Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting
about
Biomarkers in autismTranscriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant miceConstrained spherical deconvolution-based tractography and tract-based spatial statistics show abnormal microstructural organization in Asperger syndromeMeta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsDisruptive CHD8 mutations define a subtype of autism early in developmentAutism risk factors: genes, environment, and gene-environment interactionsAdvances in understanding - genetic basis of intellectual disabilitySynaptic Wnt/GSK3β Signaling Hub in AutismPerspective Biological Markers for Autism Spectrum Disorders: Advantages of the Use of Receiver Operating Characteristic Curves in Evaluating Marker Sensitivity and SpecificityMoving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disordersRisk Factors for Depression in Children and Adolescents with High Functioning Autism Spectrum DisordersFollowing the genes: a framework for animal modeling of psychiatric disordersγ-band abnormalities as markers of autism spectrum disordersNetworking in autism: leveraging genetic, biomarker and model system findings in the search for new treatmentsAutism spectrum disorders and neuropathology of the cerebellumSniffing around oxytocin: review and meta-analyses of trials in healthy and clinical groups with implications for pharmacotherapyCellular and synaptic network defects in autismThe molecular basis of cognitive deficits in pervasive developmental disordersThe role of glutamate and its receptors in autism and the use of glutamate receptor antagonists in treatment.The promise of multi-omics and clinical data integration to identify and target personalized healthcare approaches in autism spectrum disordersNINDS epilepsy and autism spectrum disorders workshop reportTherapeutic approaches for shankopathiesTwo knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.Somatosensory cortex functional connectivity abnormalities in autism show opposite trends, depending on direction and spatial scale.Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathologyActin-Dependent Alterations of Dendritic Spine Morphology in ShankopathiesThe bowel and beyond: the enteric nervous system in neurological disordersAdvancing the understanding of autism disease mechanisms through geneticsAberrant Development of Speech Processing in Young Children with Autism: New Insights from Neuroimaging Biomarkers.Beyond Lumping and Splitting: A Review of Computational Approaches for Stratifying Psychiatric DisordersAutism Spectrum Disorder Updates - Relevant Information for Early Interventionists to ConsiderEvaluating historical candidate genes for schizophreniaSynaptic, transcriptional and chromatin genes disrupted in autismPatterns and rates of exonic de novo mutations in autism spectrum disordersAutism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlationsMultiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disordersGenome-wide association analysis identifies 13 new risk loci for schizophreniaLetting a typical mouse judge whether mouse social interactions are atypicalInfant siblings and the investigation of autism risk factorsMice genetically depleted of brain serotonin display social impairments, communication deficits and repetitive behaviors: possible relevance to autism
P2860
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P2860
Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Etiological heterogeneity in a ...... c disorders and still counting
@ast
Etiological heterogeneity in a ...... c disorders and still counting
@en
type
label
Etiological heterogeneity in a ...... c disorders and still counting
@ast
Etiological heterogeneity in a ...... c disorders and still counting
@en
prefLabel
Etiological heterogeneity in a ...... c disorders and still counting
@ast
Etiological heterogeneity in a ...... c disorders and still counting
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P3181
P1433
P1476
Etiological heterogeneity in a ...... c disorders and still counting
@en
P2093
Betancur C
P3181
P356
10.1016/J.BRAINRES.2010.11.078
P407
P577
2011-03-22T00:00:00Z