Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome (Q31037536)

5 September 2017

Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome (English)

1 reference

5 September 2017

5

Chantal Kemner

1 reference

5 September 2017

2

Victor A F Lamme

1 reference

5 September 2017

Maurice J C M Magnée

1

1 reference

5 September 2017

Monique G M de Sain-van der Velden

series ordinal

3

1 reference

5 September 2017

Jacob A S Vorstman

series ordinal

4

1 reference

5 September 2017

language of work or name

English

0 references

publication date

5 October 2011

1 reference

5 September 2017

1 reference

5 September 2017

6

1 reference

5 September 2017

10

1 reference

5 September 2017

e25882

1 reference

Creative Commons Attribution 4.0 International

5 September 2017

start time

5 October 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

21 June 2018

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Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

21 June 2018

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Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group.

21 June 2018

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Functional consequences of PRODH missense mutations

21 June 2018

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

21 June 2018

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Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

21 June 2018

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Anatomical substrates for glutamate-dopamine interactions: evidence for specificity of connections and extrasynaptic actions

21 June 2018

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Genomic disorders on 22q11

21 June 2018

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Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia

21 June 2018

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Neuropsychiatric disorders in the 22q11 deletion syndrome

21 June 2018

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Dopamine transporter immunoreactivity in monkey cerebral cortex: regional, laminar, and ultrastructural localization

21 June 2018

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The distinct modes of vision offered by feedforward and recurrent processing

21 June 2018

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Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).

21 June 2018

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

21 June 2018

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A common molecular basis for rearrangement disorders on chromosome 22q11

21 June 2018

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A population study of chromosome 22q11 deletions in infancy

21 June 2018

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Proline-induced inhibition of glutamate release in hippocampal area CA1.

21 June 2018

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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

21 June 2018

1 reference

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Proline-induced potentiation of glutamate transmission

21 June 2018

1 reference

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Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

21 June 2018

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Prevalence of 22q11 microdeletion

21 June 2018

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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 June 2018

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Ocular findings in the velo-cardio-facial syndrome.

21 June 2018

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Recent advances in the phencyclidine model of schizophrenia

21 June 2018

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Molecular cloning and expression of a high affinity L-proline transporter expressed in putative glutamatergic pathways of rat brain

21 June 2018

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Parvocellular and magnocellular contributions to the initial generators of the visual evoked potential: high-density electrical mapping of the "C1" component.

21 June 2018

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A neural substrate for atypical low-level visual processing in autism spectrum disorder.

25 November 2018

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Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome.

25 November 2018

1 reference

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Processing speed in recurrent visual networks correlates with general intelligence.

25 November 2018

1 reference

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Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

25 November 2018

1 reference

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Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

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

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

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

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

Figure-ground segregation in a recurrent network architecture.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

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

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

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

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

Texture segregation is processed by primary visual cortex in man and monkey. Evidence from VEP experiments

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3187802

The neurophysiology of figure-ground segregation in primary visual cortex

25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21998713

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Age-specific distribution of plasma amino acid concentrations in a healthy pediatric population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21998713

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0025882

1 reference

5 September 2017

0 references

1 reference

5 September 2017

1 reference