Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia (Q33608652)

28 July 2017

Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia (English)

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28 July 2017

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4

Jean-Paul Selten

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28 July 2017

7

René S Kahn

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28 July 2017

Mechteld L C Hoogendoorn

1

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28 July 2017

Jacob A S Vorstman

2

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28 July 2017

Gholam R Jalali

3

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28 July 2017

Richard J Sinke

5

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28 July 2017

Beverly S Emanuel

6

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28 July 2017

language of work or name

English

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publication date

26 October 2007

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28 July 2017

5

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inferred from page(s)

published in

Schizophrenia Research

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28 July 2017

98

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28 July 2017

1-3

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28 July 2017

84-88

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MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

The schizophrenia phenotype in 22q11 deletion syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Childhood-onset schizophrenia: research update

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Neuropsychiatric disorders in the 22q11 deletion syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

A separate disease within the syndrome of schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Deficit psychopathology and a paradigm shift in schizophrenia research

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

A common molecular basis for rearrangement disorders on chromosome 22q11

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

A population study of chromosome 22q11 deletions in infancy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Prevalence of 22q11 microdeletion

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

The Schedule for the Deficit syndrome: an instrument for research in schizophrenia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

The Comprehensive Assessment of Symptoms and History (CASH). An instrument for assessing diagnosis and psychopathology.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Assessment of the frequency of the 22q11 deletion in Afrikaner schizophrenic patients

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Screening for 22q11 deletions in a schizophrenia population.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Velocardiofacial syndrome in childhood-onset schizophrenia.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

22q11 deletion syndrome in childhood onset schizophrenia: an update

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810966

Family characteristics of deficit and nondeficit schizophrenia in the Roscommon Family Study

30 October 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1016/J.SCHRES.2007.09.025

Identifiers

DOI

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28 July 2017

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28 July 2017

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