about
Emerging pharmacotherapies for neurodevelopmental disordersAntibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan's syndrome and acquired neuromyotoniaAutismNeurexin 1 (NRXN1) deletions in schizophreniaGenomics and autism spectrum disorderBlood manganese concentrations in Jamaican children with and without autism spectrum disordersRole of fruits, grains, and seafood consumption in blood cadmium concentrations of Jamaican children with and without Autism Spectrum DisorderCharacterization of the deleted in autism 1 protein family: implications for studying cognitive disorders.Heterozygous ambra1 deficiency in mice: a genetic trait with autism-like behavior restricted to the female genderMultiple autism-like behaviors in a novel transgenic mouse model.Uncovering molecular biomarkers that correlate cognitive decline with the changes of hippocampus' gene expression profiles in Alzheimer's disease.Low but increasing prevalence of autism spectrum disorders in a French area from register-based data.The genetics of autism: key issues, recent findings, and clinical implications.A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.Association of NCAM1 polymorphisms with autism and parental age at conception in a Chinese Han population.Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models.A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traitsBlood lead concentrations in Jamaican children with and without autism spectrum disorder.Defining the contribution of CNTNAP2 to autism susceptibility.Interaction between GSTT1 and GSTP1 allele variants as a risk modulating-factor for autism spectrum disorders.Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescenceLithium as a rescue therapy for regression and catatonia features in two SHANK3 patients with autism spectrum disorder: case reports.DNA methylation, the early-life social environment and behavioral disordersAutism candidate genes via mouse phenomicsIntegrative gene network analysis provides novel regulatory relationships, genetic contributions and susceptible targets in autism spectrum disordersRecurrent Transmission of a 17q12 Microdeletion and a Variable Clinical SpectrumHuman Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome.The role of drinking water sources, consumption of vegetables and seafood in relation to blood arsenic concentrations of Jamaican children with and without Autism Spectrum Disorders.Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling.Shank3 Is Part of a Zinc-Sensitive Signaling System That Regulates Excitatory Synaptic Strength.Shank mutant mice as an animal model of autism.Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.Social Communication is an Emerging Target for Pharmacotherapy in Autism Spectrum Disorder - A Review of the Literature on Potential Agents.MLPA analysis in a cohort of patients with autism.Seafood consumption and blood mercury concentrations in Jamaican children with and without autism spectrum disordersThe contribution of oxytocin and vasopressin to mammalian social behavior: potential role in autism spectrum disorder.The contribution of epigenetics to understanding genetic factors in autism.Immune dysregulation in autism spectrum disorder.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genetics of autism spectrum disorders.
@ast
Genetics of autism spectrum disorders.
@en
Genetics of autism spectrum disorders.
@nl
type
label
Genetics of autism spectrum disorders.
@ast
Genetics of autism spectrum disorders.
@en
Genetics of autism spectrum disorders.
@nl
prefLabel
Genetics of autism spectrum disorders.
@ast
Genetics of autism spectrum disorders.
@en
Genetics of autism spectrum disorders.
@nl
P1476
Genetics of autism spectrum disorders.
@en
P2093
Ravinesh A Kumar
Susan L Christian
P2888
P304
P356
10.1007/S11910-009-0029-2
P577
2009-05-01T00:00:00Z
P6179
1033404346