![Jeremy Hall Hodge Professor Of Psychiatry](https://profiles-cardiff.imgix.net/attachments/2444?w=200&h=200&auto=format&crop=faces&fit=crop&q=90")
Professor Jeremy Hall
Hodge Professor Of Psychiatry
Director of Division of Psychological Medicine and Clinical Neuroscience, Co-Director of Neuroscience and Mental Health Innovation Institute, Hon. Consultant Psychiatrist.
- Media commentator
Overview
I am the Hodge Professor of Psychiatry and Neuroscience at Cardiff University.
My overarching interest is in the role of genetic and environmental risk factors in the development of serious mental illness. In my work I employ a translational approach spanning human and laboratory studies.
I am particularly interested in how identified genetic risk factors affect learning processes in the brain; abnormalities in which underlie key symptoms.
Overall I believe that understanding how genetic risk factors influence the brain and how these responses are modulated by environmental stimuli is crucial to the development of new treatments for psychiatric symptoms. In addition to my research work I am also clinically active and conduct clinics in neuropsychiatry.
Publication
2024
- Hunt, M., Underwood, J., Hubbard, L. and Hall, J. 2024. Risk of physical health comorbidities in autistic adults: a clinical nested cross-sectional study. BJPsych Open 10(6), article number: e182. (10.1192/bjo.2024.777)
- Hall, J. H. et al. 2024. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational Psychiatry 14(1), article number: 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), article number: 256. (10.1038/s41398-024-02969-x)
- 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 (10.1111/jir.13139)
- 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), article number: 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., Clifton, N. E., Rees, E., Thomas, K. L. and Hall, J. 2024. The association of hippocampal long-term potentiation-induced gene expression with genetic risk for psychosis. International Journal of Molecular Sciences 25(2), article number: 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), article number: 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), article number: 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)
- Kopal, J. et al. 2023. Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence. Nature Human Behaviour 7, pp. 1001-1007. (10.1038/s41562-023-01541-9)
- Chawner, S. J. et al. 2023. Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions. JCPP Advances 3(2), article number: e12162. (10.1002/jcv2.12162)
- 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., Alsaqati, M., Morgan, J., Deshpande, S., Wood, J., Hall, J. and Harwood, A. J. 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, article number: 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., Manahan-Vaughan, D., Dwyer, D. M., Hall, J. and Méndez-Couz, M. 2023. Characterisation of the neural basis underlying appetitive extinction & renewal in a Cacna1c rats. Neuropharmacology 227, article number: 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), article number: 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, article number: e12128. (10.1002/jcv2.12128)
- Chawner, S. J. R. A., Evans, A., IMAGINE-ID consortium, ., Williams, N., Owen, M. J., Hall, J. and van den Bree, M. B. M. 2023. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational Psychiatry 13, article number: 7. (10.1038/s41398-022-02296-z)
- Levy, R., Timothy, K., Underwood, J., Hall, J., Bernstein, J. and Pasca, S. 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., Hall, J., Kutrowski, T. and Cheer, A. 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., Clifton, N. E., Wellard, N., Thomas, K. L., Hall, J. and Brydges, N. M. 2022. Social interaction following prepubertal stress alters prefrontal gene expression associated with cell signalling and oligodendrocytes. Translational Psychiatry 12(1), article number: 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, article number: 438. (10.1038/s41398-022-02199-z)
- Underwood, J., DelPozo-Banos, M., Frizzati, A., Rai, D., John, A. and Hall, J. 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., DelPozo-Banos, M., Frizzati, A., John, A. and Hall, J. 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, article number: e75482. (10.7554/elife.75482)
- Daughters, K., Rees, A., Hunnikin, L., Wells, A., Hall, J. and van Goozen, S. 2022. Oxytocin administration versus emotion training in healthy males: Considerations for future research. Philosophical Transactions of the Royal Society B: Biological Sciences 377(1858), article number: 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)
- 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), article number: e12797. (10.1111/gbb.12797)
- Pass, R., Haan, N., Humby, T., Wilkinson, L. S., Hall, J. and Thomas, K. L. 2022. Selective behavioural impairments in mice heterozygous for the cross disorder psychiatric risk gene DLG2. Genes, Brain and Behavior 21(4), article number: e12799. (10.1111/gbb.12799)
- 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., Thomas, K. L., Hall, J. and Sawa, A. 2022. Parsing neural circuits of fear learning and extinction across basic and clinical neuroscience: Towards better translation. Neuroscience and Biobehavioral Reviews 134, article number: 104502. (10.1016/j.neubiorev.2021.12.025)
- Cunningham, A. C., Hall, J., Owen, M. and van den Bree, M. B. M. 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., Romaniuk, L., Milad, M. R., Goff, D. C., Hall, J. and Holt, D. J. 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), article number: 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, article number: 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), article number: 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., Yang, J., Watkin, H., Hall, J. and Brydges, N. M. 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., Westacott, L. J., Carter, J., Owen, M. J., Gray, W. P., Hall, J. and Wilkinson, L. S. 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), article number: 313. (10.1038/s41398-021-01415-6)
- Cunningham, A., Hall, J., Owen, M. and Van den Bree, M. 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., Hall, J., Owen, M., Van Den Bree, M., Linden, D., Silva, A. and Doherty, J. 2021. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry 11, article number: 182. (10.1038/s41398-021-01213-0)
2020
- Moon, A. L., Brydges, N. M., Wilkinson, L. S., Hall, J. and Thomas, K. L. 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, article number: 324. (10.1038/s41398-020-00998-w)
- Cunningham, A., Fung, W., Massey, T., Hall, J., Owen, M., Van Den Bree, M. and Peall, K. 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 35(7), pp. 1272-1274. (10.1002/mds.28078)
- Corcoran, M., Hawkins, E. L., O'Hora, D., Whalley, H. C., Hall, J., Lawrie, S. M. and Dauvermann, M. R. 2020. Are working memory and glutamate concentrations involved in early-life stress and severity of psychosis?. Brain and Behavior 10(6), article number: e01616. (10.1002/brb3.1616)
- Moulding, H., Bartsch, U., Hall, J., Jones, M., Linden, D., Owen, M. and Van Den Bree, M. 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., Thomas, K. L., Wilkinson, L. S., Hall, J. and Trent, S. 2020. FMRP and CYFIP1 at the synapse and their role in psychiatric vulnerability. Complex Psychiatry (10.1159/000506858)
2019
- Ranson, A., Broom, E., Powell, A., Chen, F., Major, G. and Hall, J. 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., Kendall, K., Berrett, J., Lewis, C., Anney, R., Van den Bree, M. and Hall, J. 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., Brandon, N., Deeb, T. Z., Hall, J. and Harwood, A. J. 2019. L-type voltage-gated calcium channel regulation of in vitro human cortical neuronal networks. Scientific Reports 9, article number: 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, article number: 3455. (10.1038/s41467-019-11119-7)
- Moon, A., Brydges, N., Thomas, K. and Hall, J. 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., Kendall, K., Berrett, J., Anney, R., Bree, M. V. D. and Hall, J. 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., Hubbard, L., Mitchell, R. E., Jones, S. A., Williams, N. M., Zammit, S. and Hall, J. 2019. Association of genetic risk for rheumatoid arthritis with cognitive and psychiatric phenotypes across childhood and adolescence. JAMA Network Open 2(6), pp. -., article number: e196118. (10.1001/jamanetworkopen.2019.6118)
- Trent, S., Hall, J., Connelly, W. M. and Errington, A. C. 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), article number: 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, article number: 8. (10.1186/s11689-019-9271-3)
- Clifton, N., Trent, S., Thomas, K. and Hall, J. 2019. Regulation and function of activity-dependent Homer in synaptic plasticity. Molecular Neuropsychiatry 5(3), pp. 147-161. (10.1159/000500267)
- 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)
- Srinivasan, R., Wolstencroft, J., Erwood, M., Raymond, F. L., Van Den Bree, M., Hall, J. and Skuse, D. 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., Owen, M. J., Holmans, P., Raymond, L., Skuse, D., Hall, J. and van den Bree, M. 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.. [Online]. BioRxiv. (10.1101/535708) Available at: https://doi.org/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), article number: 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, article number: 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. -., article number: 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, article number: 139. (10.1186/s12955-019-1204-z)
2018
- Brydges, N. M., Moon, A., Rule, L., Watkin, H., Thomas, K. L. and Hall, J. 2018. Sex specific effects of pre-pubertal stress on hippocampal neurogenesis and behaviour. Translational Psychiatry 8, article number: 271. (10.1038/s41398-018-0322-4)
- Sykes, L., Clifton, N., Hall, J. and Thomas, K. L. 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., Hall, J., Wilkinson, L. S., Dwyer, D. M. and Honey, R. C. 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., Chamberlain, S. E. L., Sadowski, J. H. L. P., Hall, J., Ashby, M. C. and Mellor, J. R. 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., Haan, N., Wilkinson, L. S., Thomas, K. L. and Hall, J. 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., Doherty, J. L., Lancaster, T., Linden, D., Walters, J. T. and Hall, J. 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., Cameron, D., Trent, S., Sykes, L. H., Thomas, K. L. and Hall, J. 2017. Hippocampal regulation of postsynaptic density Homer1 by associative learning. Neural Plasticity 2017, article number: 5959182. (10.1155/2017/5959182)
- Stanfield, A. M., Philip, R. C. M., Whalley, H., Romaniuk, L., Hall, J., Johnstone, E. C. and Lawrie, S. M. 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)
- Trent, S., Phillip, B., Hall, J. and Thomas, K. 2017. AMPA receptors control fear extinction through an Arc-dependent mechanism. Learning and Memory 24, pp. 375-380. (10.1101/lm.045013.117)
- Radtke, F., Chapman, G., Hall, J. and Syed, Y. A. 2017. Modulating neuroinflammation to treat neuropsychiatric disorders. BioMed Research International, article number: 5071786.
- 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.
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, article number: 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., Doidge, A. N., Barnes, P., Hall, J., Wilkinson, L. S. and Thomas, K. L. 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), article number: 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., Barnes, P., Hall, J. and Thomas, K. L. 2015. Rescue of long-term memory after reconsolidation blockade. Nature Communications 6, article number: 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), article number: e0130900. (10.1371/journal.pone.0130900)
- Brydges, N., Holmes, M. C., Harris, A. P., Cardinal, R. N. and Hall, J. 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. Dysfunction of emotional brain systems in individuals at high risk of mood disorder with depression and predictive features prior to illness. Psychological Medicine 45(6), pp. 1207. (10.1017/S0033291714002256)
- 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., Trent, S., Thomas, K. L., O'Donovan, M. C. and Owen, M. J. 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., Pope, M., Romaniuk, L. and Hall, J. 2015. Childhood trauma, midbrain activation and psychotic symptoms in borderline personality disorder. Translational Psychiatry 5(5), article number: e559. (10.1038/tp.2015.53)
- Zeng, Y., Brydges, N., Wood, E. R., Drake, A. J. and Hall, J. 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., Wood, E. R., Holmes, M. C. and Hall, J. 2014. Prepubertal stress and hippocampal function: Sex-specific effects. Hippocampus 24(6), pp. 684-692. (10.1002/hipo.22259)
- Barker, V., Pope, M., Smith, S., Brown, V. and Hall, J. 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., Seckl, J., Torrance, H. S., Holmes, M. C., Evans, K. L. and Hall, J. 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., Jin, R., Seckl, J., Holmes, M. C., Drake, A. J. and Hall, J. 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)
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., Pope, M., Sprengelmeyer, R., Young, A. W. and Hall, J. 2013. Social judgement in borderline personality disorder. PLoS ONE 8(11), article number: 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)
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- 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)
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- 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)
- Brydges, N. et al. 2013. Imaging conditioned fear circuitry using awake rodent fMRI. PLoS ONE 8(1), article number: e54197. (10.1371/journal.pone.0054197)
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)
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- Mukherjee, P., Whalley, H. C., McKirdy, J. W., McIntosh, A. M., Johnstone, E. C., Lawrie, S. M. and Hall, J. 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)
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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)
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- 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., Olabi, B., Hall, J. and McIntosh, A. M. 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., Thomson, P. A., Hall, J., McIntosh, A. M., Lawrie, S. M. and Porteous, D. J. 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., Hall, J., McIntosh, A. M., Owens, D. G. C. and Johnstone, E. C. 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)
- 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)
- 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(5), pp. 761-770. (10.1017/S0033291709991000)
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., Hall, J., Lymer, G. K. S., Sussmann, J. E. and Lawrie, S. M. 2009. Genetic risk for white matter abnormalities in bipolar disorder. International Review of Psychiatry 21(4), pp. 387-393. (10.1080/09540260902962180)
- Whalley, H., Steele, J., Mukherjee, P., Romaniuk, L., McIntosh, A., Hall, J. and Lawrie, S. 2009. Connecting the brain and new drug targets for schizophrenia. Current Pharmaceutical Design 15(22), pp. 2615-2631. (10.2174/138161209788957500)
- 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)
- McKirdy, J., Sussmann, J. E. D., Hall, J., Lawrie, S. M., Johnstone, E. C. and McIntosh, A. M. 2009. Set shifting and reversal learning in patients with bipolar disorder or schizophrenia. Psychological Medicine 39(8), pp. 1289-1293. (10.1017/S0033291708004935)
- Whalley, H. C. et al. 2009. fMRI changes over time and reproducibility in unmedicated subjects at high genetic risk of schizophrenia. Psychological Medicine 39(7), pp. 1189-1199. (10.1017/S0033291708004923)
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- 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)
- 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)
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- 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)
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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)
- 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)
- 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)
- 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)
- Whalley, H., Mowatt, L., Stanfield, A., Hall, J., Johnstone, E., Lawrie, S. and McIntosh, A. 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)
- 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)
- Lawrie, S. M., McIntosh, A. M., Hall, J., Owens, D. G. and Johnstone, E. C. 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)
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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)
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2006
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2004
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2002
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2001
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Articles
- Hunt, M., Underwood, J., Hubbard, L. and Hall, J. 2024. Risk of physical health comorbidities in autistic adults: a clinical nested cross-sectional study. BJPsych Open 10(6), article number: e182. (10.1192/bjo.2024.777)
- Hall, J. H. et al. 2024. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational Psychiatry 14(1), article number: 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), article number: 256. (10.1038/s41398-024-02969-x)
- 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 (10.1111/jir.13139)
- 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), article number: 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., Clifton, N. E., Rees, E., Thomas, K. L. and Hall, J. 2024. The association of hippocampal long-term potentiation-induced gene expression with genetic risk for psychosis. International Journal of Molecular Sciences 25(2), article number: 946. (10.3390/ijms25020946)
- 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), article number: 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), article number: 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)
- Kopal, J. et al. 2023. Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence. Nature Human Behaviour 7, pp. 1001-1007. (10.1038/s41562-023-01541-9)
- Chawner, S. J. et al. 2023. Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions. JCPP Advances 3(2), article number: e12162. (10.1002/jcv2.12162)
- 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., Alsaqati, M., Morgan, J., Deshpande, S., Wood, J., Hall, J. and Harwood, A. J. 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, article number: 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., Manahan-Vaughan, D., Dwyer, D. M., Hall, J. and Méndez-Couz, M. 2023. Characterisation of the neural basis underlying appetitive extinction & renewal in a Cacna1c rats. Neuropharmacology 227, article number: 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), article number: 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, article number: e12128. (10.1002/jcv2.12128)
- Chawner, S. J. R. A., Evans, A., IMAGINE-ID consortium, ., Williams, N., Owen, M. J., Hall, J. and van den Bree, M. B. M. 2023. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational Psychiatry 13, article number: 7. (10.1038/s41398-022-02296-z)
- Levy, R., Timothy, K., Underwood, J., Hall, J., Bernstein, J. and Pasca, S. 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)
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- Johnstone, M., Thomson, P. A., Hall, J., McIntosh, A. M., Lawrie, S. M. and Porteous, D. J. 2011. DISC1 in schizophrenia: Genetic mouse models and human genomic imaging. Schizophrenia Bulletin 37(1), pp. 14-20. (10.1093/schbul/sbq135)
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Book sections
- Reddaway, J., Doherty, J. L., Lancaster, T., Linden, D., Walters, J. T. and Hall, J. 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)
- 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.
Websites
- Chawner, S., Owen, M. J., Holmans, P., Raymond, L., Skuse, D., Hall, J. and van den Bree, M. 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.. [Online]. BioRxiv. (10.1101/535708) Available at: https://doi.org/10.1101/535708
Research
Current Research Projects
- Role of psychiatric risk genes in learning and memory
- Expression and regulation of autism and schizophrenia associated genes
- Modulatory effects of early life experience on gene expression and psychiatric risk
- Genetic effects on brain function and structure
Supervisions
Current supervision
Contact Details
HallJ10@cardiff.ac.uk
+44 29206 88342
Hadyn Ellis Building, Room 3.35, Maindy Road, Cardiff, CF24 4HQ
+44 29206 88342
Hadyn Ellis Building, Room 3.35, Maindy Road, Cardiff, CF24 4HQ
Research themes
Specialisms
- Schizophrenia
- Huntington's disease
- Autism
- Neurosciences
- Psychiatry
