A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population (Q44312171)

1 December 2017

title

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

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1 December 2017

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Jin-Bo Fan

1

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1 December 2017

Jie Ma

2

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1 December 2017

Chang-Shun Zhang

3

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1 December 2017

Jun-Xia Tang

4

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1 December 2017

Niu-Fan Gu

5

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1 December 2017

Guo-Ying Feng

6

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1 December 2017

David St Clair

7

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1 December 2017

Lin He

8

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1 December 2017

language of work or name

English

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publication date

1 March 2003

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1 December 2017

number of pages

3

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inferred from page(s)

published in

Neuroscience Letters

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1 December 2017

volume

338

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1 December 2017

issue

3

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1 December 2017

page(s)

252-254

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Screening for 22q11 deletions in a schizophrenia population.

1 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

Genetics of schizophrenia and the new millennium: progress and pitfalls

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

A family-based and case-control association study of the NOTCH4 gene and schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

Genetic linkage in schizophrenia: perspectives from genetic epidemiology

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

Linkage and associated studies of schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

Schizophrenia: genes and environment

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

Velocardiofacial syndrome in childhood-onset schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901362-9

7 January 2021

10.1016/S0304-3940(02)01362-9

Identifiers

DOI

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1 December 2017

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