Gene-set analysis shows association between FMRP targets and autism spectrum disorder

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A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

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Myelination-related genes are associated with decreased white matter integrity in schizophrenia

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

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MAGMA: Generalized Gene-Set Analysis of GWAS Data

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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

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The role of glutamate and its receptors in autism and the use of glutamate receptor antagonists in treatment

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Synaptic, transcriptional and chromatin genes disrupted in autism

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De novo mutations in schizophrenia implicate synaptic networks

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A polygenic burden of rare disruptive mutations in schizophrenia

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The contribution of de novo coding mutations to autism spectrum disorder

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Biological insights from 108 schizophrenia-associated genetic loci

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Pathway Analyses Implicate Glial Cells in Schizophrenia

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Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models

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The FMRP regulon: from targets to disease convergence

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Individual common variants exert weak effects on the risk for autism spectrum disorders

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FMRP targets distinct mRNA sequence elements to regulate protein expression

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

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De Novo Gene Disruptions in Children on the Autistic Spectrum

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Age-Dependent Brain Gene Expression and Copy Number Anomalies in Autism Suggest Distinct Pathological Processes at Young Versus Mature Ages

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FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism

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Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders

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Rare structural variation of synapse and neurotransmission genes in autism

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Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia

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Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis

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A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

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Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability

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A genome-wide scan for common alleles affecting risk for autism

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

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A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1

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A Genome-Wide Association Study of Social and Non-Social Autistic-Like Traits in the General Population Using Pooled DNA, 500 K SNP Microarrays and Both Community and Diagnosed Autism Replication Samples

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Common genetic variants on 5p14.1 associate with autism spectrum disorders

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Pathway analysis of seven common diseases assessed by genome-wide association

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