The Simons Simplex Collection: a resource for identification of autism genetic risk factors.
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Human-specific histone methylation signatures at transcription start sites in prefrontal neuronsDisruptive CHD8 mutations define a subtype of autism early in developmentEvolution of human-specific neural SRGAP2 genes by incomplete segmental duplicationRefinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorderPrenatal Neurogenesis in Autism Spectrum DisordersMoving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disordersSharing heterogeneous data: the national database for autism researchA genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?The contribution of de novo coding mutations to autism spectrum disorderLow load for disruptive mutations in autism genes and their biased transmissionGenome-wide prediction and functional characterization of the genetic basis of autism spectrum disorderMultiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disordersUse of machine learning to shorten observation-based screening and diagnosis of autismMultiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with AutismSporadic autism exomes reveal a highly interconnected protein network of de novo mutationsDe Novo Gene Disruptions in Children on the Autistic SpectrumDe novo mutations revealed by whole-exome sequencing are strongly associated with autismExome sequencing in sporadic autism spectrum disorders identifies severe de novo mutationsCNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersRare deleterious mutations of the gene EFR3A in autism spectrum disorders.Brief report: impact of child problem behaviors and parental broad autism phenotype traits on substance use among parents of children with ASD.Effects of child characteristics on the Autism Diagnostic Interview-Revised: implications for use of scores as a measure of ASD severity.Common genetic variants, acting additively, are a major source of risk for autismRare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.Accurate de novo and transmitted indel detection in exome-capture data using microassembly.Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataStatistical analysis of twenty years (1993 to 2012) of data from mainland China's first intervention center for children with autism spectrum disorder.Increasing prevalence, changes in diagnostic criteria, and nutritional risk factors for autism spectrum disorders.Bio-collections in autism research.The autism diagnostic observation schedule, module 4: revised algorithm and standardized severity scores.Transcriptional dysregulation of neocortical circuit assembly in ASDUse of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHEA higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.Quantifying and modeling birth order effects in autism.Relative burden of large CNVs on a range of neurodevelopmental phenotypes.The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism.Refining analyses of copy number variation identifies specific genes associated with developmental delayExploring the relationship between anxiety and insistence on sameness in autism spectrum disorders.De novo mutations in histone-modifying genes in congenital heart disease.Use of artificial intelligence to shorten the behavioral diagnosis of autism.
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P2860
The Simons Simplex Collection: a resource for identification of autism genetic risk factors.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
The Simons Simplex Collection: ...... f autism genetic risk factors.
@ast
The Simons Simplex Collection: ...... f autism genetic risk factors.
@en
The Simons Simplex Collection: ...... f autism genetic risk factors.
@nl
type
label
The Simons Simplex Collection: ...... f autism genetic risk factors.
@ast
The Simons Simplex Collection: ...... f autism genetic risk factors.
@en
The Simons Simplex Collection: ...... f autism genetic risk factors.
@nl
prefLabel
The Simons Simplex Collection: ...... f autism genetic risk factors.
@ast
The Simons Simplex Collection: ...... f autism genetic risk factors.
@en
The Simons Simplex Collection: ...... f autism genetic risk factors.
@nl
P1433
P1476
The Simons Simplex Collection: ...... f autism genetic risk factors.
@en
P304
P356
10.1016/J.NEURON.2010.10.006
P407
P577
2010-10-01T00:00:00Z