Author: Kirov George

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Preprints

Genomewide association study identifies 30 loci associated with bipolar disorder

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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

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Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

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Sex-biased reduction in reproductive success drives selective constraint on human genes

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank

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Genetic association study of psychotic experiences in UK Biobank

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Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

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Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

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Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes.

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Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

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Genetic association of FMRP targets with psychiatric disorders

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Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank

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The role of rare copy number variants in depression

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Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

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Characterization of single gene copy number variants in schizophrenia

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The rate of de novo CNVs in healthy controls

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Effects of pathogenic CNVs on biochemical markers: a study on the UK Biobank

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A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder

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Characterization of Age and Polarity at Onset in Bipolar Disorder

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COVID-19 and mortality risk in patients with psychiatric disorders

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Analysis of diffusion tensor imaging data from UK Biobank confirms dosage effect of 15q11.2 copy-number variation on white matter and shows association with cognition

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