Individual common variants exert weak effects on the risk for autism spectrum disorders - Wikidata - wikimedia - TriplyDB

Individual common variants exert weak effects on the risk for autism spectrum disorders

Individual common variants exert weak effects on the risk for autism spectrum disorders

http://www.wikidata.org/entity/Q28943296

about

A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism.Synaptic Wnt/GSK3β Signaling Hub in Autism Decoding the non-coding genome: elucidating genetic risk outside the coding genome Moving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disorders Genetics and genomics of psychiatric disease Cerebral asymmetry and language development: cause, correlate, or consequence?A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Advancing the understanding of autism disease mechanisms through genetics A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Protein interaction networks reveal novel autism risk genes within GWAS statistical noise Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.Evolutionary conservation in genes underlying human psychiatric disorders Shining a light on CNTNAP2: complex functions to complex disorders.Whole-genome sequencing in an autism multiplex family An Overview of Autism Spectrum Disorder, Heterogeneity and Treatment Options.Learning delays in a mouse model of Autism Spectrum Disorder.Antipurinergic therapy corrects the autism-like features in the Fragile X (Fmr1 knockout) mouse model.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Towards identification of individual etiologies by resolving genomic and biological conundrums in patients with autism spectrum disorders.Common genetic variants, acting additively, are a major source of risk for autism The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders.Reversal of autism-like behaviors and metabolism in adult mice with single-dose antipurinergic therapy.Data mining the ScanBrit study of a gluten- and casein-free dietary intervention for children with autism spectrum disorders: behavioural and psychometric measures of dietary response.Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.Support vector machine model of developmental brain gene expression data for prioritization of Autism risk gene candidates.DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.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.Neurexins.Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder Family-based clinical associations and functional characterization of the serotonin 2A receptor gene (HTR2A) in autism spectrum disorder.Most genetic risk for autism resides with common variation.Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.A candidate gene association study further corroborates involvement of contactin genes in autism Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.De novo TBR1 mutations in sporadic autism disrupt protein functions.De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.Research review: Polygenic methods and their application to psychiatric traits.

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P2860

Individual common variants exert weak effects on the risk for autism spectrum disorders

http://www.wikidata.org/entity/Q28943296

description

2012 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

artículu científicu espublizáu en 2012

@ast

im November 2012 veröffentlichter wissenschaftlicher Artikel

@de

scientific journal article

@en

wetenschappelijk artikel (gepubliceerd op 2012/11/01)

@nl

наукова стаття, опублікована в листопаді 2012

@uk

مقالة علمية (نشرت في نوفمبر 2012)

@ar

name

Individual common variants exert weak effects on the risk for autism spectrum disorders

@ast

Individual common variants exert weak effects on the risk for autism spectrum disorders

@en

type

label

Individual common variants exert weak effects on the risk for autism spectrum disorders

@ast

Individual common variants exert weak effects on the risk for autism spectrum disorders

@en

prefLabel

Individual common variants exert weak effects on the risk for autism spectrum disorders

@ast

Individual common variants exert weak effects on the risk for autism spectrum disorders

@en

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P356

P1433

Human Molecular Genetics

P1476

Individual common variants exert weak effects on the risk for autism spectrum disorders

@en

P2093

Agatino Battaglia

http://www.w3.org/2001/XMLSchema#string

Alexander Kolevzon

http://www.w3.org/2001/XMLSchema#string

Alison Merikangas

http://www.w3.org/2001/XMLSchema#string

Alistair T. Pagnamenta

http://www.w3.org/2001/XMLSchema#string

Ana Tryfon

http://www.w3.org/2001/XMLSchema#string

Ann Le Couteur

http://www.w3.org/2001/XMLSchema#string

Ann P. Thompson

http://www.w3.org/2001/XMLSchema#string

Anthony J. Bailey

http://www.w3.org/2001/XMLSchema#string

Barbara Parrini

http://www.w3.org/2001/XMLSchema#string

Bernadette Roge

http://www.w3.org/2001/XMLSchema#string

P2860

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Copy-number variations associated with neuropsychiatric conditions

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

Rare deletions at the neurexin 3 locus in autism spectrum disorder

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

A functional genetic link between distinct developmental language disorders

SHANK1 Deletions in Males with Autism Spectrum Disorder

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

P304

4781–4792

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scholarly article

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5027800

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P356

10.1093/HMG/DDS301

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P433

21

http://www.w3.org/2001/XMLSchema#string

P478

21

http://www.w3.org/2001/XMLSchema#string

P50

Fred R. Volkmar

Christopher Gillberg

Thomas Bourgeron

Hakon Hakonarson

Jiannis Ragoussis

Joseph D. Buxbaum

Catalina Betancur

Ellen M. Wijsman

Louise Gallagher

P577

2012-11-01T00:00:00Z

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P5875

230585895

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P698

22843504

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P921

Autism spectrum

P932

3471395

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