(Q36253405)

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Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms

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Europe PubMed Central

PMC publication ID

13 August 2017

Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Matcheri S Keshavan

10

object named as

Matcheri S Keshavan

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

7

object named as

Edward Ip

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

8

object named as

Neeraj Tandon

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Stephen R. Hooper

3

object named as

Stephen R Hooper

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

author name string

Vandana Shashi

1

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Alan Francis

2

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Peter G Kranz

4

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Michael Zapadka

5

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Kelly Schoch

6

1 reference

Europe PubMed Central

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13 August 2017

Timothy D Howard

9

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

publication date

27 June 2012

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

European Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

20

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

1051-1057

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Developmental malformation of the corpus callosum: a review of typical callosal development and examples of developmental disorders with callosal involvement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

The development of the corpus callosum in the healthy human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

MRI-derived measurements of human subcortical, ventricular and intracranial brain volumes: Reliability effects of scan sessions, acquisition sequences, data analyses, scanner upgrade, scanner vendors and field strengths

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Meta-analysis of diffusion tensor imaging studies in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

A new account of the neurocognitive foundations of impairments in space, time and number processing in children with chromosome 22q11.2 deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Microstructural integrity of the corpus callosum linked with neuropsychological performance in adolescents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Microstructural maturation of the human brain from childhood to adulthood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Interpreting scan data acquired from multiple scanners: a study with Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Positive correlations between corpus callosum thickness and intelligence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Social skills and executive function deficits in children with the 22q11 Deletion Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Callosal morphology in Williams syndrome: a new evaluation of shape and thickness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Reliability in multi-site structural MRI studies: effects of gradient non-linearity correction on phantom and human data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

The role of the corpus callosum in interhemispheric transfer of information: excitation or inhibition?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

The molecular genetics of the 22q11-associated schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Association study of a promoter polymorphism of UFD1L gene with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Brain development during childhood and adolescence: a longitudinal MRI study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Brain connections: interhemispheric fiber systems and anatomical brain asymmetries in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

30 September 2017

Discordance in Diagnoses and Treatment of Psychiatric Disorders in Children and Adolescents with 22q11.2 Deletion Syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

29 June 2018

Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

29 June 2018

Development of the corpus callosum in childhood, adolescence and early adulthood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

29 June 2018

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

A quantitative MRI study of posterior fossa development in velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

A meta-analysis of diffusion tensor imaging studies of the corpus callosum in schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome).

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Neuroanatomy in adolescents and young adults with 22q11 deletion syndrome: comparison to an IQ-matched group.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Reliability of MRI-derived measurements of human cerebral cortical thickness: the effects of field strength, scanner upgrade and manufacturer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Brain volume in children with neurofibromatosis type 1: relation to neuropsychological status.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Mapping callosal morphology and cognitive correlates: effects of heavy prenatal alcohol exposure

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

22 September 2018

Topography of the human corpus callosum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449066

22 September 2018

Meta-analysis of magnetic resonance imaging studies of the corpus callosum in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.138

21 January 2018

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update

1 reference

https://pubmed.ncbi.nlm.nih.gov/22763378

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/22763378

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22763378

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/EJHG.2012.138

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

ResearchGate publication ID

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