Rare inherited variation in autism: beginning to see the forest and a few trees.
about
From mouse to human: evolutionary genomics analysis of human orthologs of essential genesThe cerebellum, sensitive periods, and autism.Disentangling the heterogeneity of autism spectrum disorder through genetic findingsAutism spectrum disorder severity reflects the average contribution of de novo and familial influences.Autism traits in the RASopathies.Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects.Performance comparison of bench-top next generation sequencers using microdroplet PCR-based enrichment for targeted sequencing in patients with autism spectrum disorderRecurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins.Sex differences in brain plasticity: a new hypothesis for sex ratio bias in autismCerebellar associative sensory learning defects in five mouse autism models.Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.Genetic research in autism spectrum disordersQuantitative autistic trait measurements index background genetic risk for ASD in Hispanic familiesInvestigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes.A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism.Human pluripotent stem cell models of autism spectrum disorder: emerging frontiers, opportunities, and challenges towards neuronal networks in a dishThe future of genomics for developmentalists.Copy-number variation in the pathogenesis of autism spectrum disorder.Epigenetic Treatment of Neuropsychiatric Disorders: Autism and Schizophrenia.Pharmacogenomics of autism spectrum disorder.mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.Increased female autosomal burden of rare copy number variants in human populations and in autism families.Motor abnormalities as a putative endophenotype for Autism Spectrum DisordersDynamic scaffolds for neuronal signaling: in silico analysis of the TANC protein family.Are We "Motorically" Wired to Others? High-Level Motor Computations and Their Role in Autism.Association of oligodendrocytes differentiation regulator gene DUSP15 with autism.Mutations (DNMs) in Autism Spectrum Disorder (ASD): Pathway and Network Analysis
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P2860
Rare inherited variation in autism: beginning to see the forest and a few trees.
description
2013 nî lūn-bûn
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2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年學術文章
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name
Rare inherited variation in autism: beginning to see the forest and a few trees.
@en
Rare inherited variation in autism: beginning to see the forest and a few trees.
@nl
type
label
Rare inherited variation in autism: beginning to see the forest and a few trees.
@en
Rare inherited variation in autism: beginning to see the forest and a few trees.
@nl
prefLabel
Rare inherited variation in autism: beginning to see the forest and a few trees.
@en
Rare inherited variation in autism: beginning to see the forest and a few trees.
@nl
P2860
P1433
P1476
Rare inherited variation in autism: beginning to see the forest and a few trees.
@en
P2093
Neelroop N Parikshak
P2860
P304
P356
10.1016/J.NEURON.2013.01.010
P407
P577
2013-01-01T00:00:00Z