Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population
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The FMRP regulon: from targets to disease convergenceCYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formationDisruption of Arp2/3 results in asymmetric structural plasticity of dendritic spines and progressive synaptic and behavioral abnormalitiesGenetics of schizophrenia from a clinicial perspective.Potential Value of Genomic Copy Number Variations in Schizophrenia.Modeling a genetic risk for schizophrenia in iPSCs and mice reveals neural stem cell deficits associated with adherens junctions and polarity.A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus.Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.Reduced CYFIP1 in Human Neural Progenitors Results in Dysregulation of Schizophrenia and Epilepsy Gene Networks.Distribution of disease-associated copy number variants across distinct disorders of cognitive development.Synaptic Actin Dysregulation, a Convergent Mechanism of Mental Disorders?A replication study of schizophrenia-related rare copy number variations in a Han Southern Chinese population.Novel treatment strategies for schizophrenia from improved understanding of genetic risk.From Prader-Willi syndrome to psychosis: translating parent-of-origin effects into schizophrenia research.Progress in genome-wide association studies of schizophrenia in Han Chinese populations.Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism.Genetic and epigenetic mechanisms of epilepsy: a review.Using mouse transgenic and human stem cell technologies to model genetic mutations associated with schizophrenia and autism.The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
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P2860
Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Rare CNVs and tag SNPs at 15q1 ...... in the Han Chinese population
@ast
Rare CNVs and tag SNPs at 15q1 ...... in the Han Chinese population
@en
type
label
Rare CNVs and tag SNPs at 15q1 ...... in the Han Chinese population
@ast
Rare CNVs and tag SNPs at 15q1 ...... in the Han Chinese population
@en
prefLabel
Rare CNVs and tag SNPs at 15q1 ...... in the Han Chinese population
@ast
Rare CNVs and tag SNPs at 15q1 ...... in the Han Chinese population
@en
P2093
P2860
P356
P1476
Rare CNVs and tag SNPs at 15q1 ...... in the Han Chinese population
@en
P2093
David St Clair
GuoYin Feng
XinZhi Zhao
P2860
P304
P356
10.1093/SCHBUL/SBR197
P407
P577
2012-02-08T00:00:00Z