Genetic variation in the 22q11 locus and susceptibility to schizophrenia (Q24543969)

6 July 2017

Genetic variation in the 22q11 locus and susceptibility to schizophrenia (English)

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6 July 2017

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6 July 2017

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Judith L Rapoport

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6 July 2017

9

Joseph A Gogos

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6 July 2017

Hui Liu

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6 July 2017

Simon C Heath

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6 July 2017

Alyson Knowles

4

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6 July 2017

Sandra Demars

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6 July 2017

Ying-Jiun Chen

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6 July 2017

J Louw Roos

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6 July 2017

Maria Karayiorgou

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6 July 2017

language of work or name

English

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publication date

11 December 2002

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Proceedings of the National Academy of Sciences of the United States of America

6 July 2017

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6 July 2017

99

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6 July 2017

16859-16864

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6 July 2017

26

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

6 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Identification of a receptor mediating Nogo-66 inhibition of axonal regeneration

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

The DHHC domain: a new highly conserved cysteine-rich motif

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Erf2, a novel gene product that affects the localization and palmitoylation of Ras2 in Saccharomyces cerevisiae

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

A common molecular basis for rearrangement disorders on chromosome 22q11

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

A genome-wide search for schizophrenia susceptibility genes

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Characterization of proteins that interact with the cell-cycle regulatory protein Ran/TC4

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Linkage disequilibrium in the human genome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Extent and distribution of linkage disequilibrium in three genomic regions

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

The 22q11 deletion syndromes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

A general test of association for quantitative traits in nuclear families

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Prevalence of 22q11 microdeletion

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

A comparison of linkage disequilibrium measures for fine-scale mapping

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Gametic disequilibrium measures: proceed with caution

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Expression of the murine RanBP1 and Htf9-c genes is regulated from a shared bidirectional promoter during cell cycle progression

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

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

30 May 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.232186099

Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.232186099

Velocardiofacial syndrome in childhood-onset schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.232186099

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.232186099

A first-generation linkage disequilibrium map of human chromosome 22

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.232186099

TRAIL-induced apoptosis in human vascular endothelium is regulated by phosphatidylinositol 3-kinase/Akt through the short form of cellular FLIP and Bcl-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.232186099

Pedigree tests of transmission disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.232186099

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.232186099

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139234

Circumventing multiple testing: a multilocus Monte Carlo approach to testing for association

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12477929

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.232186099

1 reference

6 July 2017

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6 July 2017

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