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

6 July 2017

title

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

Judith L Rapoport

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6 July 2017

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

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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

published in

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6 July 2017

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6 July 2017

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6 July 2017

page(s)

16859-16864

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

6 July 2017

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24 March 2017

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24 March 2017

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24 March 2017

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A common molecular basis for rearrangement disorders on chromosome 22q11

24 March 2017

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24 March 2017

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24 March 2017

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24 March 2017

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24 March 2017

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27 September 2017

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27 September 2017

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A general test of association for quantitative traits in nuclear families

27 September 2017

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

27 September 2017

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Prevalence of 22q11 microdeletion

27 September 2017

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A comparison of linkage disequilibrium measures for fine-scale mapping

27 September 2017

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27 September 2017

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

27 September 2017

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Gametic disequilibrium measures: proceed with caution

27 September 2017

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

27 September 2017

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30 May 2018

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

30 May 2018

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

21 January 2018

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Velocardiofacial syndrome in childhood-onset schizophrenia.

21 January 2018

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

21 January 2018

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A first-generation linkage disequilibrium map of human chromosome 22

21 January 2018

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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

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21 January 2018

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

21 January 2018

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

21 January 2018

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

29 November 2018

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PubMed

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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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