Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes - Wikidata - awgldk - TriplyDB

Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes

Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes

http://www.wikidata.org/entity/Q35103491

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DISC1: a key lead in studying cortical development and associated brain disorders RNA Sequencing in Schizophrenia Transcriptomics of cortical gray matter thickness decline during normal aging Analysis of schizophrenia-related genes and electrophysiological measures reveals ZNF804A association with amplitude of P300b elicited by novel sounds.Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk.Type I interferon signaling genes in recurrent major depression: increased expression detected by whole-blood RNA sequencing Allele-specific regulation of DISC1 expression by miR-135b-5p Role of disrupted in schizophrenia 1 (DISC1) in stress-induced prefrontal cognitive dysfunction.708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.Category fluency, latent semantic analysis and schizophrenia: a candidate gene approach Selected rapporteur summaries from the XX World Congress of Psychiatric Genetics, Hamburg, Germany, October 14-18, 2012.A sequence variant in human KALRN impairs protein function and coincides with reduced cortical thickness.Linking neurodevelopmental and synaptic theories of mental illness through DISC1 Shared intermediate phenotypes for schizophrenia and bipolar disorder: neuroanatomical features of subtypes distinguished by executive dysfunction.Disrupted-in-Schizophrenia-1 SNPs and Susceptibility to Schizophrenia: Evidence from Malaysia.Association between 5q23.2-located polymorphism of CTXN3 gene (Cortexin 3) and schizophrenia in European-Caucasian males; implications for the aetiology of schizophrenia.DISC1 and Striatal Volume: A Potential Risk Phenotype For mental Illness.The cortical thickness phenotype of individuals with DISC1 translocation resembles schizophrenia.Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.DISC1 Protein Regulates γ-Aminobutyric Acid, Type A (GABAA) Receptor Trafficking and Inhibitory Synaptic Transmission in Cortical Neurons.DISC1 genetics, biology and psychiatric illness Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function.Evidence for single nucleotide polymorphisms and their association with bipolar disorder.DISC1 as a therapeutic target for mental illnesses.Disorders and borders: psychiatric genetics and nosology.Voluntary exercise improves cognitive deficits in female dominant-negative DISC1 transgenic mouse model of neuropsychiatric disorders.Psychiatric behaviors associated with cytoskeletal defects in radial neuronal migration.Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31.Effect of DISC1 SNPs on brain structure in healthy controls and patients with a history of psychosis.Additive sex-specific influence of common non-synonymous DISC1 variants on amygdala, basal ganglia, and white cortical surface area in healthy young adults.Association of DISC1 variants with age of onset in a population-based sample of recurrent major depression.Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia.Altered DNA methylation associated with a translocation linked to major mental illness.Shared effects of DISC1 disruption and elevated WNT signaling in human cerebral organoids.DISC1 is a coordinator of intracellular trafficking to shape neuronal development and connectivity.Mammalian TRIM67 Functions in Brain Development and Behavior.Convergence of independent DISC1 mutations on impaired neurite growth via decreased UNC5D expression

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Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes

http://www.wikidata.org/entity/Q35103491

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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2011年の論文

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Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes

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Molecular Psychiatry

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Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes

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R Duggirala

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P2860

The DISC1 pathway modulates expression of neurodevelopmental, synaptogenic and sensory perception genes

Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia

Dorsal anterior cingulate cortex: a role in reward-based decision making

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

Cortical Surface-Based Analysis

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

Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

Chromosome 1 loci in Finnish schizophrenia families

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