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Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryPrenatal risk factors for autism: comprehensive meta-analysisDensity and function of central serotonin (5-HT) transporters, 5-HT1A and 5-HT2A receptors, and effects of their targeting on BTBR T+tf/J mouse social behaviorPerinatal and neonatal risk factors for autism: a comprehensive meta-analysisLinkage and candidate gene studies of autism spectrum disorders in European populationsDisruption of neurexin 1 associated with autism spectrum disorder.Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorderGene expression profiling of lymphoblasts from autistic and nonaffected sib pairs: altered pathways in neuronal development and steroid biosynthesisUsing animal models of enriched environments to inform research on sensory integration intervention for the rehabilitation of neurodevelopmental disordersAn inside job: how endosomal Na(+)/H(+) exchangers link to autism and neurological diseaseDIA1R is an X-linked gene related to Deleted In Autism-1.Pathophysiology of autism spectrum disorders: revisiting gastrointestinal involvement and immune imbalanceCommon genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders.Mothers of autistic children: lower plasma levels of oxytocin and Arg-vasopressin and a higher level of testosteroneOntogeny and regulation of the serotonin transporter: providing insights into human disorders.Links between genetics and pathophysiology in the autism spectrum disorders.Detecting autism spectrum disorders in the general practitioner's practice.Heritability estimates for cognitive factors and brain white matter integrity as markers of schizophrenia.Hippocampal Transcriptomic and Proteomic Alterations in the BTBR Mouse Model of Autism Spectrum Disorder.Altered gene expression in early postnatal monoamine oxidase A knockout mice.Large-scale mutagenesis and phenotypic screens for the nervous system and behavior in mice.Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables.Functional evaluation of autism-associated mutations in NHE9.Regulation of cerebral cortical size and neuron number by fibroblast growth factors: implications for autismNovel clustering of items from the Autism Diagnostic Interview-Revised to define phenotypes within autism spectrum disorders.Association of Aryl Hydrocarbon Receptor-Related Gene Variants with the Severity of Autism Spectrum Disorders.Mutation analysis of the NRXN1 gene in autism spectrum disorders.Convergence of circuit dysfunction in ASD: a common bridge between diverse genetic and environmental risk factors and common clinical electrophysiology.Finding genes in child psychology and psychiatry: when are we going to be there?MIR137 is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
What is known about autism: genes, brain, and behavior.
@ast
What is known about autism: genes, brain, and behavior.
@en
type
label
What is known about autism: genes, brain, and behavior.
@ast
What is known about autism: genes, brain, and behavior.
@en
prefLabel
What is known about autism: genes, brain, and behavior.
@ast
What is known about autism: genes, brain, and behavior.
@en
P356
P1476
What is known about autism: genes, brain, and behavior.
@en
P2093
Katherine Tsatsanis
Susan L Santangelo
P2888
P356
10.1038/SJ.TPJ.6500307
P577
2005-01-01T00:00:00Z
P6179
1022876934