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Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2010, Volume 49, Issue 8, pp. 794 - 809
Objective Current research suggests that the causes of autism spectrum disorders (ASD) are multifactorial and include both genetic and environmental factors.... 
Pediatrics | Psychiatry | autism spectrum disorders | epigenetics | genetics | GENOTYPE-PHENOTYPE CORRELATIONS | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | NEUROTROPHIC FACTOR BDNF | CHINESE HAN POPULATION | SEROTONIN TRANSPORTER GENE | PERVASIVE DEVELOPMENTAL DISORDERS | BECKWITH-WIEDEMANN-SYNDROME | FRAGILE-X-SYNDROME | PEDIATRICS | IN-VITRO FERTILIZATION | SYNDROME CRITICAL REGION | PRADER-WILLI-SYNDROME | Autism | Etiology | Pervasive Developmental Disorders | Mental Retardation | Evidence | Genetics | Environmental Influences | Cognitive Development | Symptoms (Individual Disorders) | Megalencephaly - psychology | Angelman Syndrome - psychology | Humans | Rett Syndrome - psychology | Angelman Syndrome - diagnosis | Social Environment | CHARGE Syndrome - psychology | Turner Syndrome - diagnosis | Prader-Willi Syndrome - psychology | Child Development Disorders, Pervasive - diagnosis | Angelman Syndrome - genetics | Prader-Willi Syndrome - genetics | Child | Fragile X Syndrome - genetics | Genetic Predisposition to Disease - psychology | Megalencephaly - genetics | Prader-Willi Syndrome - diagnosis | Genetic Predisposition to Disease - genetics | Genetic Association Studies | Rett Syndrome - diagnosis | Comorbidity | Risk Factors | CHARGE Syndrome - diagnosis | Chromosomes, Human, Pair 15 - genetics | Megalencephaly - diagnosis | Child Development Disorders, Pervasive - psychology | Child Development Disorders, Pervasive - genetics | Epigenesis, Genetic - genetics | Fragile X Syndrome - psychology | Adolescent | Turner Syndrome - genetics | CHARGE Syndrome - genetics | Rett Syndrome - genetics | Fragile X Syndrome - diagnosis | Psychological aspects | Epigenetic inheritance | Genetic aspects | Epigenetics | Child psychology | Gene expression | Genomics | Deoxyribonucleic acid--DNA
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 9/2017, Volume 47, Issue 9, pp. 2911 - 2917
Journal Article
Autism Research, ISSN 1939-3792, 05/2017, Volume 10, Issue 5, pp. 711 - 722
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 9/2013, Volume 43, Issue 9, pp. 2026 - 2037
Journal Article
Journal Article
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 7/2012, Volume 42, Issue 7, pp. 1470 - 1476
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2017, Volume 12, Issue 1, p. e0170386
It has been proposed that copy number variations (CNVs) are associated with increased risk of autism spectrum disorder (ASD) and, in conjunction with other... 
AXON INITIAL SEGMENTS | READ ALIGNMENT | RECEPTOR-GENE CLUSTERS | HUMAN-DISEASE | DE-NOVO MUTATIONS | MULTIDISCIPLINARY SCIENCES | HIGH-FREQUENCY | DNA-SEQUENCING DATA | BIPOLAR DISORDER | COPY-NUMBER VARIATION | BURROWS-WHEELER TRANSFORM | Gene Duplication | Chromosomes, Human, Pair 8 - genetics | Sequence Deletion | Translocation, Genetic | Humans | Male | Chromosomes, Human, Pair 4 - genetics | Gene Regulatory Networks | Nucleic Acid Amplification Techniques | DNA Copy Number Variations | Intellectual Disability - genetics | Female | Chromosomes, Human, Pair 4 - ultrastructure | Child | Chromosomes, Human, Pair 8 - ultrastructure | Siblings | Megalencephaly - genetics | Autism Spectrum Disorder - genetics | Genetic Association Studies | In Situ Hybridization, Fluorescence | Nerve Tissue Proteins - genetics | Syndrome | Exome - genetics | Comparative Genomic Hybridization | Learning Disorders - genetics | Usage | Comparative genomic hybridization | Copy number variations | Pervasive developmental disorders | Genetic aspects | Research | Health aspects | Risk factors | Translocation | Copy number | Genes | Schizophrenia | Data processing | Bipolar disorder | Genomes | Hybridization | Medicine | Studies | Autism | Heterogeneity | Clonal deletion | Evolutionary biology | Etiology | Network analysis | Deletion | Genetics | Mutation | Variation | Psychiatry | Genotypes
Journal Article