Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
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From Linkage Studies to Epigenetics: What We Know and What We Need to Know in the Neurobiology of SchizophreniaTowards medication-enhancement of cognitive interventions in schizophreniaGenetic Sources of Subcomponents of Event-Related Potential in the Dimension of Psychosis Analyzed From the B-SNIP StudyNeuregulin-1 signalling and antipsychotic treatment: potential therapeutic targets in a schizophrenia candidate signalling pathwayThe involvement of Type II Neuregulin-1 in rat visuospatial learning and memoryConfluence of genes, environment, development, and behavior in a post Genome-Wide Association Study worldCharacterization of neurophysiologic and neurocognitive biomarkers for use in genomic and clinical outcome studies of schizophreniaGluN2D N-Methyl-d-Aspartate Receptor Subunit Contribution to the Stimulation of Brain Activity and Gamma Oscillations by Ketamine: Implications for SchizophreniaFronto-temporal-mesolimbic gene expression and heritable differences in amphetamine-disrupted sensorimotor gating in rats.Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family Study. Association Between Neuregulin-1 Gene Variant (rs2439272) and Schizophrenia and Its Negative Symptoms in an Iranian Population.Sensory processing dysfunction in the personal experience and neuronal machinery of schizophrenia.Heritability and molecular genetic basis of antisaccade eye tracking error rate: a genome-wide association study.Comparison of the heritability of schizophrenia and endophenotypes in the COGS-1 family study.Deficient prepulse inhibition in schizophrenia detected by the multi-site COGS.Coupling of gene expression in medial prefrontal cortex and nucleus accumbens after neonatal ventral hippocampal lesions accompanies deficits in sensorimotor gating and auditory processing in ratsForebrain gene expression predicts deficits in sensorimotor gating after isolation rearing in male rats.Between-site reliability of startle prepulse inhibition across two early psychosis consortia.Developmental vulnerability of synapses and circuits associated with neuropsychiatric disorders.Phenotype ontologies and cross-species analysis for translational researchMultivariate Genetic Correlates of the Auditory Paired Stimuli-Based P2 Event-Related Potential in the Psychosis Dimension From the BSNIP Study.PhenoVar: a phenotype-driven approach in clinical genomics for the diagnosis of polymalformative syndromes.Association study of neuregulin-1 gene polymorphisms in a North Indian schizophrenia sample.Patient-controlled encrypted genomic data: an approach to advance clinical genomics.Genetic association analysis of complex diseases incorporating intermediate phenotype informationThe DAO gene is associated with schizophrenia and interacts with other genes in the Taiwan Han Chinese population.Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis.ERBB4 polymorphism and family history of psychiatric disorders on age-related cortical changes in healthy childrenMultivariate genetic determinants of EEG oscillations in schizophrenia and psychotic bipolar disorder from the BSNIP study.Cognitive endophenotypes inform genome-wide expression profiling in schizophrenia.The interaction of disrupted type II neuregulin 1 and chronic adolescent stress on adult anxiety- and fear-related behaviors.Novel molecular changes induced by Nrg1 hypomorphism and Nrg1-cannabinoid interaction in adolescence: a hippocampal proteomic study in miceAntipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes.Lack of use in the literature from the last 20 years supports dropping traditional schizophrenia subtypes from DSM-5 and ICD-11.Mismatch negativity is a breakthrough biomarker for understanding and treating psychotic disorders.Antisaccade task reflects cortical involvement in mild cognitive impairmentSensory encoding in Neuregulin 1 mutantsThe Major Histocompatibility Complex (MHC) in Schizophrenia: A Review.Global signaling effects of a schizophrenia-associated missense mutation in neuregulin 1: an exploratory study using whole genome and novel kinome approaches.Modeling heterogeneous patients with a clinical diagnosis of schizophrenia with induced pluripotent stem cells.
P2860
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P2860
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes
@nl
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
@ast
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
@en
type
label
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes
@nl
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
@ast
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
@en
prefLabel
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes
@nl
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
@ast
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
@en
P2093
P2860
P3181
P1433
P1476
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes.
@en
P2093
Allen D Radant
David L Braff
Gregory A Light
Neal R Swerdlow
P2860
P304
P3181
P356
10.1371/JOURNAL.PONE.0029630
P407
P577
2012-01-13T00:00:00Z