Professor Jeremy Hall

Hodge Professor Of Psychiatry

2026

• 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)
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2014

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2013

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2012

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2011

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2010

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2009

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2008

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2007

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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)
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