, Sled JG, et al. Behavioral phenotypes of Disc1 missense mutations in mice. Neuron. 54: 387-402. PMID 17481393 DOI: 10.1016/J.Neuron.2007.04.015  0.601
2007 Xie G, Clapcote SJ, Nieman BJ, Tallerico T, Huang Y, Vukobradovic I, Cordes SP, Osborne LR, Rossant J, Sled JG, Henderson JT, Roder JC. Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A. Genes, Brain, and Behavior. 6: 717-27. PMID 17376154 DOI: 10.1111/J.1601-183X.2007.00302.X  0.497
2006 Abramow-Newerly W, Lipina T, Abramow-Newerly M, Kim D, Bechard AR, Xie G, Clapcote SJ, Roder JC. Methods to rapidly and accurately screen a large number of ENU mutagenized mice for abnormal motor phenotypes. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 7: 112-8. PMID 16753976 DOI: 10.1080/14660820500443000  0.472
2006 Clapcote SJ, Roder JC. Deletion polymorphism of Disc1 is common to all 129 mouse substrains: implications for gene-targeting studies of brain function. Genetics. 173: 2407-10. PMID 16751659 DOI: 10.1534/Genetics.106.060749  0.537
2006 Snead OC, Clapcote SJ, Roder JC, Boulianne GL. Novel strategies for the development of animal models of refractory epilepsy. Advances in Neurology. 97: 155-71. PMID 16383125  0.385
2005 Clapcote SJ, Lazar NL, Bechard AR, Roder JC. Effects of the rd1 mutation and host strain on hippocampal learning in mice. Behavior Genetics. 35: 591-601. PMID 16184487 DOI: 10.1007/S10519-005-5634-5  0.496
2005 Clapcote SJ, Lazar NL, Bechard AR, Wood GA, Roder JC. NIH Swiss and Black Swiss mice have retinal degeneration and performance deficits in cognitive tests. Comparative Medicine. 55: 310-6. PMID 16158906  0.507
2005 Clapcote SJ, Roder JC. Simplex PCR assay for sex determination in mice. Biotechniques. 38: 702, 704, 706. PMID 15945368 DOI: 10.2144/05385Bm05  0.475
2004 Churchill GA, Airey DC, Allayee H, Angel JM, Attie AD, Beatty J, Beavis WD, Belknap JK, Bennett B, Berrettini W, Bleich A, Bogue M, Broman KW, Buck KJ, Buckler E, ... ... Clapcote S, et al. The Collaborative Cross, a community resource for the genetic analysis of complex traits. Nature Genetics. 36: 1133-7. PMID 15514660 DOI: 10.1038/Ng1104-1133  0.475
2004 Clapcote SJ, Roder JC. Survey of embryonic stem cell line source strains in the water maze reveals superior reversal learning of 129S6/SvEvTac mice. Behavioural Brain Research. 152: 35-48. PMID 15135967 DOI: 10.1016/J.Bbr.2003.09.030  0.525
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