Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit. - Wikidata - awgldk - TriplyDB

Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit.

Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit.

http://www.wikidata.org/entity/Q34021154

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Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings Competing definitions of schizophrenia: what can be learned from polydiagnostic studies?Deleterious GRM1 mutations in schizophrenia Parkinson's disease and low frequency alleles found together throughout LRRK2.Patterns of deficits in brain function in bipolar disorder and schizophrenia: a cluster analytic study.Neurocognitive allied phenotypes for schizophrenia and bipolar disorder.Association study of the trinucleotide repeat polymorphism within SMARCA2 and schizophrenia.Hierarchical Classes Analysis (HICLAS): A novel data reduction method to examine associations between biallelic SNPs and perceptual organization phenotypes in schizophrenia.Cognitive heterogeneity in schizophrenia.A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry A genome-wide linkage scan for distinct subsets of schizophrenia characterized by age at onset and neurocognitive deficits.A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.Neurological soft signs in schizophrenia: a meta-analysis.Reduced dysbindin expression mediates N-methyl-D-aspartate receptor hypofunction and impaired working memory performance.Multivariate neuroanatomical classification of cognitive subtypes in schizophrenia: a support vector machine learning approach.Genetic variation in DTNBP1 influences general cognitive ability.Subtyping schizophrenia: implications for genetic research.The genetic deconstruction of psychosis Parkinson's disease in relation to pesticide exposure and nuclear encoded mitochondrial complex I gene variants.Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p.The diagnostic concept of schizophrenia: its history, evolution, and future prospects.Can genomics help usher schizophrenia into the age of RDoC and DSM-6?Using human brain imaging studies as a guide toward animal models of schizophrenia.The Consortium on the Genetics of Schizophrenia: neurocognitive endophenotypes.Variation and validation: the example of schizophrenia The power of linkage analysis of a disease-related endophenotype using asymmetrically ascertained sib pairs.Psychiatric research: psychoproteomics, degradomics and systems biology.Role of the cholinergic system in the pathology and treatment of schizophrenia.Schizophrenia: from the brain to peripheral markers. A consensus paper of the WFSBP task force on biological markers.No association observed between schizophrenia and non-HLA coeliac disease genes: integration with the initial MYO9B association with coeliac disease.Can genetics inform the management of cognitive deficits in schizophrenia?The disease entity in psychiatry: fact or fiction?Differences in cognitive impairment between schizophrenia and bipolar disorder: Considering the role of heterogeneity.Neurocognitive impairment in deficit and non-deficit schizophrenia: a meta-analysis.Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.Evidence of aberrant DNA damage response signalling but normal rates of DNA repair in dividing lymphoblasts from patients with schizophrenia.Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia.Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia.Chromosome 13q13-q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype.Increased familiarity of intellectual deficits in early-onset schizophrenia spectrum disorders.

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P2860

Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit.

http://www.wikidata.org/entity/Q34021154

description

2005 nî lūn-bûn

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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Genetic evidence for a distinc ...... y pervasive cognitive deficit.

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P2093

Assen Jablensky

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Daniel Rock

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David Vile

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Elizabeth H Corder

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Joachim F Hallmayer

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Johanna Badcock

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Kate Hollingsworth

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Luba Kalaydjieva

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Milan Dragovic

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Patricia T Michie

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P2860

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

The endophenotype concept in psychiatry: etymology and strategic intentions

Cognitive deficits in relatives of patients with schizophrenia: a meta-analysis

The SPQ: A Scale for the Assessment of Schizotypal Personality Based on DSM-III-R Criteria

The inheritance of neuropsychological dysfunction in twins discordant for schizophrenia.

Studies of individuals with schizophrenia never treated with antipsychotic medications: a review.

Allele-sharing models: LOD scores and accurate linkage tests.

The molecular genetics of schizophrenia: new findings promise new insights.

Meta-analysis and the science of schizophrenia: variant evidence or evidence of variants?

SCAN. Schedules for Clinical Assessment in Neuropsychiatry.

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10.1086/432816

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