(Q35085481)

6 August 2017

title

Clinically detectable copy number variations in a Canadian catchment population of schizophrenia (English)

1 reference

6 August 2017

0 references

Anne S Bassett

1

1 reference

6 August 2017

Gregory Costain

2

1 reference

6 August 2017

Wai Lun Alan Fung

3

1 reference

6 August 2017

Kathryn J Russell

4

1 reference

6 August 2017

Laura Pierce

5

1 reference

6 August 2017

Ronak Kapadia

6

1 reference

6 August 2017

Ronald F Carter

7

1 reference

6 August 2017

Eva W C Chow

8

1 reference

6 August 2017

Pamela J Forsythe

9

1 reference

6 August 2017

publication date

1 November 2010

1 reference

Journal of Psychiatric Research

6 August 2017

published in

1 reference

6 August 2017

volume

44

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6 August 2017

issue

15

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6 August 2017

page(s)

1005-1009

1 reference

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

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Origins and functional impact of copy number variation in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Clinical application of microarray-based molecular cytogenetics: an emerging new era of genomic medicine

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Premature death in adults with 22q11.2 deletion syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Application of array-based comparative genome hybridization in children with developmental delay or mental retardation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Genomic microarrays in mental retardation: a practical workflow for diagnostic applications

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Strong association of de novo copy number mutations with sporadic schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Schizophrenia and 22q11.2 deletion syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Large-scale copy number polymorphism in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Genetic insights into the neurodevelopmental hypothesis of schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Genetic insights into schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Genetic counselling for schizophrenia in the era of molecular genetics

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Chromosomal abnormalities and schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

22q11 deletion syndrome: a genetic subtype of schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

A population study of chromosome 22q11 deletions in infancy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

[A study on the occurrence of the deletion 22q11.2 in patients affected with a psychiatric disease].

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Screening for 22q11 deletions in a schizophrenia population.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

No evidence of increased risk for schizophrenia or bipolar affective disorder in persons with aneuploidies of the sex chromosomes.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3129333

Systematic mutation analysis of the catechol O-methyltransferase gene as a candidate gene for schizophrenia

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20643418

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20643418

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.JPSYCHIRES.2010.06.013

1 reference

6 August 2017

1 reference

6 August 2017

1 reference