(Q48167083)

9 February 2018

title

Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia. (English)

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9 February 2018

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2

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Frank Baas

5

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9 February 2018

author name string

Zinkstok J

1

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9 February 2018

van Amelsvoort T

3

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9 February 2018

Moeton M

4

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9 February 2018

Linszen D

6

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9 February 2018

language of work or name

English

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publication date

14 May 2007

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9 February 2018

Genes, Brain and Behavior

published in

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9 February 2018

volume

7

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9 February 2018

issue

1

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9 February 2018

page(s)

61-69

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9 February 2018

Voxel-based morphometry–the methods

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

The problem of functional localization in the human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Cortex mapping reveals regionally specific patterns of genetic and disease-specific gray-matter deficits in twins discordant for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Converging Evidence of NMDA Receptor Hypofunction in the Pathophysiology of Schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

White matter changes in schizophrenia: evidence for myelin-related dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Variation in GRM3 affects cognition, prefrontal glutamate, and risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Children and adolescents with velocardiofacial syndrome: a volumetric MRI study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Receptor mechanisms and circuitry underlying NMDA antagonist neurotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

The emerging role of glutamate in the pathophysiology and treatment of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Human catechol-O-methyltransferase down-regulation by estradiol

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Brain structure, genetic liability, and psychotic symptoms in subjects at high risk of developing schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

MRI anatomy of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Impact of complex genetic variation in COMT on human brain function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case-control studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Dopamine and the regulation of cognition and attention

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

A review of MRI findings in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Structural abnormalities in frontal, temporal, and limbic regions and interconnecting white matter tracts in schizophrenic patients with prominent negative symptoms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Glutamate modulation of dopamine measured in vivo with positron emission tomography (PET) and 11C-raclopride in normal human subjects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Prefrontal neurons and the genetics of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

Association between PRODH and schizophrenia is not confirmed

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00326.X

10.1111/J.1601-183X.2007.00326.X

21 January 2018

Identifiers

DOI

1 reference

9 February 2018

PubMed ID

17504246

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9 February 2018