Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder
about
An Overview of Autism Spectrum Disorder, Heterogeneity and Treatment Options.Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism.The connectomes of males and females with autism spectrum disorder have significantly different white matter connectivity densities.Advanced paternal age effects in neurodevelopmental disorders-review of potential underlying mechanisms.Ephrin-A2 regulates excitatory neuron differentiation and interneuron migration in the developing neocortex.Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.Integrating regulatory features data for prediction of functional disease-associated SNPs.Heritable genotype contrast mining reveals novel gene associations specific to autism subgroups.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.Multidimensional Neuroanatomical Subtyping of Autism Spectrum Disorder.Revealing Alzheimer's disease genes spectrum in the whole-genome by machine learning.Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder.A Cell Type-Specific Expression Signature Predicts Haploinsufficient Autism-Susceptibility Genes.Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing.Brain-specific functional relationship networks inform autism spectrum disorder gene prediction.Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibility.The integrated landscape of causal genes and pathways in schizophrenia.A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literature.Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster.Integrated multifactor analysis explores core dysfunctional modules in autism spectrum disorder.Prioritization and functional assessment of noncoding variants associated with complex diseases.Mutations (DNMs) in Autism Spectrum Disorder (ASD): Pathway and Network Analysis
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P2860
Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder
description
2016 nî lūn-bûn
@nan
2016 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Genome-wide prediction and fun ...... is of autism spectrum disorder
@ast
Genome-wide prediction and fun ...... is of autism spectrum disorder
@en
Genome-wide prediction and fun ...... is of autism spectrum disorder
@nl
type
label
Genome-wide prediction and fun ...... is of autism spectrum disorder
@ast
Genome-wide prediction and fun ...... is of autism spectrum disorder
@en
Genome-wide prediction and fun ...... is of autism spectrum disorder
@nl
prefLabel
Genome-wide prediction and fun ...... is of autism spectrum disorder
@ast
Genome-wide prediction and fun ...... is of autism spectrum disorder
@en
Genome-wide prediction and fun ...... is of autism spectrum disorder
@nl
P2093
P2860
P50
P356
P1433
P1476
Genome-wide prediction and fun ...... is of autism spectrum disorder
@en
P2093
Alan Packer
Alicja Tadych
Chandra L Theesfeld
Natalia Volfovsky
Olga G Troyanskaya
P2860
P2888
P304
P356
10.1038/NN.4353
P407
P577
2016-08-01T00:00:00Z