Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

Genetics of Depression: Progress at Last

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Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

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Identification of 15 genetic loci associated with risk of major depression in individuals of European descent

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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

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The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)

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Integrative analysis of 111 reference human epigenomes

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Sparse whole-genome sequencing identifies two loci for major depressive disorder

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A gene-based association method for mapping traits using reference transcriptome data

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Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

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Genetic studies in intellectual disability and related disorders

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The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

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Efficient Test and Visualization of Multi-Set Intersections

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The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease

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Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

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GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database

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Copy number variation in schizophrenia in Sweden

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De novo mutations in schizophrenia implicate synaptic networks

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Biological insights from 108 schizophrenia-associated genetic loci

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Refining analyses of copy number variation identifies specific genes associated with developmental delay

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Efficient multivariate linear mixed model algorithms for genome-wide association studies

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The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

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Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network

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CFEOM1-Associated Kinesin KIF21A Is a Cortical Microtubule Growth Inhibitor

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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

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Evidence that duplications of 22q11.2 protect against schizophrenia

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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

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The Database of Genomic Variants: a curated collection of structural variation in the human genome

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ParseCNV integrative copy number variation association software with quality tracking

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GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

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An integrated encyclopedia of DNA elements in the human genome

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Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

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Exome sequencing supports a de novo mutational paradigm for schizophrenia

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

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Genome-wide association study identifies five new schizophrenia loci

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

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A copy number variation morbidity map of developmental delay

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A Versatile Gene-Based Test for Genome-wide Association Studies

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Dedicator of cytokinesis 8 (DOCK8) deficiency

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Analysing biological pathways in genome-wide association studies

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Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

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Strong synaptic transmission impact by copy number variations in schizophrenia

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DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

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A major mutation of KIF21A associated with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) enhances translocation of Kank1 to the membrane

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Kank proteins: structure, functions and diseases

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Kank attenuates actin remodeling by preventing interaction between IRSp53 and Rac1

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

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Neurexin 1 (NRXN1) Deletions in Schizophrenia

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Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projects

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Kank regulates RhoA-dependent formation of actin stress fibers and cell migration via 14-3-3 in PI3K–Akt signaling

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Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities

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