Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia (Q37402422)

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scientific article published on 27 October 2009

Language	Label	Description	Also known as
English	Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia	scientific article published on 27 October 2009

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

0 references

whole genome sequencing

1 reference

based on heuristic

inferred from title

Michael C O'Donovan

12

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Europe PubMed Central

PMC publication ID

20 August 2017

13

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Europe PubMed Central

PMC publication ID

20 August 2017

author name string

Yang Liu

1

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Europe PubMed Central

PMC publication ID

20 August 2017

Gang Chen

2

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Europe PubMed Central

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20 August 2017

Nadine Norton

3

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Europe PubMed Central

PMC publication ID

20 August 2017

Wenmin Liu

4

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Europe PubMed Central

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20 August 2017

Haining Zhu

5

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Europe PubMed Central

PMC publication ID

20 August 2017

Peng Zhou

6

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Meng Luan

7

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Shulin Yang

8

1 reference

Europe PubMed Central

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20 August 2017

Xing Chen

9

1 reference

Europe PubMed Central

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20 August 2017

Liam Carroll

10

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Europe PubMed Central

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20 August 2017

Nigel M Williams

11

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Europe PubMed Central

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20 August 2017

Michael J Owen

14

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Europe PubMed Central

PMC publication ID

20 August 2017

publication date

27 October 2009

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Europe PubMed Central

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20 August 2017

Journal of Biomedicine and Biotechnology

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Europe PubMed Central

PMC publication ID

20 August 2017

2009

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

536918

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

copyright license

Creative Commons Attribution 3.0 Unported

1 January 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

Rheumatoid arthritis association at 6q23.

1 reference

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Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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6 September 2017

Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia

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6 September 2017

Positive association of schizophrenia to JARID2 gene

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6 September 2017

Making the case for a candidate vulnerability gene in schizophrenia: Convergent evidence for regulator of G-protein signaling 4 (RGS4)

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Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the disease

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Genomic approaches to schizophrenia

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Schizophrenia: genes at last?

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Whole genome association study of rheumatoid arthritis using 27 039 microsatellites

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6 September 2017

Finding schizophrenia genes

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Complement factor H polymorphism in age-related macular degeneration

1 reference

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Association of the DTNBP1 locus with schizophrenia in a U.S. population

1 reference

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Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia

1 reference

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Haploview: analysis and visualization of LD and haplotype maps

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Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

1 reference

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Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768871

6 September 2017

The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768871

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Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768871

6 September 2017

Neuregulin 1 and susceptibility to schizophrenia

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768871

6 September 2017

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

1 reference

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High-throughput SNP genotyping by allele-specific PCR with universal energy-transfer-labeled primers

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New gene found for inherited macular degeneration

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Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families

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27 July 2018

The dysbindin gene (DTNBP1) and schizophrenia: no support for an association in the Korean population

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2 September 2018

Dysbindin genotype and negative symptoms in schizophrenia.

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2 September 2018

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.

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Linkage disequlibrium in the DTNBP1 (dysbindin) gene region and on chromosome 1p36 among psychotic patients from a genetic isolate in Israel: findings from identity by descent haplotype sharing analysis

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Human dysbindin (DTNBP1) gene expression in normal brain and in schizophrenic prefrontal cortex and midbrain

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2 September 2018

Pedigree disequilibrium tests for multilocus haplotypes.

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HUMAN GENETICS:New Gene Found for Inherited Macular Degeneration

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Miniaturized sealed-tube allele-specific PCR

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21 January 2018

Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations

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https://api.crossref.org/works/10.1155%2F2009%2F536918

21 January 2018

No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families

1 reference

https://api.crossref.org/works/10.1155%2F2009%2F536918

21 January 2018

No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study

1 reference

https://api.crossref.org/works/10.1155%2F2009%2F536918

21 January 2018

The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland

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21 January 2018

The contribution of three strong candidate schizophrenia susceptibility genes in demographically distinct populations

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https://pubmed.ncbi.nlm.nih.gov/19884986

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family-based association study of DTNBP1 in 6p22.3 and schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19884986

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/19884986

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene offers insight into macular degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/19884986

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1155/2009/536918

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

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