{"id":"00947100","next":"","publications":{"selected_publication":[{"html":"

Greer SK; Steven JC; Steven D; Christian RB; Janne P; Karolina JJ; Yeni HY; Miguel AC; Snead OC; Bente V; John HP; Martin RR; John CR<\/span> (2011)<\/span> Mania-like behavior induced by genetic dysfunction of the neuron-specific Na\n +<\/sup>\n ,K\n +<\/sup>\n -ATPase \u03b13 sodium pump<\/span>. Proceedings of the National Academy of Sciences<\/span>, 108<\/span>, (44)<\/span>, pp. 18144-18149<\/span>. <\/a><\/p>","publicationid":"155279","date":"2011-10-24","publicationtype":"Journal article","isfavourite":"1"},{"html":"

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; Vilsen B; Roder JC<\/span> (2009)<\/span> Mutation I810N in the alpha3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS<\/span>. Proc Natl Acad Sci U S A<\/span>, 106<\/span>, (33)<\/span>, pp. 14085-14090<\/span>. <\/a><\/p>","publicationid":"50443","date":"2009-08-18","publicationtype":"Journal article","isfavourite":"1"},{"html":"

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; Gondo Y; Porteous DJ; Roder JC<\/span> (2007)<\/span> Behavioral phenotypes of Disc1 missense mutations in mice<\/span>. Neuron<\/span>, 54<\/span>, (3)<\/span>, pp. 387-402<\/span>. <\/a><\/p>","publicationid":"61604","date":"2007-05-03","publicationtype":"Journal article","isfavourite":"1"}],"favourites":[],"journal_article":[{"html":"

Simpson AJ; McLellan A; Behl KE; Brown J; Clapcote SJ; Cross JH; van den Maagdenberg AMJM; Vezyroglou AN; Balestrini S; Sisodiya SM<\/span> (2025)<\/span> Alternating Hemiplegia of Childhood and ATP1A3-Related Diseases: Insights From a Decade of Discovery and Collaboration<\/span>. Neurol Genet<\/span>, 11<\/span>, (5)<\/span>, pp. e200308<\/span>. <\/a> <\/a><\/p>","publicationid":"1110291","date":"2025-10-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Pantiru AD; Van de Sompele S; Ligneul C; Chatelain C; Barrea C; Lerch JP; Filippi BM; Alkan S; De Baere E; Johnston J; Clapcote SJ<\/span> (2025)<\/span> Autistic behavior is a common outcome of biallelic disruption of PDZD8 in humans and mice<\/span>. Mol Autism<\/span>, 16<\/span>, (1)<\/span>, pp. 14<\/span>. <\/a> <\/a><\/p>","publicationid":"966723","date":"2025-02-27","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Lipina TV; Li S; Petrova ES; Amstislavskaya TG; Cameron RT; Elliott C; Gondo Y; McGirr A; Mullins JGL; Baillie GS; Woodgett JR; Clapcote SJ<\/span> (2024)<\/span> PDE4B Missense Variant Increases Susceptibility to Post-traumatic Stress Disorder-Relevant Phenotypes in Mice<\/span>. J Neurosci<\/span>, 44<\/span>, (43)<\/span>, pp. e0137242024<\/span>. <\/a> <\/a><\/p>","publicationid":"842078","date":"2024-10-23","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Armstrong P; G\u00fcng\u00f6r H; Anongjanya P; Tweedy C; Parkin E; Johnston J; Carr IM; Dawson N; Clapcote SJ<\/span> (2024)<\/span> Protective effect of PDE4B subtype-specific inhibition in an App knock-in mouse model for Alzheimer's disease<\/span>. Neuropsychopharmacology<\/span>, 49<\/span>, (10)<\/span>, pp. 1559-1568<\/span>. <\/a> <\/a><\/p>","publicationid":"648981","date":"2024-09-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Cardno AG; el din SN; Toit DD; Rehman F-U; McIlrae S; Variend H; Hussein N-R; Dasi R; Clapcote SJ; Jones LA; Jones WR; Stephenson C; Shora S; Mahmood T<\/span> (2024)<\/span> Relationships between psychotic and affective symptoms, schizotypal and dissociative phenomena, and adverse life events among individuals with psychotic disorders<\/span>. Journal of Psychiatric Intensive Care<\/span>, 20<\/span>, (1)<\/span>, pp. 9-17<\/span>. <\/a> <\/a><\/p>","publicationid":"647350","date":"2024-04-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Chofflet N; Naito Y; Pastore AJ; Padmanabhan N; Nguyen PT; Poitras C; Feller B; Yi N; Van Prooijen J; Khaled H; Coulombe B; Clapcote SJ; Bourgault S; Siddiqui TJ; Rudenko G; Takahashi H<\/span> (2024)<\/span> Structural and functional characterization of the IgSF21-neurexin2\u03b1 complex and its related signaling pathways in the regulation of inhibitory synapse organization<\/span>. Front Mol Neurosci<\/span>, 17<\/span>, pp. 1371145<\/span>. <\/a> <\/a><\/p>","publicationid":"650630","date":"2024-01-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Wilkinson ID; Mahmood T; Yasmin SF; Tomlinson A; Nazari J; Alhaj H; El Din SN; Neill J; Pandit C; Ashraf S; Cardno AG; Clapcote SJ; Inglehearn CF; Woodruff PW<\/span> (2023)<\/span> In memory of Professor Iain Wilkinson: cognitive and neuroimaging endophenotypes in a consanguineous schizophrenia multiplex family<\/span>. Psychol Med<\/span>, 53<\/span>, (7)<\/span>, pp. 3178-3186<\/span>. <\/a> <\/a><\/p>","publicationid":"579364","date":"2023-05-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Clapcote SJ<\/span> (2022)<\/span> How can we obtain truly translational mouse models to improve clinical outcomes in schizophrenia?<\/span> Dis Model Mech<\/span>, 15<\/span>, (11)<\/span>, pp. dmm049970<\/span>. <\/a> <\/a><\/p>","publicationid":"598301","date":"2022-11-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Al-Amri AH; Armstrong P; Amici M; Ligneul C; Rouse J; El-Asrag ME; Pantiru A; Vancollie VE; Ng HWY; Ogbeta JA; Goodchild K; Ellegood J; Lelliott CJ; Mullins JGL; Bretman A; Al-Ali R; Beetz C; Al-Gazali L; Al Shamsi A; Lerch JP; Mellor JR; Al Sayegh A; Ali M; Inglehearn CF; Clapcote SJ<\/span> (2022)<\/span> PDZD8 Disruption Causes Cognitive Impairment in Humans, Mice, and Fruit Flies<\/span>. Biol Psychiatry<\/span>, 92<\/span>, (4)<\/span>, pp. 323-334<\/span>. <\/a> <\/a><\/p>","publicationid":"576522","date":"2022-08-15","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Hughes RB; Whittingham-Dowd J; Clapcote SJ; Broughton SJ; Dawson N<\/span> (2022)<\/span> Altered medial prefrontal cortex and dorsal raph\u00e9 activity predict genotype and correlate with abnormal learning behavior in a mouse model of autism-associated 2p16.3 deletion<\/span>. Autism Res<\/span>, 15<\/span>, (4)<\/span>, pp. 614-627<\/span>. <\/a> <\/a><\/p>","publicationid":"579365","date":"2022-04-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Ng HWY; Ogbeta JA; Clapcote SJ<\/span> (2021)<\/span> Genetically altered animal models for ATP1A3-related disorders<\/span>. Dis Model Mech<\/span>, 14<\/span>, (10)<\/span>, pp. dmm048938<\/span>. <\/a> <\/a><\/p>","publicationid":"569125","date":"2021-10-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Hosalli P; Cardno A; Brewin A; Nazari J; Clapcote SJ; Inglehearn CF; Mahmood T<\/span> (2021)<\/span> Risk of psychosis in Yorkshire African, Caribbean and Mixed Ethnic communities<\/span>. Journal of Psychiatric Intensive Care<\/span>, 17<\/span>, (2)<\/span>, pp. 107-111<\/span>. <\/a> <\/a><\/p>","publicationid":"564527","date":"2021-09-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Cole BA; Clapcote SJ; Muench SP; Lippiat JD<\/span> (2021)<\/span> Targeting KNa1.1 channels in KCNT1-associated epilepsy<\/span>. Trends Pharmacol Sci<\/span>, 42<\/span>, (8)<\/span>, pp. 700-713<\/span>. <\/a> <\/a><\/p>","publicationid":"560002","date":"2021-08-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Mahmood T; El-Asrag ME; Poulter JA; Cardno AG; Tomlinson A; Ahmed S; Al-Amri A; Nazari J; Neill J; Chamali RS; Kiwan N; Ghuloum S; Alhaj HA; Randerson Moor J; Khan S; Al-Amin H; Johnson CA; Woodruff P; Wilkinson ID; Ali M; Clapcote SJ; Inglehearn CF<\/span> (2021)<\/span> A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to Schizophrenia<\/span>. Schizophr Bull<\/span>, 47<\/span>, (3)<\/span>, pp. 796-802<\/span>. <\/a> <\/a><\/p>","publicationid":"541365","date":"2021-04-29","publicationtype":"Journal article","isfavourite":"0"},{"html":"

B Hughes R; Whittingham-Dowd J; Simmons RE; Clapcote SJ; Broughton SJ; Dawson N<\/span> (2020)<\/span> Ketamine Restores Thalamic-Prefrontal Cortex Functional Connectivity in a Mouse Model of Neurodevelopmental Disorder-Associated 2p16.3 Deletion<\/span>. Cereb Cortex<\/span>, 30<\/span>, (4)<\/span>, pp. 2358-2371<\/span>. <\/a> <\/a><\/p>","publicationid":"515941","date":"2020-04-14","publicationtype":"Journal article","isfavourite":"0"},{"html":"

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<\/span> (2019)<\/span> LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss<\/span>. Eur J Med Genet<\/span>, 62<\/span>, (12)<\/span>, pp. 103592<\/span>. <\/a> <\/a><\/p>","publicationid":"486352","date":"2019-12-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Clapcote S; Inglehearn CF; Ali M; Al-Amri AH; Bretman A; Rouse J; Wainwright T; Armstrong P<\/span> (2019)<\/span> Truncation mutation of PDZD8 in a family with intellectual disability and autistic features<\/span>. IBRO Reports<\/span>, 6<\/span>, pp. S94<\/span>. <\/a><\/p>","publicationid":"663189","date":"2019-09-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Alsaady I; Tedford E; Alsaad M; Bristow G; Kohli S; Murray M; Reeves M; Vijayabaskar MS; Clapcote SJ; Wastling J; McConkey GA<\/span> (2019)<\/span> Downregulation of the Central Noradrenergic System by Toxoplasma gondii Infection<\/span>. Infect Immun<\/span>, 87<\/span>, (2)<\/span>, pp. e00789-e00718<\/span>. <\/a> <\/a><\/p>","publicationid":"484273","date":"2019-02-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Pervolaraki E; Tyson AL; Pibiri F; Poulter SL; Reichelt AC; Rodgers RJ; Clapcote SJ; Lever C; Andreae LC; Dachtler J<\/span> (2019)<\/span> The within-subject application of diffusion tensor MRI and CLARITY reveals brain structural changes in Nrxn2 deletion mice<\/span>. Mol Autism<\/span>, 10<\/span>, (1)<\/span>, pp. 8<\/span>. <\/a> <\/a><\/p>","publicationid":"493987","date":"2019-01-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Timothy JWS; Klas N; Sanghani HR; Al-Mansouri T; Hughes ATL; Kirshenbaum GS; Brienza V; Belle MDC; Ralph MR; Clapcote SJ; Piggins HD<\/span> (2018)<\/span> Circadian Disruptions in the Myshkin Mouse Model of Mania Are Independent of Deficits in Suprachiasmatic Molecular Clock Function<\/span>. Biol Psychiatry<\/span>, 84<\/span>, (11)<\/span>, pp. 827-837<\/span>. <\/a> <\/a><\/p>","publicationid":"381538","date":"2018-12-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

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; Christmann M; Waldmann H; Abbas SK; Beech DJ; Vasudev NS<\/span> (2018)<\/span> TRPC4\/TRPC5 channels mediate adverse reaction to the cancer cell cytotoxic agent (-)-Englerin A<\/span>. Oncotarget<\/span>, 9<\/span>, (51)<\/span>, pp. 29634-29643<\/span>. <\/a> <\/a><\/p>","publicationid":"472102","date":"2018-07-03","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Liu M; Fitzgibbon M; Wang Y; Reilly J; Qian X; O'Brien T; Clapcote S; Shen S; Roche M<\/span> (2018)<\/span> Ulk4 regulates GABAergic signaling and anxiety-related behavior<\/span>. Transl Psychiatry<\/span>, 8<\/span>, (1)<\/span>, pp. 43<\/span>. <\/a> <\/a><\/p>","publicationid":"457116","date":"2018-02-02","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Al-Amri A; Saegh AA; Al-Mamari W; El-Asrag ME; Ivorra JL; Cardno AG; Inglehearn CF; Clapcote SJ; Ali M<\/span> (2016)<\/span> Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family<\/span>. Am J Med Genet A<\/span>, 170<\/span>, (7)<\/span>, pp. 1826-1831<\/span>. <\/a> <\/a><\/p>","publicationid":"355153","date":"2016-07-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Kirshenbaum GS; Idris NF; Dachtler J; Roder JC; Clapcote SJ<\/span> (2016)<\/span> Deficits in social behavioral tests in a mouse model of alternating hemiplegia of childhood<\/span>. J Neurogenet<\/span>, 30<\/span>, (1)<\/span>, pp. 42-49<\/span>. <\/a> <\/a><\/p>","publicationid":"357766","date":"2016-03-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

McGirr A; Lipina TV; Mun H-S; Georgiou J; Al-Amri AH; Ng E; Zhai D; Elliott C; Cameron RT; Mullins JGL; Liu F; Baillie GS; Clapcote SJ; Roder JC<\/span> (2016)<\/span> Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition<\/span>. Neuropsychopharmacology<\/span>, 41<\/span>, (4)<\/span>, pp. 1080-1092<\/span>. <\/a> <\/a><\/p>","publicationid":"331730","date":"2016-03-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Dachtler J; Elliott C; Rodgers RJ; Baillie GS; Clapcote SJ<\/span> (2016)<\/span> Missense mutation in DISC1 C-terminal coiled-coil has GSK3\u03b2 signaling and sex-dependent behavioral effects in mice<\/span>. Sci Rep<\/span>, 6<\/span>, (1)<\/span>, pp. 18748<\/span>. <\/a> <\/a><\/p>","publicationid":"342808","date":"2016-01-05","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Kirshenbaum GS; Dachtler J; Roder JC; Clapcote SJ<\/span> (2016)<\/span> Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood<\/span>. Neurogenetics<\/span>, 17<\/span>, (1)<\/span>, pp. 57-63<\/span>. <\/a> <\/a><\/p>","publicationid":"336856","date":"2016-01-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Dachtler J; Ivorra JL; Rowland TE; Lever C; Rodgers RJ; Clapcote SJ<\/span> (2015)<\/span> Heterozygous deletion of \u03b1-neurexin I or \u03b1-neurexin II results in behaviors relevant to autism and schizophrenia<\/span>. Behav Neurosci<\/span>, 129<\/span>, (6)<\/span>, pp. 765-776<\/span>. <\/a> <\/a><\/p>","publicationid":"336855","date":"2015-12-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Kirshenbaum GS; Dachtler J; Roder JC; Clapcote SJ<\/span> (2015)<\/span> Characterization of cognitive deficits in mice with an alternating hemiplegia-linked mutation<\/span>. Behav Neurosci<\/span>, 129<\/span>, (6)<\/span>, pp. 822-831<\/span>. <\/a> <\/a><\/p>","publicationid":"331717","date":"2015-12-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Dachtler J; Glasper J; Cohen RN; Ivorra JL; Swiffen DJ; Jackson AJ; Harte MK; Rodgers RJ; Clapcote SJ<\/span> (2014)<\/span> Deletion of \u03b1-neurexin II results in autism-related behaviors in mice<\/span>. Transl Psychiatry<\/span>, 4<\/span>, (11)<\/span>, pp. e484<\/span>. <\/a> <\/a><\/p>","publicationid":"309056","date":"2014-11-25","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Heinzen EL; Arzimanoglou A; Brashear A; Clapcote SJ; Gurrieri F; Goldstein DB; J\u00f3hannesson SH; Mikati MA; Neville B; Nicole S; Ozelius LJ; Poulsen H; Schyns T; Sweadner KJ; van den Maagdenberg A; Vilsen B; ATP1A3 Working Group<\/span> (2014)<\/span> Distinct neurological disorders with ATP1A3 mutations<\/span>. The Lancet. Neurology<\/span>, 13<\/span>, (5)<\/span>, pp. 503-514<\/span>. <\/a><\/p>","publicationid":"283198","date":"2014-05-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

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; McIntosh AM; St Clair D; Blackwood DH<\/span> (2014)<\/span> DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan<\/span>. Molecular psychiatry<\/span>, 19<\/span>, (2)<\/span>, pp. 141-143<\/span>. <\/a><\/p>","publicationid":"277303","date":"2014-02-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Chandran JS; Kazanis I; Clapcote SJ; Ogawa F; Millar JK; Porteous DJ; Ffrench-Constant C<\/span> (2014)<\/span> Disc1 variation leads to specific alterations in adult neurogenesis<\/span>. PLoS One<\/span>, 9<\/span>, (10)<\/span>, pp. e108088<\/span>. <\/a> <\/a><\/p>","publicationid":"306609","date":"2014-01-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Ritchie DJ; Clapcote SJ<\/span> (2013)<\/span> Disc1 deletion is present in Swiss-derived inbred mouse strains: implications for transgenic studies of learning and memory<\/span>. Lab Anim<\/span>, 47<\/span>, (3)<\/span>, pp. 162-167<\/span>. <\/a> <\/a><\/p>","publicationid":"255906","date":"2013-07-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Edwards IJ; Bruce G; Lawrenson C; Howe L; Clapcote SJ; Deuchars SA; Deuchars J<\/span> (2013)<\/span> Na+\/K+ ATPase \u03b11 and \u03b13 isoforms are differentially expressed in \u03b1- and \u03b3-motoneurons<\/span>. The Journal of neuroscience : the official journal of the Society for Neuroscience<\/span>, 33<\/span>, (24)<\/span>, pp. 9913-9919<\/span>. <\/a> <\/a><\/p>","publicationid":"259649","date":"2013-06-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Kirshenbaum GS; Dawson N; Mullins JGL; Johnston TH; Drinkhill MJ; Edwards IJ; Fox SH; Pratt JA; Brotchie JM; Roder JC; Clapcote SJ<\/span> (2013)<\/span> Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase \u03b13 missense mutant mice<\/span>. PloS one<\/span>, 8<\/span>, (3)<\/span>, pp. e60141<\/span>. <\/a><\/p>","publicationid":"255106","date":"2013-01-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Kirshenbaum GS; Clapcote SJ; Petersen J; Vilsen B; Ralph MR; Roder JC<\/span> (2012)<\/span> Genetic suppression of agrin reduces mania-like behavior in Na+ , K+ -ATPase \u03b13 mutant mice<\/span>. Genes, brain, and behavior<\/span>, 11<\/span>, (4)<\/span>, pp. 436-443<\/span>. <\/a><\/p>","publicationid":"210735","date":"2012-06-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Sha L; MacIntyre L; Machell JA; Kelly MP; Porteous DJ; Brandon NJ; Muir WJ; Blackwood DH; Watson DG; Clapcote SJ; Pickard BS<\/span> (2012)<\/span> Transcriptional regulation of neurodevelopmental and metabolic pathways by NPAS3<\/span>. Molecular psychiatry<\/span>, 17<\/span>, (3)<\/span>, pp. 267-279<\/span>. <\/a><\/p>","publicationid":"143352","date":"2012-03-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Reichelt AC; Rodgers RJ; Clapcote SJ<\/span> (2012)<\/span> The role of neurexins in schizophrenia and autistic spectrum disorder<\/span>. Neuropharmacology<\/span>, 62<\/span>, (3)<\/span>, pp. 1519-1526<\/span>. <\/a><\/p>","publicationid":"133505","date":"2012-03-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Zhang L; Fu D; Belichenko PV; Liu C; Kleschevnikov AM; Pao A; Liang P; Clapcote SJ; Mobley WC; Yu YE<\/span> (2012)<\/span> Genetic analysis of Down syndrome facilitated by mouse chromosome engineering<\/span>. Bioengineered bugs<\/span>, 3<\/span>, (1)<\/span>, pp. 8-12<\/span>. <\/a><\/p>","publicationid":"158610","date":"2012-01-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Greer SK; Steven JC; Steven D; Christian RB; Janne P; Karolina JJ; Yeni HY; Miguel AC; Snead OC; Bente V; John HP; Martin RR; John CR<\/span> (2011)<\/span> Mania-like behavior induced by genetic dysfunction of the neuron-specific Na\n +<\/sup>\n ,K\n +<\/sup>\n -ATPase \u03b13 sodium pump<\/span>. Proceedings of the National Academy of Sciences<\/span>, 108<\/span>, (44)<\/span>, pp. 18144-18149<\/span>. <\/a><\/p>","publicationid":"155279","date":"2011-10-24","publicationtype":"Journal article","isfavourite":"1"},{"html":"

Lazar NL; Singh S; Paton T; Clapcote SJ; Gondo Y; Fukumura R; Roder JC; Cain DP<\/span> (2011)<\/span> Missense mutation of the reticulon-4 receptor alters spatial memory and social interaction in mice<\/span>. Behav Brain Res<\/span>, 224<\/span>, (1)<\/span>, pp. 73-79<\/span>. <\/a><\/p>","publicationid":"142014","date":"2011-10-10","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Brown SM; Clapcote SJ; Millar JK; Torrance HS; Anderson SM; Walker R; Rampino A; Roder JC; Thomson PA; Porteous DJ; Evans KL<\/span> (2011)<\/span> Synaptic modulators Nrxn1 and Nrxn3 are disregulated in a Disc1 mouse model of schizophrenia<\/span>. MOL PSYCHIATR<\/span>, 16<\/span>, (6)<\/span>, pp. 585-587<\/span>. <\/a><\/p>","publicationid":"134962","date":"2011-06-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Lee FHF; Fadel MP; Preston-Maher K; Cordes SP; Clapcote SJ; Price DJ; Roder JC; Wong AHC<\/span> (2011)<\/span> Disc1 point mutations in mice affect development of the cerebral cortex<\/span>. J Neurosci<\/span>, 31<\/span>, (9)<\/span>, pp. 3197-3206<\/span>. <\/a><\/p>","publicationid":"137265","date":"2011-03-02","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Lipina TV; Kaidanovich-Beilin O; Patel S; Wang M; Clapcote SJ; Liu F; Woodgett JR; Roder JC<\/span> (2011)<\/span> Genetic and pharmacological evidence for schizophrenia-related Disc1 interaction with GSK-3<\/span>. Synapse<\/span>, 65<\/span>, (3)<\/span>, pp. 234-248<\/span>. <\/a><\/p>","publicationid":"123302","date":"2011-03-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

d'Isa R; Clapcote SJ; Voikar V; Wolfer DP; Giese KP; Brambilla R; Fasano S<\/span> (2011)<\/span> Mice Lacking Ras-GRF1 Show Contextual Fear Conditioning but not Spatial Memory Impairments: Convergent Evidence from Two Independently Generated Mouse Mutant Lines<\/span>. Front Behav Neurosci<\/span>, 5<\/span>, (DECEMBER)<\/span>, pp. 78-11<\/span>. <\/a><\/p>","publicationid":"164599","date":"2011-01-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

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; Liu B; Baldini A; Mobley WC; Yu YE<\/span> (2010)<\/span> Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice<\/span>. Brain Res<\/span>, 1366<\/span>, pp. 162-171<\/span>. <\/a><\/p>","publicationid":"128642","date":"2010-12-17","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Xie G; Harrison J; Clapcote SJ; Huang Y; Zhang J-Y; Wang L-Y; Roder JC<\/span> (2010)<\/span> A new Kv1.2 channelopathy underlying cerebellar ataxia<\/span>. J Biol Chem<\/span>, 285<\/span>, (42)<\/span>, pp. 32160-32173<\/span>. <\/a><\/p>","publicationid":"123315","date":"2010-10-15","publicationtype":"Journal article","isfavourite":"0"},{"html":"

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; Matsui S-I; Nowak NJ; Roder JC; Chen C; Bradley A; Yu YE<\/span> (2010)<\/span> A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions<\/span>. Hum Mol Genet<\/span>, 19<\/span>, (14)<\/span>, pp. 2780-2791<\/span>. <\/a><\/p>","publicationid":"72502","date":"2010-07-15","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Yu T; Clapcote SJ; Li Z; Liu C; Pao A; Bechard AR; Carattini-Rivera S; Matsui S-I; Roder JC; Baldini A; Mobley WC; Bradley A; Yu YE<\/span> (2010)<\/span> Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice<\/span>. Mamm Genome<\/span>, 21<\/span>, (5-6)<\/span>, pp. 258-267<\/span>. <\/a><\/p>","publicationid":"65970","date":"2010-06-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

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; Vilsen B; Roder JC<\/span> (2009)<\/span> Mutation I810N in the alpha3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS<\/span>. Proc Natl Acad Sci U S A<\/span>, 106<\/span>, (33)<\/span>, pp. 14085-14090<\/span>. <\/a><\/p>","publicationid":"50443","date":"2009-08-18","publicationtype":"Journal article","isfavourite":"1"},{"html":"

Ng D; Pitcher GM; Szilard RK; Serti\u00e9 A; Kanisek M; Clapcote SJ; Lipina T; Kalia LV; Joo D; McKerlie C; Cortez M; Roder JC; Salter MW; McInnes RR<\/span> (2009)<\/span> Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning<\/span>. PLoS Biol<\/span>, 7<\/span>, (2)<\/span>, pp. e41-0300<\/span>. <\/a><\/p>","publicationid":"22036","date":"2009-02-24","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Labrie V; Clapcote SJ; Roder JC<\/span> (2009)<\/span> Mutant mice with reduced NMDA-NR1 glycine affinity or lack of D-amino acid oxidase function exhibit altered anxiety-like behaviors<\/span>. Pharmacol Biochem Behav<\/span>, 91<\/span>, (4)<\/span>, pp. 610-620<\/span>. <\/a><\/p>","publicationid":"92397","date":"2009-02-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Young EJ; Lipina T; Tam E; Mandel A; Clapcote SJ; Bechard AR; Chambers J; Mount HTJ; Fletcher PJ; Roder JC; Osborne LR<\/span> (2008)<\/span> Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice<\/span>. Genes Brain Behav<\/span>, 7<\/span>, (2)<\/span>, pp. 224-234<\/span>. <\/a><\/p>","publicationid":"93376","date":"2008-03-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Xie G; Clapcote SJ; Nieman BJ; Tallerico T; Huang Y; Vukobradovic I; Cordes SP; Osborne LR; Rossant J; Sled JG; Henderson JT; Roder JC<\/span> (2007)<\/span> Forward genetic screen of mouse reveals dominant missense mutation in the P\/Q-type voltage-dependent calcium channel, CACNA1A<\/span>. Genes Brain Behav<\/span>, 6<\/span>, (8)<\/span>, pp. 717-727<\/span>. <\/a><\/p>","publicationid":"117798","date":"2007-11-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Millar JK; Mackie S; Clapcote SJ; Murdoch H; Pickard BS; Christie S; Muir WJ; Blackwood DH; Roder JC; Houslay MD; Porteous DJ<\/span> (2007)<\/span> Disrupted in schizophrenia 1 and phosphodiesterase 4B: towards an understanding of psychiatric illness<\/span>. J Physiol<\/span>, 584<\/span>, (Pt 2)<\/span>, pp. 401-405<\/span>. <\/a><\/p>","publicationid":"95864","date":"2007-10-15","publicationtype":"Journal article","isfavourite":"0"},{"html":"

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; Silva AJ; Cannon TD; Kaibuchi K; Brandon NJ; Weinberger DR; Sawa A<\/span> (2007)<\/span> Evidence that many of the DISC1 isoforms in C57BL\/6J mice are also expressed in 129S6\/SvEv mice<\/span>. Mol Psychiatry<\/span>, 12<\/span>, (10)<\/span>, pp. 897-899<\/span>. <\/a><\/p>","publicationid":"87005","date":"2007-10-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

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; Gondo Y; Porteous DJ; Roder JC<\/span> (2007)<\/span> Behavioral phenotypes of Disc1 missense mutations in mice<\/span>. Neuron<\/span>, 54<\/span>, (3)<\/span>, pp. 387-402<\/span>. <\/a><\/p>","publicationid":"61604","date":"2007-05-03","publicationtype":"Journal article","isfavourite":"1"},{"html":"

Clapcote SJ; Roder JC<\/span> (2006)<\/span> Deletion polymorphism of Disc1 is common to all 129 mouse substrains: implications for gene-targeting studies of brain function<\/span>. Genetics<\/span>, 173<\/span>, (4)<\/span>, pp. 2407-2410<\/span>. <\/a><\/p>","publicationid":"107665","date":"2006-08-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Abramow-Newerly W; Lipina T; Abramow-Newerly M; Kim D; Bechard AR; Xie G; Clapcote SJ; Roder JC<\/span> (2006)<\/span> Methods to rapidly and accurately screen a large number of ENU mutagenized mice for abnormal motor phenotypes<\/span>. Amyotroph Lateral Scler<\/span>, 7<\/span>, (2)<\/span>, pp. 112-118<\/span>. <\/a><\/p>","publicationid":"48773","date":"2006-06-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Snead OC; Clapcote SJ; Roder JC; Boulianne GL<\/span> (2006)<\/span> Novel strategies for the development of animal models of refractory epilepsy<\/span>. Advances in neurology<\/span>, 97<\/span>, pp. 155-171<\/span>.<\/p>","publicationid":"49400","date":"2006-01-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Clapcote SJ; Lazar NL; Bechard AR; Roder JC<\/span> (2005)<\/span> Effects of the rd1 mutation and host strain on hippocampal learning in mice<\/span>. Behav Genet<\/span>, 35<\/span>, (5)<\/span>, pp. 591-601<\/span>. <\/a><\/p>","publicationid":"114304","date":"2005-09-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Clapcote SJ; Lazar NL; Bechard AR; Wood GA; Roder JC<\/span> (2005)<\/span> NIH Swiss and Black Swiss mice have retinal degeneration and performance deficits in cognitive tests<\/span>. COMPARATIVE MED<\/span>, 55<\/span>, (4)<\/span>, pp. 310-316<\/span>.<\/p>","publicationid":"96224","date":"2005-08-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Clapcote SJ; Roder JC<\/span> (2005)<\/span> Simplex PCR assay for sex determination in mice<\/span>. BIOTECHNIQUES<\/span>, 38<\/span>, (5)<\/span>, pp. 702-+<\/span>. <\/a><\/p>","publicationid":"14043","date":"2005-05-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Churchill G; 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; Burmeister M; Chesler EJ; Cheverud JM; Clapcote S; Cook MN; Cox RD; Crabbe JC; Crusio WE; Darvasi A; Deschnepper CF; Doerge RW; Farber CR; Forejt J; Gaile D; Garlow SJ; Geiger H; Gershenfeld H; Gordon T; Gu J; Gu WK; de Haan G; Hayes NL; Heller C; Himmelbauer H; Hitzemann R; Hunter K; Hsu HC; Iraqi FA; Ivandic B; Jacob HJ; Jansen RC; Jjepsen KJ; Johnson DK; Johnson TE; Kempermann G; Kendziorski C; Kotb M; Kooy RF; Llamas B; Lammert F; Lassalle JM; Lowenstein PR; Lu L; Lusiss A; Manly KF; Marcucio R; Matthews D; Medrano JF; Miller DR; Mittleman G; Mock BA; Mogil JS; Montagutelli X; Morahan G; Morris DG; Mott R; Nadeau JH; Nagase H; Nowakowski RS; O'Hara BF; Osadchuk AV; Page GP; Paigen B; Paigen K; Palmer AA; Pan HJ; Peltonen-Palotie L; Peirce J; Pomp D; Pravenec M; Prows DR; Qi ZH; Reeves RH; Roder J; Rosen GD; Schadt EE; Schalkwyk LC; Seltzer Z; Shimomura K; Shou SM; Sillanpaa MJ; Siracusa LD; Snoeck HW; Spearow JL; Svenson K; Tarantino LM; Threadgill D; Toth LA; Valdar W; de Villena FPM; Warden C; Whatley S; Williams RW; Wiltshire T; Yi NJ; Zhang DB; Zhang M; Zou F; Complex Trait Consortium<\/span> (2004)<\/span> The Collaborative Cross, a community resource for the genetic analysis of complex traits<\/span>. NAT GENET<\/span>, 36<\/span>, (11)<\/span>, pp. 1133-1137<\/span>. <\/a><\/p>","publicationid":"60959","date":"2004-11-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Clapcote SJ; Roder JC<\/span> (2004)<\/span> Survey of embryonic stem cell line source strains in the water maze reveals superior reversal learning of 129S6\/SvEvTac mice<\/span>. Behav Brain Res<\/span>, 152<\/span>, (1)<\/span>, pp. 35-48<\/span>. <\/a><\/p>","publicationid":"63992","date":"2004-06-04","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Clapcott SJ; Peters J; Orban PC; Brambilla R; Graham CF<\/span> (2003)<\/span> Two ENU-induced mutations in Rasgrf1 and early mouse growth retardation<\/span>. MAMM GENOME<\/span>, 14<\/span>, (8)<\/span>, pp. 495-505<\/span>. <\/a><\/p>","publicationid":"97030","date":"2003-08-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Iraqi F; Clapcott SJ; Kumari P; Haley CS; Kemp SJ; Teale AJ<\/span> (2000)<\/span> Fine mapping of trypanosomiasis resistance loci in murine advanced intercross lines<\/span>. MAMM GENOME<\/span>, 11<\/span>, (8)<\/span>, pp. 645-648<\/span>. <\/a><\/p>","publicationid":"113223","date":"2000-08-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Clapcott SJ; Teale AJ; Kemp SJ<\/span> (2000)<\/span> Evidence for genomic imprinting of the major QTL controlling susceptibility to trypanosomiasis in mice<\/span>. Parasite Immunol<\/span>, 22<\/span>, (5)<\/span>, pp. 259-263<\/span>. <\/a><\/p>","publicationid":"64228","date":"2000-05-01","publicationtype":"Journal article","isfavourite":"0"},{"html":"

Teale A; Agaba M; Clapcott S; Gelhaus A; Haley C; Hanotte O; Horstmann R; Iraqi F; Kemp S; Nilsson P; Schwerin M; Sekikawa K; Soller M; Sugimoto Y; Womack J<\/span> (1999)<\/span> Resistance to trypanosomosis: Of markers, genes and mechanisms<\/span>. Archiv Fur Tierzucht<\/span>, 42<\/span>, pp. 36-41<\/span>.<\/p>","publicationid":"69761","date":"1999-12-01","publicationtype":"Journal article","isfavourite":"0"}],"conference_paper":[{"html":"

Clapcote SJ; Lipina TV; Roder JC<\/span> (2010)<\/span> Endophenotypes of Disc1 missense mutations in mice<\/span>. EUROPEAN NEUROPSYCHOPHARMACOLOGY<\/span>, pp. S200<\/span>.<\/p>","publicationid":"129232","date":"2010-08-01","publicationtype":"Conference paper","isfavourite":"0"},{"html":"

Clapcote SJ; Lipina TV; Roder JC<\/span> (2010)<\/span> Endophenotypes of Disc1 missense mutations in mice<\/span>. EUROPEAN NEUROPSYCHOPHARMACOLOGY<\/span>, pp. S200<\/span>. <\/a><\/p>","publicationid":"132651","date":"2010-01-01","publicationtype":"Conference paper","isfavourite":"0"},{"html":"

Lipina TV; Clapcote SJ; Lerch JP; Sled JG; Uchiyama M; Gondo Y; Roder JC<\/span> (2007)<\/span> The point mutation in disc1 gene is associated with schizophrenia-like behavior and neuroanatomical abnormalities in mice<\/span>. SCHIZOPHRENIA BULLETIN<\/span>, pp. 300<\/span>.<\/p>","publicationid":"51573","date":"2007-01-01","publicationtype":"Conference paper","isfavourite":"0"},{"html":"

Ng D; Sertie A; Szilard RK; Pitcher GM; Clapcote S; Kalia LV; Salter MW; Roder JC; Cortez MA; McInnes RR<\/span> (2003)<\/span> Loss of Neto1, a component of the NMDA receptor complex, is associated with decreased synaptic plasticity and impaired extinction of memories<\/span>. AMERICAN JOURNAL OF HUMAN GENETICS<\/span>, pp. 549<\/span>.<\/p>","publicationid":"107785","date":"2003-01-01","publicationtype":"Conference paper","isfavourite":"0"}],"presentation_conference_workshop_etc_":[{"html":"

Al-Amin H; El-Asrag M; Ghuloum S; Cardno A; Chamali R; Kiwan N; Clapcote S; Ali M; Inglehearn C<\/span> (2019)<\/span> Screening for major risk alleles for Schizophrenia in Qatari population<\/span>. BEHAVIOR GENETICS<\/span>, pp. 534<\/span>.<\/p>","publicationid":"528824","date":"2019-01-01","publicationtype":"Presentation (conference\/workshop etc)","isfavourite":"0"},{"html":"

Hughes R; Whittingham-Dowd J; Bristow G; Clapcote S; Broughton S; Dawson N<\/span> (2018)<\/span> NEUREXIN-1A (NRNX1A) HYPOFUNCTION INDUCES SCHIZOPHRENIA-RELEVANT DEFICITS IN CEREBRAL METABOLISM, COGNITIVE PROCESSING SPEED AND COGNITIVE FLEXIBILITY<\/span>. SCHIZOPHRENIA BULLETIN<\/span>, pp. S234<\/span>. <\/a><\/p>","publicationid":"465828","date":"2018-01-01","publicationtype":"Presentation (conference\/workshop etc)","isfavourite":"0"},{"html":"

Ivorra J; Mahmood T; Ali M; Pervo-Laraki E; Khan S; Logan C; Cardno AG; Johnson C; Wilkinson LD; Woodruff P; Clapcote SJ; Inglehearn CF<\/span> (2017)<\/span> IDENTIFICATION OF A SUSCEPTIBILITY LOCUS IN A CONSANGUINEOUS FAMILY WITH MULTIPLE SCHIZOPHRENIA AFFECTED MEMBERS<\/span>. EUROPEAN NEUROPSYCHOPHARMACOLOGY<\/span>, pp. S201<\/span>.<\/p>","publicationid":"451057","date":"2017-01-01","publicationtype":"Presentation (conference\/workshop etc)","isfavourite":"0"},{"html":"

Al Amri A; Ivorra JL; Cardno AG; Logan C; Mullins J; Mahmood T; Nazar Q; Dachtler J; Abdelhamed Z; Khan S; Khan K; Johnson C; Ali M; Inglehearn CF; Clapcote SJ<\/span> (2017)<\/span> EVIDENCE FOR THE INVOLVEMENT OF DFNB31 VARIANTS IN PSYCHOTIC DISORDERS<\/span>. EUROPEAN NEUROPSYCHOPHARMACOLOGY<\/span>, pp. S348<\/span>.<\/p>","publicationid":"451056","date":"2017-01-01","publicationtype":"Presentation (conference\/workshop etc)","isfavourite":"0"},{"html":"

Ivorra JL; Ali M; Logan C; Mahmood T; Khan S; Cardno AG; Johnson C; Inglehearn CF; Clapcote S<\/span> (2014)<\/span> IDENTIFICATION OF A SUSCEPTIBILITY LOCUS IN A CONSANGUINEOUS FAMILY WITH MULTIPLE SCHIZOPHRENIA-AFFECTED MEMBERS<\/span>. SCHIZOPHRENIA RESEARCH<\/span>, pp. S325-S326<\/span>. <\/a><\/p>","publicationid":"457548","date":"2014-01-01","publicationtype":"Presentation (conference\/workshop etc)","isfavourite":"0"},{"html":"

Mahmood T; Cardno A; Nazar Q; Clapcote S; Inglehearn C<\/span> (2013)<\/span> 891 \u2013 Consanguinity Multiplex And Schizophrenia - The Royal Road To Genes Of Major Effect<\/span>. European Psychiatry<\/span>, pp. 1<\/span>. <\/a><\/p>","publicationid":"663355","date":"2013-01-01","publicationtype":"Presentation (conference\/workshop etc)","isfavourite":"0"}],"book":[],"chapter":[{"html":"

Clapcote SJ<\/span> (2024)<\/span> Therapeutic Implications of Recent Genomic Discoveries in Schizophrenia<\/span>. Drug Discovery for Schizophrenia<\/span>, Royal Society of Chemistry<\/a>, pp. 225-241<\/span>. <\/a><\/p>","publicationid":"915259","date":"2024-12-06","publicationtype":"Chapter","isfavourite":"0"},{"html":"

Clapcote SJ<\/span> (2017)<\/span> Phosphodiesterase-4B as a Therapeutic Target for Cognitive Impairment and Obesity-Related Metabolic Diseases<\/span>. Advances in Neurobiology<\/span>, Advances in Neurobiology<\/span>, 17<\/span>, Springer International Publishing<\/a>, pp. 103-131<\/span>. <\/a><\/p>","publicationid":"440882","date":"2017-01-01","publicationtype":"Chapter","isfavourite":"0"}],"conference_abstract":[{"html":"

Lewis D; Al-Banaa I; Chakrabarty S; Clapcote SJ; Pickles AR<\/span> (2026)<\/span> Re-imaging pharmacology modules and assessments to better address the requirements of graduates, employers and professional, statutory and regulatory bodies<\/span>.<\/p>","publicationid":"1269303","date":"2026-01-01","publicationtype":"Conference abstract","isfavourite":"0"}],"preprint":[{"html":"

Pervolaraki E; Tyson AL; Pibiri F; Poulter SL; Reichelt AC; Rodgers RJ; Clapcote SJ; Lever C; Andreae LC; Dachtler J<\/span> (2018)<\/span> The within-subject application of diffusion tensor MRI and CLARITY reveals brain structural changes in\n Nrxn2<\/i>\n deletion mice<\/span>. openRxiv<\/span>. <\/a><\/p>","publicationid":"667551","date":"2018-04-14","publicationtype":"Preprint","isfavourite":"0"},{"html":"

Alsaady I; Tedford E; Alsaad M; Bristow G; Kohli S; Murray M; Reeves M; Vijayabaskar MS; Clapcote S; Wastling J; McConkey G<\/span> (2018)<\/span> Downregulation of the central noradrenergic system byToxoplasma gondii<\/i>infection<\/span>. bioRxiv<\/span>. <\/a> <\/a><\/p>","publicationid":"597531","date":"2018-01-01","publicationtype":"Preprint","isfavourite":"0"}],"report":[],"internet_publication":[],"performance":[],"composition":[],"exhibition":[],"poster":[],"artefact":[],"design":[],"patent":[],"scholarly_edition":[],"software_code":[],"thesis_dissertation":[],"other":[{"html":"

McGirr A; Lipina TV; Mun H-S; Georgiou J; Al-Amri AH; Ng E; Zhai D; Elliott C; Cameron RT; Mullins JG; Liu F; Baillie GS; Clapcote SJ; Roder JC<\/span> (2017)<\/span> Specific Inhibition of Phosphodiesterase-4B Results in Anxiolysis and Facilitates Memory Acquisition<\/span>. England<\/span>, 42<\/span>, (5)<\/span>. <\/a><\/p>","publicationid":"378072","date":"2017-04-01","publicationtype":"Other","isfavourite":"0"}],"dataset":[],"media":[],"working_paper":[]}}