Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
about
Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.Etiology in psychiatry: embracing the reality of poly-gene-environmental causation of mental illnessVariability of DNA Methylation within Schizophrenia Risk Loci across Subregions of Human Hippocampus.Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.Comparative analysis of MBD-seq and MeDIP-seq and estimation of gene expression changes in a rodent model of schizophrenia.Schizophrenia genetics in the genome-wide era: a review of Japanese studies.Mapping the Consequences of Impaired Synaptic Plasticity in Schizophrenia through Development: An Integrative Model for Diverse Clinical Features.A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.10 Years of GWAS Discovery: Biology, Function, and Translation.Translating advances in the molecular basis of schizophrenia into novel cognitive treatment strategies.Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.Genetics of Schizophrenia: Ready to Translate?Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci.Schizophrenia and the dynamic genome.Evaluating Synthetic Activation and Repression of Neuropsychiatric-Related Genes in hiPSC-Derived NPCs, Neurons, and Astrocytes.Dosage-sensitive genes in evolution and disease.Schizophrenia and the neurodevelopmental continuum:evidence from genomicsDivergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis.Schizophrenia: What's Arc Got to Do with It?CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.Decreased Brain pH as a Shared Endophenotype of Psychiatric Disorders.A Upf3b-mutant mouse model with behavioral and neurogenesis defects.Whole genome sequencing in psychiatric disorders: the WGSPD consortium.The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project.Psychiatric Genomics: An Update and an Agenda.Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains.Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.The association between gene variants and longitudinal structural brain changes in psychosis: a systematic review of longitudinal neuroimaging genetics studies.Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders.Synaptic Neurexin Complexes: A Molecular Code for the Logic of Neural Circuits.Critical Reappraisal of Mechanistic Links of Copy Number Variants to Dimensional Constructs of Neuropsychiatric Disorders in Mouse Models.CHRFAM7A gene expression in schizophrenia: clinical correlates and the effect of antipsychotic treatment.A mouse model of the schizophrenia-associated 1q21.1 microdeletion syndrome exhibits altered mesolimbic dopamine transmission.White matter abnormalities in 22q11.2 deletion syndrome patients showing cognitive decline.Advancing psychiatric genetics through dissecting heterogeneity.Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?Ulk4 regulates GABAergic signaling and anxiety-related behavior.Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.Genetic and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus.
P2860
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P2860
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Contribution of copy number va ...... wide study of 41,321 subjects.
@en
Contribution of copy number va ...... wide study of 41,321 subjects.
@nl
type
label
Contribution of copy number va ...... wide study of 41,321 subjects.
@en
Contribution of copy number va ...... wide study of 41,321 subjects.
@nl
prefLabel
Contribution of copy number va ...... wide study of 41,321 subjects.
@en
Contribution of copy number va ...... wide study of 41,321 subjects.
@nl
P2093
P2860
P50
P356
P1433
P1476
Contribution of copy number va ...... wide study of 41,321 subjects.
@en
P2093
Aaron R Wolen
Abraham Reichenberg
Adam Savitz
Aiden Corvin
Alan R Sanders
Alexander L Richards
Alkes Price
Andrea Hofman
Andreas J Forstner
Andrew McQuillin
P2507
P2860
P2888
P356
10.1038/NG.3725
P407
P50
P577
2016-11-21T00:00:00Z