Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network. - Wikidata - awgldk - TriplyDB

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.

http://www.wikidata.org/entity/Q37487752

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Disruptive CHD8 mutations define a subtype of autism early in development Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies Genetics and genomics of psychiatric disease Toward a Deeper Understanding of the Genetics of Bipolar Disorder Genetic changes shaping the human brain Consortium on the Genetics of Schizophrenia (COGS) assessment of endophenotypes for schizophrenia: an introduction to this Special Issue of Schizophrenia Research.The developmental transcriptome of the human brain: implications for neurodevelopmental disorders The SLC6 transporters: perspectives on structure, functions, regulation, and models for transporter dysfunction Beyond modules and hubs: the potential of gene coexpression networks for investigating molecular mechanisms of complex brain disorders Circadian rhythms and mood: opportunities for multi-level analyses in genomics and neuroscience: circadian rhythm dysregulation in mood disorders provides clues to the brain's organizing principles, and a touchstone for genomics and neuroscience Genome-scale neurogenetics: methodology and meaning Schizophrenia as a disorder of molecular pathways Nonsense-mediated mRNA decay: inter-individual variability and human disease Genetic and genomic analyses as a basis for new diagnostic nosologies The contribution of de novo coding mutations to autism spectrum disorder Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia Genetic variants in Alzheimer disease - molecular and brain network approaches De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome Comparison of the heritability of schizophrenia and endophenotypes in the COGS-1 family study.Toll-like receptor-2 deficiency induces schizophrenia-like behaviors in mice Network analysis of GWAS data Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery.Genome-wide analysis of differential RNA editing in epilepsy.Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics.Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability Rare damaging variants in DNA repair and cell cycle pathways are associated with hippocampal and cognitive dysfunction: a combined genetic imaging study in first-episode treatment-naive patients with schizophrenia.De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activity.Transcriptomic evidence for immaturity of the prefrontal cortex in patients with schizophrenia.Prioritization of neurodevelopmental disease genes by discovery of new mutations.Psychiatric disorders: diagnosis to therapy Dysregulated nitric oxide signaling as a candidate mechanism of fragile X syndrome and other neuropsychiatric disorders.Telomere length, family history, and paternal age in schizophrenia.Prenatal expression patterns of genes associated with neuropsychiatric disorders.Refining analyses of copy number variation identifies specific genes associated with developmental delay Phenotypic differences in hiPSC NPCs derived from patients with schizophrenia.Association of NCAM1 polymorphisms with autism and parental age at conception in a Chinese Han population.Systematic prioritization and integrative analysis of copy number variations in schizophrenia reveal key schizophrenia susceptibility genes.

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Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.

http://www.wikidata.org/entity/Q37487752

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Spatial and temporal mapping o ...... l prefrontal cortical network.

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J.CELL.2013.06.049

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Spatial and temporal mapping o ...... l prefrontal cortical network.

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Amanda C Watts

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Anne M Thornton

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Caitlin Rippey

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Consortium on the Genetics of Schizophrenia (COGS)

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David L Braff

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Hashem Shahin

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Jon M McClellan

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Ming K Lee

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Neal R Swerdlow

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PAARTNERS Study Group

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P2860

Rare chromosomal deletions and duplications increase risk of schizophrenia

Dynamic mapping of human cortical development during childhood through early adulthood.

Medicine. The future of psychiatric research: genomes and neural circuits

Experience and the developing prefrontal cortex

Rate of de novo mutations and the importance of father's age to disease risk

Modelling schizophrenia using human induced pluripotent stem cells.

Strong association of de novo copy number mutations with autism

Specific contribution of human T-type calcium channel isotypes (alpha(1G), alpha(1H) and alpha(1I)) to neuronal excitability

GeneMANIA: a real-time multiple association network integration algorithm for predicting gene function

Large recurrent microdeletions associated with schizophrenia

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10.1016/J.CELL.2013.06.049

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Mary-Claire King

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2013-08-01T00:00:00Z

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