|
| 38086109 | The schizophrenia syndrome, circa 2024: What we know and how that informs its nature. | Schizophr Res | 2024 |
| 35144709 | Psychopathology in adults with copy number variants. | Psychological Medicine | 2023 |
| 36372570 | Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry. | Biol Psychiatry | 2023 |
| 36059063 | Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions. | Brain | 2023 |
| 36446581 | Psychopathology in mothers of children with pathogenic Copy Number Variants. | J Med Genet | 2023 |
| 37853064 | Genomic findings in schizophrenia and their implications. | | 2023 |
| 37853043 | Mediation and longitudinal analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count. | | 2023 |
| 38001363 | Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes. | | 2023 |
| 37881570 | Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive Performance. | | 2023 |
| 37777856 | GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. | Am J Psychiatry | 2023 |
| 37402765 | Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders. | | 2023 |
| 36958377 | Pathogenic Mis-splicing of CPEB4 in Schizophrenia. | | 2023 |
| 37131672 | Using rare genetic mutations to revisit structural brain asymmetry. | bioRxiv | 2023 |
| 36752340 | DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts. | | 2023 |
| 36869225 | Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. | Mol Psychiatry | 2023 |
| 36804072 | Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: a longitudinal analysis and genome-wide association study using UK clinical monitoring data. | | 2023 |
| 37437579 | Specificity of polygenic signatures across symptom dimensions in bipolar disorder: an analysis of UK Bipolar Disorder Research Network data. | | 2023 |
| 37434504 | Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants. | Am J Psychiatry | 2023 |
| 36864136 | Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence. | Nat Hum Behav | 2023 |
| 37431317 | Mental health impact of autism on families of children with intellectual and developmental disabilities of genetic origin. | JCPP Adv | 2023 |
| 36925053 | The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases. | Neurobiol Dis | 2023 |
| 36914811 | Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia. | | 2023 |
| 36844807 | Genomic insights into schizophrenia. | | 2023 |
| 33966571 | Mental Health Research, shared goals. | Journal of Mental Health | 2023 |
| 34158623 | Correction: Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study. | Molecular Psychiatry | 2023 |
| 33981004 | Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study. | Molecular Psychiatry | 2023 |
| 34756599 | The nature of schizophrenia: As broad as it is long. | Schizophrenia Research | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 36044200 | Genetic Liabilities Differentiating Bipolar Disorder, Schizophrenia, and Major Depressive Disorder, and Phenotypic Heterogeneity in Bipolar Disorder. | JAMA Psychiatry | 2022 |
| 36039635 | 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 | 2022 |
| 36216811 | 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 | 2022 |
| 35674151 | Schizophrenia Polygenic Risk and Experiences of Childhood Adversity: A Systematic Review and Meta-analysis. | Schizophrenia Bulletin | 2022 |
| 36260540 | The Contribution of the Rüdin School to Psychiatric Genetics: The Light and the Darkness. | Schizophrenia Bulletin | 2022 |
| 35410376 | Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. | Nat Genet | 2022 |
| 36117659 | Autism: A model of neurodevelopmental diversity informed by genomics. | Frontiers in Psychiatry | 2022 |
| 35976659 | Ultrarare Coding Variants and Cognitive Function in Schizophrenia. | JAMA Psychiatry | 2022 |
| 35779327 | Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank. | Schizophrenia Research | 2022 |
| 34112971 | Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome. | Molecular Psychiatry | 2022 |
| 33782512 | A normative chart for cognitive development in a genetically selected population. | Neuropsychopharmacology | 2022 |
| 33987677 | Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia. | Schizophr Bull | 2022 |
| 32643597 | Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs. | Psychological Medicine | 2022 |
| 32515721 | Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence. | Psychol Med | 2022 |
| 35031607 | Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. | Nat Commun | 2022 |
| 35019943 | Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia. | JAMA Psychiatry | 2022 |
| 34543680 | Complement C3 and C3aR mediate different aspects of emotional behaviours; relevance to risk for psychiatric disorder. | Brain Behav Immun | 2022 |
| 34715029 | Post-partum psychosis and its association with bipolar disorder in the UK: a case-control study using polygenic risk scores. | Lancet Psychiatry,The | 2021 |
| 32015465 | Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. | Mol Psychiatry | 2021 |
| 31739810 | Coordination difficulties, IQ and psychopathology in children with high-risk copy number variants. | Psychological Medicine | 2021 |
| 32366953 | Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders. | Mol Psychiatry | 2021 |