O’Donovan, Michael C.
Cardiff University
47 papers on CoChatORCID 0000-0001-7073-2379
Most cited papers
- Verified
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects
Kendall, K. M., Rees, E., Escott-Price, V., Einon, M., Thomas, R., Hewitt, J., O’Donovan, M. C., Owen, M. J., Walters, J. T. R., & Kirov, G. (2017) · Biological Psychiatry
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 226
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A Replicated Molecular Genetic Basis for Subtyping Antisocial Behavior in Children With Attention-Deficit/Hyperactivity Disorder
Caspi, A., Langley, K., Milne, B., Moffitt, T. E., O’Donovan, M., Owen, M. J., Polo Tomas, M., Poulton, R., Rutter, M., Taylor, A., et al. (2008) · Archives of General Psychiatry
Attention Deficit Hyperactivity DisorderNeurotransmitter Receptor Influence on Behavior
Cited by 221
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Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia
Pocklington, A. J., Rees, E., Walters, J. T. R., Han, J., Kavanagh, D. H., Chambert, K. D., Holmans, P., Moran, J. L., McCarroll, S. A., Kirov, G., et al. (2015) · Neuron
Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities
Cited by 193
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Genetic Risk for Attention-Deficit/Hyperactivity Disorder Contributes to Neurodevelopmental Traits in the General Population
Martin, J., Hamshere, M. L., Stergiakouli, E., O’Donovan, M. C., & Thapar, A. (2014) · Biological Psychiatry
Attention Deficit Hyperactivity DisorderAutism Spectrum Disorder Research
Cited by 187
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A Population-Based Cohort Study Examining the Incidence and Impact of Psychotic Experiences From Childhood to Adulthood, and Prediction of Psychotic Disorder
Sullivan, S. A., Kounali, D., Cannon, M., David, A. S., Fletcher, P. C., Holmans, P., Jones, H., Jones, P. B., Linden, D. E. J., Lewis, G., et al. (2020) · American Journal of Psychiatry
Schizophrenia research and treatmentMental Health Treatment and Access
Cited by 176
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Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank
Crawford, K., Bracher-Smith, M., Owen, D., Kendall, K. M., Rees, E., Pardiñas, A. F., Einon, M., Escott-Price, V., Walters, J. T. R., O’Donovan, M. C., et al. (2019) · Journal of Medical Genetics
Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology
Cited by 175
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Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia
Bergen, S. E., Ploner, A., Howrigan, D., CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium, O’Donovan, M. C., Smoller, J. W., Sullivan, P. F., Sebat, J., Neale, B., & Kendler, K. S. (2019) · American Journal of Psychiatry
Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities
Cited by 171
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Characterizing Developmental Trajectories and the Role of Neuropsychiatric Genetic Risk Variants in Early-Onset Depression
Rice, F., Riglin, L., Thapar, A. K., Heron, J., Anney, R., O’Donovan, M. C., & Thapar, A. (2019) · JAMA Psychiatry
Child and Adolescent Psychosocial and Emotional DevelopmentGenetic Associations and Epidemiology
Cited by 167
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Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia
Rees, E., Kendall, K., Pardiñas, A. F., Legge, S. E., Pocklington, A., Escott-Price, V., MacCabe, J. H., Collier, D. A., Holmans, P., O’Donovan, M. C., et al. (2016) · JAMA Psychiatry
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 162
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Association of genetic risk variants with attention-deficit/hyperactivity disorder trajectories in the general population
Riglin, L., Collishaw, S., Thapar, A. K., Dalsgaard, S., Langley, K., Smith, G. D., Stergiakouli, E., Maughan, B., O’Donovan, M. C., & Thapar, A. (2016) · JAMA Psychiatry
Attention Deficit Hyperactivity DisorderAutism Spectrum Disorder Research
Cited by 161
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GWAS meta-analysis of suicide attempt: identification of 12 genome-wide significant loci and implication of genetic risks for specific health factors
Docherty, A. R., Mullins, N., Ashley-Koch, A. E., Qin, X., Coleman, J. R. I., Shabalin, A., Kang, J., Murnyak, B., Wendt, F., Adams, M., et al. (2023) · American Journal of Psychiatry
Genetic Associations and EpidemiologySuicide and Self-Harm Studies
Cited by 160
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Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease
Desikan, R. S., Schork, A. J., Wang, Y., Thompson, W. K., Dehghan, A., Ridker, P. M., Chasman, D. I., McEvoy, L. K., Holland, D., Chen, C.-H., et al. (2015) · Circulation
Alzheimer's disease research and treatmentsGenetic Associations and Epidemiology
Cited by 154
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High Loading of Polygenic Risk for ADHD in Children With Comorbid Aggression
Hamshere, M. L., Langley, K., Martin, J., Agha, S. S., Stergiakouli, E., Anney, R. J. L., Buitelaar, J., Faraone, S. V., Lesch, K.-P., Neale, B. M., et al. (2013) · American Journal of Psychiatry
Attention Deficit Hyperactivity DisorderGenetic Associations and Epidemiology
Cited by 144
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Association of Rare Copy Number Variants With Risk of Depression
Kendall, K. M., Rees, E., Bracher-Smith, M., Legge, S., Riglin, L., Zammit, S., O’Donovan, M. C., Owen, M. J., Jones, I., Kirov, G., et al. (2019) · JAMA Psychiatry
Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology
Cited by 144
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Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns
Czamara, D., Eraslan, G., Page, C. M., Lahti, J., Lahti-Pulkkinen, M., Hämäläinen, E., Kajantie, E., Laivuori, H., Villa, P. M., Reynolds, R. M., et al. (2019) · Nature Communications
Epigenetics and DNA MethylationBirth, Development, and Health
Cited by 143
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Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders
Arloth, J., Bogdan, R., Weber, P., Frishman, G., Menke, A., Wagner, K. V., Balsevich, G., Schmidt, M. V., Karbalai, N., Czamara, D., et al. (2015) · Neuron
Stress Responses and CortisolGenetic Associations and Epidemiology
Cited by 142
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De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia
GROUP Investigators, Rees, E., Han, J., Morgan, J., Carrera, N., Escott-Price, V., Pocklington, A. J., Duffield, M., Hall, L. S., Legge, S. E., et al. (2020) · Nature Neuroscience
Schizophrenia research and treatmentGenetic Associations and Epidemiology
Cited by 129
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Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases
Yuan, K., Longchamps, R. J., Pardiñas, A. F., Yu, M., Chen, T.-T., Lin, S.-C., Chen, Y., Lam, M., Liu, R., Xia, Y., et al. (2023) · Nature Genetics
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 94
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Effects of Differential Genotyping Error Rate on the Type I Error Probability of Case-Control Studies
Moskvina, V., Craddock, N., Holmans, P., Owen, M. J., & O’Donovan, M. C. (2006) · Human Heredity
Genetic Associations and EpidemiologyGenetic diversity and population structure
Cited by 88
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Investigating the genetic architecture of general and specific psychopathology in adolescence
Jones, H. J., Heron, J., Hammerton, G., Stochl, J., Jones, P. B., Cannon, M., Smith, G. D., Holmans, P., Lewis, G., Linden, D. E. J., et al. (2018) · Translational Psychiatry
Schizophrenia research and treatmentGenetic Associations and Epidemiology
Cited by 59
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Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation
Carroll, L. S., Woolf, R., Ibrahim, Y., Williams, H. J., Dwyer, S., Walters, J., Kirov, G., O’Donovan, M. C., & Owen, M. J. (2016) · Psychiatric Genetics
Schizophrenia research and treatmentIon channel regulation and function
Cited by 54
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Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder
Langley, K., Fowler, T. A., Grady, D. L., Moyzis, R. K., Holmans, P. A., van den Bree, M. B. M., Owen, M. J., O’Donovan, M. C., & Thapar, A. (2009) · European Child & Adolescent Psychiatry
Attention Deficit Hyperactivity DisorderNeurotransmitter Receptor Influence on Behavior
Cited by 47
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Genetic Differences between Five European Populations
Moskvina, V., Smith, M., Ivanov, D., Blackwood, D., StClair, D., Hultman, C., Toncheva, D., Gill, M., Corvin, A., O’Dushlaine, C., et al. (2010) · Human Heredity
Forensic and Genetic ResearchGenetic Associations and Epidemiology
Cited by 38
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