Author: Michael C O’Donovan

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Preprints

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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Contrasting regional architectures of schizophrenia and other complex diseases using fast variance components analysis

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Haplotypes of common SNPs can explain missing heritability of complex diseases

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

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Conditional GWAS analysis identifies putative disorder-specific SNPs for psychiatric disorders

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

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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

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Using genetics to examine a general liability to childhood psychopathology

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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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