Common genetic variants on 1p13.2 associate with risk of autism.
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Psychiatric genetics in China: achievements and challengesAssociation of genetic variants of GRIN2B with autism.Employment and financial burden of families with preschool children diagnosed with autism spectrum disorders in urban China: results from a descriptive study.Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in China.BCAS2 Regulates Delta-Notch Signaling Activity through Delta Pre-mRNA Splicing in Drosophila Wing DevelopmentEvidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.Potential serum biomarkers from a metabolomics study of autismConditional Knockout of Breast Carcinoma Amplified Sequence 2 (BCAS2) in Mouse Forebrain Causes Dendritic Malformation via β-catenin.Neuropsychiatric genomics in precision medicine: diagnostics, gene discovery, and translation.Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression.Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.Genetic architecture, epigenetic influence and environment exposure in the pathogenesis of Autism.Identification of likely associations between cerebral folate deficiency and complex genetic- and metabolic pathogenesis of autism spectrum disorders by utilization of a pilot interaction modeling approach.Autism genetics - an overview.TRIM proteins and diseases.Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population.Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism.High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.Progress in Genetic Studies of Tourette's Syndrome.Excessive UBE3A dosage impairs retinoic acid signaling and synaptic plasticity in autism spectrum disorders.Association of oligodendrocytes differentiation regulator gene DUSP15 with autism.Novel functional variants at the GWAS-implicated loci might confer risk to major depressive disorder, bipolar affective disorder and schizophrenia.Low-Rank Graph-Regularized Structured Sparse Regression for Identifying Genetic Biomarkers.
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P2860
Common genetic variants on 1p13.2 associate with risk of autism.
description
2013 nî lūn-bûn
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2013年の論文
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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
@zh-hans
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2013年學術文章
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name
Common genetic variants on 1p13.2 associate with risk of autism.
@en
Common genetic variants on 1p13.2 associate with risk of autism.
@nl
type
label
Common genetic variants on 1p13.2 associate with risk of autism.
@en
Common genetic variants on 1p13.2 associate with risk of autism.
@nl
prefLabel
Common genetic variants on 1p13.2 associate with risk of autism.
@en
Common genetic variants on 1p13.2 associate with risk of autism.
@nl
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Common genetic variants on 1p13.2 associate with risk of autism
@en
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D St Clair
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10.1038/MP.2013.146
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P50
P577
2013-11-05T00:00:00Z