Owen, Michael J.

De Novo Rates and Selection of Schizophrenia-Associated Copy Number Variants

Rees, E., Moskvina, V., Owen, M. J., O'Donovan, M. C., & Kirov, G. (2011) · Biological Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 94

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

Gur, R. E., Bassett, A. S., McDonald-McGinn, D. M., Bearden, C. E., Chow, E., Emanuel, B. S., Owen, M., Swillen, A., Van den Bree, M., Vermeesch, J., et al. (2017) · Molecular Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 93

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome

Monks, S., Niarchou, M., Davies, A. R., Walters, J. T. R., Williams, N., Owen, M. J., van den Bree, M. B. M., & Murphy, K. C. (2014) · Schizophrenia Research

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 93

A cross-sectional and a prospective study of thyroid disorders in lithium-treated patients

Kirov, G., Tredget, J., John, R., Owen, M. J., & Lazarus, J. H. (2005) · Journal of Affective Disorders

Bipolar Disorder and TreatmentThyroid Disorders and Treatments

Cited by 90

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

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

Writing Committee for the ENIGMA-CNV Working Group, van der Meer, D., Sønderby, I. E., Kaufmann, T., Walters, G. B., Abdellaoui, A., Ames, D., Amunts, K., Andersson, M., Armstrong, N. J., et al. (2020) · JAMA Psychiatry

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 87

Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene

Buxbaum, J. D., Georgieva, L., Young, J. J., Plescia, C., Kajiwara, Y., Jiang, Y., Moskvina, V, Norton, N., Peirce, T., Williams, H., et al. (2008) · Molecular Psychiatry

Schizophrenia research and treatmentProtein Tyrosine Phosphatases

Cited by 86

Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility

Silva, A. I., Haddon, J. E., Ahmed Syed, Y., Trent, S., Lin, T.-C. E., Patel, Y., Carter, J., Haan, N., Honey, R. C., Humby, T., et al. (2019) · Nature Communications

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 71

APOE ε4 influences the manifestation of Alzheimer's disease in adults with Down's syndrome

Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, J., & Owen, M. J. (2000) · British Journal of Psychiatry

Down syndrome and intellectual disability researchAlzheimer's disease research and treatments

Cited by 71

Charting the landscape of priority problems in psychiatry, part 2: pathogenesis and aetiology

Stephan, K. E., Binder, E. B., Breakspear, M., Dayan, P., Johnstone, E. C., Meyer-Lindenberg, A., Schnyder, U., Wang, X.-J., Bach, D. R., Fletcher, P. C., et al. (2016) · The Lancet Psychiatry

Mental Health and PsychiatryPsychology and Mental Health

Cited by 64

Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression

Hagenaars, S. P., Coleman, J. R. I., Choi, S. W., Gaspar, H., Adams, M. J., Howard, D. M., Hodgson, K., Traylor, M., Air, T. M., Andlauer, T. F. M., et al. (2020) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 61

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

Association between a promoter variant in the monoamine oxidase A gene and schizophrenia

Jönsson, E. G., Norton, N., Forslund, K., Mattila-Evenden, M., Rylander, G., Åsberg, M., Owen, M. J., & Sedvall, G. C. (2003) · Schizophrenia Research

Schizophrenia research and treatmentNeurotransmitter Receptor Influence on Behavior

Cited by 57

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

Genome-wide association analysis of copy number variation in recurrent depressive disorder

Rucker, J. J. H., Breen, G., Pinto, D., Pedroso, I., Lewis, C. M., Cohen-Woods, S., Uher, R., Schosser, A., Rivera, M., Aitchison, K. J., et al. (2013) · Molecular Psychiatry

Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Cited by 51

Misconceptions about gene-environment interactions in psychiatry

Zammit, S., Owen, M. J., & Lewis, G. (2010) · Evidence Based Mental Health

Genetic Associations and EpidemiologyHealth, Environment, Cognitive Aging

Cited by 50

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

Allelic expression of APOE in human brain: Effects of epsilon status and promoter haplotypes

Bray, N. J., Jehu, L., Moskvina, V., Buxbaum, J. D., Dracheva, S., Haroutunian, V., Williams, J., Buckland, P. R., Owen, M. J., & O'Donovan, M. C. (2004) · Human Molecular Genetics

Alzheimer's disease research and treatmentsGenetic Associations and Epidemiology

Cited by 45

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

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study

Silva, A. I., Ulfarsson, M. O., Stefansson, H., Gustafsson, O., Walters, G. B., Linden, D. E. J., Wilkinson, L. S., Drakesmith, M., Owen, M. J., Hall, J., et al. (2019) · Biological Psychiatry

Genomic variations and chromosomal abnormalitiesAdvanced Neuroimaging Techniques and Applications

Cited by 36

A Multi-Center Study of ACE and the Risk of Late-Onset Alzheimer's Disease

Belbin, O., Brown, K., Shi, H., Medway, C., Abraham, R., Passmore, P., Mann, D., Smith, A. D., Holmes, C., McGuinness, B., et al. (2011) · Journal of Alzheimer's Disease

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 34

Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures

Drakesmith, M., Parker, G. D., Smith, J., Linden, S. C., Rees, E., Williams, N., Owen, M. J., van den Bree, M., Hall, J., Jones, D. K., et al. (2019) · Translational Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 31

Haploinsufficiency of the schizophrenia and autism risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through microglial and Arp2/3 mediated actin dependent mechanisms

Haan, N., Westacott, L. J., Carter, J., Owen, M. J., Gray, W. P., Hall, J., & Wilkinson, L. S. (2021) · Translational Psychiatry

Neurogenesis and neuroplasticity mechanismsNeuroinflammation and Neurodegeneration Mechanisms

Cited by 29

A family-based study of common polygenic variation and risk of schizophrenia

Ruderfer, D. M., Kirov, G., Chambert, K., Moran, J. L., Owen, M. J., O'Donovan, M. C., Sklar, P., & Purcell, S. M. (2011) · Molecular Psychiatry

Genetic Associations and EpidemiologySchizophrenia research and treatment

Cited by 28