Yr Athro Jeremy Hall

Hodge Professor Of Psychiatry

2026

• Berndt, L. C. S. et al., 2026. Sleep as a window into thalamocortical pathology: generative modeling implicates NMDA receptor hypofunction in 22q11.2 deletion syndrome. Translational Psychiatry (10.1038/s41398-026-04368-w)
• Gergel, T. et al., 2026. A tool to evaluate the impact of lived experience involvement in research: the Brain and Genomics Hub Impact Log protocol. Wellcome Open Research 11 562. (10.12688/wellcomeopenres.27426.1)
• Singh, T. et al., 2026. Human induced pluripotent stem cell-derived microglia with 1q21.1 deletion and duplication exhibit aberrant inflammatory response. Genes & diseases 13 (4) 101923. (10.1016/j.gendis.2025.101923)
• Wilkinson, G. et al. 2026. CACNA1C genetic variants differentially affect neuronal networks through divergent pathways. Biological Psychiatry Global Open Science 100792. (10.1016/j.bpsgos.2026.100792)
• Underwood, J. F. et al. 2026. Timothy syndrome and CACNA1C-Related Disorder: first international language and management guidelines consensus statement. European Journal of Human Genetics (10.1038/s41431-026-02178-8)
• Námešná, A. et al. 2026. Synaptic and circuit mechanisms shaping neurodevelopmental and psychiatric outcomes associated with 16p11.2 copy number variation. Genes 17 (6) 716. (10.3390/genes17060716)
• Underwood, J. F. and Hall, J. 2026. Cannabis and psychosis: genomic methods shed light on pathophysiological processes [Commentary]. Biological Psychiatry Global Open Science 6 (5) 100759. (10.1016/j.bpsgos.2026.100759)
• Underwood, J. F. et al. 2026. Childhood trauma as a mediator between autistic traits and depression: evidence from the ALSPAC birth cohort. Psychological Medicine 56 e169. (10.1017/S0033291726104267)
• Alsaqati, M. et al. 2026. Effects of acute fluctuations of extracellular Zinc on network activity of human iPSC-derived neurons; impact of NMDA Receptor and L-Type Calcium Channel Activation. Neuropharmacology 292 110952. (10.1016/j.neuropharm.2026.110952)
• Saka, A. et al., 2026. The Sleep Detectives: a co-designed protocol for longitudinal tracking of sleep health, sleep neurophysiology and cognition in children and young people at risk of neurodevelopmental disorders [Abstract]. Sleep Medicine 138 106934. (10.1016/j.sleep.2025.106934)
• Lee, I. O. et al., 2026. The influence of genetic factors on education health and care plan obtainment for pupils with intellectual developmental disabilities. Scientific Reports 16 9181. (10.1038/s41598-026-36227-5)
• Berndt, L. et al., 2026. Sleep as a window into circuit pathology in 22q11.2 deletion syndrome: a thalamocortical computational psychiatry approach [Abstract]. Neuroscience Applied 5 (S1) 106589. (10.1016/j.nsa.2025.106589)

2025

• Lee, I. et al., 2025. Inequalities of the waiting time for education health and care plan provision for pupils with intellectual developmental disabilities: a brief report. Journal of Intellectual Disability Research 69 (11), pp.1325-1336. (10.1111/jir.13239)
• Varney, L. et al., 2025. Effect of polygenic scores on the relationship between psychosis and cognition. Translational Psychiatry 15 (1) 491. (10.1038/s41398-025-03666-z)
• Silva, A. et al. 2025. Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging 10 (10), pp.1093-1106. (10.1016/j.bpsc.2025.05.010)
• Lilford, P. et al., 2025. Examining whether inflammation mediates effects of genetic risk and trauma on psychopathology. BJPsych Open 11 (5) e181. (10.1192/bjo.2025.10054)
• Gasalla, P. et al. 2025. Reduced cacna1c expression produces anhedonic reactions to palatable sucrose in rats: No interactions with juvenile or adult stress. Genes, Brain and Behavior 24 (2) e70021. (10.1111/gbb.70021)

2024

• Hunt, M. et al., 2024. Risk of physical health comorbidities in autistic adults: a clinical nested cross-sectional study. BJPsych Open 10 (6) e182. (10.1192/bjo.2024.777)
• Lee, I. O. et al., 2024. The inequity of education, health and care plan provision for children and young people with intellectual and developmental disabilities. Journal of Intellectual Disability Research 68 (10), pp.1167-1183. (10.1111/jir.13139)
• Hall, J. H. et al. 2024. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational Psychiatry 14 (1) 259. (10.1038/s41398-024-02975-z)
• Haddon, J. E. et al. 2024. Linking haploinsufficiency of the autism- and schizophrenia-associated gene Cyfip1 with striatal-limbic-cortical network dysfunction and cognitive inflexibility. Translational Psychiatry 14 (1) 256. (10.1038/s41398-024-02969-x)
• Cabezas De La Fuente, D. et al. 2024. Impaired oxysterol-liver X receptor signaling underlies aberrant cortical neurogenesis in a human stem cell model of neurodevelopmental disorder. Cell Reports 43 (3) 113946. (10.1016/j.celrep.2024.113946)
• Peall, K. J. , Owen, M. J. and Hall, J. 2024. Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes. Nature Reviews Neurology 20 (1), pp.7-21. (10.1038/s41582-023-00896-x)
• Wellard, N. L. et al. 2024. The association of hippocampal long-term potentiation-induced gene expression with genetic risk for psychosis. International Journal of Molecular Sciences 25 (2) 946. (10.3390/ijms25020946)

2023

• Griesius, S. et al., 2023. A mild impairment in reversal learning in a bowl-digging substrate deterministic task but not other cognitive tests in the Dlg2+/- rat model of genetic risk for psychiatric disorder. Genes, Brain and Behavior 22 (6) e12865. (10.1111/gbb.12865)
• Wang, B. et al., 2023. Psychosis endophenotypes: A gene-set-specific polygenic risk score analysis. Schizophrenia Bulletin 49 (6), pp.1625-1636. (10.1093/schbul/sbad088)
• Indrigo, M. et al., 2023. Nuclear ERK1/2 signaling potentiation enhances neuroprotection and cognition via Importinα1/KPNA2. EMBO Molecular Medicine 15 (11) e15984. (10.15252/emmm.202215984)
• Kumar, K. et al., 2023. Subcortical brain alterations in carriers of genomic copy number variants. The American Journal of Psychiatry 180 (9), pp.685-698. (10.1176/appi.ajp.20220304)
• Chawner, S. J. et al. 2023. Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions. JCPP Advances 3 (2) e12162. (10.1002/jcv2.12162)
• Kopal, J. et al., 2023. Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence. Nature Human Behaviour 7 , pp.1001-1017. (10.1038/s41562-023-01541-9)
• Niarchou, M. et al., 2023. Psychopathology in mothers of children with pathogenic copy number variants. Journal of Medical Genetics 60 , pp.706-711. (10.1136/jmg-2022-108752)
• Dec, K. et al. 2023. A high ratio of linoleic acid (n-6 PUFA) to alpha-linolenic acid (n-3 PUFA) adversely affects early stage of human neuronal differentiation and electrophysiological activity of glutamatergic neurons in vitro. Frontiers in Cell and Developmental Biology 11 1166808. (10.3389/fcell.2023.1166808)
• Moreau, C. A. et al., 2023. Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions. Brain 146 (4), pp.1686-1696. (10.1093/brain/awac315)
• Gasalla Canto, P. et al. 2023. Characterisation of the neural basis underlying appetitive extinction & renewal in a Cacna1c rats. Neuropharmacology 227 109444. (10.1016/j.neuropharm.2023.109444)
• Lynham, A. J. et al. 2023. DRAGON-Data: A platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts. BJPsych Open 9 (2) e32. (10.1192/bjo.2022.636)
• Dimitriadis, S. I. et al. 2023. Genetic risk for schizophrenia is associated with increased proportion of indirect connections in brain networks revealed by a semi-metric analysis: evidence from population sample stratified for polygenic risk. Cerebral Cortex 33 (6), pp.2997-3011. (10.1093/cercor/bhac256)
• Wolstencroft, J. et al., 2023. Mental health impact of autism on families of children with intellectual and developmental disabilities of genetic origin. JCPP Advances e12128. (10.1002/jcv2.12128)
• Chawner, S. J. R. A. et al. 2023. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational Psychiatry 13 7. (10.1038/s41398-022-02296-z)
• Levy, R. et al., 2023. A cross-sectional study of the neuropsychiatric phenotype of CACNA1C-related disorder. Pediatric Neurology 138 , pp.101-106. (10.1016/j.pediatrneurol.2022.10.013)

2022

• Zurek, S. et al., 2022. Experimental verification of 2.4 kVAr and 12 kVAr prototype variable inductors controlled by virtual air gaps with magnetic orthogonality. IEEE Transactions on Power Delivery 37 (6), pp.4880-4887. (10.1109/TPWRD.2022.3162174)
• Moon, A. L. et al. 2022. Social interaction following prepubertal stress alters prefrontal gene expression associated with cell signalling and oligodendrocytes. Translational Psychiatry 12 (1) 516. (10.1038/s41398-022-02280-7)
• Alsaqati, M. et al. 2022. NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia. Translational Psychiatry 12 438. (10.1038/s41398-022-02199-z)
• Underwood, J. et al. 2022. Neurological and psychiatric disorders among autistic adults: a population healthcare record study. Psychological Medicine (10.1017/S0033291722002884)
• Clifton, N. et al. 2022. Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function. Human Molecular Genetics 31 (18), pp.3095-3106. (10.1093/hmg/ddac105)
• Silva, A. I. et al. 2022. Neuroimaging findings in neurodevelopmental copy number variants: identifying molecular pathways to convergent phenotypes. Biological Psychiatry 92 (5), pp.341-361. (10.1016/j.biopsych.2022.03.018)
• Wolstencroft, J. et al., 2022. Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study. The Lancet Psychiatry 9 (9), pp.715-724. (10.1016/S2215-0366(22)00207-3)
• Underwood, J. F. G. et al. 2022. Evidence of increasing recorded diagnosis of autism spectrum disorders in Wales, UK – an e-cohort study. Autism 26 (6), pp.1499-1508. (10.1177/13623613211059674)
• Donnelly, N. A. et al., 2022. Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms. eLife 11 e75482. (10.7554/elife.75482)
• Daughters, K. et al. 2022. Oxytocin administration versus emotion training in healthy males: Considerations for future research. Philosophical Transactions of the Royal Society B: Biological Sciences 377 (1858) 20210056. (10.1098/rstb.2021.0056)
• Griesius, S. et al., 2022. Reduced expression of the psychiatric risk gene DLG2 (PSD93) impairs hippocampal synaptic integration and plasticity. Neuropsychopharmacology 47 , pp.1367-1378. (10.1038/s41386-022-01277-6)
• Pass, R. et al. 2022. Selective behavioural impairments in mice heterozygous for the cross disorder psychiatric risk gene DLG2. Genes, Brain and Behavior 21 (4) e12799. (10.1111/gbb.12799)
• Waldron, S. et al. 2022. Behavioural and molecular characterisation of the Dlg2 haploinsufficiency rat model of genetic risk for psychiatric disorder. Genes, Brain and Behavior 21 (4) e12797. (10.1111/gbb.12797)
• Hall, J. and Bray, N. J. 2022. Schizophrenia genomics: convergence on synaptic development, adult synaptic plasticity, or both?. Biological Psychiatry 91 (8), pp.709-717. (10.1016/j.biopsych.2021.10.018)
• Namkung, H. et al., 2022. Parsing neural circuits of fear learning and extinction across basic and clinical neuroscience: Towards better translation. Neuroscience and Biobehavioral Reviews 134 104502. (10.1016/j.neubiorev.2021.12.025)
• Cunningham, A. C. et al. 2022. Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs. Psychological Medicine 52 (3), pp.574-586. (10.1017/S0033291720002330)
• Tuominen, L. et al., 2022. Impairment in acquisition of conditioned fear in schizophrenia. Neuropsychopharmacology 47 , pp.681-686. (10.1038/s41386-021-01193-1)
• Warne, N. et al. 2022. Collecting genetic samples and linked mental health data from adolescents in schools: protocol co-production and a mixed-methods pilot of feasibility and acceptability. BMJ Open 12 (2) e049283. (10.1136/bmjopen-2021-049283)
• Westacott, L. J. et al. 2022. Complement C3 and C3aR mediate different aspects of emotional behaviours; relevance to risk for psychiatric disorder. Brain, Behavior, and Immunity 99 , pp.70-82. (10.1016/j.bbi.2021.09.005)

2021

• Dimitriadis, S. I. et al. 2021. Global brain flexibility during working memory is reduced in a high genetic risk group for schizophrenia. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging 6 (12), pp.1176-1184. (10.1016/j.bpsc.2021.01.007)
• Westacott, L. J. et al. 2021. Dissociable effects of complement C3 and C3aR on survival and morphology of adult born hippocampal neurons, pattern separation, and cognitive flexibility in male mice. Brain, Behavior, and Immunity 98 , pp.136-150. (10.1016/j.bbi.2021.08.215)
• Dimitriadis, S. I. et al. 2021. Genetic risk for schizophrenia is associated with altered visually-induced gamma band activity: evidence from a population sample stratified polygenic risk. Translational Psychiatry 11 592. (10.1038/s41398-021-01678-z)
• Thygesen, J. H. et al., 2021. Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study. Molecular Psychiatry 26 , pp.5307-5319. (10.1038/s41380-020-0820-7)
• Clifton, N. E. et al. 2021. Developmental profile of psychiatric risk associated with voltage-gated cation channel activity. Biological Psychiatry 90 (6)(10.1016/j.biopsych.2021.03.009)
• Silva, A. I. et al. 2021. Analysis of diffusion tensor imaging data from the UK Biobank confirms dosage effect of 15q11.2 copy number variation on white matter and shows association with cognition. Biological Psychiatry 90 (5), pp.307-316. (10.1016/j.biopsych.2021.02.969)
• Clifton, N. E. et al. 2021. Genetic association of FMRP targets with psychiatric disorders. Molecular Psychiatry 26 , pp.2977-2990. (10.1038/s41380-020-00912-2)
• Modenato, C. et al., 2021. Effects of eight neuropsychiatric copy number variants on human brain structure. Translational Psychiatry 11 (1) 399. (10.1038/s41398-021-01490-9)
• Hubbard, L. et al. 2021. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 90 (1), pp.28-34. (10.1016/j.biopsych.2020.11.025)
• Notter, T. et al. 2021. Neuronal activity increases translocator protein (TSPO) levels. Molecular Psychiatry 26 , pp.2025-2037. (10.1038/s41380-020-0745-1)
• Rule, L. et al., 2021. Environmental enrichment rescues survival and function of adult-born neurons following early life stress. Molecular Psychiatry 26 , pp.1898-1908. (10.1038/s41380-020-0718-4)
• Tigaret, C. M. et al. 2021. Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by hemizygosity of the psychiatric risk gene Cacna1c. Molecular Psychiatry 26 , pp.1748-1760. (10.1038/s41380-020-01001-0)
• Haan, N. et al. 2021. Haploinsufficiency of the schizophrenia and autism risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through microglial and Arp2/3 mediated actin dependent mechanisms. Translational Psychiatry 11 (1) 313. (10.1038/s41398-021-01415-6)
• Cunningham, A. et al. 2021. Coordination difficulties, IQ and psychopathology in children with high-risk Copy Number Variants. Psychological Medicine 51 (2), pp.290-299. (10.1017/S0033291719003210)
• Chawner, S. et al. 2021. A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants. American Journal of Psychiatry 178 (1), pp.77-86. (10.1176/appi.ajp.2020.20010015)
• Sønderby, I. E. et al., 2021. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry 11 182. (10.1038/s41398-021-01213-0)

2020

• Moon, A. L. et al. 2020. Cacna1c hemizygosity results in aberrant fear conditioning to neutral stimuli. Schizophrenia Bulletin 46 (5), pp.1231-1238. (10.1093/schbul/sbz127)
• Dima, D. C. et al. 2020. Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk. Translational Psychiatry 10 324. (10.1038/s41398-020-00998-w)
• Cunningham, A. et al. 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 35 (7), pp.1272-1274. (10.1002/mds.28078)
• Corcoran, M. et al., 2020. Are working memory and glutamate concentrations involved in early-life stress and severity of psychosis?. Brain and Behavior 10 (6) e01616. (10.1002/brb3.1616)
• Moulding, H. et al. 2020. Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS). Psychological Medicine 50 , pp.1191-1202. (10.1017/S0033291719001119)
• Clifton, N. E. et al. 2020. FMRP and CYFIP1 at the synapse and their role in psychiatric vulnerability. Complex Psychiatry (10.1159/000506858)

2019

• Ranson, A. et al. 2019. Top-down suppression of sensory cortex in an NMDAR hypofunction model of psychosis. Schizophrenia Bulletin 45 (6), pp.1349-1357. (10.1093/schbul/sby190)
• Underwood, J. et al. 2019. Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort. British Journal of Psychiatry 215 (5), pp.647-653. (10.1192/bjp.2019.30)
• Sykes, L. et al. 2019. Genetic variation in the psychiatric risk gene CACNA1C modulates reversal learning across species. Schizophrenia Bulletin 45 (5), pp.1024-1032. (10.1093/schbul/sby146)
• Plumbly, W. et al. 2019. L-type voltage-gated calcium channel regulation of in vitro human cortical neuronal networks. Scientific Reports 9 13810. (10.1038/s41598-019-50226-9)
• Silva, A. I. et al., 2019. Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility. Nature Communications 10 3455. (10.1038/s41467-019-11119-7)
• Moon, A. et al. 2019. Su13: Genetic variation in 'calcium voltage-gated channel subunit alpha1c (cacna1c): interactions with prepubertal stress and impact on hippocampal dependent learning. European Neuropsychopharmacology 29 (S4), pp.S1274-S1275. (10.1016/j.euroneuro.2018.08.377)
• Underwood, J. et al. 2019. SA20COPY Number variants and polygenic risk scores in adults with autism spectrum disorder (ASD): results from the NCMH adult ASD cohort. European Neuropsychopharmacology 29 (S4), pp.S1198-S1199. (10.1016/j.euroneuro.2018.08.242)
• Jones, H. J. et al. 2019. Association of genetic risk for rheumatoid arthritis with cognitive and psychiatric phenotypes across childhood and adolescence. JAMA Network Open 2 (6), pp.-. e196118. (10.1001/jamanetworkopen.2019.6118)
• Trent, S. et al. 2019. Cyfip1 haploinsufficiency does not alter GABAA receptor δ-subunit expression and tonic inhibition in dentate gyrus PV+ interneurons and granule cells. eNeuro 6 (3) ENEURO.0364-18.2019. (10.1523/ENEURO.0364-18.2019)
• Cunningham, A. et al. 2019. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion Syndrome. Journal of Neurodevelopmental Disorders 11 8. (10.1186/s11689-019-9271-3)
• Chawner, S. J. R. A. et al. 2019. Genotype–phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study. Lancet Psychiatry 6 (6), pp.493 - 505. (10.1016/S2215-0366(19)30123-3)
• Clifton, N. et al. 2019. Regulation and function of activity-dependent Homer in synaptic plasticity. Molecular Neuropsychiatry 5 (3), pp.147-161. (10.1159/000500267)
• Srinivasan, R. et al. 2019. Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities. Journal of Intellectual Disability Research 63 (5), pp.477-488. (10.1111/jir.12607)
• Silva, A. I. et al. 2019. Reciprocal white matter changes associated with copy number variation at 15q11.2 BP1-BP2: A diffusion tensor imaging study. Biological Psychiatry 85 (7), pp.563-572. (10.1016/j.biopsych.2018.11.004)
• Lancaster, T. M. et al. 2019. Structural and functional neuroimaging of polygenic risk for schizophrenia: a recall-by-genotype-based approach. Schizophrenia Bulletin 45 (2), pp.405-414. (10.1093/schbul/sby037)
• Chawner, S. et al. 2019. Genotype-phenotype relationships in children with copy number variants associated with high neuropsychiatric risk: Findings from the Intellectual Disability & Mental Health: Assessing the Genomic Impact on Neurodevelopment (IMAGINE-ID) study.. bioRxiv (10.1101/535708)
• Drakesmith, M. et al. 2019. Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures. Translational Psychiatry 9 (1) 102. (10.1038/s41398-019-0440-7)
• Clifton, N. E. et al. 2019. Dynamic expression of genes associated with schizophrenia and bipolar disorder across development. Translational Psychiatry 9 74. (10.1038/s41398-019-0405-x)
• Schwarz, E. et al., 2019. Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder. Translational Psychiatry 9 (1), pp.-. 12. (10.1038/s41398-018-0225-4)
• Niarchou, M. et al. 2019. Psychiatric disorders in children with 16p11.2 deletion and duplication. Translational Psychiatry (10.1038/s41398-018-0339-8)
• Melendez-Torres, G. et al. 2019. Measurement invariance properties and external construct validity of the Short Warwick-Edinburgh Mental Wellbeing Scale in a large national sample of secondary school students in Wales. Health and Quality of Life Outcomes 17 139. (10.1186/s12955-019-1204-z)

2018

• Brydges, N. M. et al. 2018. Sex specific effects of pre-pubertal stress on hippocampal neurogenesis and behaviour. Translational Psychiatry 8 271. (10.1038/s41398-018-0322-4)
• Sykes, L. et al., 2018. Regulation of the expression of the psychiatric risk gene Cacna1c during associative learning. Molecular Neuropsychiatry 4 , pp.149-157. (10.1159/000493917)
• Iliescu, A. F. et al. 2018. The nature of phenotypic variation in Pavlovian conditioning. Journal of Experimental Psychology: Animal Learning and Cognition 44 (4), pp.358-369. (10.1037/xan0000177)
• Tigaret, C. M. et al. 2018. Convergent metabotropic signalling pathways inhibit SK channels to promote synaptic plasticity in the hippocampus. Journal of Neuroscience 38 (43), pp.9252-9262. (10.1523/JNEUROSCI.1160-18.2018)
• Moon, A. L. et al. 2018. CACNA1C: Association with pychiatric disorders, behavior, and neurogenesis. Schizophrenia Bulletin 44 (5), pp.958-965. (10.1093/schbul/sby096)
• Kamath, A. et al., 2018. Chromosome 17q12 duplications: Further delineation of the range of psychiatric and clinical phenotypes. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 (5), pp.520-528. (10.1002/ajmg.b.32643)
• Pratt, J. and Hall, J. 2018. Biomarkers in neuropsychiatry: a prospect for the twenty-first century?. Current Topics in Behavioral Neuroscience 40 , pp.3-10. (10.1007/7854_2018_58)
• Ruderfer, D. M. et al., 2018. Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes. Cell 173 (7), pp.1705-1715.e16. (10.1016/j.cell.2018.05.046)
• Reddaway, J. et al. 2018. Genomic and imaging biomarkers in schizophrenia. In: Current Topics in Behavioral Neurosciences. Berlin and Heidelberg: Springer. , pp.325-352. (10.1007/7854_2018_52)
• Clifton, N. , Thomas, K. and Hall, J. 2018. The effect of ketamine on the consolidation and extinction of contextual fear memory. Journal of Psychopharmacology 32 (2), pp.156-162. (10.1177/0269881117748903)
• Cunningham, A. C. et al. 2018. Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome. British Journal of Psychiatry 212 (1), pp.27-33. (10.1192/bjp.2017.6)

2017

• Clifton, N. et al. 2017. Hippocampal regulation of postsynaptic density Homer1 by associative learning. Neural Plasticity 2017 5959182. (10.1155/2017/5959182)
• Stanfield, A. M. et al., 2017. Dissociation of brain activation in autism and schizotypal personality disorder during social judgements. Schizophrenia Bulletin 43 (6), pp.1220-1228. (10.1093/schbul/sbx083)
• Schmaal, L. et al., 2017. Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group. Molecular Psychiatry 22 (6), pp.900-909. (10.1038/mp.2016.60)
• Neilson, E. et al., 2017. Effects of environmental risks and polygenic loading for schizophrenia on cortical thickness. Schizophrenia Research 184 , pp.128-136. (10.1016/j.schres.2016.12.011)
• Clifton, N. E. et al. 2017. Schizophrenia copy number variants and associative learning. Molecular Psychiatry 22 (2), pp.178-182. (10.1038/mp.2016.227)
• Foley, S. F. et al. 2017. Multimodal brain imaging reveals structural differences in Alzheimer's disease polygenic risk carriers: A study in healthy young adults. Biological Psychiatry 81 (2), pp.154-161. (10.1016/j.biopsych.2016.02.033)
• Hall, J. H. and Harwood, J. L. 2017. Brain lipids in health and disease. In: Food Lipids: Chemistry, Nutrition, and Biotechnology, Fourth Edition. CRC Press. , pp.747-764.
• Radtke, F. et al. 2017. Modulating neuroinflammation to treat neuropsychiatric disorders. BioMed Research International 5071786.
• Trent, S. et al. 2017. AMPA receptors control fear extinction through an Arc-dependent mechanism. Learning and Memory 24 , pp.375-380. (10.1101/lm.045013.117)

2016

• Chan, S. W. et al., 2016. Deactivation in anterior cingulate cortex during facial processing in young individuals with high familial risk and early development of depression: fMRI findings from the Scottish Bipolar Family Study. Journal of Child Psychology and Psychiatry 57 (11), pp.1277-1286. (10.1111/jcpp.12591)
• Thomson, P. A. et al., 2016. Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function. npj Schizophrenia 2 16024. (10.1038/npjschz.2016.24)
• Nickson, T. et al., 2016. Prospective longitudinal voxel-based morphometry study of major depressive disorder in young individuals at high familial risk. Psychological Medicine 46 (11), pp.2351-2361. (10.1017/S0033291716000519)
• Scholz, B. et al., 2016. The regulation of cytokine networks in hippocampal CA1 differentiates extinction from those required for the maintenance of contextual fear memory after recall. PLoS ONE 11 (5) e0153102. (10.1371/journal.pone.0153102)

2015

• Papmeyer, M. et al., 2015. Neurocognition in individuals at high familial risk of mood disorders with or without subsequent onset of depression. Psychological Medicine 45 (15), pp.3317-3327. (10.1017/S0033291715001324)
• Johnstone, M. et al., 2015. Copy number variations in DISC1 and DISC1-interacting partners in major mental illness. Molecular Neuropsychiatry 1 (3), pp.175-190. (10.1159/000438788)
• Hall, J. and Owen, M. J. 2015. Psychiatric classification - a developmental perspective. British Journal of Psychiatry 207 (4), pp.281-282. (10.1192/bjp.bp.114.159996)
• Trent, S. et al. 2015. Rescue of long-term memory after reconsolidation blockade. Nature Communications 6 7897. (10.1038/ncomms8897)
• van Amelsvoort, T. et al., 2015. Effects of a balanced translocation between chromosomes 1 and 11 disrupting the DISC1 locus on white matter integrity. PLoS ONE 10 (6) e0130900. (10.1371/journal.pone.0130900)
• Brydges, N. et al. 2015. Early life stress produces compulsive-like, but not impulsive, behavior in females. Behavioral Neuroscience 129 (3), pp.300-308. (10.1037/bne0000059)
• Whalley, H. C. et al., 2015. White matter integrity and its association with affective and interpersonal symptoms in borderline personality disorder. NeuroImage: Clinical 7 , pp.476-481. (10.1016/j.nicl.2015.01.016)
• Hall, J. et al. 2015. Genetic risk for schizophrenia: convergence on synaptic pathways Involved in plasticity. Biological Psychiatry 77 (1), pp.52-68. (10.1016/j.biopsych.2014.07.011)
• Nicol, K. et al., 2015. Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder. Translational Psychiatry 5 (5) e559. (10.1038/tp.2015.53)
• Whalley, H. C. et al., 2015. Dysfunction of emotional brain systems in individuals at high risk of mood disorder with depression and predictive features prior to illness. Psychological Medicine 45 (06), pp.1207. (10.1017/S0033291714002256)
• Zeng, Y. et al., 2015. Prenatal glucocorticoid exposure in rats: programming effects on stress reactivity and cognition in adult offspring. Stress 18 (3), pp.353-361. (10.3109/10253890.2015.1055725)

2014

• Nicol, K. , Pope, M. and Hall, J. 2014. Facial emotion recognition in borderline personality: An association, with childhood experience. Psychiatry Research 218 (1-2), pp.256-258. (10.1016/j.psychres.2014.04.017)
• Thompson, P. M. et al., 2014. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior , pp.153-82. (10.1007/s11682-013-9269-5)
• Brydges, N. et al. 2014. Juvenile stress produces long-lasting changes in hippocampal DISC1, GSK3ß and NRG1 expression. Molecular Psychiatry 19 (8), pp.854. (10.1038/mp.2013.193)
• Brydges, N. et al. 2014. Juvenile stress enhances anxiety and alters corticosteroid receptor expression in adulthood. Brain and Behavior 4 (1), pp.4-13. (10.1002/brb3.182)
• Mukherjee, P. et al., 2014. Altered amygdala connectivity within the social brain in schizophrenia. Schizophrenia Bulletin 40 (1), pp.152-60. (10.1093/schbul/sbt086)
• Barker, V. et al., 2014. Set shifting and reversal learning in borderline personality disorder. Personality and Mental Health 8 (1), pp.1-13. (10.1002/pmh.1235)
• Brydges, N. et al. 2014. Prepubertal stress and hippocampal function: Sex-specific effects. Hippocampus 24 (6), pp.684-692. (10.1002/hipo.22259)

2013

• Sprooten, E. et al., 2013. Cortical thickness in first-episode schizophrenia patients and individuals at high familial risk: A cross-sectional comparison. Schizophrenia Research 151 (1-3), pp.259-64. (10.1016/j.schres.2013.09.024)
• Nicol, K. et al., 2013. Social judgement in borderline personality disorder. PLoS ONE 8 (11) e73440. (10.1371/journal.pone.0073440)
• Ripke, S. et al., 2013. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics 45 (10), pp.1150-1159. (10.1038/ng.2742)
• McIntosh, A. M. et al., 2013. Neuroticism, depressive symptoms and white-matter integrity in the Lothian Birth Cohort 1936. Psychological Medicine 43 (06), pp.1197-1206. (10.1017/S003329171200150X)
• McIntosh, A. M. et al., 2013. Polygenic risk for schizophrenia is associated with cognitive change between childhood and old age. Biological Psychiatry 73 (10), pp.938-943. (10.1016/j.biopsych.2013.01.011)
• Parra, M. A. et al., 2013. Medial temporal lobe function during emotional memory in early Alzheimer's disease, mild cognitive impairment and healthy ageing: an fMRI study. BMC Psychiatry 13 (1) 76. (10.1186/1471-244X-13-76)
• Gradin, V. B. et al., 2013. Salience network-midbrain dysconnectivity and blunted reward signals in schizophrenia. Psychiatry Research: Neuroimaging 211 (2), pp.104-111. (10.1016/j.pscychresns.2012.06.003)
• Brydges, N. et al. 2013. Imaging conditioned fear circuitry using awake rodent fMRI. PLoS ONE 8 (1) e54197. (10.1371/journal.pone.0054197)
• Whalley, H. C. et al., 2013. Polygenic risk and white matter integrity in individuals at high risk of mood disorder. Biological Psychiatry 74 (4), pp.280-286. (10.1016/j.biopsych.2013.01.027)
• Whalley, H. C. et al., 2013. Prediction of depression in individuals at high familial risk of mood disorders using functional magnetic resonance imaging [Article]. PLoS ONE 8 (3), pp.e57357. (10.1371/journal.pone.0057357)

2012

• Sprooten, E. et al., 2012. An investigation of a genomewide supported psychosis variant in ZNF804A and white matter integrity in the human brain. Magnetic Resonance Imaging 30 (10), pp.1373-1380. (10.1016/j.mri.2012.05.013)
• Whalley, H. C. et al., 2012. Impact of a microRNA MIR137 susceptibility variant on brain function in people at high genetic risk of schizophrenia or bipolar disorder. Neuropsychopharmacology 37 (12), pp.2720-2729. (10.1038/npp.2012.137)
• Brydges, N. M. et al. 2012. The effects of juvenile stress on anxiety, cognitive bias and decision making in adulthood: A rat model. PLoS ONE 7 (10), pp.e48143. (10.1371/journal.pone.0048143)
• Gradin, V. B. et al., 2012. Abnormal neural responses to social exclusion in schizophrenia. PLoS ONE 7 (8) e42608. (10.1371/journal.pone.0042608)
• Whalley, H. C. et al., 2012. The influence of polygenic risk for bipolar disorder on neural activation assessed using fMRI. Translational Psychiatry 2 (7) e130. (10.1038/tp.2012.60)
• McIntosh, A. M. et al., 2012. Genetic variation in hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression. Frontiers in Genetics 3 , pp.116. (10.3389/fgene.2012.00116)
• McAlonan, G. M. et al., 2012. Evaluation of a screening instrument for autism spectrum disorders in prisoners. PLoS ONE 7 (5) e36078. (10.1371/journal.pone.0036078)
• Stein, J. L. et al., 2012. Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics 44 (5), pp.552-561. (10.1038/ng.2250)
• Whalley, H. C. et al., 2012. Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159B (3), pp.343-353. (10.1002/ajmg.b.32035)
• Whalley, H. C. et al., 2012. Effect of variation in diacylglycerol kinase η (DGKH) gene on brain function in a cohort at familial risk of bipolar disorder. Neuropsychopharmacology 37 (4), pp.919-928. (10.1038/npp.2011.272)
• Mukherjee, P. et al., 2012. Lower effective connectivity between amygdala and parietal regions in response to fearful faces in schizophrenia. Schizophrenia Research 134 (2-3), pp.118-124. (10.1016/j.schres.2011.09.033)
• Robinson, L. et al., 2012. Facial emotion recognition in Scottish prisoners. International Journal of Law and Psychiatry 35 (1), pp.57-61. (10.1016/j.ijlp.2011.11.009)

2011

• Whalley, H. C. et al., 2011. Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8), pp.941-948. (10.1002/ajmg.b.31241)
• Welch, K. A. et al., 2011. The impact of substance use on brain structure in people at high risk of developing schizophrenia. Schizophrenia Bulletin 37 (5), pp.1066-1076. (10.1093/schbul/sbq013)
• O'Connell, G. et al., 2011. Schizophrenia risk genes: Implications for future drug development and discovery [Review]. Biochemical Pharmacology 81 (12), pp.1367-1373. (10.1016/j.bcp.2010.11.009)
• Gradin, V. B. et al., 2011. Expected value and prediction error abnormalities in depression and schizophrenia. Brain 134 (6), pp.1751-1764. (10.1093/brain/awr059)
• McIntosh, A. M. et al., 2011. Longitudinal volume reductions in people at high genetic risk of schizophrenia as they develop psychosis. Biological psychiatry 69 (10), pp.953-958. (10.1016/j.biopsych.2010.11.003)
• Chakirova, G. et al., 2011. The effects of DISC1 risk variants on brain activation in controls, patients with bipolar disorder and patients with schizophrenia. Psychiatry Research: Neuroimaging 192 (1), pp.20-28. (10.1016/j.pscychresns.2011.01.015)
• Lawrie, S. M. et al., 2011. Do we have any solid evidence of clinical utility about the pathophysiology of schizophrenia? [Editorial]. World Psychiatry 10 (1), pp.19-31. (10.1002/j.2051-5545.2011.tb00004.x)
• Johnstone, M. et al., 2011. DISC1 in schizophrenia: Genetic mouse models and human genomic imaging. Schizophrenia Bulletin 37 (1), pp.14-20. (10.1093/schbul/sbq135)

2010

• Whalley, H. C. et al., 2010. Effects of the BDNF val66met polymorphism on prefrontal brain function in a population at high genetic risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8), pp.1474-1482. (10.1002/ajmg.b.31128)
• Lawrie, S. M. et al., 2010. The 'continuum of psychosis': scientifically unproven and clinically impractical [Editorial]. British Journal of Psychiatry 197 (6), pp.423-425. (10.1192/bjp.bp.109.072827)
• Philip, R. C. M. et al., 2010. Deficits in facial, body movement and vocal emotional processing in autism spectrum disorders. Psychological Medicine 40 (11), pp.1919-1929. (10.1017/S0033291709992364)
• Chakirova, G. et al., 2010. Orbitofrontal morphology in people at high risk of developing schizophrenia. European Psychiatry 25 (6), pp.366-372. (10.1016/j.eurpsy.2010.03.001)
• Baig, B. J. et al., 2010. Functional magnetic resonance imaging of BDNF val66met polymorphism in unmedicated subjects at high genetic risk of schizophrenia performing a verbal memory task. Psychiatry Research: Neuroimaging 183 (3), pp.195-201. (10.1016/j.pscychresns.2010.06.009)
• Hall, J. et al. 2010. Hippocampal function in schizophrenia and bipolar disorder. Psychological Medicine 40 (05), pp.761-770. (10.1017/S0033291709991000)
• Romaniuk, L. et al., 2010. Midbrain activation during Pavlovian conditioning and delusional symptoms in schizophrenia. JAMA Psychiatry 67 (12), pp.1246-1254. (10.1001/archgenpsychiatry.2010.169)

2009

• Whalley, H. C. et al., 2009. Functional imaging of emotional memory in bipolar disorder and schizophrenia. Bipolar Disorders 11 (8), pp.840-856. (10.1111/j.1399-5618.2009.00768.x)
• Moorhead, T. W. J. et al., 2009. Progressive temporal lobe grey matter loss in adolescents with schizotypal traits and mild intellectual impairment. Psychiatry Research: Neuroimaging 174 (2), pp.105-109. (10.1016/j.pscychresns.2009.04.003)
• Zuliani, R. et al., 2009. Genetic variation in the G72 (DAOA) gene affects temporal lobe and amygdala structure in subjects affected by bipolar disorder. Bipolar Disorders 11 (6), pp.621-627. (10.1111/j.1399-5618.2009.00731.x)
• McIntosh, A. M. et al., 2009. Genetic risk for white matter abnormalities in bipolar disorder. International Review of Psychiatry 21 (4), pp.387-393. (10.1080/09540260902962180)
• McKirdy, J. et al., 2009. Set shifting and reversal learning in patients with bipolar disorder or schizophrenia. Psychological Medicine 39 (08), pp.1289-1293. (10.1017/S0033291708004935)
• Mirakhur, A. et al., 2009. Changes in gyrification over 4 years in bipolar disorder and their association with the brain-derived neurotrophic factor valine66 methionine variant. Biological psychiatry 66 (3), pp.293-297. (10.1016/j.biopsych.2008.12.006)
• Whalley, H. et al., 2009. Connecting the brain and new drug targets for schizophrenia. Current Pharmaceutical Design 15 (22), pp.2615-2631. (10.2174/138161209788957500)
• Whalley, H. C. et al., 2009. fMRI changes over time and reproducibility in unmedicated subjects at high genetic risk of schizophrenia. Psychological Medicine 39 (07), pp.1189-1199. (10.1017/S0033291708004923)
• Hall, J. et al. 2009. Associative learning and the genetics of schizophrenia [Review]. Trends in Neurosciences 32 (6), pp.359-365. (10.1016/j.tins.2009.01.011)
• Whalley, H. C. et al., 2009. A GRIK4 variant conferring protection against bipolar disorder modulates hippocampal function [Letter]. Molecular Psychiatry 14 (5), pp.467-468. (10.1038/mp.2009.7)
• McIntosh, A. M. et al., 2009. Prefrontal gyral folding and its cognitive correlates in bipolar disorder and schizophrenia. Acta Psychiatrica Scandinavica 119 (3), pp.192-198. (10.1111/j.1600-0447.2008.01286.x)
• Sprooten, E. et al., 2009. The relationship of anterior thalamic radiation integrity to psychosis risk associated neuregulin-1 variants [Letter]. Molecular Psychiatry 14 (3), pp.237-238. (10.1038/mp.2008.136)
• Stanfield, A. C. et al., 2009. Structural abnormalities of ventrolateral and orbitofrontal cortex in patients with familial bipolar disorder. Bipolar Disorders 11 (2), pp.135-144. (10.1111/j.1399-5618.2009.00666.x)
• Sussmann, J. E. et al., 2009. White matter abnormalities in bipolar disorder and schizophrenia detected using diffusion tensor magnetic resonance imaging. Bipolar Disorders 11 (1), pp.11-18. (10.1111/j.1399-5618.2008.00646.x)

2008

• McIntosh, A. M. et al., 2008. White matter tractography in bipolar disorder and schizophrenia. Biological psychiatry 64 (12), pp.1088-1092. (10.1016/j.biopsych.2008.07.026)
• Hall, J. 2008. DISConnectivity in schizophrenia (Commentary on Di Giorgioet al.) [Commentary]. European Journal of Neuroscience 28 (10), pp.2128-2128. (10.1111/j.1460-9568.2008.06542.x)
• Marwick, K. and Hall, J. 2008. Social cognition in schizophrenia: a review of face processing. British Medical Bulletin 88 (1), pp.43-58. (10.1093/bmb/ldn035)
• Whalley, H. et al., 2008. Hypofrontality in subjects at high genetic risk of schizophrenia with depressive symptoms. Journal of affective disorders 109 (1-2), pp.99-106. (10.1016/j.jad.2007.11.009)
• Lawrie, S. M. et al., 2008. Neuroimaging and molecular genetics of schizophrenia: pathophysiological advances and therapeutic potential. British Journal of Pharmacology 153 (S1), pp.S120-S124. (10.1038/sj.bjp.0707655)
• Lawrie, S. M. et al., 2008. Brain structure and function changes during the development of schizophrenia: The evidence from studies of subjects at increased genetic risk. Schizophrenia Bulletin 34 (2), pp.330-340. (10.1093/schbul/sbm158)
• McIntosh, A. M. et al., 2008. Prefrontal function and activation in bipolar disorder and schizophrenia. American Journal of Psychiatry 165 (3), pp.378-384. (10.1176/appi.ajp.2007.07020365)
• Hall, J. et al. 2008. Overactivation of fear systems to neutral faces in schizophrenia. Biological Psychiatry 64 (1), pp.70-73. (10.1016/j.biopsych.2007.12.014)
• Hall, J. et al. 2008. Genetic variation in the DAOA (G72) gene modulates hippocampal function in subjects at high risk of schizophrenia. Biological Psychiatry 64 (5), pp.428-433. (10.1016/j.biopsych.2008.03.009)
• McIntosh, A. M. et al., 2008. The effects of a neuregulin 1 variant on white matter density and integrity. Molecular Psychiatry 13 (11), pp.1054-1059. (10.1038/sj.mp.4002103)

2007

• Whalley, H. C. et al., 2007. Correlations between fMRI activation and individual psychotic symptoms in un-medicated subjects at high genetic risk of schizophrenia. BMC Psychiatry 7 (1), pp.61-61. (10.1186/1471-244X-7-61)
• Moorhead, T. W. J. et al., 2007. Progressive gray matter loss in patients with bipolar disorder. Biological psychiatry 62 (8), pp.894-900. (10.1016/j.biopsych.2007.03.005)
• McIntosh, A. M. et al., 2007. Relationship of catechol-o-methyltransferase variants to brain structure and function in a population at high risk of psychosis. Biological Psychiatry 61 (10), pp.1127-34. (10.1016/j.biopsych.2006.05.020)
• Hall, J. et al. 2007. Emotional memory in schizophrenia. Neuropsychologia 45 (6), pp.1152-1159. (10.1016/j.neuropsychologia.2006.10.012)

2004

• Hall, J. et al. 2004. Social cognition and face processing in schizophrenia. The British Journal of Psychiatry 185 (2), pp.169-170. (10.1192/bjp.185.2.169)

2002

• Thomas, K. L. , Hall, J. and Everitt, B. J. 2002. Cellular imaging with zif268 expression in the rat nucleus accumbens and frontal cortex further dissociates the neural pathways activated following the retrieval of contextual and cued fear memory. European Journal of Neuroscience 16 (9), pp.1789-1796. (10.1046/j.1460-9568.2002.02247.x)

2001

• Hall, J. , Thomas, K. L. and Everitt, B. J. 2001. Cellular imaging of zif268 Expression in the hippocampus and amygdala during contextual and cued fear memory retrieval: selective activation of hippocampal CA1 neurons during the recall of contextual memories. Journal of Neuroscience Vol 21 (6), pp.2186-2193. (10.1523/JNEUROSCI.21-06-02186.2001)
• Hall, J. , Thomas, K. L. and Everitt, B. J. 2001. Fear memory retrieval induces CREB phosphorylation and Fos expression within the amygdala. European Journal of Neuroscience 13 (7), pp.1453-1458. (10.1046/j.0953-816x.2001.01531.x)