Multiple rare variants in the etiology of autism spectrum disorders
about
Behavioral and Neuroanatomical Phenotypes in Mouse Models of AutismNegative allosteric modulation of the mGluR5 receptor reduces repetitive behaviors and rescues social deficits in mouse models of autism.Histopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesisSociability and motor functions in Shank1 mutant miceRecurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.Exome sequencing of a multigenerational human pedigreeBehavioural phenotyping assays for mouse models of autismAnimal models of neuropsychiatric disordersValproate-induced neurodevelopmental deficits in Xenopus laevis tadpoles.Translational animal models of autism and neurodevelopmental disorders.Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant miceMultiple autism-like behaviors in a novel transgenic mouse model.Low stress reactivity and neuroendocrine factors in the BTBR T+tf/J mouse model of autismDopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention.Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID.Adjusting family relatedness in data-driven burden test of rare variantsRepetitive self-grooming behavior in the BTBR mouse model of autism is blocked by the mGluR5 antagonist MPEP.Communication, interventions, and scientific advances in autism: a commentary.A data-driven method for identifying rare variants with heterogeneous trait effects.Polymorphisms of BDNF gene and autism spectrum disorders: family based association study with korean trios.Candidate gene study of HOXB1 in autism spectrum disorderA functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autismNeural stem cell regulation, fibroblast growth factors, and the developmental origins of neuropsychiatric disorders.Neurobehavioral manifestations of developmental impairment of the brain.Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.Absence of preference for social novelty and increased grooming in integrin β3 knockout mice: initial studies and future directions.MAOA, DBH, and SLC6A4 variants in CHARGE: a case-control study of autism spectrum disorders.Predictable enriched environment prevents development of hyper-emotionality in the VPA rat model of autismTARGETED TREATMENTS IN AUTISM AND FRAGILE X SYNDROMEConditioning adaptive combination of P-values method to analyze case-parent trios with or without population controls.Association of the catechol-o-methyltransferase gene polymorphisms with Korean autism spectrum disordersModeling autism by SHANK gene mutations in mice.Perspectives on the use of stem cells for autism treatmentTouchscreen learning deficits and normal social approach behavior in the Shank3B model of Phelan-McDermid Syndrome and autismMutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese populationGenome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disordersA Review of Oxytocin and Arginine-Vasopressin Receptors and Their Modulation of Autism Spectrum Disorder.Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder.Integrated multifactor analysis explores core dysfunctional modules in autism spectrum disorder.
P2860
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P2860
Multiple rare variants in the etiology of autism spectrum disorders
description
2009 nî lūn-bûn
@nan
2009 թուականին հրատարակուած գիտական յօդուած
@hyw
2009 թվականին 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
Multiple rare variants in the etiology of autism spectrum disorders
@ast
Multiple rare variants in the etiology of autism spectrum disorders
@en
Multiple rare variants in the etiology of autism spectrum disorders
@nl
type
label
Multiple rare variants in the etiology of autism spectrum disorders
@ast
Multiple rare variants in the etiology of autism spectrum disorders
@en
Multiple rare variants in the etiology of autism spectrum disorders
@nl
prefLabel
Multiple rare variants in the etiology of autism spectrum disorders
@ast
Multiple rare variants in the etiology of autism spectrum disorders
@en
Multiple rare variants in the etiology of autism spectrum disorders
@nl
P2860
P921
P3181
P1476
Multiple rare variants in the etiology of autism spectrum disorders
@en
P2093
Joseph D Buxbaum
P2860
P3181
P407
P5008
P577
2009-01-01T00:00:00Z