A compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility (Q24534073)

4 July 2017

A compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility (English)

1 reference

4 July 2017

0 references

Aravinda Chakravarti

1

1 reference

PubMed ID

11959925

4 July 2017

language of work or name

English

0 references

publication date

1 April 2002

1 reference

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

4 July 2017

1 reference

4 July 2017

99

1 reference

4 July 2017

4755-4756

1 reference

4 July 2017

8

1 reference

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

4 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122660

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=122660

The DNA sequence of human chromosome 22

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122660

Genetic dissection of complex traits

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122660

Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122660

Genetics of schizophrenia and the new millennium: progress and pitfalls

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122660

Understanding the molecular basis of fragile X syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122660

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=122660

Path analysis of qualitative data on pairs of relatives: application to 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=122660

Linkage strategies for genetically complex traits. I. Multilocus models

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122660

The marker (X) syndrome: a cytogenetic and genetic analysis.

27 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.092158299

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.092158299

Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11959925

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Population genetics--making sense out of sequence

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11959925

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.092158299

1 reference

4 July 2017

0 references

1 reference

4 July 2017

1 reference

PubMed ID

11959925