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List of works by Michael Owen

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

scientific article published on 22 March 2021

A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia

scientific article published on 15 January 2019

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study

scientific article published on 29 July 2019

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders

scientific article published on 04 May 2020

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

scientific article published on 26 February 2018

Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders

scientific article published on 12 May 2020

Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication

scientific article published on 05 March 2019

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

scientific article published on 01 August 2019

De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia

scientific article published on 13 January 2020

Dynamic expression of genes associated with schizophrenia and bipolar disorder across development

scientific article published on 04 February 2019

Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk

scientific article published on 21 September 2020

Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders

scientific article published on 11 April 2019

Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference.

scientific article published on 19 February 2018

Gender differences in CNV burden do not confound schizophrenia CNV associations.

scientific article published on 17 May 2016

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

article

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

scientific article

Genetic association of FMRP targets with psychiatric disorders

scientific article published on 19 October 2020

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

scientific article published on 03 February 2020

Genetic identification of brain cell types underlying schizophrenia

scientific article published on 21 May 2018

Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank

scientific article published on 04 January 2019

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 28 February 2019

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Genome-wide Significant Associations for Cannabis Dependence Severity: Relevance to Psychiatric Disorders

scientific article

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

scientific article published in October 2013

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scientific article

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

scientific article

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Integrative functional genomic analysis of human brain development and neuropsychiatric risks

scientific article published on 01 December 2018

Investigating the genetic architecture of general and specific psychopathology in adolescence

scientific article published on 08 August 2018

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

scientific article published on 13 June 2018

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder ⬇️

scientific article published on August 1, 2010

NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia

scientific article published in 2022

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.

scientific article

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

scientific article

Psychiatric disorders in children with 16p11.2 deletion and duplication

scientific article published on 16 January 2019

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

scientific article published on 01 July 2019

Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

scientific article published on 01 June 2019

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

scientific article

Reasons for discontinuing clozapine: A cohort study of patients commencing treatment

scientific article

Response to letter to editor: "Knowing when and how to use epilepsy screening questionnaires"

scientific article published on 02 March 2020

Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS)

scientific article published on 30 May 2019

The Contribution of the Rüdin School to Psychiatric Genetics: The Light and the Darkness

scientific article published in 2022

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

scientific article published on 26 June 2017

The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome

scientific article published on 05 November 2018

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

scientific article published on 09 November 2020

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