Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments. - Wikidata - awgldk - TriplyDB

Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.

Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.

http://www.wikidata.org/entity/Q52580896

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Isolated populations and complex disease gene identification The genetics of bipolar disorder GRM7 variants confer susceptibility to age-related hearing impairment Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort DISC1-binding proteins in neural development, signalling and schizophrenia Database of genetic studies of bipolar disorder Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders.Effects of background mutations and single nucleotide polymorphisms (SNPs) on the Disc1 L100P behavioral phenotype associated with schizophrenia in mice.DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis Category fluency, latent semantic analysis and schizophrenia: a candidate gene approach A Gene-Based Analysis of Acoustic Startle Latency.Neurocognitive-genetic and neuroimaging-genetic research paradigms in schizophrenia and bipolar disorder.Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.Differential effects of prenatal and postnatal expressions of mutant human DISC1 on neurobehavioral phenotypes in transgenic mice: evidence for neurodevelopmental origin of major psychiatric disorders.Zinc finger protein 804A (ZNF804A) and verbal deficits in individuals with autism.Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.DISC1 Ser704Cys impacts thalamic-prefrontal connectivity.Association of variants in DISC1 with psychosis-related traits in a large population cohort Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes Common functional polymorphisms of DISC1 and cortical maturation in typically developing children and adolescents.Association between 5q23.2-located polymorphism of CTXN3 gene (Cortexin 3) and schizophrenia in European-Caucasian males; implications for the aetiology of schizophrenia.Nature and nurture in neuropsychiatric genetics: where do we stand?Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex Aggregated proteins in schizophrenia and other chronic mental diseases: DISC1opathies Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.Beyond the brain: disrupted in schizophrenia 1 regulates pancreatic β-cell function via glycogen synthase kinase-3β.Effect of DISC1 on the P300 waveform in psychosis Genetic association of cyclic AMP signaling genes with bipolar disorder.DISC1 genetics, biology and psychiatric illness Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.Intermediate: cognitive phenotypes in bipolar disorder.Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample.Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.Power of genetic association studies in the presence of linkage disequilibrium and allelic heterogeneity.Gene expression alterations related to mania and psychosis in peripheral blood of patients with a first episode of psychosis.DISCopathies: brain disorders related to DISC1 dysfunction.Biological roles of translin and translin-associated factor-X: RNA metabolism comes to the fore.Ndel1, Nudel (Noodle): flexible in the cell?Neurodevelopmental Perspectives on Wnt Signaling in Psychiatry.

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Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.

http://www.wikidata.org/entity/Q52580896

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2007 nî lūn-bûn

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Association of distinct alleli ...... erlying cognitive impairments.

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Association of distinct alleli ...... erlying cognitive impairments.

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Association of distinct alleli ...... erlying cognitive impairments.

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Human Molecular Genetics

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Association of distinct alleli ...... erlying cognitive impairments.

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Mervi Antila

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Outi M Palo

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Pia Soronen

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Tiina Paunio

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Tuula Kieseppä

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P2860

DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

DISC1-NDEL1/NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1

Isolation and characterization of a cDNA encoding a Translin-like protein, TRAX

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

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

The endophenotype concept in psychiatry: etymology and strategic intentions

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

Chromosome 1 loci in Finnish schizophrenia families

Disrupted in Schizophrenia 1 and Nudel form a neurodevelopmentally regulated protein complex: implications for schizophrenia and other major neurological disorders

A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder

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20

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16

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Leena Peltonen-Palotie

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Leena Helena Kilpinen-barrett

Annamari Tuulio-Henriksson

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