Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.
about
Isolated populations and complex disease gene identificationThe genetics of bipolar disorderGRM7 variants confer susceptibility to age-related hearing impairmentFindings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohortDISC1-binding proteins in neural development, signalling and schizophreniaDatabase of genetic studies of bipolar disorderAnnual 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 disorderA Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode PsychosisCategory fluency, latent semantic analysis and schizophrenia: a candidate gene approachA 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 cohortImpact of DISC1 variation on neuroanatomical and neurocognitive phenotypesCommon 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 neocortexAggregated proteins in schizophrenia and other chronic mental diseases: DISC1opathiesConvergent 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 psychosisGenetic association of cyclic AMP signaling genes with bipolar disorder.DISC1 genetics, biology and psychiatric illnessCopy 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.
P2860
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P2860
Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Association of distinct alleli ...... erlying cognitive impairments.
@en
Association of distinct alleli ...... erlying cognitive impairments.
@nl
type
label
Association of distinct alleli ...... erlying cognitive impairments.
@en
Association of distinct alleli ...... erlying cognitive impairments.
@nl
prefLabel
Association of distinct alleli ...... erlying cognitive impairments.
@en
Association of distinct alleli ...... erlying cognitive impairments.
@nl
P2093
P2860
P50
P356
P1476
Association of distinct alleli ...... erlying cognitive impairments.
@en
P2093
Mervi Antila
Outi M Palo
Pia Soronen
Tiina Paunio
Tuula Kieseppä
P2860
P304
P356
10.1093/HMG/DDM207
P50
P577
2007-08-02T00:00:00Z