Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume.
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No association of COMT (Val158Met) genotype with brain structure differences between men and womenMeta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity.Imaging phenotypes of major depressive disorder: genetic correlatesEffects of the Val158Met catechol-O-methyltransferase polymorphism on cortical structure in children and adolescents.Toward dysfunctional connectivity: a review of neuroimaging findings in pediatric major depressive disorder.COMT Val158Met × SLC6A4 5-HTTLPR interaction impacts on gray matter volume of regions supporting emotion processing.Catechol-O-methyltransferase Val158Met polymorphism modulates gray matter volume and functional connectivity of the default mode network.COMT Val158Met Genotype and Individual Differences in Executive Function in Healthy Adults.Imaging genetics and psychiatric disorders.Genetic Variation in the Catechol-O-Methyl Transferase Val108/158Met Is Linked to the Caudate and Posterior Cingulate Cortex Volume in Healthy Subjects: Voxel-Based Morphometry Analysis of Brain Magnetic Resonance Imaging.Imaging genetics of mood disorders.COMT Genetic Reduction Produces Sexually Divergent Effects on Cortical Anatomy and Working Memory in Mice and Humans.COMT, neuropsychological function and brain structure in schizophrenia: a systematic review and neurobiological interpretation.COMT genotype and resting brain perfusion in children.Interactions of genetic variants reveal inverse modulation patterns of dopamine system on brain gray matter volume and resting-state functional connectivity in healthy young adults.The genetics of episodic memory.Common variants in psychiatric risk genes predict brain structure at birth.Ethnic differences in COMT genetic effects on striatal grey matter alterations associated with childhood ADHD: A voxel-based morphometry study in a Japanese sample.White matter alterations related to attention-deficit hyperactivity disorder and COMT val(158)met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (ciMorphological changes in gray matter volume correlate with catechol-O-methyl transferase gene Val158Met polymorphism in first-episode treatment-naïve patients with schizophrenia.Structural correlates of COMT Val158Met polymorphism in childhood ADHD: a voxel-based morphometry study.COMT rs4680 Met is not always the 'smart allele': Val allele is associated with better working memory and larger hippocampal volume in healthy Chinese.Opportunities for an enhanced integration of neuroscience and genomics.Imaging genetics: implications for research on variable antidepressant drug response.Prefrontal Volume Mediates Effect of COMT Polymorphism on Interference Resolution Capacity in Healthy Male Adults.Modulative effects of COMT haplotype on age-related associations with brain morphology.
P2860
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P2860
Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Impact of catechol-O-methyltransferase Val
@nl
Impact of catechol-O-methyltra ...... prefrontal gray matter volume.
@en
type
label
Impact of catechol-O-methyltransferase Val
@nl
Impact of catechol-O-methyltra ...... prefrontal gray matter volume.
@en
prefLabel
Impact of catechol-O-methyltransferase Val
@nl
Impact of catechol-O-methyltra ...... prefrontal gray matter volume.
@en
P50
P1433
P1476
Impact of catechol-O-methyltra ...... prefrontal gray matter volume.
@en
P2093
Maria C Gioia
Pierluigi Lanza
P304
P356
10.1097/WNR.0B013E3282F5F784
P577
2008-03-01T00:00:00Z