A genome-wide scan for common alleles affecting risk for autism
about
Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS dataAutism risk factors: genes, environment, and gene-environment interactionsA novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism.Allelic diversity in human developmental neurogenetics: insights into biology and diseaseThe Evolving Diagnostic and Genetic Landscapes of Autism Spectrum DisorderIn Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric DisordersGenetics of Autism Spectrum Disorder: Current Status and Possible Clinical ApplicationsFollowing the genes: a framework for animal modeling of psychiatric disordersObesity in children with autism spectrum disorderSialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regenerationProgress in the genetics of polygenic brain disorders: significant new challenges for neurobiologyAlterations in sociability and functional brain connectivity caused by early-life seizures are prevented by bumetanide.Mechanism of enzymatic reaction and protein-protein interactions of PLD from a 3D structural model.A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in miceThe phospholipase D superfamily as therapeutic targetsLoci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait lociInfant siblings and the investigation of autism risk factorsProtocadherin α (PCDHA) as a novel susceptibility gene for autismBurden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsiesProtein interaction networks reveal novel autism risk genes within GWAS statistical noiseRecurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.Evolutionary conservation in genes underlying human psychiatric disordersWhole-genome sequencing in an autism multiplex familyIndividual common variants exert weak effects on the risk for autism spectrum disordersGenome-wide association study of comorbid depressive syndrome and alcohol dependenceMultiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with AutismInfluence of stimulant-induced hyperactivity on social approach in the BTBR mouse model of autismIdentification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorderThe clinical-basic interface in defining pathogenesis in disorders of neurodevelopmental origin.Autism-associated promoter variant in MET impacts functional and structural brain networks.Common genetic variants, acting additively, are a major source of risk for autismDopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention.Autism as early neurodevelopmental disorder: evidence for an sAPPα-mediated anabolic pathwayUncovering the etiology of autism spectrum disorders: genomics, bioinformatics, environment, data collection and exploration, and future possibilities.Epilepsy and Autism.Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism.Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.Bio-collections in autism research.Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder.
P2860
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P2860
A genome-wide scan for common alleles affecting risk for autism
description
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2010
@ast
im Oktober 2010 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2010/10/15)
@nl
наукова стаття, опублікована в жовтні 2010
@uk
مقالة علمية (نشرت في 15-10-2010)
@ar
name
A genome-wide scan for common alleles affecting risk for autism
@ast
A genome-wide scan for common alleles affecting risk for autism
@en
type
label
A genome-wide scan for common alleles affecting risk for autism
@ast
A genome-wide scan for common alleles affecting risk for autism
@en
prefLabel
A genome-wide scan for common alleles affecting risk for autism
@ast
A genome-wide scan for common alleles affecting risk for autism
@en
P2093
P2860
P50
P3181
P356
P1476
A genome-wide scan for common alleles affecting risk for autism
@en
P2093
Abdul Noor
Agatino Battaglia
Alexander Kolevzon
Alison Merikangas
Alistair T. Pagnamenta
Ana Tryfon
Anath C. Lionel
Andrew Crossett
Andrew R. Carson
Ann Le Couteur
P2860
P304
P3181
P356
10.1093/HMG/DDQ307
P50
P577
2010-10-15T00:00:00Z