Relative burden of large CNVs on a range of neurodevelopmental phenotypes. - Test2 - elhamkhani - TriplyDB

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

http://www.wikidata.org/entity/Q34079175

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Lamarckian evolution explains human brain evolution and psychiatric disorders Autism risk factors: genes, environment, and gene-environment interactions Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder Genetic screening for the risk of type 2 diabetes: worthless or valuable?A genetic model for neurodevelopmental disease Investigating the effects of copy number variants on reading and language performance.Function and regulation of AUTS2, a gene implicated in autism and human evolution Functional consequences of 17q21.31/WNT3-WNT9B amplification in hPSCs with respect to neural differentiation Evidence for the role of EPHX2 gene variants in anorexia nervosa Possible functional links among brain- and skull-related genes selected in modern humans Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population ASD-relevant Animal Models of the Foxp Family of Transcription Factors RhoGTPase Regulators Orchestrate Distinct Stages of Synaptic Development.The Correlation-Base-Selection Algorithm for Diagnostic Schizophrenia Based on Blood-Based Gene Expression Signatures Heterozygous Disruption of Autism susceptibility candidate 2 Causes Impaired Emotional Control and Cognitive Memory The genetics of reading disabilities: from phenotypes to candidate genes Translational animal models of autism and neurodevelopmental disorders.Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications.Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis.Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins.Genetics of schizophrenia from a clinicial perspective.Neuronal Migration and AUTS2 Syndrome.Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants Identification of structural variation in mouse genomes.Selected rapporteur summaries from the XX World Congress of Psychiatric Genetics, Hamburg, Germany, October 14-18, 2012.Bio-collections in autism research.Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID).The genetic variability and commonality of neurodevelopmental disease.Schizophrenia: an integrated sociodevelopmental-cognitive model.Genomic studies in fragile X premutation carriers.Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy.Phenotypic impact of genomic structural variation: insights from and for human disease.Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes.Lessons from model organisms: phenotypic robustness and missing heritability in complex disease.An integrated map of structural variation in 2,504 human genomes.Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.

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P2860

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

http://www.wikidata.org/entity/Q34079175

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2011 nî lūn-bûn

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2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2011年の論文

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2011年論文

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2011年論文

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2011年论文

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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prefLabel

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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Evan E Eichler

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Laura Vives

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Neil Shafer

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11

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Margherita Cirillo Silengo

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2011-11-10T00:00:00Z

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51816942

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