Large recurrent microdeletions associated with schizophrenia - sprookjes - yvandenbroek - TriplyDB

Large recurrent microdeletions associated with schizophrenia

Large recurrent microdeletions associated with schizophrenia

http://www.wikidata.org/entity/Q24654741

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Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy Understanding the impact of 1q21.1 copy number variant BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1 Finding the missing heritability of complex diseases The shock of the new: progress in schizophrenia genomics The Kraepelinian dichotomy - going, going... but still not gone A review of anti-inflammatory agents for symptoms of schizophrenia The dopamine hypothesis of schizophrenia: version III--the final common pathway Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia DUF1220 domains, cognitive disease, and human brain evolution The chimeric gene CHRFAM7A, a partial duplication of the CHRNA7 gene, is a dominant negative regulator of α7*nAChR function Structure and control of the actin regulatory WAVE complex Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling Chemical modulation of mutant mGlu1 receptors derived from deleterious GRM1 mutations found in schizophrenics Schizophrenia is associated with an increase in cortical microRNA biogenesis Common genetic variation and performance on standardized cognitive tests Diversity of human copy number variation and multicopy genes CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 Using ERDS to infer copy-number variants in high-coverage genomes Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes The genetic basis of addictive disorders Common variants conferring risk of schizophrenia Mapping copy number variation by population-scale genome sequencing Direct measure of the de novo mutation rate in autism and schizophrenia cohorts An arrayed human genomic library constructed in the PAC shuttle vector pJCPAC-Mam2 for genome-wide association studies and gene therapy Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.Large, rare chromosomal deletions associated with severe early-onset obesity Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus Strong 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 schizophrenia Copy number variation at 1q21.1 associated with neuroblastoma A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB 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 schizophrenia

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P2860

Large recurrent microdeletions associated with schizophrenia

http://www.wikidata.org/entity/Q24654741

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

Large recurrent microdeletions associated with schizophrenia

@ast

Large recurrent microdeletions associated with schizophrenia

@en

Large recurrent microdeletions associated with schizophrenia

@nl

type

label

Large recurrent microdeletions associated with schizophrenia

@ast

Large recurrent microdeletions associated with schizophrenia

@en

Large recurrent microdeletions associated with schizophrenia

@nl

prefLabel

Large recurrent microdeletions associated with schizophrenia

@ast

Large recurrent microdeletions associated with schizophrenia

@en

Large recurrent microdeletions associated with schizophrenia

@nl

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Large recurrent microdeletions associated with schizophrenia

@en

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Andres Ingason

http://www.w3.org/2001/XMLSchema#string

Annamarie Tuulio-Henriksson

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Annette Hartmann

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Arnaldur Gylfason

http://www.w3.org/2001/XMLSchema#string

Asgeir Bjornsson

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Asgeir Sigurdsson

http://www.w3.org/2001/XMLSchema#string

August G Wang

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Bjarni V Halldorsson

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Brynja B Magnusdottir

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Caroline Crombie

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Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

Rare chromosomal deletions and duplications increase risk of schizophrenia

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

Connexin 50 gene on human chromosome 1q21 is associated with schizophrenia in matched case control and family-based studies

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

Disruption of two novel genes by a translocation co-segregating with schizophrenia

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

Association between microdeletion and microduplication at 16p11.2 and autism

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

Performance deficit of alpha7 nicotinic receptor knockout mice in a delayed matching-to-place task suggests a mild impairment of working/episodic-like memory

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232-6

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scholarly article

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379835

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10.1038/NATURE07229

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7210

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455

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Hans-Jürgen Möller

Marcella Rietschel

Leena Peltonen-Palotie

Hreinn Stefansson

Unnur Þorsteinsdóttir

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2008-09-11T00:00:00Z

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23138435

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1038869319

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18668039

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2687075

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