Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders
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The shock of the new: progress in schizophrenia genomicsWhat causes attention deficit hyperactivity disorder?forestSV: structural variant discovery through statistical learningConverging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndromeFollowing the genes: a framework for animal modeling of psychiatric disordersToward developmental models of psychiatric disorders in zebrafishChild development and molecular genetics: 14 years laterCNVs: harbingers of a rare variant revolution in psychiatric geneticsAmish revisited: next-generation sequencing studies of psychiatric disorders among the Plain peopleMutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathologyGenetic aspects of autism spectrum disorders: insights from animal modelsGenetic Counseling for Autism Spectrum Disorder in an Evolving Theoretical LandscapePatterns and rates of exonic de novo mutations in autism spectrum disordersGenetics of smoking and depressionDUF1220 copy number is associated with schizophrenia risk and severity: implications for understanding autism and schizophrenia as related diseasesReconciling evidence-based medicine and precision medicine in the era of big data: challenges and opportunitiesGenome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorderNeural mechanisms underlying stress resilience in Ahi1 knockout mice: relevance to neuropsychiatric disordersDetection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes.Reductions in synaptic proteins and selective alteration of prepulse inhibition in male C57BL/6 mice after postnatal administration of a VIP receptor (VIPR2) agonist.Characterization of the deleted in autism 1 protein family: implications for studying cognitive disorders.Potential Impact of miR-137 and Its Targets in Schizophrenia.New frontiers in animal research of psychiatric illnessHierarchical Classes Analysis (HICLAS): A novel data reduction method to examine associations between biallelic SNPs and perceptual organization phenotypes in schizophrenia.De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.Genetics of schizophrenia from a clinicial perspective.Neuroscience. Preventable forms of autism?Large-scale genomics unveils the genetic architecture of psychiatric disordersThe genetics of Autism Spectrum Disorders--a guide for clinicians.CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree.High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.The psychosis susceptibility gene ZNF804A: associations, functions, and phenotypesEffects of genetic variations on microRNA: target interactionsDISC1 in schizophrenia: genetic mouse models and human genomic imaging.Construction and analysis of the protein-protein interaction networks for schizophrenia, bipolar disorder, and major depressionA sequence variant in human KALRN impairs protein function and coincides with reduced cortical thickness.Avoiding mouse traps in schizophrenia genetics: lessons and promises from current and emerging mouse models.A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.The hunt for gene effects pertinent to behavioral traits and psychiatric disorders: from mouse to human.An inherited small microdeletion at 15q13.3 in a patient with early-onset obsessive-compulsive disorder
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P2860
Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Rare structural variants in sc ...... e mutation, multiple disorders
@ast
Rare structural variants in sc ...... e mutation, multiple disorders
@en
type
label
Rare structural variants in sc ...... e mutation, multiple disorders
@ast
Rare structural variants in sc ...... e mutation, multiple disorders
@en
prefLabel
Rare structural variants in sc ...... e mutation, multiple disorders
@ast
Rare structural variants in sc ...... e mutation, multiple disorders
@en
P2860
P1433
P1476
Rare structural variants in sc ...... e mutation, multiple disorders
@en
P2093
Deborah L Levy
Shane E McCarthy
P2860
P304
P356
10.1016/J.TIG.2009.10.004
P577
2009-10-31T00:00:00Z