Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. - Wikidata - awgldk - TriplyDB

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

http://www.wikidata.org/entity/Q36736904

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Why are autism spectrum conditions more prevalent in males?Recent advances in the pathogenesis of syndromic autisms Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13 Autism risk factors: genes, environment, and gene-environment interactions A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism.Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation Multiple rare variants in the etiology of autism spectrum disorders The Evolving Diagnostic and Genetic Landscapes of Autism Spectrum Disorder Networking in autism: leveraging genetic, biomarker and model system findings in the search for new treatments Genetic aspects of autism spectrum disorders: insights from animal models A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics.Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population The role of genetics in the etiology of schizophrenia 16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder Increased de novo copy number variants in the offspring of older males The clinical-basic interface in defining pathogenesis in disorders of neurodevelopmental origin.New perspectives on rodent models of advanced paternal age: relevance to autism.Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females.High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.Axonal localization of Ca2+-dependent activator protein for secretion 2 is critical for subcellular locality of brain-derived neurotrophic factor and neurotrophin-3 release affecting proper development of postnatal mouse cerebellum.Association and mutation analyses of 16p11.2 autism candidate genes.Molecular cytogenetics and cytogenomics of brain diseases.Whole genome scanning: resolving clinical diagnosis and management amidst complex data.Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.Autism Genetic Database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites.The correlation between rates of cancer and autism: an exploratory ecological investigation.[Genetic and brain structure anomalies in autism spectrum disorders. Towards an understanding of the aetiopathogenesis?].Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies Genome-wide linkage in Utah autism pedigrees Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q.Genetics of psychiatric disorders methods: molecular approaches.

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P2860

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

http://www.wikidata.org/entity/Q36736904

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2008年论文

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2008年论文

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

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type

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

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J.BIOPSYCH.2008.01.009

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Biological Psychiatry

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

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Camille W Brune

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Devin McQuaid

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Eli Hatchwell

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Elliot S Gershon

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James Gergel

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Jeffrey Conroy

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Judith A Badner

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Jyotsna Sudi

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Norma J Nowak

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Ravinesh A Kumar

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P2860

Genetics of austim: complex aetiology for a heterogeneous disorder

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

Strong association of de novo copy number mutations with autism

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Epidemiology of autistic disorder and other pervasive developmental disorders

GeneWays: a system for extracting, analyzing, visualizing, and integrating molecular pathway data.

Pervasive developmental disorders in preschool children: confirmation of high prevalence.

1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.

Get ready to GO! A biologist's guide to the Gene Ontology.

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1111-1117

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12

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William B. Dobyns

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Autism spectrum

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