(Q28300576)

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A framework for interpreting genome-wide association studies of psychiatric disorders

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Europe PubMed Central

A framework for interpreting genome-wide association studies of psychiatric disorders (English)

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genome-wide association study

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language of work or name

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publication date

January 2009

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Molecular Psychiatry

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14

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1

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10-7

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A searchable database of genetic evidence for psychiatric disorders

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https://api.crossref.org/works/10.1038/MP.2008.126

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Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

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Association between microdeletion and microduplication at 16p11.2 and autism

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Rare chromosomal deletions and duplications increase risk of schizophrenia

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Large recurrent microdeletions associated with schizophrenia

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Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

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Replicating genotype-phenotype associations

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A HapMap harvest of insights into the genetics of common disease

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How to interpret a genome-wide association study

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Guilt beyond a reasonable doubt

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Phenotypic and genetic complexity of psychosis

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New models of collaboration in genome-wide association studies: the Genetic Association Information Network

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Heterogeneity in meta-analyses of genome-wide association investigations

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A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

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A new multipoint method for genome-wide association studies by imputation of genotypes

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Simple and efficient analysis of disease association with missing genotype data

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A haplotype map of the human genome

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A second generation human haplotype map of over 3.1 million SNPs

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Schizophrenia as a Genetic Morphism

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The endophenotype concept in psychiatry: etymology and strategic intentions

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