Yr Athro Syr Michael Owen

BSc, MB ChB, PhD, FRCPsych, FMedSci, FLSW

2026

• Cheng, M. et al., 2026. Genome-wide tandem repeat expansions modify schizophrenia risk in the presence of a 22q11.2 deletion. Molecular Psychiatry 31 , pp.4934-4946. (10.1038/s41380-026-03574-8)
• Fenner, E. et al. 2026. Analysis of rare coding variants in schizophrenia-associated genes and generalised cognition in the UK Biobank. Molecular Psychiatry 31 , pp.5104-5113. (10.1038/s41380-026-03601-8)
• Fiksinski, A. M. et al., 2026. The uneven landscape of cognitive domains in 22q11.2 deletion syndrome: A large consortium study. Psychological Medicine 56 e283. (10.1017/S0033291726105224)
• Rammos, A. et al., 2026. Common variant contributions to neurodevelopmental risk in orofacial clefts.
• Rossi, F. et al., 2026. Co-expression-based models improve eQTL predictions for transcriptome-wide association studies and highlight new schizophrenia-associated genes. Nature Genetics 58 , pp.1559-1572. (10.1038/s41588-026-02646-3)
• 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)
• Yao, K. et al., 2026. Integrating genome-wide and epigenome-wide associations for antipsychotic induced extrapyramidal side effects. Psychopharmacology 243 , pp.1631-1642. (10.1007/s00213-025-06912-w)
• Alvarez-Jimenez, M. et al., 2026. Two decades of progress in schizophrenia: Evolution, current insights, and future directions. Spanish Journal of Psychiatry and Mental Health (10.1016/j.sjpmh.2026.06.003)
• Escott-Price, V. et al. 2026. Genetic investigation of non-affective psychosis and depression as causal risk factors for dementia. BMJ Mental Health 29 (1) e302424. (10.1136/bmjment-2025-302424)
• Katzourou, I. K. et al. 2026. Neurodevelopmental copy-number variants increase risk of internalizing and cardiometabolic multimorbidity: Findings from the UK Biobank. American Journal of Human Genetics 113 (6), pp.1319-1329. (10.1016/j.ajhg.2026.02.021)
• Owen, M. J. and O'Donovan, M. C. 2026. Rethinking schizophrenia: insights from genomics and implications for research. Molecular Psychiatry (10.1038/s41380-026-03654-9)
• Tsang, R. S. M. et al., 2026. Immunometabolic blood biomarkers of developmental trajectories of depressive symptoms: findings from the ALSPAC birth cohort. Molecular Psychiatry 31 , pp.1746-1756. (10.1038/s41380-025-03311-7)
• Owen, M. J. 2026. A genetic perspective on Kraepelin’s nosology. In: Ikkos, G. and Becker, T. eds. Psychiatry after Kraepelin: Ambition Images Practices 1926-2026. Cham, Switzerland: Springer. , pp.73-86. (10.1007/978-3-032-09475-9_6)
• Wray, N. R. and Owen, M. J. 2026. Psychiatric nosology should include genetic syndromes [Commentary]. Biological Psychiatry 99 (7), pp.508-510. (10.1016/j.biopsych.2026.01.008)
• 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)
• Smart, S. E. et al. 2026. Genetics to Improve Outcomes in Schizophrenia (GENios): A within-case molecular genetic study protocol. PLoS ONE 21 (2) e0340584. (10.1371/journal.pone.0340584)
• Grotzinger, A. D. et al., 2026. Mapping the genetic landscape across 14 psychiatric disorders. Nature 649 , pp.406-415. (10.1038/s41586-025-09820-3)

2025

• Colbert, S. M. C. et al., 2025. Defining suicidality phenotypes for genetic studies: perspectives of the Psychiatric Genomics Consortium Suicide Working Group. Molecular Psychiatry 30 , pp.6144-6154. (10.1038/s41380-025-03271-y)
• Owen, M. J. et al. 2025. Genomics of schizophrenia, bipolar disorder and major depressive disorder. Nature Reviews Genetics 26 , pp.862-877. (10.1038/s41576-025-00843-0)
• Dennison, C. A. et al. 2025. Early manifestations of neurodevelopmental copy number variants in children: A population-based investigation. Biological Psychiatry 98 (12), pp.924-933. (10.1016/j.biopsych.2025.03.004)
• 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)
• Richards, A. L. et al. 2025. Effects of shared and nonshared schizophrenia and bipolar disorder alleles on cognition and educational attainment in the UK Biobank. Biological Society: Global Open Science 5 (6) 100601. (10.1016/j.bpsgos.2025.100601)
• Gudmundsson, S. et al., 2025. Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database. Nature Communications 16 9623. (10.1038/s41467-025-61698-x)
• 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)
• Smart, S. E. et al. 2025. The role of SLC39A8.p.( Ala391Thr ) in schizophrenia symptom severity and cognitive ability: cross‐sectional studies of schizophrenia and the general UK population. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 198 (7), pp.135-146. (10.1002/ajmg.b.33037)
• Rammos, A. et al., 2025. Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palate. Human Molecular Genetics 34 (18), pp.1563-1574. (10.1093/hmg/ddaf115)
• Chick, S. L. et al. 2025. Whole-exome sequencing analysis identifies risk genes for schizophrenia. Nature Communications 16 (1) 7102. (10.1038/s41467-025-62429-y)
• Koromina, M. et al., 2025. Fine-mapping genomic loci refines bipolar disorder risk genes. Nature Neuroscience 28 (7), pp.1393-1403. (10.1038/s41593-025-01998-z)
• Kappel, D. et al. 2025. Association between genetic liability to physical health conditions and comorbidities in individuals with severe mental illness: an analysis of two cross-sectional observational studies in the UK. The Lancet Psychiatry 12 (6), pp.447-456. (10.1016/S2215-0366(25)00123-3)
• Lock, S. K. et al. 2025. Antipsychotic and pharmacogenomic effects on cross-sectional symptom severity and cognitive ability in schizophrenia. EBioMedicine 116 105745. (10.1016/j.ebiom.2025.105745)
• Katzourou, I. et al. 2025. Contributions of common and rare genetic variation to different measures of mood and anxiety disorder in UK Biobank. BJPsych Open 11 (3) e97. (10.1192/bjo.2025.43)
• Ali, N. M. et al. 2025. Comparison of autism domains across thirty rare variant genotypes. EBioMedicine 112 105521. (10.1016/j.ebiom.2024.105521)
• Panagiotaropoulou, G. et al., 2025. Identifying genetic differences between bipolar disorder and major depression through multiple genome-wide association analyses. The British Journal of Psychiatry 226 , pp.79-90. (10.1192/bjp.2024.125)
• Owen, M. J. and O'Donovan, M. C. 2025. The genetics of cognition in schizophrenia. Genomic Psychiatry 1 (1), pp.28-35. (10.61373/gp024i.0040)

2024

• Woolway, G. E. et al., 2024. Assessing the validity of a self-reported clinical diagnosis of schizophrenia. Schizophrenia 10 (1) 99. (10.1038/s41537-024-00526-5)
• Benger, L. et al. 2024. Adverse childhood experiences and multimorbidity of internalising and cardiometabolic conditions in an older-age population. Presented at: International Population Data Linkage Conference Chicago, USA 15-18 September 2025. Conference Proceedings for International Population Data Linkage Conference. Vol. 9.Vol. 5. Swansea University. , pp.133. (10.23889/ijpds.v9i5.2617)
• Koromina, M. et al., 2024. Fine-mapping genomic loci refines bipolar disorder risk genes. [Online].medRxiv: OpenRxiv. (10.1101/2024.02.12.24302716)Available at: https://doi.org/10.1101/2024.02.12.24302716.
• Legge, S. E. et al. 2024. Genetic and phenotypic features of Schizophrenia in the UK Biobank. JAMA Psychiatry 81 , pp.681-690. (10.1001/jamapsychiatry.2024.0200)
• Trastulla, L. et al., 2024. Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nature Communications 15 5534. (10.1038/s41467-024-49338-2)
• 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)
• Stevenson-Hoare, J. et al. 2024. Severe psychiatric disorders are associated with increased risk of dementia. BMJ Mental Health 27 (1) e301097. (10.1136/bmjment-2024-301097)
• 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)
• Kopal, J. et al., 2024. Using rare genetic mutations to revisit structural brain asymmetry. Nature Communications 15 (1) 2639. (10.1038/s41467-024-46784-w)
• Kappel, D. et al. 2024. Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia. European Neuropsychopharmacology 80 , pp.47-54. (10.1016/j.euroneuro.2023.12.007)
• Tandon, R. et al., 2024. The schizophrenia syndrome, circa 2024: What we know and how that informs its nature. Schizophrenia Research 264 , pp.1-28. (10.1016/j.schres.2023.11.015)
• Boen, R. et al., 2024. Beyond the global brain differences: Intra-individual variability differences in 1q21.1 distal and 15q11.2 BP1-BP2 deletion carriers. Biological Psychiatry 95 (2), pp.147-160. (10.1016/j.biopsych.2023.08.018)
• Doherty, J. L. et al. 2024. Atypical cortical networks in children at high-genetic risk of psychiatric and eurodevelopmental disorders. Neuropsychopharmacology 49 , pp.368-376. (10.1038/s41386-023-01628-x)
• 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)
• Ge, R. et al., 2024. Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human Brain Mapping 45 (1) e26553. (10.1002/hbm.26553)

2023

• Wang, S. et al., 2023. Rare X-linked variants carry predominantly male risk in Autism, Tourette Syndrome, and ADHD. Nature Communications 14 8077. (10.1038/s41467-023-43776-0)
• Chilvers, C. and Owen, M. J. 2023. Mental Health Research, shared goals. Journal of Mental Health 32 1017. (10.1080/09638237.2021.1898562)
• Caseras, X. et al. 2023. Copy Number Variants increasing risk for schizophrenia: shared and distinct effects on brain morphometry and cognitive performance. Biological Psychiatry: Global Open Science 3 (4), pp.902-911. (10.1016/j.bpsgos.2022.10.006)
• Lock, S. K. et al. 2023. Mediation and longitudinal analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count. Schizophrenia 9 74. (10.1038/s41537-023-00404-6)
• Doherty, A. et al., 2023. Genome-wide association study meta-analysis of suicide attempt identifies twelve genome-wide significant loci and implicates genetic risks for specific health factors. The American Journal of Psychiatry 180 (10), pp.723-738. (10.1176/appi.ajp.21121266)
• Owen, M. et al. 2023. Genomic findings in schizophrenia and their implications. Molecular Psychiatry 28 , pp.3638-3647. (10.1038/s41380-023-02293-8)
• 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)
• Le Guen, Y. et al., 2023. Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes. Proceedings of the National Academy of Sciences 120 (36) e2302720120. (10.1073/pnas.2302720120)
• Ollà, I. et al., 2023. Pathogenic mis-splicing of CPEB4 in schizophrenia. Biological Psychiatry 94 (4), pp.341-351. (10.1016/j.biopsych.2023.03.010)
• Zhao, Y. et al., 2023. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. npj Genomic Medicine 8 (1) 17. (10.1038/s41525-023-00363-y)
• Allardyce, J. et al. 2023. Specificity of polygenic signatures across symptom dimensions in bipolar disorder: an analysis of UK Bipolar Disorder Research Network data. The Lancet Psychiatry 10 (8), pp.623-631. (10.1016/S2215-0366(23)00186-4)
• 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)
• Adams, R. L. et al. 2023. Psychopathology in adults with copy number variants. Psychological Medicine 53 (7), pp.3142-3149. (10.1017/S0033291721005201)
• Chen, Z. et al., 2023. The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases. Neurobiology of Disease 180 106082. (10.1016/j.nbd.2023.106082)
• Lin, J. et al., 2023. Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular Psychiatry 28 , pp.2071-2080. (10.1038/s41380-023-02009-y)
• Rogdaki, M. et al., 2023. 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 28 , pp.1995-2006. (10.1038/s41380-021-01108-y)
• 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)
• 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)
• Pardinas, A. F. et al. 2023. Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: a longitudinal analysis and genome-wide association study using UK clinical monitoring data. The Lancet Psychiatry 10 (3), pp.209-219. (10.1016/S2215-0366(23)00002-0)
• Rammos, A. et al. 2023. Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia. Molecular Psychiatry 28 , pp.2081-2087. (10.1038/s41380-023-02013-2)
• 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)
• Liu, D. et al., 2023. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature Genetics 55 , pp.369-376. (10.1038/s41588-023-01305-1)
• Owen, M. J. 2023. Genomic insights into schizophrenia. Royal Society Open Science 10 (2) 230125. (10.1098/rsos.230125)
• Moreau, C. A. et al., 2023. Genetic heterogeneity shapes brain connectivity in psychiatry. Biological Psychiatry 93 (1), pp.45-58. (10.1016/j.biopsych.2022.08.024)
• Kappel, D. B. et al. 2023. Genomic stratification of clozapine prescription patterns using schizophrenia polygenic scores. Biological Psychiatry 93 , pp.149-156. (10.1016/j.biopsych.2022.07.014)
• 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)

2022

• Owen, M. J. 2022. The contribution of the Rüdin school to psychiatric genetics: the light and the darkness. Schizophrenia Bulletin: The Journal of Psychoses and Related Disorders 48 (Supple), pp.S1-S3. (10.1093/schbul/sbac119)
• 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)
• Woolway, G. et al. 2022. Schizophrenia polygenic risk and experiences of childhood adversity: a systematic review and meta-analysis. Schizophrenia Bulletin 48 (5), pp.967-980. (10.1093/schbul/sbac049)
• Chawner, S. and Owen, M. 2022. Autism: a model of neurodevelopmental diversity informed by genomics. Frontiers in Psychiatry 13 981691. (10.3389/fpsyt.2022.981691)
• 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)
• Bracher-Smith, M. et al. 2022. Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK Biobank. Schizophrenia Research 246 , pp.156-164. (10.1016/j.schres.2022.06.006)
• Richards, A. et al. 2022. Genetic liabilities differentiating bipolar disorder, schizophrenia and major depression and phenotypic heterogeneity in bipolar disorder. JAMA Psychiatry 79 (10), pp.1032-1039. (10.1001/jamapsychiatry.2022.2594)
• 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)
• Creeth, H. D. J. et al. 2022. Ultrarare coding variants and cognitive function in schizophrenia. JAMA Psychiatry 79 (10), pp.963-970. (10.1001/jamapsychiatry.2022.2289)
• Fiksinski, A. M. et al., 2022. A normative chart for cognitive development in a genetically selected population. Neuropsychopharmacology 47 (7), pp.1379–1386. (10.1038/s41386-021-00988-6)
• Palmer, D. et al., 2022. Exome sequencing in bipolar disorder reveals AKAP11 as a risk gene shared with schizophrenia. Nature Genetics (10.1038/s41588-022-01034-x)
• Bellenguez, C. et al., 2022. New insights into the genetic etiology of Alzheimer's disease and related dementias. Nature Genetics 54 (4), pp.412-436. (10.1038/s41588-022-01024-z)
• Owen, M. and Legge, S. 2022. The nature of schizophrenia: as broad as it is long. Schizophrenia Research 242 , pp.109-112. (10.1016/j.schres.2021.10.012)
• Singh, T. et al., 2022. Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 604 , pp.509-516. (10.1038/s41586-022-04556-w)
• Trubetskoy, V. et al., 2022. Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia. Nature 604 , pp.502-508. (10.1038/s41586-022-04434-5)
• Chapman, G. et al. 2022. Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome. Molecular Psychiatry 27 , pp.819-830. (10.1038/s41380-021-01182-2)
• 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)
• Wolstencroft, J. et al., 2022. Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE - The UK National Cohort Study. SSRN (10.2139/ssrn.4028542)
• Mullins, N. et al., 2022. Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors. Biological Psychiatry 91 (3), pp.313-327. (10.1016/j.biopsych.2021.05.029)
• Jones, H. J. et al., 2022. Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence. Psychological Medicine 52 (1), pp.132-139. (10.1017/S0033291720001798)
• Vassos, E. et al., 2022. Lack of support for the genes by early environment interaction hypothesis in the pathogenesis of schizophrenia. Schizophrenia Bulletin 48 (1), pp.20-26. (10.1093/schbul/sbab052)
• 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)
• Sanders, B. et al. 2022. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature Communications 13 (1) 27. (10.1038/s41467-021-27601-0)
• Pardinas, A. et al. 2022. Interaction testing and polygenic risk scoring to estimate the contribution of common genetic variants to treatment resistance in schizophrenia. JAMA Psychiatry 79 (3), pp.260-269. (10.1001/jamapsychiatry.2021.3799)

2021

• Di Florio, A. et al. 2021. Post-partum psychosis and its association with bipolar disorder in the UK: a case-control study using polygenic risk scores. The Lancet Psychiatry 8 (12), pp.1045-1052. (10.1016/S2215-0366(21)00253-4)
• 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)
• Kalman, J. L. et al., 2021. Characterisation of age and polarity at onset in bipolar disorder. The British Journal of Psychiatry 219 (6), pp.659-669. (10.1192/bjp.2021.102)
• Pardinas, A. F. , Owen, M. J. and Walters, J. T. 2021. Pharmacogenomics: A road ahead for precision medicine in psychiatry. Neuron 109 (24), pp.3914-3929. (10.1016/j.neuron.2021.09.011)
• 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)
• Dennison, C. et al. 2021. Risk factors, clinical features, and polygenic risk scores in schizophrenia and schizoaffective disorder depressive-type. Schizophrenia Bulletin 47 (5), pp.1375-1384. (10.1093/schbul/sbab036)
• Jia, X. et al., 2021. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry 26 , pp.5239-5250. (10.1038/s41380-020-01006-9)
• 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)
• Rees, E. et al. 2021. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations. Nature Communications 12 5353. (10.1038/s41467-021-25532-4)
• Cleynen, I. et al., 2021. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry , pp.4496-4510. (10.1038/s41380-020-0654-3)
• Legge, S. et al. 2021. Associations between schizophrenia polygenic liability, symptom dimensions, and cognitive ability in schizophrenia. JAMA Psychiatry 78 (10), pp.1143-1151. (10.1001/jamapsychiatry.2021.1961)
• 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)
• Forsyth, J. K. et al., 2021. Prioritizing genetic contributors to cortical alterations in 22q11.2 deletion syndrome using imaging transcriptomics. Cerebral Cortex 31 (7), pp.3285-3298. (10.1093/cercor/bhab008)
• 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)
• Amare, A. T. et al., 2021. Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. Molecular Psychiatry 26 , pp.2457-2470. (10.1038/s41380-020-0689-5)
• Byrne, E. et al., 2021. Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders. Molecular Psychiatry 26 , pp.2070-2081. (10.1038/s41380-020-0705-9)
• Hall, L. S. et al. 2021. Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders. Molecular Psychiatry 26 , pp.2082-2088. (10.1038/s41380-020-0743-3)
• Mullins, N. et al., 2021. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics 53 , pp.817-829. (10.1038/s41588-021-00857-4)
• Owen, M. J. and Williams, N. M. 2021. Explaining the missing heritability of psychiatric disorders. World Psychiatry 20 (2), pp.294-295. (10.1002/wps.20870)
• 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)
• Peterson, R. E. et al., 2021. Genome-wide analyses of smoking behaviors in schizophrenia: findings from the Psychiatric Genomics Consortium. Journal of Psychiatric Research 137 , pp.215-225. (10.1016/j.jpsychires.2021.02.027)
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2020

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2019

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2018

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2017

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2016

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2015

• Tansey, K. E. et al. 2015. Common alleles contribute to schizophrenia in CNV carriers [Erratum]. Molecular Psychiatry 21 1153. (10.1038/mp.2015.170)
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• Heyes, S. et al., 2015. Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders. Progress in Neurobiology 134 , pp.36-54. (10.1016/j.pneurobio.2015.09.002)
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• Lee, S. H. et al., 2015. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology 44 (5), pp.1706-1721. (10.1093/ije/dyv136)
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• Lloyd, K. et al., 2015. A national population-based e-cohort of people with psychosis (PsyCymru) linking prospectively ascertained phenotypically rich and genetic data to routinely collected records: Overview, recruitment and linkage. Schizophrenia Research 166 (1-3), pp.131-6. (10.1016/j.schres.2015.05.036)
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• Jones, L. et al. 2015. Convergent genetic and expression data implicate immunity in Alzheimer's disease. Alzheimer's and Dementia 11 (6), pp.658-671. (10.1016/j.jalz.2014.05.1757)
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• Stergiakouli, E. et al., 2015. Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD. Journal of the American Academy of Child and Adolescent Psychiatry 54 (4), pp.322-327. (10.1016/j.jaac.2015.01.010)
• Oertel-Knöchel, V. et al., 2015. Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: Evidence from two independent cohorts. NeuroImage: Clinical 7 , pp.764-770. (10.1016/j.nicl.2015.03.005)
• Vivian-Griffiths, T. et al. 2015. Utilising machine-learning algorithms to uncover complex genetic interactions in schizophrenia [Conference Abstract]. Human Heredity 79 (1), pp.48-48. A46. (10.1159/000381109)
• Farrell, M. S. et al., 2015. Evaluating historical candidate genes for schizophrenia. Molecular Psychiatry 20 (5), pp.555-562. (10.1038/mp.2015.16)
• Taylor, P. N. et al. 2015. Whole-genome sequence-based analysis of thyroid function. Nature Communications 6 5681. (10.1038/ncomms6681)
• O'Dushlaine, C. et al., 2015. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience 18 (2), pp.199-209. (10.1038/nn.3922)
• Desikan, R. S. et al., 2015. Genetic overlap between Alzheimer's Disease and Parkinson's Disease at the MAPT locus. Molecular Psychiatry 20 (12), pp.1588-1595. (10.1038/mp.2015.6)
• Maier, R. et al., 2015. Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. American Journal of Human Genetics 96 (2), pp.283-294. (10.1016/j.ajhg.2014.12.006)
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• Green, E. K. et al., 2015. Copy number variation in bipolar disorder. Molecular Psychiatry 21 (1), pp.89-93. (10.1038/mp.2014.174)
• 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)
• Tansey, K. E. , Owen, M. J. and O'Donovan, M. C. 2015. Schizophrenia genetics: Building the foundations of the future. Schizophrenia Bulletin 41 (1), pp.15-19. (10.1093/schbul/sbu162)
• Rees, E. et al. 2015. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational Psychiatry 5 (7) e607. (10.1038/tp.2015.99)
• Rees, E. , O'Donovan, M. C. and Owen, M. J. 2015. Genetics of schizophrenia. Current Opinion in Behavioral Sciences 2 , pp.8-14. (10.1016/j.cobeha.2014.07.001)

2014

• Peall, K. J. et al. 2014. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. Journal of Neurology 261 (12), pp.2296-2304. (10.1007/s00415-014-7488-3)
• Georgieva, L. et al. 2014. De novo CNVs in bipolar affective disorder and schizophrenia. Human Molecular Genetics 23 (24), pp.6677-6683. (10.1093/hmg/ddu379)
• De Rubeis, S. et al., 2014. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 515 , pp.209-215. (10.1038/nature13772)
• Gusev, A. et al., 2014. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. American Journal of Human Genetics 95 (5), pp.535-552. (10.1016/j.ajhg.2014.10.004)
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• Timpson, N. J. et al., 2014. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. Nature Communications 5 4871. (10.1038/ncomms5871)
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• Szatkiewicz, J. P. et al., 2014. Copy number variation in schizophrenia in Sweden. Molecular Psychiatry 19 (7), pp.762-773. (10.1038/mp.2014.40)
• Ripke, S. et al., 2014. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511 (7510), pp.421-427. (10.1038/nature13595)
• Hung, C. et al., 2014. Relationship between obesity and the risk of clinically significant depression: Mendelian randomisation study. British Journal of Psychiatry 205 (1), pp.24-28. (10.1192/bjp.bp.113.130419)
• Niarchou, M. et al. 2014. Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 (5), pp.410-420. (10.1002/ajmg.b.32245)
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• Schneider, M. et al., 2014. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: Results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. American Journal of Psychiatry 171 (6), pp.627-639. (10.1176/appi.ajp.2013.13070864)
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• Ferentinos, P. et al., 2014. Investigating the genetic variation underlying episodicity in major depressive disorder: Suggestive evidence for a bipolar contribution. Journal of Affective Disorders 155 , pp.81-89. (10.1016/j.jad.2013.10.027)
• Pocklington, A. , O'Donovan, M. C. and Owen, M. J. 2014. The synapse in schizophrenia. European Journal of Neuroscience 39 (7), pp.1059-1067. (10.1111/ejn.12489)

2013

• Green, E. K. et al. 2013. Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample. Molecular Psychiatry 18 (12), pp.1302-1307. (10.1038/mp.2012.142)
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• Donohoe, G. et al., 2013. Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. Genes, Brain and Behavior 12 (2), pp.203-209. (10.1111/gbb.12016)
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• Kim, Y. et al., 2013. Non-random mating, parent-of-origin, and maternal-fetal incompatibility effects in schizophrenia. Schizophrenia Research 143 (1), pp.11-17. (10.1016/j.schres.2012.11.002)
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• Rucker, J. J. H. et al., 2013. Genome-wide association analysis of copy number variation in recurrent depressive disorder. Molecular Psychiatry 18 , pp.183-189. (10.1038/mp.2011.144)
• Ruderfer, D. et al., 2013. Mosaic copy number variation in schizophrenia. European Journal of Human Genetics 21 (9), pp.1007-1011. (10.1038/ejhg.2012.287)
• Tandon, R. et al., 2013. Catatonia in DSM-5. Schizophrenia Research 150 (1), pp.26-30. (10.1016/j.schres.2013.04.034)
• van den Bree, M. B. et al. 2013. The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS). European Journal of Medical Genetics 56 (8), pp.439-441. (10.1016/j.ejmg.2013.05.001)
• Williams, H. J. et al. 2013. Schizophrenia two-hit hypothesis in velo-cardio facial syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 (2), pp.177-182. (10.1002/ajmg.b.32129)
• Yang, L. et al., 2013. Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome-wide association study of both common and rare variants. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 (5), pp.419-430. (10.1002/ajmg.b.32169)

2012

• Hollingworth, P. et al. 2012. Genome-wide association study of Alzheimer's disease with psychotic symptoms. Molecular Psychiatry 17 (12), pp.1316-1327. (10.1038/mp.2011.125)
• Cooper, J. D. et al., 2012. Seven newly identified loci for autoimmune thyroid disease. Human Molecular Genetics 21 (23), pp.5202-5208. (10.1093/hmg/dds357)
• Eyre, S. et al., 2012. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics 44 (12), pp.1336-1340. (10.1038/ng.2462)
• Jostins, L. et al., 2012. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 491 (7422), pp.119-124. (10.1038/nature11582)
• O'Donovan, M. C. et al. 2012. Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia. Biological psychiatry 72 (8), pp.620-628. (10.1016/j.biopsych.2012.05.035)
• Sellers, R. et al. 2012. Risk of psychopathology in adolescent offspring of mothers with psychopathology and recurrent depression. British Journal of Psychiatry 202 (2), pp.108-114. (10.1192/bjp.bp.111.104984)
• Hamilton, G. et al., 2012. The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159B (6), pp.696-709. (10.1002/ajmg.b.32073)
• Levinson, D. F. et al., 2012. Genome-wide association study of multiplex schizophrenia pedigrees. American Journal of Psychiatry 169 (9), pp.963-973. (10.1176/appi.ajp.2012.11091423)
• Hamilton, G. et al., 2012. Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. Neurobiology of Aging 33 (8) 1848.e1. (10.1016/j.neurobiolaging.2012.02.005)
• Owen, M. J. 2012. The origins of schizophrenia [Review]. British Journal of Psychiatry 201 (2), pp.162. (10.1192/bjp.bp.111.107300)
• Shi, H. et al., 2012. Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS). Neurobiology of Aging 33 (8) 1849.e5. (10.1016/j.neurobiolaging.2012.02.014)
• Derks, E. M. et al., 2012. Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: A polygenic risk score analysis. PLoS ONE 7 (6) e37852. (10.1371/journal.pone.0037852)
• Hudson, G. et al., 2012. No consistent evidence for association between mtDNA variants and Alzheimer disease. Neurology 78 (14), pp.1038-1042. (10.1212/WNL.0b013e31824e8f1d)
• Owen, M. J. 2012. Intellectual disability and major psychiatric disorders: a continuum of neurodevelopmental causality. British Journal of Psychiatry 200 (4), pp.268-269. (10.1192/bjp.bp.111.105551)
• Grozeva, D. et al. 2012. Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia. Schizophrenia Research 135 (1-3), pp.1-7. (10.1016/j.schres.2011.11.004)
• Lambert, J. C. et al., 2012. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Molecular Psychiatry 18 , pp.461-470. (10.1038/mp.2012.14)
• Economou, A. et al. 2012. The health informatics cohort enhancement project (HICE): using routinely collected primary care data to identify people with a lifetime diagnosis of psychotic disorder. BMC Research Notes 5 (1), pp.95-100. (10.1186/1756-0500-5-95)
• Jia, P. et al., 2012. A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia. Journal of Medical Genetics 49 (2), pp.96-103. (10.1136/jmedgenet-2011-100397)
• Kirov, G. et al. 2012. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Molecular Psychiatry 17 (2), pp.142-153. (10.1038/mp.2011.154)
• Gerrish, A. et al. 2012. The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's Disease. Journal of Alzheimer's Disease 28 (2), pp.377-387. (10.3233/JAD-2011-110824)
• Sullivan, P. et al., 2012. Don't give up on GWAS [Letter]. Molecular Psychiatry 17 (1), pp.2-3. (10.1038/mp.2011.94)
• Baig, S. et al., 2012. Clusterin mRNA and protein in Alzheimer's disease. Journal of Alzheimer's Disease 28 (2), pp.337-344. (10.3233/JAD-2011-110473)
• Doherty, J. L. , O'Donovan, M. C. and Owen, M. J. 2012. Recent genomic advances in schizophrenia. Clinical Genetics 81 (2), pp.103-109. (10.1111/j.1399-0004.2011.01773.x)
• Escott-Price, V. et al. 2012. Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis. European Journal of Human Genetics 20 (8), pp.890-896. (10.1038/ejhg.2012.8)
• Fisher, H. L. et al., 2012. Stressful life events and the serotonin transporter gene (5-HTT) in recurrent clinical depression. Journal of Affective Disorders 136 (1-2), pp.189-193. (10.1016/j.jad.2011.09.016)
• Fowler, T. et al., 2012. A population-based study of shared genetic variation between premorbid IQ and psychosis among male twin pairs and sibling pairs from Sweden. Archives of General Psychiatry 69 (5), pp.460-466. (10.1001/archgenpsychiatry.2011.1370)
• Fromer, M. et al., 2012. Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. American Journal of Human Genetics 91 (4), pp.597-607. (10.1016/j.ajhg.2012.08.005)
• Håvik, B. et al., 2012. DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS ONE 7 (4), pp.e35424. (10.1371/journal.pone.0035424)
• Keller, M. C. et al., 2012. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. Plos Genetics 8 (4) e1002656. (10.1371/journal.pgen.1002656)
• Owen, M. J. 2012. Implications of genetic findings for understanding schizophrenia. Schizophrenia Bulletin 38 (5), pp.904-907. (10.1093/schbul/sbs103)
• Peall, K. J. et al. 2012. Myoclonus dystonia syndrome: SGCE mutations and psychiatric disease [Abstract]. Journal of Neurology 259 , pp.S30-S30.
• Power, R. A. et al., 2012. Dissecting the genetic heterogeneity of depression through age at onset. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159B (7), pp.859-868. (10.1002/ajmg.b.32093)
• Proitsi, P. et al., 2012. Association of serotonin and dopamine gene pathways with behavioral subphenotypes in dementia. Neurobiology of Aging 33 (4), pp.791-803. (10.1016/j.neurobiolaging.2010.06.011)
• Rees, E. et al. 2012. De Novo mutation in schizophrenia. Schizophrenia Bulletin 38 (3), pp.377-381. (10.1093/schbul/sbs047)
• Richards, A. et al. 2012. Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry 17 (2), pp.193-201. (10.1038/mp.2011.11)
• Stergiakouli, E. et al. 2012. Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. American Journal of Psychiatry 169 (2), pp.186-194. (10.1176/appi.ajp.2011.11040551)
• Thapar, A. K. et al. 2012. Trajectories of change in self-reported psychotic-like experiences in childhood and adolescence. Schizophrenia Research 140 (1-3), pp.104-109. (10.1016/j.schres.2012.06.024)
• Williams, H. J. et al. 2012. Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample [Letter]. Schizophrenia Research 141 (2-3), pp.274-276. (10.1016/j.schres.2012.08.024)
• Williams, N. M. et al. 2012. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. American Journal of Psychiatry 169 (2), pp.195-204. (10.1176/appi.ajp.2011.11060822)

2011

• Cardno, A. G. et al., 2011. A genomewide linkage study of age at onset in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (8), pp.929-940. (10.1002/ajmg.1404)
• Hinney, A. et al., 2011. Genome-wide association study in German patients with attention deficit/hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8), pp.888-897. (10.1002/ajmg.b.31246)
• Sklar, P. et al., 2011. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 [Letter]. Nature Genetics 43 (10), pp.977-983. (10.1038/ng.943)
• Ripke, S. et al., 2011. Genome-wide association study identifies five new schizophrenia loci [Letter]. Nature Genetics 43 (10), pp.969-976. (10.1038/ng.940)
• Chen, J. et al., 2011. Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia. Schizophrenia Research 131 (1-3), pp.43-51.
• Escott-Price, V. et al. 2011. An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction. Biological Psychiatry 70 (2), pp.198-203. (10.1016/j.biopsych.2011.01.034)
• Chen, J. et al., 2011. Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia. Schizophrenia Research 131 (1-3), pp.43-51. (10.1016/j.schres.2011.06.023)
• Hollingworth, P. et al. 2011. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature Genetics 43 (5), pp.429-435. (10.1038/ng.803)
• Williams, H. J. et al. 2011. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Molecular Psychiatry 16 (4), pp.429-441. (10.1038/mp.2010.36)
• Stergiakouli, E. et al., 2011. Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder. Genes Brain and Behavior 10 (3), pp.334-344. (10.1111/j.1601-183x.2010.00672.x)
• Ikeda, M. et al., 2011. Genome-Wide Association Study of Schizophrenia in a Japanese Population. Biological Psychiatry 69 (5), pp.472-478. (10.1016/j.biopsych.2010.07.010)
• O'Dushlaine, C. et al., 2011. Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Molecular Psychiatry 16 (3), pp.286-292. (10.1038/mp.2010.7)
• Belbin, O. et al., 2011. A multi-center study of ACE and the risk of late-onset Alzheimer's disease. Journal of Alzheimer's Disease 24 (3), pp.587-597. (10.3233/JAD-2011-101914)
• Owen, M. J. 2011. Is there a schizophrenia to diagnose? [Editorial]. World Psychiatry 10 (1), pp.34-35. (10.1002/j.2051-5545.2011.tb00007.x)
• Reilly, M. P. et al., 2011. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. The Lancet 377 (9763), pp.383-392. (10.1016/S0140-6736(10)61996-4)
• Bridges, M. et al., 2011. Genetic classification of populations using supervised learning. PLoS ONE 6 (5) e14802. (10.1371/journal.pone.0014802)
• Hamshere, M. L. et al. 2011. Polygenic dissection of the bipolar phenotype. British Journal of Psychiatry 198 (4), pp.284-288. (10.1192/bjp.bp.110.087866)
• Williams, H. J. et al. 2011. Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Human Molecular Genetics 20 (2), pp.387-391. (10.1093/hmg/ddq471)
• Schosser, A. et al., 2011. P02-217 - COMT in major depression - UK candidate gene association study [Meeting Abstract]. European Psychiatry 26 , pp.813. (10.1016/S0924-9338(11)72518-4)
• Boot, E. et al., 2011. COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome. Synapse 65 (9), pp.967-970. (10.1002/syn.20932)
• Breen, G. et al., 2011. A genome-wide significant linkage for severe depression on chromosome 3: the depression network study. American Journal of Psychiatry 168 (8), pp.840-847. (10.1176/appi.ajp.2011.10091342)
• Carroll, L. S. et al. 2011. Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7), pp.844-849. (10.1002/ajmg.b.31231)
• Cichon, S. et al., 2011. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics 88 (3), pp.372-381. (10.1016/j.ajhg.2011.01.017)
• Donohoe, G. et al., 2011. A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809 [Letter]. Schizophrenia Research 125 (2-3), pp.304-306. (10.1016/j.schres.2010.10.019)
• Dwyer, S. L. et al. 2011. Investigation of rare non-synonymous variants at ABCA13 in schizophrenia and bipolar disorder [letter]. Molecular Psychiatry 16 (8), pp.790-791. (10.1038/mp.2011.2)
• Green, E. K. et al. 2011. DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (4), pp.490-492. (10.1002/ajmg.b.31187)
• Hamshere, M. L. et al. 2011. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8), pp.929-940. (10.1002/ajmg.b.31240)
• Hansen, T. et al., 2011. At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia. Biological Psychiatry 70 (1), pp.59-63. (10.1016/j.biopsych.2011.01.031)
• Ingason, A. et al., 2011. Maternally derived microduplications at 15q11-q13: Implication of imprinted genes in psychotic illness. American Journal of Psychiatry 168 (4), pp.408-417. (10.1176/appi.ajp.2010.09111660)
• Langley, K. et al. 2011. Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. British Journal of Psychiatry 199 (5), pp.398-403.
• Owen, M. J. et al. 2011. Neurodevelopmental hypothesis of schizophrenia. British Journal of Psychiatry 198 (3), pp.173-175. (10.1192/bjp.bp.110.084384)
• Peall, K. J. et al. 2011. Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review. Movement Disorders 26 (10), pp.1939-1942. (10.1002/mds.23791)
• Proitsi, P. et al., 2011. A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD). Neurobiology of Aging 32 (3), pp.434-442. (10.1016/j.neurobiolaging.2009.03.005)
• Rees, E. et al. 2011. De novo rates and selection of schizophrenia-associated copy number variants. Biological Psychiatry 70 (12), pp.1109-1114. (10.1016/j.biopsych.2011.07.011)
• Reitz, C. et al., 2011. Meta-analysis of the association between variants in SORL1 and Alzheimer Disease. Archives of Neurology 68 (1), pp.99-106. (10.1001/archneurol.2010.346)
• Rietschel, M. et al., 2011. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Molecular Psychiatry , pp.1-12. (10.1038/mp.2011.80)
• Rivera, M. et al., 2011. Depressive disorder moderates the effect of the FTO gene on body mass index. Molecular Psychiatry 17 (6), pp.604-611. (10.1038/mp.2011.45)
• Ruderfer, D. M. et al., 2011. A family-based study of common polygenic variation and risk of schizophrenia [Letter]. Molecular Psychiatry 16 (9), pp.887-888. (10.1038/mp.2011.34)
• Samaan, Z. et al., 2011. Methylenetetrahydrofolate reductase gene variant (MTHFR C677T) and migraine: a case control study and meta-analysis. BMC Neurology 11 , pp.66-74. (10.1186/1471-2377-11-66)
• Schosser, A. et al., 2011. A follow-up case-control association study of tractable (druggable) genes in recurrent major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (6), pp.640-650. (10.1002/ajmg.b.31204)
• Schosser, A. et al., 2011. Genomewide association scan of suicidal thoughts and behaviour in major depression. PLoS ONE 6 (7) e20690. (10.1371/journal.pone.0020690)
• Sims, R. et al. 2011. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7), pp.764-771. (10.1002/ajmg.b.31216)
• Smith, R. L. et al. 2011. Analysis of neurogranin (NRGN) in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (5), pp.532-535. (10.1002/ajmg.b.31191)
• Steinberg, S. et al., 2011. Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Human Molecular Genetics 20 (20), pp.4076-4081. (10.1093/hmg/ddr325)
• Williams, H. J. et al. 2011. Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7), pp.781-784. (10.1002/ajmg.b.31219)
• Williams, N. M. et al. 2011. Structural variations in attention-deficit hyperactivity disorder - Authors' reply [Letter]. The Lancet 377 (9763), pp.378. (10.1016/S0140-6736(11)60121-9)
• Yosifova, A. et al., 2011. Genome-wide association study on bipolar disorder in the Bulgarian population. Genes, Brain and Behavior 10 (7), pp.789-797. (10.1111/j.1601-183X.2011.00721.x)
• Zammit, S. et al. 2011. Cannabis, COMT and psychotic experiences. British Journal of Psychiatry 199 (5), pp.380-385. (10.1192/bjp.bp.111.091421)
• Zuliani, R. et al., 2011. Genetic variants in the ErbB4 gene are associated with white matter integrity. Psychiatry Research: Neuroimaging 191 (2), pp.133-137. (10.1016/j.pscychresns.2010.11.001)

2010

• Carroll, L. S. et al. 2010. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha. Molecular Psychiatry 15 (11), pp.1101-1111. (10.1038/mp.2009.96)
• Craddock, N. J. et al. 2010. Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype [Corrigendum]. Molecular Psychiatry 15 (11), pp.1121-1121. (10.1038/mp.2010.62)
• Jones, L. et al. 2010. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. PLoS ONE 5 (11) e13950. (10.1371/journal.pone.0013950)
• Williams, N. M. et al. 2010. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. The Lancet 376 (9750), pp.1401-1408. (10.1016/S0140-6736(10)61109-9)
• Green, E. K. et al. 2010. The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia. Molecular Psychiatry 15 (10), pp.1016-1022. (10.1038/mp.2009.49)
• Nishikawa, K. et al., 2010. Maf promotes osteoblast differentiation in mice by mediating the age-related switch in mesenchymal cell differentiation. The Journal of Clinical Investigation 120 (10), pp.3455-3465. (10.1172/JCI42528)
• Allison, D. B. et al., 2010. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics 6 (9) e1001097. (10.1371/journal.pgen.1001097)
• Zammit, S. , Owen, M. J. and Lewis, G. 2010. Misconceptions about gene-environment interactions in psychiatry. Evidence Based Mental Health 13 (3), pp.65-68. (10.1136/ebmh.13.3.65)
• Escott-Price, V. et al. 2010. Genetic differences between five European populations. Human Heredity 70 (2), pp.141-149. (10.1159/000313854)
• Craddock, N. J. et al. 2010. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature 464 (7289), pp.713-720. (10.1038/nature08979)
• Grozeva, D. et al. 2010. Rare copy number variants: A point of rarity in genetic risk for bipolar disorder and schizophrenia. Archives of General Psychiatry 67 (4), pp.318-327. (10.1001/archgenpsychiatry.2010.25)
• Craddock, N. J. et al. 2010. Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype. Molecular Psychiatry 15 (2), pp.146-153. (10.1038/mp.2008.66)
• Baig, S. et al., 2010. Distribution and expression of picalm in alzheimer disease. Journal of Neuropathology and Experimental Neurology 69 (10), pp.1071-1077. (10.1097/NEN.0b013e3181f52e01)
• Blake, D. J. et al., 2010. TCF4, Schizophrenia, and Pitt-Hopkins Syndrome. Schizophrenia Bulletin 36 (3), pp.443-447. (10.1093/schbul/sbq035)
• Butler, A. W. et al., 2010. A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8), pp.1465-1473. (10.1002/ajmg.b.31127)
• Chen, X. et al., 2010. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry 16 (11), pp.1117-1129. (10.1038/mp.2010.96)
• Cohen-Woods, S. et al., 2010. The Bipolar Association Case-Control Study (BACCS) and meta-analysis: No association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (7), pp.1298-1304. (10.1002/ajmg.b.31101)
• Craddock, N. J. and Owen, M. J. 2010. Authors' reply:. British Journal of Psychiatry 196 (6), pp.495-496. (10.1192/bjp.196.6.495a)
• Craddock, N. J. and Owen, M. J. 2010. Data and clinical utility should be the drivers of changes to psychiatric classification [Letter]. British Journal of Psychiatry 197 (2), pp.158. (10.1192/bjp.197.2.158)
• Craddock, N. J. and Owen, M. J. 2010. Molecular genetics and the kraepelinian dichotomy: one disorder, two disorders, or do we need to start thinking afresh?. Psychiatric Annals 40 (2), pp.88-91. (10.3928/00485718-20100127-04)
• Craddock, N. J. and Owen, M. J. 2010. Molecular genetics and the relationship between epilepsy and psychosis [Letter]. British Journal of Psychiatry 197 (1), pp.75-76. (10.1192/bjp.197.1.75a)
• Craddock, N. J. and Owen, M. J. 2010. The Kraepelinian dichotomy - going, going... but still not gone (Reappraisal). British Journal of Psychiatry 196 (2), pp.92-95. (10.1192/bjp.bp.109.073429)
• Cruchaga, C. et al., 2010. SNPS associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease. PLoS Genetics 6 (9) e1001101. (10.1371/journal.pgen.1001101)
• Dwyer, S. L. et al. 2010. No evidence that rare coding variants in ZNF804A confer risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8), pp.1411-1416. (10.1002/ajmg.b.31117)
• Green, E. K. et al. 2010. Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (7), pp.1347-1349. (10.1002/ajmg.b.31108)
• Hollingworth, P. et al. 2010. Alzheimer's disease genetics: current knowledge and future challenges. International Journal of Geriatric Psychiatry 26 (8), pp.793-802. (10.1002/gps.2628)
• Ikeda, M. et al. 2010. Copy number variation in schizophrenia in the Japanese population. Biological Psychiatry 67 (3), pp.283-286. (10.1016/j.biopsych.2009.08.034)
• Ikeda, M. et al. 2010. Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approaches. Biological psychiatry 67 (3), pp.263-269. (10.1016/j.biopsych.2009.08.030)
• Ikeda, M. et al. 2010. Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (4), pp.980-982. (10.1002/ajmg.b.31060)
• Langley, K. et al. 2010. Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder. British Journal of Psychiatry 196 (3), pp.235-240. (10.1192/bjp.bp.109.066274)
• Langley, K. et al. 2010. Genotype link with extreme antisocial behavior: The contribution of cognitive pathways. Archives of General Psychiatry 67 (12), pp.1317-1323. (10.1001/archgenpsychiatry.2010.163)
• Lewis, C. M. et al., 2010. Genome-wide association study of major recurrent depression in the U.K. population. American Journal of Psychiatry 167 (8), pp.949-957. (10.1176/appi.ajp.2010.09091380)
• Liu, Y. et al., 2010. Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder [Letter]. Molecular Psychiatry 16 (1), pp.2-4. (10.1038/mp.2009.107)
• Lupton, M. K. et al., 2010. Education, occupation and retirement age effects on the age of onset of Alzheimer's disease. International Journal of Geriatric Psychiatry 25 (1), pp.30-36. (10.1002/gps.2294)
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2009

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2008

• Barton, A. et al., 2008. Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13. Nature Genetics 40 (10), pp.1156-1159. (10.1038/ng.218)
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2007

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2006

• Harold, D. et al., 2006. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry 11 (12), pp.1085-91. (10.1038/sj.mp.4001904)
• van Amelsvoort, T. et al., 2006. Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging. British Journal of Psychiatry 189 (6), pp.560-561. (10.1192/bjp.bp.105.019876)
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• Grupe, A. et al., 2006. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. The American Journal of Human Genetics 78 (1), pp.78-88.
• Peirce, T. R. et al. 2006. Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophrenia. Archives of general psychiatry 63 (1), pp.18-24. (10.1001/archpsyc.63.1.18)
• Smemo, S. et al., 2006. Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. Annals of Neurology 59 (1), pp.21-26. (10.1002/ana.20673)
• Williams, N. M. , O'Donovan, M. C. and Owen, M. J. 2006. Chromosome 22 deletion syndrome and schizophrenia. International Review of Neurobiology 73 , pp.1-27. (10.1016/S0074-7742(06)73001-X)
• Blair, I. P. et al., 2006. Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele. Molecular Psychiatry 11 (4), pp.372-383. (10.1038/sj.mp.4001784)
• Bray, N. J. et al. 2006. Cis- and trans-acting loci influence expression of DTNBP1, a susceptibility gene for schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7), pp.723-724.
• Craddock, N. J. , Owen, M. J. and O'Donovan, M. C. 2006. The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons. Molecular Psychiatry 11 (5), pp.446-458. (10.1038/sj.mp.4001808)
• Green, E. K. et al., 2006. Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation. Molecular Psychiatry 11 (9), pp.798-799. (10.1038/sj.mp.4001853)
• Green, E. K. et al., 2006. Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UK. British Journal of Psychiatry 188 (1), pp.21-25. (10.1192/bjp.bp.105.009969)
• Hamilton, G. et al., 2006. Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease. Neuroscience Letters 401 (1-2), pp.77-80. (10.1016/j.neulet.2006.03.021)
• Hamshere, M. L. et al. 2006. Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes. Journal of Medical Genetics 43 (7), pp.563-567. (10.1136/jmg.2005.035345)
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• Lambert, D. et al., 2006. Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22 - Corrigendum. Molecular Psychiatry 11 (12), pp.1140-1143. (10.1038/sj.mp.4001917)
• Norton, N. et al. 2006. Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (1), pp.96-101. (10.1002/ajmg.b.30236)
• Norton, N. , Williams, H. J. and Owen, M. J. 2006. An update on the genetics of schizophrenia. Current Opinion in Psychiatry 19 (2), pp.158-164. (10.1097/01.yco.0000214341.52249.59)
• Thapar, A. et al. 2006. Refining the attention deficit hyperactivity disorder phenotype for molecular genetic studies. Molecular Psychiatry 11 (8), pp.714-20. (10.1038/sj.mp.4001831)

2005

• Langley, K. et al. 2005. No support for association between the dopamine transporter (DAT1) gene and ADHD. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 139B (1), pp.7-10. (10.1002/ajmg.b.30206)
• Craddock, N. J. and Owen, M. J. 2005. Kraepelinian dichotomy - Author's reply. British Journal of Psychiatry 187 , pp.485-486.
• Thapar, A. et al. 2005. Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder. Archives of General Psychiatry 62 (11), pp.1275-1278. (10.1001/archpsyc.62.11.1275)
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• Williams, N. M. , O'Donovan, M. C. and Owen, M. J. 2005. Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia?. Schizophrenia Bulletin 31 (4), pp.800-805. (10.1093/schbul/sbi061)
• Li, Y. et al., 2005. The BDNF Val66Met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples. Molecular Psychiatry 10 (9), pp.809-810. (10.1038/sj.mp.4001702)
• Williams, H. J. et al., 2005. No association between schizophrenia and polymorphisms in COMT in two large samples. American Journal of Psychiatry 162 (9), pp.1736-1738. (10.1176/appi.ajp.162.9.1736)
• Kirov, G. et al. 2005. A cross-sectional and a prospective study of thyroid disorders in lithium-treated patients. Journal of affective disorders 87 (2-3), pp.313-317. (10.1016/j.jad.2005.03.010)
• Glaser, B. et al., 2005. No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biological psychiatry 58 (1), pp.78-80.
• Green, E. K. et al. 2005. Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. Archives of general psychiatry 62 (6), pp.642-648. (10.1001/archpsyc.62.6.642)
• Kirov, G. , O'Donovan, M. C. and Owen, M. J. 2005. Finding schizophrenia genes. The Journal of Clinical Investigation 115 (6), pp.1440-1448. (10.1172/JCI24759)
• Turic, D. et al., 2005. A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder. Biological psychiatry 57 (11), pp.1461-1466. (10.1016/j.biopsych.2005.03.025)
• Norton, N. et al., 2005. No evidence for association between polymorphisms in GRM3 and schizophrenia. BMC Psychiatry 5 23. (10.1186/1471-244X-5-23)
• Holmans, P. A. et al. 2005. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 135B (1), pp.24-32. (10.1002/ajmg.b.30114)
• Lambert, D. et al., 2005. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. Molecular psychiatry 10 (9), pp.831-841. (10.1038/sj.mp.4001684)
• Bray, N. J. et al. 2005. Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. Human Molecular Genetics 14 (14), pp.1947-1954. (10.1093/hmg/ddi199)
• Cope, N. A. et al., 2005. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics 76 (4), pp.581-591. (10.1086/429131)
• Cope, N. A. et al., 2005. No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia. Molecular Psychiatry 10 (3), pp.237-238. (10.1038/sj.mp.4001596)
• Li, Y. et al., 2005. Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Human Mutation 25 (3), pp.270-277. (10.1002/humu.20138)
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• Turic, D. et al., 2005. A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD).. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 133B (1), pp.64-67. (10.1002/ajmg.b.30123)
• Owen, M. J. , O'Donovan, M. C. and Harrison, P. J. 2005. Schizophrenia: a genetic disorder of the synapse?. British Medical Journal (BMJ) 330 (7484), pp.158-159. (10.1136/bmj.330.7484.158)
• Glaser, B. et al., 2005. Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 132B (1), pp.38-45. (10.1002/ajmg.b.30081)
• Dimitrova, A. et al., 2005. Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment.. The Pharmacogenomics Journal 5 (1), pp.35-41. (10.1038/sj.tpj.6500273)
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• Owen, M. J. 2005. Genomic approaches to schizophrenia. Clinical Therapeutics 27 (A), pp.S2-S7.
• Ahuja, A. , Thapar, A. and Owen, M. J. 2005. Genetics of mental retardation. Indian Journal of Medical Sciences 59 (9), pp.407-417. (10.4103/0019-5359.16820)
• Craddock, N. J. , O'Donovan, M. C. and Owen, M. J. 2005. Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology. Schizophrenia Bulletin 32 (1), pp.9-16. (10.1093/schbul/sbj033)
• Craddock, N. J. , O'Donovan, M. C. and Owen, M. J. 2005. The genetics of schizophrenia and bipolar disorder: dissecting psychosis. Journal of Medical Genetics 42 (3), pp.193-204. (10.1136/jmg.2005.030718)
• Escott-Price, V. et al. 2005. Streamlined analysis of pooled genotype data in SNP-based association studies. Genetic Epidemiology 28 (3), pp.273-282. (10.1002/gepi.20062)
• Glaser, B. et al., 2005. Identification of a potential Bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4. Molecular Psychiatry 10 (10), pp.920-927. (10.1038/sj.mp.4001689)
• Green, E. et al., 2005. Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease. American Journal of Psychiatry 162 (1), pp.35-42. (10.1176/appi.ajp.162.1.35)
• Kent, L. et al., 2005. Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Molecular Psychiatry 10 (10), pp.939-943. (10.1038/sj.mp.4001696)
• McGuffin, P. et al., 2005. Whole genome linkage scan of recurrent depressive disorder from the depression network study. Human Molecular Genetics 14 (22), pp.3337-3345. (10.1093/hmg/ddi363)
• Owen, M. J. , Craddock, N. J. and O'Donovan, M. C. 2005. Schizophrenia: genes at last?. Trends in Genetics 21 (9), pp.518-525. (10.1016/j.tig.2005.06.011)
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2004

• Farmer, A. et al., 2004. The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic study. BMC Psychiatry 4 42. (10.1186/1471-244X-4-42)
• Jones, G. and Owen, M. J. 2004. Genetics: The implications for forensic psychiatry. Journal of Forensic Psychiatry & Psychology 15 (4), pp.696-704. (10.1080/14789940410001729509)
• Li, Y. et al., 2004. Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. Proceedings of the National Academy of Sciences 101 (44), pp.15688-15693. (10.1073/pnas.0403535101)
• van Amelsvoort, T. et al., 2004. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. Archives of General Psychiatry 61 (11), pp.1085-1096. (10.1001/archpsyc.61.11.1085)
• van Amelsvoort, T. et al., 2004. Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome. Schizophrenia Research 70 (2-3), pp.223-232. (10.1016/j.schres.2003.10.004)
• Bray, N. J. et al. 2004. Allelic variation in the expression of neuropsychiatric candidate genes [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1), pp.25-25.
• Fowler, T. A. et al., 2004. Early onset antisocial behaviour in children with ADHD is associated with a functional variant in the catechol-O-methyltransferase (COMT) gene [Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1), pp.98-98. (10.1002/ajmg.b.30101)
• Peirce, T. R. et al., 2004. Convergent functional genomics, association and linkage analysis suggests 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase (CNP) as a potential susceptibility gene for schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1), pp.81-81. (10.1002/ajmg.b.30101)
• Farbrother, J. E. et al., 2004. Family aggregation of high myopia: estimation of the sibling recurrence risk ratio. Investigative Ophthalmology and Visual Science 45 (9), pp.2873-2878. (10.1167/iovs.03-1155)
• Farbrother, J. E. et al., 2004. Linkage analysis of the genetic loci for high myopia on chromosomes 18p, 12q and 17q in 51 UK families. Investigative Ophthalmology and Visual Science 45 (9), pp.2879-2885. (10.1167/iovs.03-1156)
• Li, Y. et al., 2004. Association of ABCA1 with late-onset Alzheimer?s disease is not observed in a case-control study. Neuroscience Letters 366 (3), pp.268-271. (10.1016/j.neulet.2004.05.047)
• Morris, D. et al., 2004. Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability. American Journal Of Medical Genetics Part A 129B (1), pp.97-103. (10.1002/ajmg.b.30033)
• Mowry, B. J. et al., 2004. Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry 9 (8), pp.784-795. (10.1038/sj.mp.4001481)
• Zammit, S. et al. 2004. Polymorphisms in the MAOA, MAOB, and COMT genes and aggressive behavior in schizophrenia. American Journal of Medical Genetics 128B (1), pp.19-20. (10.1002/ajmg.b.30021)
• Harvey, K. et al., 2004. The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering. Journal of neuroscience 24 (25), pp.5816-5826. (10.1523/JNEUROSCI.1184-04.2004)
• Reid, S. J. et al., 2004. TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's disease. Molecular Brain Research 125 (1-2), pp.120-128. (10.1016/j.molbrainres.2004.03.018)
• Mills, S. et al., 2004. No evidence of association between Catechol-O-Methyltransferase (COMT) Val(158)Met genotype and performance on neuropsychological tasks in children with ADHD: A case-control study. BMC Psychiatry 4 , pp.15-15. (10.1186/1471-244X-4-15)
• Plomin, R. et al., 2004. A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability. Molecular Psychiatry 9 (6), pp.582-586. (10.1038/sj.mp.4001441)
• Williams, N. M. and Owen, M. J. 2004. Genetic abnormalities of chromosome 22 and the development of psychosis. Current Psychiatry Reports 6 (3), pp.176-182. (10.1007/s11920-004-0062-4)
• Zammit, S. et al. 2004. Parental age difference and schizophrenia - Reply. British Journal of Psychiatry 184 , pp.540-541.
• Kirov, G. et al. 2004. Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria. Biological psychiatry 55 (10), pp.971-975. (10.1016/j.biopsych.2004.01.025)
• Turic, D. et al., 2004. Direct analysis of the genes encoding G proteins G alpha T2, G alpha o, G alpha Z in ADHD. American Journal of Medical Genetics 127B (1), pp.68-72. (10.1002/ajmg.b.20173)
• Korszun, A. et al., 2004. Familiarity of symptom dimensions in depression. Archives of General Psychiatry 61 (5), pp.468-474. (10.1001/archpsyc.61.5.468)
• Cook, L. J. et al., 2004. Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease. Neuroscience Letters 358 (2), pp.142-146. (10.1016/j.neulet.2004.01.016)
• Williams, N. M. et al. 2004. Support for RGS4 as a susceptibility gene for schizophrenia. Biological Psychiatry 55 (2), pp.192-195. (10.1016/j.biopsych.2003.11.002)
• Langley, K. et al. 2004. Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD. American Journal of Psychiatry 161 (1), pp.133-138. (10.1176/appi.ajp.161.1.133)
• Williams, N. M. et al. 2004. Identification in two independent samples of a novel schizophrenia risk haplotype of the dystobrevin binding protein gene (DTNBP1). Archives of general psychiatry 61 (4), pp.336-344. (10.1001/archpsyc.61.4.336)
• Bray, N. J. et al. 2004. The serotonin-2A receptor gene locus does not contain common polymorphism affecting mRNA levels in adult brain. Molecular Psychiatry 9 (1), pp.109-114. (10.1038/sj.mp.4001366)
• Bray, N. J. et al. 2004. Allelic expression of APOE in brain [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1), pp.61-61.
• Bray, N. J. et al. 2004. P4-101 Allelic expression of APOE in brain [Conference Abstract]. Neurobiology of Aging 25 , pp.S503-S503. (10.1016/S0197-4580(04)81659-2)
• Bray, N. J. et al. 2004. Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes. Human Molecular Genetics 13 (22), pp.2885-2892. (10.1093/hmg/ddh299)
• Busby, V. et al., 2004. Alpha-T-Catenin Is Expressed in Human Brain and Interacts With the Wnt Signaling Pathway But Is Not Responsible for Linkage to Chromosome 10 in Alzheimer's Disease. Neuromolecular Medicine 5 (2), pp.133-146. (10.1385/NMM:5:2:133)
• Cichon, S. et al., 2004. Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nature Genetics 36 (8), pp.783-784. (10.1038/ng0804-783)
• Fekadu, A. et al., 2004. Bipolar disorder among an isolated island community in Ethiopia. Journal of affective disorders 80 (1), pp.1-10. (10.1016/S0165-0327(02)00345-2)
• Murphy, K. et al., 2004. What can velo-cardio-facial syndrome tell us about the genetics of schizophrenia?. European Psychiatry 19 (Supp1), pp.96S-96S.
• Myers, A. J. et al., 2004. Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American Journal of Medical Genetics 124B (1), pp.29-37. (10.1002/ajmg.b.20036)
• Norton, N. et al., 2004. Interaction between neuregulin 1 and its receptor ERBB4 increases susceptibility to schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1), pp.18-18.
• Norton, N. et al., 2004. DNA pooling as a tool for large-scale association studies in complex traits. Annals of Medicine 36 (2), pp.146-152. (10.1080/07853890310021724)
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• Turic, D. et al. 2004. Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD. Molecular Psychiatry 9 (2), pp.169-173. (10.1038/sj.mp.4001387)
• Williams, N. M. et al. 2004. Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). Archives of General Psychiatry 61 (4), pp.336-344. (10.1001/archpsyc.61.4.336)

2003

• Marchbanks, R. et al., 2003. A mitochondrial DNA sequence variant associated with schizophrenia and oxidative stress. Schizophrenia Research 65 (1), pp.33-38. (10.1016/S0920-9964(03)00011-2)
• Williams, N. M. et al. 2003. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. The American journal of human genetics 73 (6), pp.1355-1367. (10.1086/380206)
• Ivanov, D. et al. 2003. Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis: Molecular genetic study. The British Journal of Psychiatry 183 (5), pp.409-413. (10.1192/bjp.183.5.409)
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2001

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2000

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• Rees, M. I. et al., 2000. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3).. Human Genetics 106 (2), pp.206-209. (10.1007/s004390051029)
• Tunstall, N. et al., 2000. Familial influence on variation in age of onset and behavioural phenotype in Alzheimer's disease. British Journal of Psychiatry 176 , pp.156-159. (10.1192/bjp.176.2.156)
• Buckland, J. et al., 2000. Co-ordination of the expression of the protein tyrosine kinase p56(lck) with the pre-T cell receptor during thymocyte development. European Journal of Immunology 30 (1), pp.8-18. (10.1002/1521-4141(200001)30:1<8::AID-IMMU8>3.0.CO;2-8)
• Cardno, A. G. , O'Donovan, M. C. and Owen, M. J. 2000. Genetic risk factors for schizophrenia. International Journal of Mental Health 29 (3), pp.13-38.
• Deb, S. et al., 2000. Presence of the Apolipoprotein E e4 allele is associated with the manifestation of Alzheimer dementia in adults with Down syndrome. Journal of Intellectual Disability Research 44 , pp.259-259.
• Kirov, G. et al. 2000. Automated genotyping of single-nucleotide polymorphisms by extension of fluorescently labelled primers: analysis of individual and pooled DNA samples. Balkan Journal of Medical Genetics 3 , pp.23-28.
• Murphy, K. , Jones, L. and Owen, M. J. 2000. High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS). Schizophrenia Research 41 (1), pp.29-29. (10.1016/S0920-9964(00)90364-5)
• Murphy, K. and Owen, M. J. 2000. No association between polymorphisms of catechol-o-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. Schizophrenia Research 41 (1), pp.96. (10.1016/S0920-9964(00)90531-0)
• Owen, M. J. , Cardno, A. G. and O'Donovan, M. C. 2000. Psychiatric genetics: back to the future. Molecular Psychiatry 5 (1), pp.22-31. (10.1038/sj.mp.4000702)
• Austin, J. et al., 2000. Association analysis of the proneurotensin gene and bipolar disorder. Psychiatric Genetics 10 (1), pp.51-54. (10.1097/00041444-200010010-00009)
• Austin, J. et al., 2000. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Molecular Psychiatry 5 (2), pp.208-212. (10.1038/sj.mp.4000693)
• Bowen, T. et al. 2000. No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder. Bipolar Disorders 2 (4), pp.328-331. (10.1034/j.1399-5618.2000.020406.x)
• Bowen, T. et al. 2000. Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia. Psychiatric Genetics 10 (1), pp.33-37. (10.1097/00041444-200010010-00006)
• Bray, N. J. et al. 2000. No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. Psychiatric Genetics 10 (2), pp.83-86. (10.1097/00041444-200010020-00005)
• Hoogendoorn, B. et al. 2000. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Human Genetics 107 (5), pp.488-493. (10.1007/s004390000397)
• Kirov, G. et al. 2000. Pooled genotyping of microsatellite markers in parent-offspring trios. Genome Research 10 (1), pp.105-115.
• Speight, G. et al., 2000. Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder. Molecular Psychiatry 5 (3), pp.327-331. (10.1038/sj.mp.4000717)
• Watts, P. et al. 2000. Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13. Eye 14 (2), pp.172-175. (10.1038/eye.2000.48)
• Williams, N. et al. 2000. Identification and characterisation of SNPs in candidate genes for schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 96 (4), pp.462.
• Williams, N. et al. 2000. Linkage disequilibrium mapping and candidate gene screening of the VCFS deleted region for mutations associated with schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 96 (4), pp.475.

1999

• Willliams, H. et al., 1999. No evidence for allelic association between schizophrenia and a functional variant of the human dopamine beta-hydroxylase gene (DBH).. American Journal Of Medical Genetics Part A 88 (5), pp.557-559. (10.1002/(SICI)1096-8628(19991015)88:5<557::AID-AJMG22>3.0.CO;2-F)
• Kirov, G. and Owen, M. J. 1999. Identification of new microsatellite markers on chromosome 4p16. American Journal of Human Genetics 65 (4), pp.A257-A257.
• Murphy, K. C. , Jones, L. A. and Owen, M. J. 1999. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Archives of General Psychiatry 56 (10), pp.940-945. (10.1001/archpsyc.56.10.940)
• Murphy, K. C. , Jones, L. A. and Owen, M. J. 1999. High rates of schizophrenia in velo-cardio-facial syndrome. American Journal of Human Genetics 65 (4), pp.A336-A336.
• Emilien, G. et al., 1999. Dopamine receptors and schizophrenia: contribution of molecular genetics and clinical neuropsychology. The International Journal of Neuropsychopharmacology 2 (3), pp.197. (10.1017/S1461145799001479)
• Fisher, P. J. et al., 1999. A high resolution genome scan made possible with DNA pooling. Molecular Psychiatry 4 (1), pp.S10-S10.
• Hill, L. et al., 1999. IGF2R and cognitive ability. Molecular Psychiatry 4 , pp.S108-S108.
• Jones, I. R. , Owen, M. J. and Craddock, N. J. 1999. Further evidence of familial cosegregation of major affective disorder and Darier's disease. Molecular Psychiatry 4 , pp.S73-S73.
• Jones, L. A. et al., 1999. Sustained and selective attention as quantitative measures of schizophrenia liability. Molecular Psychiatry 4 , pp.S117-S117.
• Jonsson, E. G. et al., 1999. Monoamine oxidase a promoter polymorphism and relationships to monoamine metabolite concentrations in CSF. Molecular Psychiatry 4 , pp.S97-S98.
• McCarthy, G. et al., 1999. Familial aggregation of clinical variables in a sibling pair study of schizophrenia. Molecular Psychiatry 4 , pp.S121-S121.
• McCarthy, G. et al., 1999. Intra-pair correlations of symptom dimensions in a sibling pair study of schizophrenia. Molecular Psychiatry 4 , pp.S26-S27.
• Middle, F. A. et al., 1999. Association studies between bipolar disorder and a polymorphism in the Wolfram gene. Molecular Psychiatry 4 , pp.S76-S76.
• Murphy, K. et al., 1999. The prevalence of chromosome 22q11 deletions in an adult congenital heart disease population. Journal of Medical Genetics 36 , pp.S59-S59.
• Murphy, K. C. and Owen, M. J. 1999. No association between polymorphisms of catechol-O-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. Journal of Medical Genetics 36 , pp.S78-S78.
• Norton, N. et al., 1999. No evidence for association between schizophrenia and MAO-A promoter polymorphism. Molecular Psychiatry 4 , pp.S96-S96.
• O'Donovan, M. C. and Owen, M. J. 1999. Candidate-gene association studies of schizophrenia. American Journal of Human Genetics 65 (3), pp.587-592. (10.1086/302560)
• Owen, M. J. 1999. Evidence of novel loci in late onset Alzheimer's disease. Molecular Psychiatry 4 (1), pp.S9-S9.
• Sanders, R. D. et al., 1999. Pre-pulse inhibition in the functional psychoses. Molecular Psychiatry 4 , pp.S121-S121.
• Thapar, A. et al. 1999. A quantitative trait loci study of attention deficit hyperactivity disorder. Molecular Psychiatry 4 , pp.S52-S53.
• Williams, H. J. et al., 1999. Characterization, mutational analysis, and association of the human proline oxidase gene: A candidate gene for schizophrenia.. Molecular Psychiatry 4 , pp.S115-S115.
• Williams, N. M. et al. 1999. A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs. Human Molecular Genetics 8 (9), pp.1729-1739. (10.1093/hmg/8.9.1729)
• Wavrant-De Vrieze, F. et al., 1999. Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease. Neuroscience Letters 269 (2), pp.67-70.
• Owen, M. J. and Cardno, A. G. 1999. Psychiatric genetics: progress, problems, and potential. The Lancet 354 (1), pp.SI11-SI14. (10.1016/S0140-6736(99)90242-8)
• Rees, M. I. et al., 1999. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry 4 (4), pp.353-359. (10.1038/sj.mp.4000521)
• Cardno, A. G. et al., 1999. CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia. Biological Psychiatry 45 (12), pp.1592-1596. (10.1016/s0006-3223(99)00033-5)
• Williams, J. , Kehoe, P. G. and Owen, M. J. 1999. Case-control study of presenelin-1 intronic polymorphism. Journal of Neurology, Neurosurgery & Psychiatry 66 (6), pp.702. (10.1136/jnnp.66.6.702)
• Fisher, P. J. et al., 1999. DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. Human Molecular Genetics 8 (5), pp.915-922. (10.1093/hmg/8.5.915)
• Amelsvoort, T. V. et al., 1999. An MRI and fMRI study on the effect of deletions on chromosome 22 on brain. Biological psychiatry 45 (8), pp.110S-111S.
• Hill, L. et al., 1999. DNA pooling and dense marker maps: a systematic search for genes for cognitive ability. NeuroReport 10 (4), pp.843-848. (10.1097/00001756-199903170-00032)
• Wavrant-DeVrieze, F. et al., 1999. No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease. Neuroscience Letters 262 (2), pp.137-139. (10.1016/S0304-3940(99)00035-X)
• Franks, E. et al., 1999. Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder. American Journal of Medical Genetics 88 (1), pp.67-70. (10.1002/(SICI)1096-8628(19990205)88:1<67::AID-AJMG12>3.0.CO;2-#)
• Guy, C. et al. 1999. No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder. American Journal of Medical Genetics 88 (1), pp.57-60. (10.1002/(sici)1096-8628(19990205)88:1%3C57::aid-ajmg10%3E3.0.co;2-6)
• Kehoe, P. et al., 1999. Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length. Journal of Medical Genetics 36 (2), pp.108-111. (10.1136/jmg.36.2.108)
• Kehoe, P. et al., 1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2), pp.237-245. (10.1093/hmg/8.2.237)
• Cardno, A. G. et al., 1999. Dimensions of psychosis in affected sibling pairs. Schizophrenia Bulletin 25 (4), pp.841-850.
• Hoogendoorn, B. et al. 1999. Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography. Human Genetics 104 (1), pp.89-93. (10.1007/s004390050915)
• Kehoe, P. G. et al., 1999. Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease. Nature Genetics 21 (1), pp.71-72. (10.1038/5009)
• Kerwin, R. and Owen, M. J. 1999. Genetics of novel therapeutic targets in schizophrenia. The British journal of psychiatry. Supplement. 38 , pp.1-4.
• Bowen, T. et al. 1999. Linkage studies of bipolar disorder with chromosome 18 markers. American Journal of Medical Genetics 15 (88), pp.503-509. (10.1002/(SICI)1096-8628(19991015)88:5<503::AID-AJMG13>3.0.CO;2-U)
• Bray, N. J. et al. 1999. Embryonic NCAM and schizophrenia: Genetic analysis of regulatory enzymes. Molecular Psychiatry 4 , pp.S32-S32.
• Guy, C. et al. 1999. CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder. Neurobiology of Disease 6 (4), pp.302-307. (10.1006/nbdi.1999.0249)
• Jacobsen, N. J. et al., 1999. Mutational analysis of phospholipase A2A: a positional candidate susceptibility gene for bipolar disorder. Molecular Psychiatry 4 (3), pp.274-279. (10.1038/sj.mp.4000476)
• Jacobsen, N. J. et al., 1999. ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes. Human Molecular Genetics 8 (9), pp.1631-1636. (10.1093/hmg/8.9.1631)
• Kirov, G. et al. 1999. Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5. Molecular Psychiatry 4 (6), pp.558-565.
• Kirov, G. et al. 1999. A functional polymorphism in the promoter of monoamine oxidase A gene and bipolar affective disorder. International Journal of Neuropsychopharmacology 2 (4), pp.293-298. (10.1017/s1461145799001601)
• Kirov, G. et al. 1999. Tryptophan hydroxylase gene and manic-depressive illness [letter]. Archives of General Psychiatry 56 (1), pp.98-99. (10.1001/archpsyc.56.1.98)
• Kirov, G. et al. 1999. Bipolar disorder and the serotonin transporter gene: a family-based association study. Psychological Medicine -London- 29 (5), pp.1249-1254. (10.1017/s003329179900882x)
• Sakuntabhai, A. et al., 1999. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nature Genetics 21 (3), pp.271-277.
• Williams, N. M. et al. 1999. Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia. Molecular Psychiatry 4 (supp1), pp.S42-S42.

1998

• Kehoe, P. G. et al., 1998. The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. Journal of Medical Genetics 35 (12), pp.1034-1035. (10.1136/jmg.35.12.1034)
• Bennett, P. et al., 1998. The Wellcome Trust UK-Irish Bipolar Sib-pair Study: Chromosome 21. American Journal of Medical Genetics 81 (6), pp.541-541.
• Fisher, P. J. et al., 1998. DNA pooling for genomic scanning - Application to an association study. American Journal of Medical Genetics 81 (6), pp.469-469.
• Hill, L. et al., 1998. QTLs for general cognitive ability in children: DNA pooling for chromosome 22. American Journal of Medical Genetics 81 (6), pp.486-486.
• Kirov, G. et al. 1998. Family-based association studies of candidate genes in bipolar disorder. American Journal of Medical Genetics 81 (6), pp.476-477.
• Poulton, K. et al., 1998. A molecular genetic study of hyperkinetic disorder/attention deficit hyperactivity disorder. American Journal of Medical Genetics 81 (6), pp.458-458.
• Spurlock, G. et al., 1998. Polymorphism screening of the human type 1 Sigma (σ) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. American Journal of Medical Genetics - Neuropsychiatric Genetics 81 (6), pp.525-526.
• Spurlock, G. et al. 1998. Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique.. American Journal of Medical Genetics 81 (6), pp.525-526.
• Williams, N. M. , Fenton, I. and Owen, M. J. 1998. PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects. American Journal of Medical Genetics 81 (6), pp.463-464.
• Williams, N. M. et al. 1998. Screening the critical region on chromosome 4p with DNA pooling for association with bipolar disorder. American Journal of Medical Genetics 81 (6), pp.486-486.
• Deb, S. et al., 1998. No significant association between a PS-1 intronic polymorphism and dementia in Down's syndrome. Alzheimers Reports 1 (6), pp.365-368.
• Murphy, K. C. and Owen, M. J. 1998. Chromosome 22qII deletions and aggressive behaviour. British Journal of Psychiatry 173 , pp.353-354. (10.1192/bjp.173.4.353b)
• Wu, W. S. et al., 1998. Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA - The Journal of the American Medical Association 280 (7), pp.619-622. (10.1001/jama.280.7.619)
• Straub, R. E. et al., 1998. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Collaborative Linkage Group for Chromosome 22. Schizophrenia Research 32 (2), pp.115-121. (10.1016/S0920-9964(98)00048-6)
• Wright, P. et al., 1998. A transmission/disequilibrium study of the DRB1*04 gene locus on chromosome 6p21.3 with schizophrenia. Schizophrenia Research 32 (2), pp.75-80. (10.1016/S0920-9964(98)00050-4)
• Cardno, A. G. et al., 1998. Sibling pairs with schizophrenia or schizoaffective disorder: associations of subtypes, symptoms and demographic variables. Psychological Medicine 28 (4), pp.815-823. (10.1017/S0033291798006783)
• Owen, M. J. and Craddock, N. J. 1998. Chromosome 11 workshop. Psychiatric Genetics 8 (2), pp.89-92.
• Owen, M. J. and McGuffin, P. 1998. The programmed alliance of two disciplines. La Recherche 311 , pp.38-39.
• Chorney, M. et al., 1998. A Quantitative Trait Locus Associated With Cognitive Ability in Children. Psychological Science 9 (3), pp.159-166. (10.1111/1467-9280.00032)
• Daniels, J. et al., 1998. A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies. American Journal of Human Genetics 62 (5), pp.1189-1197. (10.1086/301816)
• Daniels, J. et al., 1998. Molecular genetic studies of cognitive ability. Human Biology 70 (2), pp.281-296.
• Williams, J. et al. 1998. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry 3 (2), pp.141-149.
• Spurlock, G. et al., 1998. European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. American Journal of Medical Genetics 81 (1), pp.24-28. (10.1002/(SICI)1096-8628(19980207)81:1<24::AID-AJMG5>3.0.CO;2-N)
• Cardno, A. G. et al., 1998. Polydactyly and psychosis. Five cases of co-occurrence. British Journal of Psychiatry 172 , pp.184-185. (10.1192/bjp.172.2.184)
• Murphy, K. C. et al., 1998. Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability. British Journal of Psychiatry 172 , pp.180-183. (10.1192/bjp.172.2.180)
• Ball, D. et al., 1998. Dopamine markers and general cognitive ability. NeuroReport 9 (2), pp.347-349. (10.1097/00001756-199801260-00031)
• Arranz, M. J. et al., 1998. Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine. Molecular Psychiatry 3 (1), pp.61-66. (10.1038/sj.mp.4000348)
• Murphy, K. C. et al., 1998. Chromosome 22q11 deletions - An under-recognized cause of idiopathic learning disability?. Schizophrenia Research 29 (1-2), pp.132-132. (10.1016/S0920-9964(97)88634-3)
• Murphy, K. C. and Owen, M. J. 1998. The behavioural phenotype in velo-cardio-facial syndrome [Conference Abstract]. Schizophrenia Research 29 (1-2), pp.132-132. (10.1016/S0920-9964(97)88633-1)
• Murphy, K. C. et al., 1998. A linkage study of chromosome 22q in SIB-pairs with schizophrenia. Schizophrenia Research 29 (1-2), pp.131-132. (10.1016/S0920-9964(97)88632-X)
• Owen, M. J. 1998. Psychiatric disorders in Wolfram syndrome heterozygotes. Molecular Psychiatry 3 (1), pp.12-13.
• Asherson, P. et al., 1998. A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder. Molecular Psychiatry 3 (4), pp.310-320. (10.1038/sj.mp.4000399)
• Bowen, T. et al. 1998. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Molecular Psychiatry 3 (3), pp.266-269. (10.1038/sj.mp.4000400)
• Bowen, T. et al. 1998. Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder. Molecular Psychiatry 3 (1), pp.67-71. (10.1038/sj.mp.4000293)
• Cardno, A. G. et al., 1998. Association between functional psychosis and expanded CAG/CTG repeats is not explained by health stratification [comparative study]. Psychiatric Genetics 8 (1), pp.29-32. (10.1097/00041444-199800810-00005)
• Kirov, G. et al. 1998. Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder. Molecular Psychiatry 3 (4), pp.342-345. (10.1038/sj.mp.4000385)
• Spurlock, G. et al. 1998. A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter. Molecular Psychiatry 3 (1), pp.42-49. (10.1038/sj.mp.4000342)
• Vallada, H. P. et al., 1998. Linkage analysis between bipolar affective disorder and markers on chromosome X. Psychiatric Genetics 8 (3), pp.183-186. (10.1097/00041444-199800830-00008)

1997

• Jones, L. et al. 1997. No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia. Molecular Psychiatry 2 (6), pp.478-482. (10.1038/sj.mp.4000297)
• Murphy, K. C. et al., 1997. Chromosome 22q11 deletions: An underrecognized cause of idiopathic learning disability?. American Journal of Medical Genetics 74 (6), pp.567-567.
• Murphy, K. C. and Owen, M. J. 1997. The behavioral phenotype in velo-cardio-facial syndrome [Poster Abstract]. American Journal of Medical Genetics 74 (6), pp.660-660. (10.1002/(SICI)1096-8628(19971121)74:6%3C641::AID-AJMG6%3E3.0.CO;2-M)
• Vallada, H. P. et al., 1997. Linkage studies in bipolar affective disorder with markers on chromosome Xq25-27. American Journal of Medical Genetics 74 (6), pp.679-680.
• Williams, J. et al. 1997. A meta analysis of association between the 5-HT2a receptor, T102C polymorphism and schizophrenia. American Journal of Medical Genetics 74 (6), pp.612-612.
• Davies, S. J. et al., 1997. Parietal foramina and multiple exostoses - familial inheritance of a molecular deletion. American Journal of Human Genetics 61 (4), pp.A95-A95.
• Kunugi, H. et al., 1997. Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families. Psychiatric Genetics 7 (3), pp.97-101. (10.1097/00041444-199723000-00001)
• Owen, M. J. and McGuffin, P. 1997. Genetics and psychiatry. British Journal of Psychiatry 171 , pp.201-202. (10.1192/bjp.171.3.201)
• Owen, M. J. , Holmans, P. A. and McGuffin, P. 1997. Association studies in psychiatric genetics. Molecular Psychiatry 2 (4), pp.270-273. (10.1038/sj.mp.4000292)
• Williams, N. M. et al. 1997. Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene. Psychiatric Genetics 7 (2), pp.83-85. (10.1097/00041444-199722000-00005)
• Daniels, J. K. et al., 1997. Linkage study of chromosome 6p in sib-pairs with schizophrenia. American Journal of Medical Genetics 74 (3), pp.319-323. (10.1002/(SICI)1096-8628(19970531)74:3<319::AID-AJMG14>3.0.CO;2-R)
• Williams, J. et al. 1997. Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia.. The Lancet 349 (9060), pp.1221. (10.1016/S0140-6736(05)62413-0)
• Speight, G. et al., 1997. Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia. American Journal of Medical Genetics 74 (2), pp.204-206. (10.1002/(SICI)1096-8628(19970418)74:2<204::AID-AJMG19>3.0.CO;2-M)
• Arranz, M. et al., 1997. Polymorphisms in the 5-HT2A receptor gene and promoter region associated with clozapine response. Schizophrenia Research 24 (1-2), pp.90. (10.1016/S0920-9964(97)82243-8)
• Spurlock, G. et al., 1997. Meta-analysis of association studies between schizophrenia and polymorphisms of the 5-hydroxytryptamine type 2A receptor gene. Schizophrenia Research 24 (1-2), pp.91. (10.1016/S0920-9964(97)82247-5)
• Williams, N. M. et al. 1997. No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283. American Journal of Medical Genetics 74 (1), pp.37-39. (10.1002/(SICI)1096-8628(19970221)74:1<37::AID-AJMG8>3.0.CO;2-S)
• Andrew, M. and Owen, M. J. 1997. Hyperekplexia: abnormal startle response due to glycine receptor mutations. British Journal of Psychiatry 170 , pp.106-108. (10.1192/bjp.170.2.106)
• Jonsson, E. G. et al., 1997. Tryptophan hydroxylase and catechol-O-methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteers. European Archives of Psychiatry and Clinical Neuroscience 247 (6), pp.297-230. (10.1007/BF02922258)
• Petrill, S. A. et al., 1997. No association between general cognitive ability and the A1 allele of the D2 dopamine receptor gene. Behavior Genetics 27 (1), pp.29-31. (10.1023/A:1025659124405)
• Craddock, N. J. et al. 1997. Expanded CAG/CTG repeats in bipolar disorder: no correlation with phenotypic measures of illness severity. Biological psychiatry 42 (10), pp.876-881. (10.1016/s0006-3223(96)00516-1)
• Guy, C. et al. 1997. Exclusion of expansion of 50 CAG/CTG trinucleotide repeats in bipolar disorder. American Journal of Psychiatry 154 (8), pp.1146-1147.
• Petrill, S. A. et al., 1997. Failure to replicate a QTL association between a DNA marker identified by EST00083 and IQ. Intelligence 25 (3), pp.179-184. (10.1016/S0160-2896(97)90041-6)
• Rees, M. et al., 1997. Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT). Molecular Psychiatry 2 (5), pp.398-402. (10.1038/sj.mp.4000256)
• Thomas, N. S. T. et al. 1997. Molecular genetic studies in familial Rett syndrome. European Child & Adolescent Psychiatry 6 (Supp 1), pp.94-94.

1996

• Craddock, N. J. , O'Donovan, M. C. and Owen, M. J. 1996. Introducing Selfcite 2.0--career enhancing software. BMJ 313 (7072), pp.1659-1660. (10.1136/bmj.313.7072.1659)
• Cardno, A. G. et al., 1996. Factor analysis of schizophrenic symptoms using the OPCRIT checklist. Schizophrenia Research 22 (3), pp.233-239. (10.1016/S0920-9964(96)00060-6)
• Cardno, A. G. et al., 1996. Expanded CAG/CTG repeats in schizophrenia. A study of clinical correlates. British Journal of Psychiatry 169 (6), pp.766-771. (10.1192/bjp.169.6.766)
• Craddock, N. J. and Owen, M. J. 1996. Candidate gene association studies in psychiatric genetics: a SERTain future?. Molecular Psychiatry 1 (6), pp.434-436.
• O'Donovan, M. C. et al. 1996. Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder. Psychological Medicine -London- 26 (6), pp.1145-1153. (10.1017/s0033291700035868)
• Levinson, D. F. et al., 1996. Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. American Journal of Medical Genetics 67 (6), pp.580-594. (10.1002/(SICI)1096-8628(19961122)67:6<580::AID-AJMG11>3.0.CO;2-P)
• Petrill, S. A. et al., 1996. DNA markers associated with general and specific cognitive abilities. Intelligence 23 (3), pp.191. (10.1016/S0160-2896(96)90003-3)
• Kunugi, H. et al., 1996. A linkage study of schizophrenia with DNA markers from chromosome 8p21-p22 in 25 multiplex families. Schizophrenia Research 22 (1), pp.61-68. (10.1016/0920-9964(96)00048-5)
• Daniels, J. , McGuffin, P. and Owen, M. J. 1996. Molecular genetic research on IQ: can it be done? Should it be done?. Journal of Biosocial Science 28 (4), pp.491-507. (10.1017/S0021932000022550)
• Kehoe, P. et al., 1996. Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease. NeuroReport 7 (13), pp.2155-2158. (10.1097/00001756-199609020-00019)
• Owen, M. J. , Kehoe, P. and Williams, J. 1996. Presenilin-1 polymorphism and Alzheimer's disease. The Lancet 348 (9024), pp.414. (10.1016/S0140-6736(05)65041-6)
• Farmer, A. and Owen, M. J. 1996. Genomics: the next psychiatric revolution?. British Journal of Psychiatry 169 (2), pp.135-138. (10.1192/bjp.169.2.135)
• Ashworth, A. et al., 1996. Linkage analysis of the fragile X gene FMR-1 and schizophrenia: no evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat. Psychiatric Genetics 6 (2), pp.81-86. (10.1097/00041444-199622000-00008)
• Craddock, N. J. et al. 1996. Concurrent validity of the OPCRIT diagnostic system. Comparison of OPCRIT diagnoses with consensus best-estimate lifetime diagnoses. British Journal of Psychiatry 169 (1), pp.58-63. (10.1192/bjp.169.1.58)
• Parfitt, E. et al., 1996. No evidence for linkage between schizophrenia and eight microsatellite markers on chromosome 19. Human Heredity 46 (4), pp.191-196. (10.1159/000154352)
• Williams, J. et al. 1996. Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. The Lancet 347 (9011), pp.1294-1296. (10.1016/S0140-6736(96)90939-3)
• Asherson, P. et al., 1996. Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia. Molecular Psychiatry 1 (2), pp.125-132.
• Kehoe, P. et al., 1996. Presenilin-1 polymorphism and Alzheimer's disease. The UK Alzheimer's Disease Collaborative Group. The Lancet 347 (9009), pp.1185.
• Murphy, K. C. and Owen, M. J. 1996. Schizophrenia, CATCH 22 and FISH. British Journal of Psychiatry 168 (4), pp.397-398.
• Gill, M. et al., 1996. A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).. American Journal of Medical Genetics 67 (1), pp.40-45. (10.1002/(SICI)1096-8628(19960216)67:1<40::AID-AJMG6>3.0.CO;2-W)
• Cardno, A. et al., 1996. Factor-derived subsyndromes of schizophrenia and familial morbid risks. Schizophrenia Research 18 (2-3), pp.IVA2-IVA2.
• Daniels, J. K. et al., 1996. No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. American Journal of Psychiatry 153 (2), pp.268-270. (10.1176/ajp.153.2.268)
• Murphy, K. C. and Owen, M. J. 1996. Minor physical anomalies and their relationship to the aetiology of schizophrenia. British Journal of Psychiatry 168 (2), pp.139-142. (10.1192/bjp.168.2.139)
• Lin, M. W. et al., 1996. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Cytogenetics and Cell Genetics 75 , pp.2-3.
• O'Donovan, M. C. and Owen, M. J. 1996. Dynamic mutations and psychiatric genetics. Psychological Medicine 26 (1), pp.1-6. (10.1017/S0033291700033663)
• Bowen, T. et al. 1996. Expansion of 50 CAG/CTG repeats excluded in schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set. American Journal of Human Genetics 59 (4), pp.912-917.
• Craddock, N. J. et al. 1996. Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairs. Molecular Psychiatry 1 (1), pp.59-64.
• Craddock, N. J. and Owen, M. J. 1996. Modern molecular genetic approaches to psychiatric disease. British Medical Bulletin 52 (3), pp.434-452. (10.1093/oxfordjournals.bmb.a011558)
• Jacobsen, N. et al., 1996. Association study of bipolar disorder at the phospholipase A2 gene (PLA2A) in the Darier's disease (DAR) region of chromosome 12q23-q24.1. Psychiatric Genetics 6 (4), pp.195-199. (10.1097/00041444-199624000-00005)
• Lim, L. C. C. et al., 1996. Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees. Behavior Genetics 26 (2), pp.113-122. (10.1007/bf02359889)
• O'Donovan, M. C. et al. 1996. Involvement of expanded trinucleotide repeats in common diseases. The Lancet 348 (9043), pp.1739-1740. (10.1016/s0140-6736(05)65870-9)
• Owen, M. J. and Craddock, N. J. 1996. Modern molecular genetic approaches to complex traits: implications for psychiatric disorders [review]. Molecular Psychiatry 1 (1), pp.21-26.
• Vallada, H. et al., 1996. Linkage studies in bipolar affective disorder with markers on chromosome 21. Journal of affective disorders 41 (3), pp.217-221. (10.1016/s0165-0327(96)00055-9)

1995

• Roberts, A. G. et al., 1995. Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23. Human Molecular Genetics 4 (12), pp.2387-2390. (10.1093/hmg/4.12.2387)
• Arranz, M. et al., 1995. Schizophrenia and the androgen receptor gene: report of a sibship showing co-segregation with Reifenstein syndrome but no evidence for linkage in 23 multiply affected families. American Journal of Medical Genetics 60 (5), pp.377-381. (10.1002/ajmg.1320600506)
• Dawson, E. et al., 1995. Systematic search for major genes in schizophrenia: methodological issues and results from chromosome 12. American Journal of Medical Genetics 60 (5), pp.424-433. (10.1002/ajmg.1320600513)
• Okoro, C. et al., 1995. No evidence for linkage between the X-chromosome marker DXS7 and schizophrenia. American Journal of Medical Genetics 60 (5), pp.461-464. (10.1002/ajmg.1320600520)
• Lin, M. W. et al., 1995. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Psychiatric Genetics 5 (3), pp.117-126. (10.1097/00041444-199505030-00004)
• Vallada, H. et al., 1995. Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia. Psychiatric Genetics 5 (3), pp.127-130. (10.1097/00041444-199505030-00005)
• McGuffin, P. , Owen, M. J. and Farmer, A. E. 1995. Genetic basis of schizophrenia. The Lancet 346 (8976), pp.678-682. (10.1016/S0140-6736(95)92285-7)
• Skuder, P. et al., 1995. A polymorphism in mitochondrial DNA associated with IQ?. Intelligence 21 (1), pp.1-11. (10.1016/0160-2896(95)90035-7)
• Vallada, H. P. et al., 1995. Linkage studies on chromosome 22 in familial schizophrenia. American Journal of Medical Genetics 60 (2), pp.139-146. (10.1002/ajmg.1320600210)
• Daniels, J. et al., 1995. No association between schizophrenia and polymorphisms within the genes for debrisoquine 4-hydroxylase (CYP2D6) and the dopamine transporter (DAT).. American Journal of Medical Genetics 60 (1), pp.85-87. (10.1002/ajmg.1320600115)
• Mullan, M. et al., 1995. Clinical features of early onset, familial Alzheimer's disease linked to chromosome 14. American Journal of Medical Genetics 60 (1), pp.44-52. (10.1002/ajmg.1320600109)
• Craddock, N. J. et al. 1995. No evidence for allelic association between bipolar disorder and monoamine oxidase A gene polymorphisms. American Journal of Medical Genetics 60 (4), pp.322-324. (10.1002/ajmg.1320600412)
• Craddock, N. J. et al. 1995. Association study of bipolar disorder using a functional polymorphism (Ser311-->Cys) in the dopamine D2 receptor gene. Psychiatric Genetics 5 (2), pp.63-65.
• Dawson, E. et al., 1995. Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1. American Journal of Medical Genetics 60 (2), pp.94-102. (10.1002/ajmg.1320600203)
• Liddell, M. B. , Bayer, A. J. and Owen, M. J. 1995. No evidence that common allelic variation in the Amyloid Precursor Protein (APP) gene confers susceptibility to Alzheimer's disease. Human Molecular Genetics 4 (5), pp.853-858. (10.1093/hmg/4.5.853)
• O'Donovan, M. C. et al. 1995. Expanded CAG repeats in schizophrenia and bipolar disorder [letter]. Nature Genetics 10 (4), pp.380-381. (10.1038/ng0895-380)
• Plomin, R. et al., 1995. Allelic associations between 100 DNA markers and high versus low IQ. Intelligence 21 (1), pp.31. (10.1016/0160-2896(95)90037-3)

1994

• Rees, M. I. et al., 1994. Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor. Human Molecular Genetics 3 (12), pp.2175-2179. (10.1093/hmg/3.12.2175)
• McGuffin, P. et al., 1994. Genetics, chance and dysmorphogenesis in schizophrenia. British Journal of Psychiatry 165 , pp.694-695. (10.1192/bjp.165.5.693b)
• Daniels, J. et al., 1994. Repeat length variation in the dopamine D4 receptor gene shows no evidence of association with schizophrenia. American Journal of Medical Genetics 54 (3), pp.256-258. (10.1002/ajmg.1320540313)
• Craddock, N. J. , McGuffin, P. and Owen, M. J. 1994. Darier's disease cosegregating with affective disorder [letter]. British Journal of Psychiatry 165 (2), pp.272-272. (10.1192/bjp.165.2.272a)
• Plomin, R. , Owen, M. J. and McGuffin, P. 1994. The genetic basis of complex human behaviors. Science 264 (5166), pp.1733-1739. (10.1126/science.8209254)
• Craddock, N. J. et al. 1994. Variation at the fragile X locus does not influence susceptibility to bipolar disorder. American Journal of Medical Genetics 54 (2), pp.141-143. (10.1002/ajmg.1320540209)
• Asherson, P. and Owen, M. J. 1994. Anticipation in mental illness. The American Journal of Human Genetics 54 (2), pp.386-387.
• Asherson, P. et al., 1994. Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia?. The British Journal of Psychiatry 164 (5), pp.619-624. (10.1192/bjp.164.5.619)
• Asherson, P. et al., 1994. DRD2 Ser311/Cys311 polymorphism in schizophrenia. The Lancet 343 (8904), pp.1045-1045.
• Craddock, N. J. et al. 1994. Bipolar affective puerperal psychosis associated with consanguinity. British Journal of Psychiatry 164 (3), pp.359-364. (10.1192/bjp.164.3.359)
• Craddock, N. J. and Owen, M. J. 1994. Chromosomal aberrations and bipolar affective disorder [review]. British Journal of Psychiatry 164 (4), pp.507-512. (10.1192/bjp.164.4.507)
• Craddock, N. J. and Owen, M. J. 1994. Is there an inverse relationship between Down's syndrome and bipolar affective disorder? literature review and genetic implications [Review]. Journal of Intellectual Disability Research 38 (6), pp.613-620. (10.1111/j.1365-2788.1994.tb00462.x)
• Craddock, N. J. et al. 1994. Familial cosegregation of major affective disorder and Darier's disease (keratosis follicularis). British Journal of Psychiatry 164 (3), pp.355-358. (10.1192/bjp.164.3.355)
• Daniels, J. et al., 1994. IQ and variation in the number of fragile X CGG repeats: No association in a normal sample. Intelligence 19 (1), pp.45-50. (10.1016/0160-2896(94)90052-3)
• James, C. M. et al., 1994. Debrisoquine hydroxylase gene polymorphism in motor-neuron disease. Neurodegeneration 3 (2), pp.149-152.
• Korner, J. et al., 1994. Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls. Psychiatric Genetics 4 (3), pp.167-175. (10.1097/00041444-199400430-00007)
• Liddell, M. B. et al. 1994. Confirmation of association between the e4 allele of apolipoprotein E and Alzheimer's disease. Journal of Medical Genetics 31 (3), pp.197-200. (10.1136/jmg.31.3.197)
• Mant, R. et al., 1994. Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia. American Journal of Medical Genetics 54 (1), pp.21-26. (10.1002/ajmg.1320540106)
• McGuffin, P. et al., 1994. The strength of the genetic effect. Is there room for an environmental influence in the aetiology of schizophrenia?. British Journal of Psychiatry 164 (5), pp.593-599. (10.1192/bjp.164.5.593)
• McGuffin, P. et al., 1994. Seminars in psychiatric genetics. Gaskell, Royal College of Psychiatrists.
• Owen, M. J. 1994. The molecular genetics of Alzheimer's disease. Molecular and Cell Biology of Human Diseases Series 1994 (4), pp.92-109.
• Owen, M. J. , Liddell, M. and McGuffin, P. 1994. Alzheimer's disease. British Medical Journal (BMJ) 308 (6930), pp.672-673. (10.1136/bmj.308.6930.672)
• Parfitt, E. et al., 1994. The gene for Darier's disease maps between D12S78 and D12S79. Human Molecular Genetics 3 (1), pp.35-38. (10.1093/hmg/3.1.35)
• Plomin, R. et al., 1994. DNA markers associated with high versus low IQ: The IQ quantitative trait loci (QTL) project. Behavior Genetics 24 (2), pp.107-118. (10.1007/BF01067815)
• Pulver, A. E. et al., 1994. Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2. American Journal of Medical Genetics 54 (1), pp.44-50. (10.1002/ajmg.1320540109)
• Shaikh, S. et al., 1994. Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia. American Journal of Medical Genetics 54 (1), pp.8-11. (10.1002/ajmg.1320540104)
• Thapar, A. et al. 1994. The genetics of mental retardation. The British Journal of Psychiatry 164 (6), pp.747. (10.1192/bjp.164.6.747)
• Vallada, H. et al., 1994. Is there a major gene for schizophrenia on chromosome-22. Schizophrenia Research 11 (2), pp.147-147.

1993

• Asherson, P. et al., 1993. Failure to find linkage between schizophrenia and genetic markers on chromosome 21. American Journal of Medical Genetics 48 (3), pp.161-165. (10.1002/ajmg.1320480310)
• Craddock, N. J. et al. 1993. Linkage is excluded between Darier's disease and the Duffy blood group locus in five British families. Annales de Genetique 36 (4), pp.211-213.
• Craddock, N. J. et al. 1993. The gene for Darier's disease maps to chromosome 12q23-q24.1. Human Molecular Genetics 2 (11), pp.1941-1943. (10.1093/hmg/2.11.1941)
• Gill, M. et al., 1993. A linkage study of schizophrenia with DNA markers from the long arm of chromosome 11. Psychological Medicine 23 (1), pp.27-44. (10.1017/S0033291700038824)
• Jones, P. B. et al., 1993. A case-control study of family history and cerebral cortical abnormalities in schizophrenia. Acta Psychiatrica Scandinavica 87 (1), pp.6-12. (10.1111/j.1600-0447.1993.tb03322.x)
• Mant, R. et al., 1993. Susceptibility to schizophrenia and the dopamine d3 receptor gene. American Journal of Human Genetics 53 (3), pp.1654-1654.
• McGuffin, P. and Owen, M. J. 1993. Molecular-genetics and schizophrenia - the current picture. Behavior Genetics 23 (6), pp.558-558.
• Owen, M. J. and McGuffin, P. 1993. Association and linkage: complementary strategies for complex disorders.. Journal of Medical Genetics 30 (8), pp.638-639. (10.1136/jmg.30.8.638)
• Saudino, K. J. et al., 1993. Applying a QTL association approach to temperament. Behavior Genetics 23 (6), pp.564-564.
• Shaikh, S. et al., 1993. The dopamine D3 receptor gene: no association with bipolar affective disorder. Journal of Medical Genetics 30 (4), pp.308-309. (10.1136/jmg.30.4.308)

1992

• Vallada, H. et al., 1992. Debrisoquine 4-hydroxylase (CYP2D) locus and possible susceptibility to schizophrenia. The Lancet 340 (8812), pp.181-182. (10.1016/0140-6736(92)93266-P)
• Asherson, P. et al., 1992. No evidence for a pseudoautosomal locus for schizophrenia. Linkage analysis of multiply affected families. British Journal of Psychiatry 161 (1), pp.63-68. (10.1192/bjp.161.1.63)
• Collier, D. et al., 1992. Linkage analysis of schizophrenia on chromosome 22. Schizophrenia Research 6 (2), pp.89-90. (10.1016/0920-9964(92)90085-J)
• Craddock, N. J. and Owen, M. J. 1992. Christmas disease and major affective disorder [letter]. British Journal of Psychiatry 160 , pp.715-715. (10.1192/bjp.160.5.715a)
• Dawson, E. et al., 1992. Genetic linkage analysis of schizophrenia using microsatellite repeat polymorphisms on chromosome 12. Schizophrenia Research 6 (2), pp.90-90. (10.1016/0920-9964(92)90086-K)
• Mant, R. et al., 1992. Schizophrenia scepticism. Nature Genetics 2 (1), pp.12-12. (10.1038/ng0992-12)
• Nanko, S. et al., 1992. Linkage Study of Schizophrenia with Markers on Chromosome 11 in Two Japanese Pedigrees. Psychiatry and Clinical Neurosciences 46 (1), pp.155-159. (10.1111/j.1440-1819.1992.tb00828.x)
• O'Donovan, M. C. and Owen, M. J. 1992. Advances and Retreats in the Molecular Genetics of Major Mental Illness. Annals of Medicine 24 (3), pp.171-177. (10.3109/07853899209147816)
• Owen, M. J. and GILL, M. 1992. Looking for genes in schizophrenia. Clinical Neuropharmacology 15 (Suppl1), pp.222A-223A. (10.1097/00002826-199201001-00116)
• Owen, M. J. and Liddell, M. 1992. Role of amyloid beta-protein in Alzheimer's disease. The Lancet 340 (8823), pp.851-851.
• Owen, M. J. et al. 1992. No association between RFLPs at the porphobilinogen deaminase gene and schizophrenia. Human Genetics 90 (1-2), pp.131-132. (10.1007/BF00210756)
• Owen, M. J. and McGuffin, P. 1992. The molecular genetics of schizophrenia.. British Medical Journal (BMJ) 305 (6855), pp.664-665. (10.1136/bmj.305.6855.664)
• Shaikh, S. , Owen, M. J. and Gill, M. 1992. DRD2 (TGn) repeat polymorphism in a large family data set. Schizophrenia Research 6 (2), pp.91-91. (10.1016/0920-9964(92)90088-M)

1991

• Mant, R. et al., 1991. Mononucleotide repeat polymorphism in the APP gene. Nucleic Acids Research 19 (16), pp.4572-4572. (10.1093/nar/19.16.4572-a)
• Owen, M. J. , Goate, A. and Hardy, J. 1991. A polymorphic microsatellite repeat sequence on chromosome 21 (D21S80). Nucleic Acids Research 19 (16), pp.4574-4571. (10.1093/nar/19.16.4574)
• Goate, A. et al., 1991. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349 (6311), pp.704-706. (10.1038/349704a0)
• Foerster, A. et al., 1991. Pre-morbid adjustment and personality in psychosis. Effects of sex and diagnosis. British Journal of Psychiatry 158 (2), pp.171-176. (10.1192/bjp.158.2.171)
• Foerster, A. et al., 1991. Low birth weight and a family history of schizophrenia predict poor premorbid functioning in psychosis. Schizophrenia Research 5 (1), pp.13-20. (10.1016/0920-9964(91)90049-W)
• Mant, R. et al., 1991. Exclusion of close linkage between GABA a receptor subunit 1a gene and schizophrenia using a microsatellite repeat marker. Cytogenetics and Cell Genetics 58 (3-4), pp.1900-1991.
• McGuffin, P. and Owen, M. J. 1991. The molecular genetics of schizophrenia: An overview and forward view. European Archives of Psychiatry and Clinical Neuroscience 240 (3), pp.169-173. (10.1007/BF02190759)
• Owen, M. J. and McGuffin, P. 1991. DNA-and classical genetic markers in schizophrenia. European Archives of Psychiatry and Clinical Neuroscience 240 (3), pp.197-203. (10.1007/BF02190764)
• Owen, M. J. et al. 1991. Linkage studies of schizophrenia with markers of chromosome-11q. American Journal of Human Genetics 49 (4), pp.354-354.
• Upadhyaya, M. et al., 1991. A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.. Journal of Medical Genetics 28 (10), pp.665-671. (10.1136/jmg.28.10.665)

1990

• Upadhyaya, M. et al., 1990. DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease. The Lancet 336 (8726), pp.1320-1321. (10.1016/0140-6736(90)93005-A)
• St George-Hyslop, P. H. et al., 1990. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature 347 (6289), pp.194-197. (10.1038/347194a0)
• Owen, M. J. , McGuffin, P. and Andrews, R. 1990. Obstetric complications and schizophrenia. The Lancet 336 (8707), pp.122-122. (10.1016/0140-6736(90)91643-O)
• Goate, A. et al., 1990. Genetics of Alzheimer's disease. Advances in Neurology -New York- Raven Press- 51 , pp.197-198.
• Owen, M. J. , Craufurd, D. and St Clair, D. 1990. Localisation of a susceptibility locus for schizophrenia on chromosome 5. British Journal of Psychiatry 157 (1), pp.123-127. (10.1192/bjp.157.1.123)
• Owen, M. J. et al. 1990. Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21.. American Journal of Human Genetics 46 (2), pp.316-322.
• Owen, M. J. and Mullan, M. J. 1990. Molecular genetic studies of manic-depression and schizophrenia. Trends in Neurosciences 13 (1), pp.29-31. (10.1016/0166-2236(90)90059-J)

1989

• Hardy, J. et al., 1989. Presenile dementia associated with mosaic trisomy 21 in a patient with a down syndrome child. The Lancet 334 (8665), pp.743-743. (10.1016/S0140-6736(89)90805-2)
• Goate, A. et al., 1989. Predisposing locus for Alzheimer's disease on chromosome 21. The Lancet 333 (8634), pp.352-355. (10.1016/S0140-6736(89)91725-X)
• HARDY, J. A. et al., 1989. Molecular genetics of Alzheimer's disease. Biochemical Society Transactions 17 (1), pp.75-76. (10.1042/bst0170075)
• Hardy, J. et al., 1989. Modelling the occurrence and pathology of Alzheimer's disease. Neurobiology of Aging 10 (5), pp.429-431. (10.1016/0197-4580(89)90084-5)
• Owen, M. J. , Lewis, S. W. and Murray, R. M. 1989. Family history and cerebral ventricular enlargement in schizophrenia. A case control study. British Journal of Psychiatry 154 (5), pp.629-634. (10.1192/bjp.154.5.629)

1988

• Owen, M. J. and Murray, R. 1988. Blue genes. British Medical Journal (BMJ) 297 (6653), pp.871-872.
• Owen, M. J. and Lewis, S. W. 1988. Risk factors in schizophrenia. British Journal of Psychiatry 153 (3), pp.407-407. (10.1192/bjp.153.3.407a)
• Owen, M. J. , Lewis, S. W. and Murray, R. M. 1988. Obstetric complications and schizophrenia: a computed tomographic study. Psychological Medicine 18 (02), pp.331-339. (10.1017/S003329170000787X)
• Owen, M. J. and Whatley, S. 1988. Polymorphic DNA markers and mental disease. Psychological Medicine 18 (3), pp.529-533.

1987

• Owen, M. J. and Nimgaonkar, V. 1987. The continuum of psychosis and the gene. British Journal of Psychiatry 150 , pp.566-567.

1986

• Owen, M. J. and Lweis, S. 1986. Lateral ventricular size in schizophrenia. The Lancet 2 (8500), pp.223-224.

1984

• Gaffan, D. et al., 1984. Effects of fornix transection upon associative memory in monkeys: role of the hippocampus in learned action. Quarterly Journal of Experimental Psychology 36 (3), pp.173-221.
• Owen, M. J. and Butler, S. 1984. Does amnesia after transection of the fornix in monkeys reflect abnormal sensitivity to proactive interference?. Behavioural Brain Research 14 (3), pp.183-192.

1981

• Owen, M. J. and Butler, S. 1981. Amnesia after transection of the fornix in monkeys: Long-term memory impaired, short-term memory intact. Behavioural Brain Research 3 (1), pp.115-123. (10.1016/0166-4328(81)90032-2)

1980

• Owen, M. J. and Butler, S. 1980. Effects of fornix lesions on recognition memory in the monkey. Journal of Anatomy 131 (DEC), pp.771-771.
• Owen, M. J. and Butler, S. 1980. The effects of fornix lesions on latent learning in the rat. Physiology & Behavior 24 (5), pp.817-822. (10.1016/0031-9384(80)90133-X)