Copy number variants and therapeutic response to antidepressant medication in major depressive disorder

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CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

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Biomarkers predicting treatment outcome in depression: what is clinically significant?

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Genetic Predictors of Response to Serotonergic and Noradrenergic Antidepressants in Major Depressive Disorder: A Genome-Wide Analysis of Individual-Level Data and a Meta-Analysis

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Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications

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Genome-wide association analysis of copy number variation in recurrent depressive disorder

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De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

(2011) Vladimir Vacic et al.   NATURE

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

(2011) Dalila Pinto et al.   NATURE BIOTECHNOLOGY

High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

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Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient sample

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Genome-Wide Pharmacogenetics of Antidepressant Response in the GENDEP Project

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Rare Copy Number VariantsA Point of Rarity in Genetic Risk for Bipolar Disorder and SchizophreniaRare Copy Number Variants

(2010) Detelina Grozeva   ARCHIVES OF GENERAL PSYCHIATRY

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

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Functional impact of global rare copy number variation in autism spectrum disorders

(2010) Dalila Pinto et al.   NATURE

A Genomewide Association Study Points to Multiple Loci That Predict Antidepressant Drug Treatment Outcome in Depression

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A Genomewide Association Study of Citalopram Response in Major Depressive Disorder

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Differential efficacy of escitalopram and nortriptyline on dimensional measures of depression

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

(2009) Joseph T. Glessner et al.   NATURE

Neurexin 1 (NRXN1) Deletions in Schizophrenia

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Copy-number variations associated with neuropsychiatric conditions

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Large recurrent microdeletions associated with schizophrenia

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GENetic and clinical Predictors Of treatment response in Depression: the GenPod randomised trial protocol

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