Common variants in psychiatric risk genes predict brain structure at birth. - Wikidata - awgldk - TriplyDB

Common variants in psychiatric risk genes predict brain structure at birth.

Common variants in psychiatric risk genes predict brain structure at birth.

http://www.wikidata.org/entity/Q37688290

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Ushering in the study and treatment of preclinical Alzheimer disease Behavioral, Neurophysiological, and Synaptic Impairment in a Transgenic Neuregulin1 (NRG1-IV) Murine Schizophrenia Model.Endophenotypes in Schizophrenia for the Perinatal Period: Criteria for Validation.White matter development and early cognition in babies and toddlers.Brain differences in infants at differential genetic risk for late-onset Alzheimer disease: a cross-sectional imaging study.ApoE4 induces Aβ42, tau, and neuronal pathology in the hippocampus of young targeted replacement apoE4 mice.FVGWAS: Fast voxelwise genome wide association analysis of large-scale imaging genetic data.Schizophrenia-risk variant rs6994992 in the neuregulin-1 gene on brain developmental trajectories in typically developing children Longitudinal change in working memory as a function of APOE genotype in midlife and old age.Maternal prenatal anxiety and child COMT genotype predict working memory and symptoms of ADHD.APOE-epsilon4 and aging of medial temporal lobe gray matter in healthy adults older than 50 years Two Alzheimer's disease risk genes increase entorhinal cortex volume in young adults Developmental heterochrony and the evolution of autistic perception, cognition and behavior Are APOE ɛ genotype and TOMM40 poly-T repeat length associations with cognitive ageing mediated by brain white matter tract integrity?Associations between DNA methylation and schizophrenia-related intermediate phenotypes - a gene set enrichment analysis Brain Imaging and Blood Biomarker Abnormalities in Children With Autosomal Dominant Alzheimer Disease: A Cross-Sectional Study.Genetic influence of apolipoprotein E4 genotype on hippocampal morphometry: An N = 725 surface-based Alzheimer's disease neuroimaging initiative study.Effects of schizophrenia risk variation in the NRG1 gene on NRG1-IV splicing during fetal and early postnatal human neocortical development.Imaging brain effects of APOE4 in cognitively normal individuals across the lifespan.Transcriptomics of maternal and fetal membranes can discriminate between gestational-age matched preterm neonates with and without cognitive impairment diagnosed at 18-24 months.Heritable influences on behavioural problems from early childhood to mid-adolescence: evidence for genetic stability and innovation.Influence of APOE Genotype on Hippocampal Atrophy over Time - An N=1925 Surface-Based ADNI Study.Association analysis of DISC1 gene polymorphisms with Attention-Deficit Hyperactivity Disorder in Iranian population Development and aging of cortical thickness correspond to genetic organization patterns Effects of the BDNF Val66Met Polymorphism on Gray Matter Volume in Typically Developing Children and Adolescents The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume A Systems View of the Differences between APOE ε4 Carriers and Non-carriers in Alzheimer's Disease.Greater medial temporal hypometabolism and lower cortical amyloid burden in ApoE4-positive AD patients.A Multi-Cohort Study of ApoE ɛ4 and Amyloid-β Effects on the Hippocampus in Alzheimer's Disease.Genetic influences on brain developmental trajectories on neuroimaging studies: from infancy to young adulthood.Apolipoprotein E as a β-amyloid-independent factor in Alzheimer's disease.Imaging markers of structural and functional brain changes that precede cognitive symptoms in risk for Alzheimer's disease Maternal immune activation and abnormal brain development across CNS disorders.Genetics and brain morphology.FGWAS: Functional genome wide association analysis.Gray matter maturation and cognition in children with different APOE ε genotypes.The role of APOE on lipid homeostasis and inflammation in normal brains.Altered Energy Metabolism Pathways in the Posterior Cingulate in Young Adult Apolipoprotein E ɛ4 Carriers.Alzheimer's Disease Genetic Risk Factor APOE-ε4 Also Affects Normal Brain Function.Tract Based Spatial Statistic Reveals No Differences in White Matter Microstructural Organization between Carriers and Non-Carriers of the APOE ɛ4 and ɛ2 Alleles in Young Healthy Adolescents.

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Common variants in psychiatric risk genes predict brain structure at birth.

http://www.wikidata.org/entity/Q37688290

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 02 January 2013

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

Common variants in psychiatric risk genes predict brain structure at birth.

@en

Common variants in psychiatric risk genes predict brain structure at birth.

@nl

type

label

Common variants in psychiatric risk genes predict brain structure at birth.

@en

Common variants in psychiatric risk genes predict brain structure at birth.

@nl

prefLabel

Common variants in psychiatric risk genes predict brain structure at birth.

@en

Common variants in psychiatric risk genes predict brain structure at birth.

@nl

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Cerebral Cortex

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Common variants in psychiatric risk genes predict brain structure at birth.

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Hongtu Zhu

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Jiaping Wang

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John H Gilmore

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Robert M Hamer

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Sandra Woolson

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Thomas Konneker

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Weili Lin

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Xiujuan Geng

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P2860

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain

Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the disease

The neurodevelopmental hypothesis of schizophrenia, revisited

Neurotrophin-regulated signalling pathways

Automated Anatomical Labeling of Activations in SPM Using a Macroscopic Anatomical Parcellation of the MNI MRI Single-Subject Brain

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

Meta-analysis shows strong positive association of the neuregulin 1 (NRG1) gene with schizophrenia

Site-specific role of catechol-O-methyltransferase in dopamine overflow within prefrontal cortex and dorsal striatum

DISC1 at 10: connecting psychiatric genetics and neuroscience

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1230-1246

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scholarly article

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10.1093/CERCOR/BHS401

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5

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24

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Rebecca Knickmeyer

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2013-01-02T00:00:00Z

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234043181

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23283688

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3977618

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