(Q30439224)

8 November 2017

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders (English)

1 reference

8 November 2017

N Hiroi

1

1 reference

8 November 2017

T Takahashi

2

1 reference

8 November 2017

A Hishimoto

3

1 reference

8 November 2017

T Izumi

4

1 reference

8 November 2017

S Boku

5

1 reference

8 November 2017

T Hiramoto

6

1 reference

8 November 2017

language of work or name

English

0 references

publication date

6 August 2013

1 reference

8 November 2017

1 reference

8 November 2017

18

1 reference

8 November 2017

11

1 reference

8 November 2017

1153-1165

1 reference

Mouse Models of 22q11.2-Associated Autism Spectrum Disorder

8 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Reimagining psychoses: an agnostic approach to diagnosis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Genotype-phenotype correlation in 22q11.2 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Common genetic variants, acting additively, are a major source of risk for autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Startle reactivity and prepulse inhibition of the acoustic startle response are modulated by catechol-O-methyl-transferase Val(158) Met polymorphism in adults with 22q11 deletion syndrome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Individual common variants exert weak effects on the risk for autism spectrum disorders

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Genetic architectures of psychiatric disorders: the emerging picture and its implications

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Functional outcomes of adults with 22q11.2 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

The social motivation theory of autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

CNVs: harbingers of a rare variant revolution in psychiatric genetics

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

The benefit of directly comparing autism and schizophrenia for revealing mechanisms of social cognitive impairment.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Decreased exploratory activity in a mouse model of 15q duplication syndrome; implications for disturbance of serotonin signaling

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Lack of developmental improvement on a face memory task during adolescence in autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Elevated prevalence of generalized anxiety disorder in adults with 22q11.2 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Chronic adolescent exposure to Δ-9-tetrahydrocannabinol in COMT mutant mice: impact on psychosis-related and other phenotypes.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Functional impact of global rare copy number variation in autism spectrum disorders

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Brief report: Sensorimotor gating in idiopathic autism and autism associated with fragile X syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

A genome-wide linkage and association scan reveals novel loci for autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Developmental changes in cognitive control through adolescence

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Common variants conferring risk of schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Common genetic variants on 5p14.1 associate with autism spectrum disorders

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Supportive evidence for reduced expression of GNB1L in schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and function

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Genetic dissection of the role of catechol-O-methyltransferase in cognition and stress reactivity in mice

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Clinical variability of the 22q11.2 duplication syndrome.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Large recurrent microdeletions associated with schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Rare chromosomal deletions and duplications increase risk of schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Schizophrenia and 22q11.2 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Structural variation of chromosomes in autism spectrum disorder

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Strong evidence that GNB1L is associated with schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotype

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Can neuroscience be integrated into the DSM-V?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Analysis of TBX1 variation in patients with psychotic and affective disorders

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

The family of sensorimotor gating disorders: comorbidities or diagnostic overlaps?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Symptoms, syndromes, and the value of psychiatric diagnostics in patients who have functional somatic disorders

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Association study of the G-protein signaling 4 (RGS4) and proline dehydrogenase (PRODH) genes with schizophrenia: a meta-analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Lower prepulse inhibition in children with the 22q11 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Microduplication and triplication of 22q11.2: a highly variable syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Networks of attention in children with the 22q11 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Executive functions in children aged 6 to 13: a dimensional and developmental study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Maturation of cognitive processes from late childhood to adulthood

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Persecutory beliefs, attributions and theory of mind: comparison of patients with paranoid delusions, Asperger's syndrome and healthy controls.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

The structure of working memory from 4 to 15 years of age.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Normative data from the CANTAB. I: development of executive function over the lifespan

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Implications for the Neural Basis of Social Cognition for the Study of Schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

The endophenotype concept in psychiatry: etymology and strategic intentions

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Knockout mice: simple solutions to the problems of genetic background and flanking genes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Evidence for early-childhood, pan-developmental impairment specific to schizophreniform disorder: results from a longitudinal birth cohort

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

A nosology of disorders of attention

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Neuropsychiatric disorders in the 22q11 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Attention, memory, and motor skills as childhood predictors of schizophrenia-related psychoses: the New York High-Risk Project.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

A prospective cohort study of neurodevelopmental processes in the genesis and epigenesis of schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

What develops in working memory? A life span perspective

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

A common molecular basis for rearrangement disorders on chromosome 22q11

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

22q11 deletion syndrome in adults with schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Research update: childhood-onset schizophrenia: implications of clinical and neurobiological research

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Another advanced test of theory of mind: evidence from very high functioning adults with autism or asperger syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Inbred strain differences in prepulse inhibition of the mouse startle response

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Social cognition in schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Looking for childhood-onset schizophrenia: the first 71 cases screened

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Child development risk factors for adult schizophrenia in the British 1946 birth cohort

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Childhood antecedents of schizophrenia and affective illness: social adjustment at ages 7 and 11

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Velo-cardio-facial syndrome: language and psychological profiles.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

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

14 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Velocardiofacial syndrome in childhood-onset schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Screening for 22q11 deletions in a schizophrenia population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Prodromal and autistic symptoms in schizotypal personality disorder and 22q11.2 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Autistic disorder and 22q11.2 duplication.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Cognitive development in children with 22q11.2 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Microduplication 22q11.2: a benign polymorphism or a syndrome with a very large clinical variability and reduced penetrance?--Report of two families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Distal 22q11.2 microduplication encompassing the BCR gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Association of syndromic mental retardation and autism with 22q11.2 duplication.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Affective disorders and other psychiatric diagnoses in children and adolescents with 22q11.2 Deletion Syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Premorbid adjustment and personality in people with schizophrenia†

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Child and adolescent (juvenile onset) schizophrenia. A case control study of premorbid developmental impairments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Influence of the COMT genotype on working memory and brain activity changes during development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

A prospective study of childhood neurocognitive functioning in schizophrenic patients and their siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Working memory impairments in children with attention-deficit hyperactivity disorder with and without comorbid language learning disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Working memory functions in children with different degrees of intellectual disability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Executive functions and memory abilities in children with 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Attentional capacities in children with autism: is there a general deficit in shifting focus?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Attentional processes in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Is it possible to be schizophrenic yet neuropsychologically normal?

21 January 2018

2 references

https://api.crossref.org/works/10.1038%2FMP.2013.92

21 January 2018

12 December 2020

Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Individual differences in executive function and central coherence predict developmental changes in theory of mind in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Schizophrenia and theory of mind.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Brain anatomy and sensorimotor gating in Asperger's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Sensorimotor gating deficits in adults with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Meta-analysis of association between genetic variants in COMT and schizophrenia: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Evaluation of six SNPs of MicroRNA machinery genes and risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Systematic association analysis of microRNA machinery genes with schizophrenia informs further study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Association study between GNB1L and three major mental disorders in Chinese Han populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Genetic vs. pharmacological inactivation of COMT influences cannabinoid-induced expression of schizophrenia-related phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Phenotypic characterization of cognition and social behavior in mice with heterozygous versus homozygous deletion of catechol-O-methyltransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Acoustic startle and prepulse inhibition in 40 inbred strains of mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia – relationship with COMT Val108/158 Met polymorphism, gender and symptomatology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.92

Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

The development of mental processing: efficiency, working memory, and thinking.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Developmental pathways to schizophrenia: behavioral subtypes.

26 November 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

26 November 2018

https://api.crossref.org/works/10.1038%2FMP.2013.92

7 January 2021

inferred from DOI database lookup

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3852900

Comparing phenotypes in patients with idiopathic autism to patients with velocardiofacial syndrome (22q11 DS) with and without autism

26 November 2018

1 reference

12 December 2020

Association study of Nogo-related genes with schizophrenia in a Japanese case-control sample

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Behavior problems and personality aspects of 40 children with velo-cardio-facial syndrome

1 reference

12 December 2020

From animal models to model animals

1 reference

12 December 2020

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

1 reference

12 December 2020

Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population

1 reference

12 December 2020

Identifiers

DOI

10.1038/MP.2013.92

1 reference

8 November 2017

1 reference

8 November 2017

PubMed publication ID

23917946

1 reference