Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.
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Role of late maternal thyroid hormones in cerebral cortex development: an experimental model for human prematurityThe neurodevelopmental hypothesis of schizophrenia, revisitedWhite matter development in the early stages of psychosis.A review of neuroimaging studies of young relatives of individuals with schizophrenia: a developmental perspective from schizotaxia to schizophrenia.Trajectories of anatomic brain development as a phenotype.Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.Developmental disruptions in neural connectivity in the pathophysiology of schizophrenia.Family-based association study of Neuregulin 1 with psychotic bipolar disorderSchizophrenia-risk variant rs6994992 in the neuregulin-1 gene on brain developmental trajectories in typically developing childrenAssociation study of neuregulin-1 gene polymorphisms in a North Indian schizophrenia sample.Childhood onset schizophrenia: support for a progressive neurodevelopmental disorderResearch review: Cholinergic mechanisms, early brain development, and risk for schizophrenia.Ablation of ErbB4 from excitatory neurons leads to reduced dendritic spine density in mouse prefrontal cortex.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.The DTNBP1 (dysbindin-1) gene variant rs2619522 is associated with variation of hippocampal and prefrontal grey matter volumes in humans.Personal reflections on observational and experimental research approaches to childhood psychopathology.Genetics of childhood-onset schizophreniaThe effect of ANK3 bipolar-risk polymorphisms on the working memory circuitry differs between loci and according to risk-status for bipolar disorder.Age of onset of schizophrenia: perspectives from structural neuroimaging studiesCortical mapping of genotype-phenotype relationships in schizophrenia.Common variants in the MKL1 gene confer risk of schizophrenia.Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorderMaternal infection leads to abnormal gene regulation and brain atrophy in mouse offspring: implications for genesis of neurodevelopmental disordersPathophysiology of early onset schizophrenia.Neuregulin 1 genotype and schizophrenia.The Association between COMT, BDNF, and NRG1 and Premorbid Social Functioning in Patients with Psychosis, Their Relatives, and ControlsThe genetics of childhood-onset schizophrenia: when madness strikes the prepubescentAnalysis of a promoter polymorphism in the SMDF neuregulin 1 isoform in Schizophrenia.Common variants in psychiatric risk genes predict brain structure at birth.Neurobiology and phenotypic expression in early onset schizophrenia.Cerebral asymmetry in schizophrenia.An environmental analysis of genes associated with schizophrenia: hypoxia and vascular factors as interacting elements in the neurodevelopmental model.Development of novel therapy of schizophrenia in children and adolescents.Forty years of structural imaging in psychosis: promises and truth.The association between gene variants and longitudinal structural brain changes in psychosis: a systematic review of longitudinal neuroimaging genetics studies.Genetic variation in neuregulin1 is associated with differences in prefrontal engagement in children.Is neuregulin 1 involved in determining cerebral volumes in schizophrenia? Preliminary results showing a decrease in superior temporal gyrus volume.Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia.Effects of NRG1 genotypes on orbitofrontal sulcogyral patterns in Japanese patients diagnosed with schizophrenia.
P2860
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P2860
Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Neuregulin 1 (8p12) and childh ...... in developmental trajectories.
@en
Neuregulin 1
@nl
type
label
Neuregulin 1 (8p12) and childh ...... in developmental trajectories.
@en
Neuregulin 1
@nl
prefLabel
Neuregulin 1 (8p12) and childh ...... in developmental trajectories.
@en
Neuregulin 1
@nl
P2093
P2860
P356
P1433
P1476
Neuregulin 1 (8p12) and childh ...... ain developmental trajectories
@en
P2093
Gornick MC
Greenstein D
Rapoport JL
P2860
P2888
P304
P356
10.1038/SJ.MP.4001906
P407
P577
2006-10-10T00:00:00Z