(Q37219660)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

review article

1 reference

title

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

author name string

Sarah E Prasad

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Sarah Howley

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

language of work or name

1 reference

1 January 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

Developmental Disabilities Research Reviews

10 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

page(s)

26-34

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

Clinical features of 78 adults with 22q11 Deletion Syndrome.

10 January 2020

cites work

1 reference

Behavioral phenotypes in organic genetic disease. Presidential address to the Society for Pediatric Research, May 1, 1971.

21 January 2018

1 reference

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

21 January 2018

1 reference

Evaluation of potential gene-gene interactions for attention deficit hyperactivity disorder in the Han Chinese population.

21 January 2018

1 reference

Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women

21 January 2018

1 reference

Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?

21 January 2018

1 reference

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

21 January 2018

1 reference

A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD).

21 January 2018

1 reference

The psychopathological phenotype of velo-cardio-facial syndrome

21 January 2018

1 reference

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome.

21 January 2018

1 reference

7 January 2021

Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders

1 reference

7 January 2021

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

1 reference

7 January 2021

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

1 reference

7 January 2021

Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome

1 reference

7 January 2021

The schizophrenia phenotype in 22q11 deletion syndrome

1 reference

7 January 2021

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome

1 reference

7 January 2021

The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.

1 reference

7 January 2021

Functional consequences of PRODH missense mutations

1 reference

7 January 2021

Human catechol-O-methyltransferase: cloning and expression of the membrane-associated form

1 reference

7 January 2021

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

1 reference

7 January 2021

Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene X environment interaction

1 reference

7 January 2021

Mutation analysis of ARVCF gene on chromosome 22q11 as a candidate for a schizophrenia gene

1 reference

7 January 2021

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

1 reference

7 January 2021

Meta-analysis of association between a catechol-O-methyltransferase gene polymorphism and attention deficit hyperactivity disorder

1 reference

7 January 2021

Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications

1 reference

7 January 2021

Proline reduces acetylcholinesterase activity in cerebral cortex of rats

1 reference

7 January 2021

Possible role for COMT in psychosis associated with velo-cardio-facial syndrome.

1 reference

7 January 2021

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

1 reference

7 January 2021

Protein palmitoylation: a regulator of neuronal development and function

1 reference

7 January 2021

Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?

1 reference

7 January 2021

Schizotypy, attention deficit hyperactivity disorder, and dopamine genes

1 reference

7 January 2021

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

1 reference

7 January 2021

The nature and heritability of attention-deficit/hyperactivity disorder.

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Analysis of TBX1 variation in patients with psychotic and affective disorders

1 reference

7 January 2021

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

1 reference

7 January 2021

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.

1 reference

7 January 2021

Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies

1 reference

7 January 2021

Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia

1 reference

7 January 2021

D(1) receptors in prefrontal cells and circuits

1 reference

7 January 2021

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

1 reference

7 January 2021

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

1 reference

7 January 2021

Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome.

1 reference

7 January 2021

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

1 reference

7 January 2021

Long-term follow-up of children with mental retardation/borderline intellectual functioning and ADHD.

1 reference

7 January 2021

Genes for schizophrenia? Recent findings and their pathophysiological implications

1 reference

7 January 2021

Genetics and genomics of behavioral and psychiatric disorders

1 reference

7 January 2021

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

1 reference

7 January 2021

Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder

1 reference

7 January 2021

The molecular genetics of the 22q11-associated schizophrenia

1 reference

7 January 2021

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

7 January 2021

Family‐based and case–control study of catechol‐O‐methyltransferase in schizophrenia among Palestinian Arabs

1 reference

7 January 2021

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

1 reference

7 January 2021

Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population

1 reference

7 January 2021

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

1 reference

7 January 2021

A neurodevelopmental model of schizophrenia: Neonatal disconnection of the hippocampus

1 reference

7 January 2021

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

1 reference

7 January 2021

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

1 reference

7 January 2021

Cloning and Characterization of Human Placental Catechol--Methyltransferase cDNA

1 reference

7 January 2021

Brain anatomy and sensorimotor gating in Asperger's syndrome.

1 reference

7 January 2021

Genomic disorders on 22q11

1 reference

7 January 2021

Association between catechol-O-methyltransferase and phobic anxiety

1 reference

7 January 2021

A comprehensive analysis of 22q11 gene expression in the developing and adult brain

1 reference

7 January 2021

Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome.

1 reference

7 January 2021

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

7 January 2021

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

1 reference

7 January 2021

Schizophrenia and velo-cardio-facial syndrome.

1 reference

7 January 2021

The behavioural phenotype in velo-cardio-facial syndrome.

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Neuropsychiatric disorders in the 22q11 deletion syndrome

1 reference

7 January 2021

Failure to find association between PRODH deletion and schizophrenia

1 reference

7 January 2021

The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia

1 reference

7 January 2021

T-box genes in human disorders

1 reference

7 January 2021

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

1 reference

7 January 2021

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

1 reference

7 January 2021

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

1 reference

7 January 2021

No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population

1 reference

7 January 2021

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1 reference

7 January 2021

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

1 reference

7 January 2021

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

7 January 2021

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

7 January 2021

A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children

1 reference

7 January 2021

Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.

1 reference

7 January 2021

T-box genes: what they do and how they do it.

1 reference

7 January 2021

Neuromotor deficits in children with the 22q11 deletion syndrome

1 reference

7 January 2021

Schizophrenia genes - famine to feast

1 reference

7 January 2021

Catechol-o-methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.

1 reference

7 January 2021

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond

1 reference

7 January 2021

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

1 reference

7 January 2021

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

1 reference

7 January 2021

Early cerebro-craniofacial dysmorphogenesis in schizophrenia: a lifetime trajectory model from neurodevelopmental basis to 'neuroprogressive' process.

1 reference

7 January 2021

Prefrontal neurons and the genetics of schizophrenia

1 reference

7 January 2021

Is COMT a susceptibility gene for schizophrenia?

1 reference

7 January 2021

Association between PRODH and schizophrenia is not confirmed

1 reference

7 January 2021

Strong evidence that GNB1L is associated with schizophrenia

1 reference

7 January 2021

Genes, dopamine and cortical signal-to-noise ratio in schizophrenia

1 reference

7 January 2021

Role of TBX1 in human del22q11.2 syndrome

1 reference

7 January 2021

Prevalence of ADHD in children with velocardiofacial syndrome: a preliminary report.

1 reference

7 January 2021

Identifiers

DOI

10.1002/DDRR.5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18636634%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference