CNVs conferring risk of autism or schizophrenia affect cognition in controls - Wikidata - awgldk - TriplyDB

CNVs conferring risk of autism or schizophrenia affect cognition in controls

CNVs conferring risk of autism or schizophrenia affect cognition in controls

http://www.wikidata.org/entity/Q29308426

about

Genetics and genomics of psychiatric disease Human molecular cytogenetics: From cells to nucleotides Brain-specific Crmp2 deletion leads to neuronal development deficits and behavioural impairments in mice Investigating the effects of copy number variants on reading and language performance.A mouse model of the 15q13.3 microdeletion syndrome shows prefrontal neurophysiological dysfunctions and attentional impairment.A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Perspective-taking abilities in the balance between autism tendencies and psychosis proneness The role of sex-differential biology in risk for autism spectrum disorder The 15q11.2 BP1-BP2 microdeletion syndrome: a review CNVs in neuropsychiatric disorders Autism As a Disorder of High Intelligence Cyfip1 Regulates Presynaptic Activity during Development Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals Directional dominance on stature and cognition in diverse human populations Extracting research-quality phenotypes from electronic health records to support precision medicine Common genetic variants associated with cognitive performance identified using the proxy-phenotype method Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.Dissecting the genetics of complex traits using summary association statistics Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice.Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.16p11.2 Deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks Periventricular white matter abnormalities and restricted repetitive behavior in autism spectrum disorder.State-dependent architecture of thalamic reticular subnetworks.Cognitive Effort and Schizophrenia Modulate Large-Scale Functional Brain Connectivity A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.Prenatal sonographic diagnosis of urorectal septum malformation sequence and chromosomal microarray analysis: A case report and review of the literature.[Neurobiology of schizophrenia: new findings from the structure to the molecules].The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data NMDA receptor-deficient mice display sexual dimorphism in the onset and severity of behavioural abnormalities.Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes."Gestaltomics": Systems Biology Schemes for the Study of Neuropsychiatric Diseases.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Reproductive fitness and genetic risk of psychiatric disorders in the general population.Prioritization of neurodevelopmental disease genes by discovery of new mutations.Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10 ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data.The importance of copy number variation in congenital heart disease

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P2860

CNVs conferring risk of autism or schizophrenia affect cognition in controls

http://www.wikidata.org/entity/Q29308426

description

2013 nî lūn-bûn

@nan

2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

CNVs conferring risk of autism or schizophrenia affect cognition in controls

@ast

CNVs conferring risk of autism or schizophrenia affect cognition in controls

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type

label

CNVs conferring risk of autism or schizophrenia affect cognition in controls

@ast

CNVs conferring risk of autism or schizophrenia affect cognition in controls

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prefLabel

CNVs conferring risk of autism or schizophrenia affect cognition in controls

@ast

CNVs conferring risk of autism or schizophrenia affect cognition in controls

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CNVs conferring risk of autism or schizophrenia affect cognition in controls

@en

P2093

Adam J. Schwarz

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

Berglind Stefansdottir

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

Birna Jonsdottir

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

Brynja Magnusdottir

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

Evald Saemundsen

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

Gudbjorn F. Jonsson

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

Gudrun A. Jonsdottir

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

Heimir Snorrason

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

Isafold Helgadottir

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

Jonas G. Halldorsson

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

P2860

Microduplications of 16p11.2 are associated with schizophrenia

Large recurrent microdeletions associated with schizophrenia

CNVs: harbingers of a rare variant revolution in psychiatric genetics

A fast diffeomorphic image registration algorithm

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

Cognitive deficits in relatives of patients with schizophrenia: a meta-analysis

Dissociable intrinsic connectivity networks for salience processing and executive control

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Unified segmentation

Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome).

P2888

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361-366

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scholarly article

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379834

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10.1038/NATURE12818

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P433

7483

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P478

505

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P50

Hreinn Stefansson

Engilbert Sigurdsson

Andreas Meyer-Lindenberg

Johan Hilge Thygesen

Gyda Bjornsdottir

G. Bragi Walters

Kári Stefánsson

P577

2013-12-18T00:00:00Z

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259386996

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1043154470

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24352232

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