Rare chromosomal deletions and duplications increase risk of schizophrenia
about
The DISC1 pathway modulates expression of neurodevelopmental, synaptogenic and sensory perception genesAdvanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhoodGenome-wide copy number analysis uncovers a new HSCR gene: NRG3Human genetics and genomics a decade after the release of the draft sequence of the human genomeBAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss familyFinding the missing heritability of complex diseasesThe shock of the new: progress in schizophrenia genomicsThe Kraepelinian dichotomy - going, going... but still not goneThe dopamine hypothesis of schizophrenia: version III--the final common pathwayEvolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophreniaDUF1220 domains, cognitive disease, and human brain evolutionGenome-wide association study of Tourette's syndromeRare deletions at the neurexin 3 locus in autism spectrum disorderDisrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signalingSchizophrenia is associated with an increase in cortical microRNA biogenesisFunctional impact of global rare copy number variation in autism spectrum disordersPopulation structure and genome-wide patterns of variation in Ireland and BritainPharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysisCNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.Using ERDS to infer copy-number variants in high-coverage genomesRare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genesEvolutionary history and genome organization of DUF1220 protein domainsCommon variants conferring risk of schizophreniaGenome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsRecurrent 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?Modelling schizophrenia using human induced pluripotent stem cells.Microduplications of 16p11.2 are associated with schizophreniaCase-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genesCopy number variation at 1q21.1 associated with neuroblastomaA genome-wide study of common SNPs and CNVs in cognitive performance in the CANTABGenome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.Disruption of the neurexin 1 gene is associated with schizophreniaRecurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalitiesNeurexin 1 (NRXN1) deletions in schizophreniaCopy number variation and schizophrenia
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P2860
Rare chromosomal deletions and duplications increase risk of schizophrenia
description
2008 nî lūn-bûn
@nan
2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի սեպտեմբերին 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
Rare chromosomal deletions and duplications increase risk of schizophrenia
@ast
Rare chromosomal deletions and duplications increase risk of schizophrenia
@en
Rare chromosomal deletions and duplications increase risk of schizophrenia
@en-gb
Rare chromosomal deletions and duplications increase risk of schizophrenia
@nl
type
label
Rare chromosomal deletions and duplications increase risk of schizophrenia
@ast
Rare chromosomal deletions and duplications increase risk of schizophrenia
@en
Rare chromosomal deletions and duplications increase risk of schizophrenia
@en-gb
Rare chromosomal deletions and duplications increase risk of schizophrenia
@nl
prefLabel
Rare chromosomal deletions and duplications increase risk of schizophrenia
@ast
Rare chromosomal deletions and duplications increase risk of schizophrenia
@en
Rare chromosomal deletions and duplications increase risk of schizophrenia
@en-gb
Rare chromosomal deletions and duplications increase risk of schizophrenia
@nl
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Rare chromosomal deletions and duplications increase risk of schizophrenia
@en
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10.1038/NATURE07239
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2008-09-11T00:00:00Z
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1040865418