Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. - Wikidata - wikimedia - TriplyDB

Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22.

Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22.

http://www.wikidata.org/entity/Q33909819

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Increased expression in dorsolateral prefrontal cortex of CAPON in schizophrenia and bipolar disorder.Association of RGS4 variants with schizotypy and cognitive endophenotypes at the population level Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia Does the CAPON gene confer susceptibility to schizophrenia?NOS1AP regulates dendrite patterning of hippocampal neurons through a carboxypeptidase E-mediated pathway NOS1AP associates with Scribble and regulates dendritic spine development.Mismatch negativity and cognitive performance for the prediction of psychosis in subjects with at-risk mental state.Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.Association of RGS2 and RGS5 variants with schizophrenia symptom severity.Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.FBXL21 association with schizophrenia in Irish family and case-control samples.Finding schizophrenia genes.Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate.A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.Oxidative stress in schizophrenia: an integrated approach.Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIalpha gene (PIP5K2A) with schizophrenia.The genetics of schizophrenia and bipolar disorder: dissecting psychosis Genome-wide linkage scan of bipolar disorder in a Colombian population isolate replicates Loci on chromosomes 7p21-22, 1p31, 16p12 and 21q21-22 and identifies a novel locus on chromosome 12q.Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls.Childhood trauma and genetic factors in familial schizophrenia associated with the NOS1AP gene Heritability of neurocognitive traits in familial schizophrenia Tumor necrosis factor promoter haplotype associated with schizophrenia reveals a linked locus on 1q44.Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples Nitric oxide synthase 1 adaptor protein, a protein implicated in schizophrenia, controls radial migration of cortical neurons.Role of nitric oxide and related molecules in schizophrenia pathogenesis: biochemical, genetic and clinical aspects.Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.New roles of carboxypeptidase E in endocrine and neural function and cancer.Early environmental exposures influence schizophrenia expression even in the presence of strong genetic predisposition.Genetics of developmental psychiatric disorders: pathways to discovery The neuropathology of autism: a review.Clustering of metabolic comorbidity in schizophrenia: a genetic contribution?Association of synapsin 2 with schizophrenia in families of Northern European ancestry Schizophrenia genetics: uncovering positional candidate genes.Generation of a cre recombinase-conditional Nos1ap over-expression transgenic mouse Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.Basic helix-loop-helix transcription factor NEUROG1 and schizophrenia: effects on illness susceptibility, MRI brain morphometry and cognitive abilities NOS1AP in schizophrenia Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland

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P2860

Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22.

http://www.wikidata.org/entity/Q33909819

description

2004 nî lūn-bûn

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2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2004 թվականի ապրիլին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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name

Linkage disequilibrium mapping ...... PON region of chromosome 1q22.

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Linkage disequilibrium mapping ...... PON region of chromosome 1q22.

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type

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Linkage disequilibrium mapping ...... PON region of chromosome 1q22.

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Linkage disequilibrium mapping ...... PON region of chromosome 1q22.

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Linkage disequilibrium mapping ...... PON region of chromosome 1q22.

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Linkage disequilibrium mapping ...... PON region of chromosome 1q22.

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American Journal of Human Genetics

P1476

Linkage disequilibrium mapping ...... PON region of chromosome 1q22.

@en

P2093

Anne S Bassett

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

Eva W C Chow

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

Jaime Simone

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

Jared E Hayter

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

Kathleen A Hodgkinson

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

Linda M Brzustowicz

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Paria Mohseni

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P2860

CAPON: a protein associated with neuronal nitric oxide synthase that regulates its interactions with PSD95

Neuronal nitric-oxide synthase localization mediated by a ternary complex with synapsin and CAPON.

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

Dexras1: a G protein specifically coupled to neuronal nitric oxide synthase via CAPON

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

Hypoxic-ischemia-related fetal/neonatal complications and risk of schizophrenia and other nonaffective psychoses: a 19-year longitudinal study

Genes for schizophrenia? Recent findings and their pathophysiological implications

Dexras1/AGS-1 inhibits signal transduction from the Gi-coupled formyl peptide receptor to Erk-1/2 MAP kinases

Nitrosopeptide mapping: a novel methodology reveals s-nitrosylation of dexras1 on a single cysteine residue

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1057-1063

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10.1086/420774

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5

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74

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2004-04-02T00:00:00Z

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8636630

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15065015

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1181969

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