(Q35738055)

English

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

scientific article published on 13 December 2011

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scholarly article

1 reference

Europe PubMed Central

10 August 2017

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

1 reference

Europe PubMed Central

10 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

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13

object named as

Raquel E Gur

1 reference

Europe PubMed Central

10 August 2017

5

object named as

Elaine Zackai

1 reference

Europe PubMed Central

10 August 2017

Monica E Calkins

2

object named as

Monica E Calkins

1 reference

Europe PubMed Central

10 August 2017

Donna M McDonald-McGinn

4

object named as

Donna McDonald-McGinn

1 reference

Europe PubMed Central

10 August 2017

12

object named as

Ruben C Gur

1 reference

Europe PubMed Central

10 August 2017

Beverly S Emanuel

7

object named as

Beverly Emanuel

1 reference

Europe PubMed Central

10 August 2017

Karin E Borgmann-Winter

9

object named as

Karin Borgmann-Winter

1 reference

Europe PubMed Central

10 August 2017

Catherine G Conroy

11

object named as

Catherine G Conroy

1 reference

Europe PubMed Central

10 August 2017

author name string

Paula C Goldenberg

1

1 reference

Europe PubMed Central

10 August 2017

Jan Richard

3

1 reference

Europe PubMed Central

10 August 2017

Nandita Mitra

6

1 reference

Europe PubMed Central

10 August 2017

Marcella Devoto

8

1 reference

Europe PubMed Central

10 August 2017

Christian Kohler

10

1 reference

Europe PubMed Central

10 August 2017

language of work or name

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based on heuristic

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publication date

13 December 2011

1 reference

Europe PubMed Central

10 August 2017

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

1 reference

Europe PubMed Central

10 August 2017

159B

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Europe PubMed Central

10 August 2017

1

1 reference

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10 August 2017

87-93

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Europe PubMed Central

10 August 2017

Cognition at illness onset as a predictor of later functional outcome in early psychosis: systematic review and methodological critique

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Attenuated positive symptoms of psychosis in adolescents 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=3272485

27 July 2018

A cognitive neuroscience-based computerized battery for efficient measurement of individual differences: standardization and initial construct validation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Large recurrent microdeletions associated with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Schizophrenia: a concise overview of incidence, prevalence, and mortality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

The neural correlates of non-spatial working memory in velocardiofacial syndrome (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=3272485

27 July 2018

Verbal short-term memory in individuals with chromosome 22q11.2 deletion: specific deficit in serial order retention capacities?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

The Consortium on the Genetics of Endophenotypes in Schizophrenia: model recruitment, assessment, and endophenotyping methods for a multisite collaboration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Assessment of adolescents at risk for psychosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

The schizophrenia phenotype in 22q11 deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Working memory for complex figures: an fMRI comparison of letter and fractal n-back tasks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Neuropsychological deficits in neuroleptic naive patients with first-episode schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Neuropsychological function in schizophrenia. Selective impairment in memory and learning

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

27 July 2018

Performance on the Modified Card Sorting Test and its relation to psychopathology in adolescents and young adults 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=3272485

25 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

Associations between performance on the Rey-Osterrieth Complex Figure and regional brain volumes in children with and without velocardiofacial syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 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=3272485

25 September 2018

Neurocognitive endophenotypes in a multiplex multigenerational family study of schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

Clinical features of 78 adults with 22q11 Deletion Syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

Computerized neurocognitive scanning: II. The profile of schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

Computerized neurocognitive scanning: I. Methodology and validation in healthy people.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

High rates of schizophrenia in adults with 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=3272485

25 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3272485

25 September 2018

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=3272485

25 September 2018

The relationship of APOE genotype to neuropsychological performance in long-term cancer survivors treated with standard dose chemotherapy

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https://api.crossref.org/works/10.1002%2FAJMG.B.32005

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22170773

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3

1 reference

https://pubmed.ncbi.nlm.nih.gov/22170773

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Potential linkage disequilibrium between schizophrenia and locus D22S278 on the long arm of chromosome 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/22170773

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The course of cognitive functioning in first episode psychosis: changes over time and impact on outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22170773

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.B.32005

1 reference

Europe PubMed Central

10 August 2017

release_podkhhja4nhfndzdurfrnaj2ka

1 reference

https://api.fatcat.wiki/v0/release/podkhhja4nhfndzdurfrnaj2ka

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

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