Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
about
Abnormal cell properties and down-regulated FAK-Src complex signaling in B lymphoblasts of autistic subjectsRare structural variation of synapse and neurotransmission genes in autismThe Impact of Neuroimmune Alterations in Autism Spectrum DisorderNetworking in autism: leveraging genetic, biomarker and model system findings in the search for new treatmentsBrinp1(-/-) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron densityCharacterization of the deleted in autism 1 protein family: implications for studying cognitive disorders.Development of individual differences in stress responsiveness: an overview of factors mediating the outcome of early life experiences.A randomised controlled trial of bumetanide in the treatment of autism in childrenFunctional autonomic nervous system profile in children with autism spectrum disorder.RNA-Seq of human neurons derived from iPS cells reveals candidate long non-coding RNAs involved in neurogenesis and neuropsychiatric disorders.Schizophrenia: an integrated sociodevelopmental-cognitive model.Fitting the pieces together: current research on the genetic basis of attention-deficit/hyperactivity disorder (ADHD)Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general populationSibling recurrence and the genetic epidemiology of autism.The therapeutic effect of memantine through the stimulation of synapse formation and dendritic spine maturation in autism and fragile X syndrome.Shared familial transmission of autism spectrum and attention-deficit/hyperactivity disorders.Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database.IL-6 is increased in the cerebellum of autistic brain and alters neural cell adhesion, migration and synaptic formationClinically detectable copy number variations in a Canadian catchment population of schizophrenia.Psychopathological aspects of dopaminergic gene polymorphisms in adolescence and young adulthoodDNA methylation, the early-life social environment and behavioral disordersBroad autism phenotype features of Chinese parents with autistic children and their associations with severity of social impairment in probands.Immunological characterization and transcription profiling of peripheral blood (PB) monocytes in children with autism spectrum disorders (ASD) and specific polysaccharide antibody deficiency (SPAD): case studyGenome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.Copy number variation and warfarin dosing: evaluation of CYP2C9, VKORC1, CYP4F2, GGCX and CALUThe molecular genetics of autism spectrum disorders: genomic mechanisms, neuroimmunopathology, and clinical implicationsThe utility of chromosomal microarray analysis in developmental and behavioral pediatrics.Newborn screening for autism: in search of candidate biomarkers.1q21.1 Microduplication expression in adults.Epigenomic strategies at the interface of genetic and environmental risk factors for autismAutistic traits below the clinical threshold: re-examining the broader autism phenotype in the 21st century.A common susceptibility factor of both autism and epilepsy: functional deficiency of GABA A receptors.Copy-number variation in the pathogenesis of autism spectrum disorder.Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era.Visual function in autism spectrum disorders: a critical review.Increasing autism prevalence in metropolitan New Jersey.Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia.Autism spectrum disorders and allergy: observation from a pediatric allergy/immunology clinic.Association between MTHFR gene polymorphisms and the risk of autism spectrum disorders: a meta-analysis.Improving emotional face perception in autism with diuretic bumetanide: a proof-of-concept behavioral and functional brain imaging pilot study.
P2860
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P2860
Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
description
2009 nî lūn-bûn
@nan
2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի նոյեմբերին 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
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@ast
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@en
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@nl
type
label
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@ast
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@en
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@nl
prefLabel
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@ast
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@en
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@nl
P2860
P356
P1476
Autism genetics: emerging data ...... nucleotide polymorphism scans.
@en
P2093
Lauren A Weiss
P2860
P304
P356
10.1586/ERM.09.59
P577
2009-11-01T00:00:00Z