Strong association of de novo copy number mutations with sporadic schizophrenia
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The DISC1 pathway modulates expression of neurodevelopmental, synaptogenic and sensory perception genesNovel association strategy with copy number variation for identifying new risk Loci of human diseasesAdvanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhoodEffects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspringFinding the missing heritability of complex diseasesEvolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophreniaThe genetics of bipolar disorderMutations in NTRK3 suggest a novel signaling pathway in human congenital heart diseaseDisease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorderSchizophrenia is associated with an increase in cortical microRNA biogenesisDual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorderRare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genesDirect measure of the de novo mutation rate in autism and schizophrenia cohortsDe novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardationMicroRNA dysregulation in psychiatric diseaseStrong synaptic transmission impact by copy number variations in schizophrenia.CNV and nervous system diseases--what's new?Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.Disruption of the neurexin 1 gene is associated with schizophreniaCopy number variation and schizophreniaMicroRNAs: Key Regulators in the Central Nervous System and Their Implication in Neurological DiseasesSomatic mutations in disorders with disrupted brain connectivityThe molecular evolution of the vertebrate behavioural repertoireConverging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndromeSynaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia.Following the genes: a framework for animal modeling of psychiatric disordersToward developmental models of psychiatric disorders in zebrafishOrchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorderCNVs: harbingers of a rare variant revolution in psychiatric geneticsEssential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.New insights into the generation and role of de novo mutations in health and diseaseGenetic and genomic analyses as a basis for new diagnostic nosologiesRecent advances in the genetics of autoimmune diseaseCommon polygenic variation contributes to risk of schizophrenia and bipolar disorderPaternal age effect mutations and selfish spermatogonial selection: causes and consequences for human diseaseThe clustering of functionally related genes contributes to CNV-mediated diseaseNovel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in SchizophreniaGene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic riskAbnormal dosage of ultraconserved elements is highly disfavored in healthy cells but not cancer cells
P2860
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P2860
Strong association of de novo copy number mutations with sporadic schizophrenia
description
2008 nî lūn-bûn
@nan
2008 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Strong association of de novo copy number mutations with sporadic schizophrenia
@ast
Strong association of de novo copy number mutations with sporadic schizophrenia
@en
Strong association of de novo copy number mutations with sporadic schizophrenia
@nl
type
label
Strong association of de novo copy number mutations with sporadic schizophrenia
@ast
Strong association of de novo copy number mutations with sporadic schizophrenia
@en
Strong association of de novo copy number mutations with sporadic schizophrenia
@nl
prefLabel
Strong association of de novo copy number mutations with sporadic schizophrenia
@ast
Strong association of de novo copy number mutations with sporadic schizophrenia
@en
Strong association of de novo copy number mutations with sporadic schizophrenia
@nl
P2093
P2860
P3181
P356
P1433
P1476
Strong association of de novo copy number mutations with sporadic schizophrenia
@en
P2093
E J van Rensburg
Joseph A Gogos
Maria Karayiorgou
P2860
P2888
P304
P3181
P356
10.1038/NG.162
P407
P577
2008-05-30T00:00:00Z