Risk factors for autism: translating genomic discoveries into diagnostics.
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Rare deletions at the neurexin 3 locus in autism spectrum disorderSHANK1 Deletions in Males with Autism Spectrum DisorderWhole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back AgainSharing heterogeneous data: the national database for autism researchInfant siblings and the investigation of autism risk factorsCurrent progress and challenges in the search for autism biomarkersRepetitive behavior profile and supersensitivity to amphetamine in the C58/J mouse model of autism.Measurement of Serum Superoxide Dismutase and Its Relevance to Disease Intensity Autistic ChildrenParents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian Sample.Increased topographical variability of task-related activation in perceptive and motor associative regions in adult autistics.Polymorphisms of BDNF gene and autism spectrum disorders: family based association study with korean trios.The social brain network and autismSocial visual engagement in infants and toddlers with autism: early developmental transitions and a model of pathogenesisNext Generation Sequencing and Health Technology Assessment in Autism Spectrum Disorder.Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disordersClassification and adaptive behavior prediction of children with autism spectrum disorder based upon multivariate data analysis of markers of oxidative stress and DNA methylation.Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular eraThe importance of autism research.A discovery resource of rare copy number variations in individuals with autism spectrum disorder.Patterns of Risk for Multiple Co-Occurring Medical Conditions Replicate Across Distinct Cohorts of Children with Autism Spectrum Disorder.Postsynaptic density scaffold SAP102 regulates cortical synapse development through EphB and PAK signaling pathway.Novel inter-hemispheric white matter connectivity in the BTBR mouse model of autismA Comparison of Logistic Regression, Logic Regression, Classification Tree, and Random Forests to Identify Effective Gene-Gene and Gene-Environmental Interactions.Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingTranscriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.Behavioral signatures related to genetic disorders in autismDivergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis.Autism spectrum disorder: advances in evidence-based practice.Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.Modeling the autism spectrum disorder phenotype.Modeling of autism genetic variations in mice: focusing on synaptic and microcircuit dysfunctions.Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder.Autism spectrum disorder model mice: Focus on copy number variation and epigenetics.Accurate Autism Screening at the 18-Month Well-Child Visit Requires Different Strategies than at 24 Months.A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.The ethics of complexity. Genetics and autism, a literature review."Set in Stone" or "Ray of Hope": Parents' Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASD.A noncoding RNA antisense to moesin at 5p14.1 in autism.Parents' perspectives on participating in genetic research in autism.
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Risk factors for autism: translating genomic discoveries into diagnostics.
description
article científic
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article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 24 June 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Risk factors for autism: translating genomic discoveries into diagnostics.
@en
Risk factors for autism: translating genomic discoveries into diagnostics.
@nl
type
label
Risk factors for autism: translating genomic discoveries into diagnostics.
@en
Risk factors for autism: translating genomic discoveries into diagnostics.
@nl
prefLabel
Risk factors for autism: translating genomic discoveries into diagnostics.
@en
Risk factors for autism: translating genomic discoveries into diagnostics.
@nl
P2860
P1433
P1476
Risk factors for autism: translating genomic discoveries into diagnostics.
@en
P2860
P2888
P304
P356
10.1007/S00439-011-1037-2
P577
2011-06-24T00:00:00Z