The genetics of autism: key issues, recent findings, and clinical implications. - Wikidata - awgldk - TriplyDB

The genetics of autism: key issues, recent findings, and clinical implications.

The genetics of autism: key issues, recent findings, and clinical implications.

http://www.wikidata.org/entity/Q33739608

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Biomarkers in autism Autism spectrum disorders: is mesenchymal stem cell personalized therapy the future?Adult restoration of Shank3 expression rescues selective autistic-like phenotypes Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders Impairment of translation in neurons as a putative causative factor for autism High-throughput sequencing of mGluR signaling pathway genes reveals enrichment of rare variants in autism A brain region-specific predictive gene map for autism derived by profiling a reference gene set DNA methylation: a mechanism linking environmental chemical exposures to risk of autism spectrum disorders?Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.Glutamate carboxypeptidase II and folate deficiencies result in reciprocal protection against cognitive and social deficits in mice: implications for neurodevelopmental disorders Translational animal models of autism and neurodevelopmental disorders.Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features The clinical-basic interface in defining pathogenesis in disorders of neurodevelopmental origin.A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report.The genetics of Autism Spectrum Disorders--a guide for clinicians.Unraveling the miswired connectome: a developmental perspective Genetics of childhood-onset schizophrenia Genetics and mitochondrial abnormalities in autism spectrum disorders: a review.Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders.New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.The Human Model: Changing Focus on Autism Research.Candidate Biomarkers in Children with Autism Spectrum Disorder: A Review of MRI Studies.Genetic testing and genetic counseling among Medicaid-enrolled children with autism spectrum disorder in 2001 and 2007.The autism risk genes MET and PLAUR differentially impact cortical development Utilization of genetic testing among children with developmental disabilities in the United States.Exploring Links between Genotypes, Phenotypes, and Clinical Predictors of Response to Early Intensive Behavioral Intervention in Autism Spectrum Disorder.Modeling the autism spectrum disorder phenotype.Risk factors for autism: translating genomic discoveries into diagnostics.Autoimmune and gastrointestinal dysfunctions: does a subset of children with autism reveal a broader connection?Modeling of autism genetic variations in mice: focusing on synaptic and microcircuit dysfunctions.Diagnostic shortfalls in early childhood chronic stress: a review of the issues.Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era.Stem cells as a good tool to investigate dysregulated biological systems in autism spectrum disorders.The molecular genetic architecture of attention deficit hyperactivity disorder.The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.A current snapshot of common genomic variants contribution in psychiatric disorders.Autism spectrum disorders: an updated guide for genetic counseling.Network- and attribute-based classifiers can prioritize genes and pathways for autism spectrum disorders and intellectual disability.Autism spectrum disorder: genetic versus environmental.No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.

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P2860

The genetics of autism: key issues, recent findings, and clinical implications.

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2010 nî lūn-bûn

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2010 թուականի Մարտին հրատարակուած գիտական յօդուած

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2010 թվականի մարտին հրատարակված գիտական հոդված

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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The genetics of autism: key issues, recent findings, and clinical implications.

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The genetics of autism: key issues, recent findings, and clinical implications.

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Identification and Evaluation of Children With Autism Spectrum Disorders

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

Autism and autism spectrum disorders: diagnostic issues for the coming decade

Fragile X: translation in action

Advances in autism genetics: on the threshold of a new neurobiology

Childhood autism and associated comorbidities

The Lifetime Distribution of the Incremental Societal Costs of Autism

A comprehensive review of genetic association studies

Disorder-associated mutations lead to functional inactivation of neuroligins

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

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