(Q35081418)

6 August 2017

title

Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome (English)

1 reference

6 August 2017

0 references

4

Herman van Engeland

1 reference

6 August 2017

6

René S Kahn

1 reference

6 August 2017

Jacob A S Vorstman

1

1 reference

6 August 2017

Eva W Chow

2

1 reference

6 August 2017

Roel A Ophoff

3

1 reference

6 August 2017

Frits A Beemer

5

1 reference

6 August 2017

Richard J Sinke

7

1 reference

6 August 2017

Anne S Bassett

8

1 reference

6 August 2017

publication date

1 April 2009

1 reference

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

6 August 2017

published in

1 reference

6 August 2017

volume

150B

1 reference

6 August 2017

issue

3

1 reference

6 August 2017

page(s)

430-433

1 reference

Schizophrenia and 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=3127866

Detailed analysis of 22q11.2 with a high density MLPA probe set

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127866

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=3127866

An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene 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=3127866

Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 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=3127866

Haploview: analysis and visualization of LD and haplotype maps

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127866

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=3127866

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127866

Cloning, expression, and localization of 230-kDa phosphatidylinositol 4-kinase

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127866

Association between polymorphism of the SNAP29 gene promoter region 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=3127866

Polymorphism in SNAP29 gene promoter region associated with schizophrenia

16 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18646052

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AJMG.B.30827

1 reference

release_yxaonrhufngsbk2xwdgrjn56wm

6 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/yxaonrhufngsbk2xwdgrjn56wm

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

3127866

1 reference

6 August 2017

1 reference