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Whole Exome Sequencing in Females with Autism Implicates Novel and Candidate Genes

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The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review

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Whole-genome sequencing of quartet families with autism spectrum disorder

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Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involvingCHD8gene, is associated with autism and macrocephaly

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Genomic and genetic aspects of autism spectrum disorder

(2014) Xiaoxi Liu et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

The discovery of integrated gene networks for autism and related disorders

(2014) Fereydoun Hormozdiari et al.   GENOME RESEARCH

The Familial Risk of Autism

(2014) Sven Sandin et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

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Synaptic, transcriptional and chromatin genes disrupted in autism

(2014) Silvia De Rubeis et al.   NATURE

The contribution of de novo coding mutations to autism spectrum disorder

(2014) Ivan Iossifov et al.   NATURE

Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder

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Protein Interaction Networks Reveal Novel Autism Risk Genes within GWAS Statistical Noise

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

(2014) Dexter Hadley et al.   Nature Communications

Biomarkers in Autism

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Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

(2013) Yong-hui Jiang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The Genetic Landscapes of Autism Spectrum Disorders

(2013) Guillaume Huguet et al.   Annual Review of Genomics and Human Genetics

Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome

(2013) Malcolm G Campbell et al.   BMC Medical Genomics

Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services

(2013) Jennifer L. Roberts et al.   GENE

Prader-Willi Syndrome: Obesity due to Genomic Imprinting

(2012) Merlin G. Butler   CURRENT GENOMICS

Common genetic variants, acting additively, are a major source of risk for autism

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Genetics and Mitochondrial Abnormalities in Autism Spectrum Disorders:A Review

(2011) Sukhbir Dhillon et al.   CURRENT GENOMICS

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(2011) Judith H Miles   GENETICS IN MEDICINE

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

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Array Comparative Genomic Hybridization Findings in a Cohort Referred for an Autism Evaluation

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Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

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

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Microdeletion syndrome 16p11.2-p12.2: Clinical and molecular characterization

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

(2009) Deqiong Ma et al.   ANNALS OF HUMAN GENETICS

Update on autism: A review of 1300 reports published in 2008

(2009) John R. Hughes   EPILEPSY & BEHAVIOR

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

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A genome-wide linkage and association scan reveals novel loci for autism

(2009) Lauren A. Weiss et al.   NATURE

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

(2009) Kai Wang et al.   NATURE

Syndromic autism: causes and pathogenetic pathways

(2009) Arianna Benvenuto et al.   World Journal of Pediatrics

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

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