Microduplications of 16p11.2 are associated with schizophrenia - Test2 - elhamkhani - TriplyDB

Microduplications of 16p11.2 are associated with schizophrenia

Microduplications of 16p11.2 are associated with schizophrenia

http://www.wikidata.org/entity/Q24634151

about

TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia Human-specific histone methylation signatures at transcription start sites in prefrontal neurons The Kraepelinian dichotomy - going, going... but still not gone Autism risk factors: genes, environment, and gene-environment interactions Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder Mapping copy number variation by population-scale genome sequencing Modelling schizophrenia using human induced pluripotent stem cells.Prenatal Neurogenesis in Autism Spectrum Disorders Genetics and genomics of psychiatric disease Characterizing autism spectrum disorders by key biochemical pathways.Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia.Predicting the risk of psychosis onset: advances and prospects CNVs: harbingers of a rare variant revolution in psychiatric genetics The impact of human copy number variation on gene expression Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes Coronin 1 regulates cognition and behavior through modulation of cAMP/protein kinase A signaling Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men Structural variation mutagenesis of the human genome: Impact on disease and evolution.CNVs in neuropsychiatric disorders Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications Evidence for the role of EPHX2 gene variants in anorexia nervosa Quaking regulates Hnrnpa1 expression through its 3' UTR in oligodendrocyte precursor cells Data use under the NIH GWAS data sharing policy and future directions The Danish 22q11 research initiative The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations The role of genetics in the etiology of schizophrenia Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism CNVs conferring risk of autism or schizophrenia affect cognition in controls Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes.16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions.Using whole-exome sequencing to identify inherited causes of autism.Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.JNK1 controls dendritic field size in L2/3 and L5 of the motor cortex, constrains soma size, and influences fine motor coordination.Imaging and genetics of language and cognition in pediatric epilepsy The interleukin 3 gene (IL3) contributes to human brain volume variation by regulating proliferation and survival of neural progenitors

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P2860

Microduplications of 16p11.2 are associated with schizophrenia

http://www.wikidata.org/entity/Q24634151

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

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

name

Microduplications of 16p11.2 are associated with schizophrenia

@ast

Microduplications of 16p11.2 are associated with schizophrenia

@en

Microduplications of 16p11.2 are associated with schizophrenia

@nl

type

label

Microduplications of 16p11.2 are associated with schizophrenia

@ast

Microduplications of 16p11.2 are associated with schizophrenia

@en

Microduplications of 16p11.2 are associated with schizophrenia

@nl

prefLabel

Microduplications of 16p11.2 are associated with schizophrenia

@ast

Microduplications of 16p11.2 are associated with schizophrenia

@en

Microduplications of 16p11.2 are associated with schizophrenia

@nl

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Nature Genetics

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Microduplications of 16p11.2 are associated with schizophrenia

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Abhishek Bhandari

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Anil K Malhotra

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Anthony Leotta

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B Lakshmi

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Chad Haldeman-Englert

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Clara M Lajonchere

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Curtis K Deutsch

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David Skuse

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

Deborah L Levy

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

Dheeraj Malhotra

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

P2860

Mapping Early Brain Development in Autism

Rare chromosomal deletions and duplications increase risk of schizophrenia

Strong association of de novo copy number mutations with autism

Disruption of neurexin 1 associated with autism spectrum disorder.

Disruption of the neurexin 1 gene is associated with schizophrenia

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

Large recurrent microdeletions associated with schizophrenia

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

Structural variation of chromosomes in autism spectrum disorder

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

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2574345

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10.1038/NG.474

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11

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41

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Marcella Rietschel

Terho Lehtimäki

Michael C O'Donovan

Francis J. McMahon

Markus M Nöthen

Detelina Grozeva

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2009-11-01T00:00:00Z

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38034818

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1011794963

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19855392

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