De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder
about
Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing TechnologyA Dishful of a Troubled Mind: Induced Pluripotent Stem Cells in Psychiatric ResearchThe role of sex-differential biology in risk for autism spectrum disorderDiscovery of Rare Mutations in Autism: Elucidating Neurodevelopmental MechanismsBio-collections in autism research.Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.The female protective effect in autism spectrum disorder is not mediated by a single genetic locus.Excess of rare, inherited truncating mutations in autism.The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity.Mixed Lineage Leukemia 5 (MLL5) Protein Stability Is Cooperatively Regulated by O-GlcNac Transferase (OGT) and Ubiquitin Specific Protease 7 (USP7).De novo mutations from sporadic schizophrenia cases highlight important signaling genes in an independent sample.Autism spectrum disorders: from genes to neurobiologyRare variants in the neurotrophin signaling pathway implicated in schizophrenia risk.Paternal sperm DNA methylation associated with early signs of autism risk in an autism-enriched cohortMulti-nucleotide de novo Mutations in Humans.Genetics and genomics of autism spectrum disorder: embracing complexity.Gene hunting in autism spectrum disorder: on the path to precision medicineA spectral approach integrating functional genomic annotations for coding and noncoding variants.Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study.Genome-wide characteristics of de novo mutations in autismNeuropsychiatric genomics in precision medicine: diagnostics, gene discovery, and translation.Advanced paternal age effects in neurodevelopmental disorders-review of potential underlying mechanisms.A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders.Mutation spectra of histone methyltransferases with canonical SET domains and EZH2-targeted therapy.Developmental neurogenetics and multimodal neuroimaging of sex differences in autism.Unifying Views of Autism Spectrum Disorders: A Consideration of Autoregulatory Feedback Loops.Defective phosphoinositide metabolism in autism.Autism genetics - an overview.Brain transcriptome atlases: a computational perspective.MLL5 (KMT2E): structure, function, and clinical relevance.Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations.High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.High-throughput sequencing of the synaptome in major depressive disorder.De Novo Coding Variants Are Strongly Associated with Tourette Disorder.Human CRMP4 mutation and disrupted Crmp4 expression in mice are associated with ASD characteristics and sexual dimorphism.Progress in Genetic Studies of Tourette's Syndrome.Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.Genetic analysis of very obese children with autism spectrum disorder.Genome-wide association studies of placebo and duloxetine response in major depressive disorder.
P2860
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P2860
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder
description
2014 nî lūn-bûn
@nan
2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
De novo insertions and deletio ...... with autism spectrum disorder
@ast
De novo insertions and deletio ...... with autism spectrum disorder
@en
De novo insertions and deletio ...... with autism spectrum disorder
@nl
type
label
De novo insertions and deletio ...... with autism spectrum disorder
@ast
De novo insertions and deletio ...... with autism spectrum disorder
@en
De novo insertions and deletio ...... with autism spectrum disorder
@nl
prefLabel
De novo insertions and deletio ...... with autism spectrum disorder
@ast
De novo insertions and deletio ...... with autism spectrum disorder
@en
De novo insertions and deletio ...... with autism spectrum disorder
@nl
P2093
P2860
P50
P1433
P1476
De novo insertions and deletio ...... with autism spectrum disorder
@en
P2093
A Gulhan Ercan-Sencicek
A Jeremy Willsey
Abha R Gupta
Andrew I Brooks
Bernie Devlin
Catherine A Sullivan
Jeanselle Dea
Jeffrey D Mandell
John D Overton
John F Keaney
P2860
P356
10.1016/J.CELREP.2014.08.068
P577
2014-10-02T00:00:00Z