Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and function (Q21145031)

11

object named as

Andreas Meyer-Lindenberg

Andreas

Meyer-Lindenberg

1 reference

17 August 2022

9

Joseph H Callicott

Joseph H

Callicott

1 reference

17 August 2022

10

Daniel R Weinberger

Daniel R

Weinberger

1 reference

17 August 2022

7

Richard E Straub

Richard E

Straub

1 reference

17 August 2022

6

Michael F Egan

Michael F

Egan

1 reference

17 August 2022

3

Bhaskar Kolachana

Bhaskar

Kolachana

1 reference

17 August 2022

Lucas Kempf

1

Lucas

Kempf

1 reference

17 August 2022

Kristin K Nicodemus

2

Kristin K

Nicodemus

1 reference

17 August 2022

Radhakrishna Vakkalanka

4

Radhakrishna

Vakkalanka

1 reference

17 August 2022

Beth A Verchinski

5

Beth A

Verchinski

1 reference

17 August 2022

Venkata A Mattay

8

Venkata A

Creative Commons CC0 License

Mattay

1 reference

17 August 2022

language of work or name

English

0 references

publication date

November 2008

0 references

published in

PLOS Genetics

0 references

volume

4

0 references

issue

11

0 references

page(s)

e1000252

0 references

copyright license

start time

7 November 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

0 references

cites work

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

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Early neurological phenotype in 4 children with biallelic PRODH mutations

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Association study of the G-protein signaling 4 (RGS4) and proline dehydrogenase (PRODH) genes with schizophrenia: a meta-analysis

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Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population

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Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

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PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

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12 September 2017

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12 September 2017

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12 September 2017

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12 September 2017

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12 September 2017

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27 September 2017

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27 September 2017

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Association between PRODH and schizophrenia is not confirmed

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573019

Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome.

30 May 2018

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

21 January 2018

1 reference

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Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

Failure to find association between PRODH deletion and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

Hyperprolinemia is not associated with childhood onset schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

Dysfunctional prefrontal regional specialization and compensation in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

Heritability of brain morphology related to schizophrenia: a large-scale automated magnetic resonance imaging segmentation study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

snp.plotter: an R-based SNP/haplotype association and linkage disequilibrium plotting package.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

The brain-derived neurotrophic factor val66met polymorphism and variation in human cortical morphology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

Abnormal fMRI response of the dorsolateral prefrontal cortex in cognitively intact siblings of patients with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

Impact of complex genetic variation in COMT on human brain function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000252

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=2573019

Schizophrenia and chromosomal deletions within 22q11.2.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573019

Novel CAG/CTG repeat expansion mutations do not contribute to the genetic risk for most cases of bipolar disorder or schizophrenia

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18989458

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Allelic discrimination using fluorogenic probes and the 5' nuclease assay

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18989458

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1000252

1 reference

2563468

2563468

1 reference

1 reference

1 reference