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Systematic meta-analyses and field synopsis of genetic association studies of violence and aggressionThe impact of CACNA1C allelic variation on effective connectivity during emotional processing in bipolar disorderGenome-Wide Association of Heroin Dependence in Han ChineseGenetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviorsHypermethylation in the ZBTB20 gene is associated with major depressive disorder.Predicting outcomes following cognitive behaviour therapy in child anxiety disorders: the influence of genetic, demographic and clinical information.Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders.NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series - further understanding of the relevance of NRXN1 to neurodevelopmental disordersMale-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.Random or stochastic monoallelic expressed genes are enriched for neurodevelopmental disorder candidate genes.Therapygenetics: the 5HTTLPR and response to psychological therapy.Effect of DISC1 on the P300 waveform in psychosisThe association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relativesEstablishing the characteristics of an effective pharmacogenetic test for clozapine-induced agranulocytosis.Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case-control sample of schizophrenia.Advanced paternal age increases the risk of schizophrenia and obsessive-compulsive disorder in a Chinese Han population.BBGRE: brain and body genetic resource exchangeThe Association between COMT, BDNF, and NRG1 and Premorbid Social Functioning in Patients with Psychosis, Their Relatives, and ControlsCommon variant at 16p11.2 conferring risk of psychosis.Ohnologs are overrepresented in pathogenic copy number mutations.A COMT gene haplotype associated with methamphetamine abuse.PACAP and PAC1 receptor in brain development and behavior.Using genetic findings in autism for the development of new pharmaceutical compounds.Novel brain expressed RNA identified at the MIR137 schizophrenia-associated locus.Identification and Potential Regulatory Properties of Evolutionary Conserved Regions (ECRs) at the Schizophrenia-Associated MIR137 Locus.Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency - molecular profiling and functional rescue.Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.Advances in the genetics of schizophrenia: toward a network and pathway view for drug discovery.Clinical utility gene card for: 16p13.11 microdeletion syndromeTranslating genome-wide association findings into new therapeutics for psychiatry.Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.Gene-set analysis based on the pharmacological profiles of drugs to identify repurposing opportunities in schizophrenia.Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.Clinical utility gene card for: 15q13.3 microdeletion syndrome.Independent modulation of engagement and connectivity of the facial network during affect processing by CACNA1C and ANK3 risk genes for bipolar disorder.Volume increases in putamen associated with positive symptom reduction in previously drug-naive schizophrenia after 6 weeks antipsychotic treatment.A genome-wide association study for quantitative traits in schizophrenia in China.Interaction between effects of genes coding for dopamine and glutamate transmission on striatal and parahippocampal function.
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D A Collier
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0000-0003-4087-1559