Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan. (Q37371260)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18332877%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan (English)

1 reference

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4 January 2020

0 references

2

1 reference

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4 January 2020

Stephen J Glatt

1

1 reference

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4 January 2020

Hai-Gwo Hwu

5

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4 January 2020

author name string

J A Lasky-Su

3

1 reference

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4 January 2020

T Kanazawa

4

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4 January 2020

M T Tsuang

6

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4 January 2020

language of work or name

English

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publication date

11 March 2008

1 reference

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4 January 2020

1 reference

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4 January 2020

volume

14

1 reference

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4 January 2020

issue

9

1 reference

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4 January 2020

page(s)

885-893

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Psychosis pathways converge via D2high dopamine receptors

4 January 2020

cites work

1 reference

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The Cys allele of the DRD2 Ser311Cys polymorphism has a dominant effect on risk for schizophrenia: evidence from fixed- and random-effects meta-analyses

6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

6 September 2017

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Power and design considerations for a general class of family-based association tests: quantitative traits

6 September 2017

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The structure of haplotype blocks in the human genome

6 September 2017

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Genomic control for association studies

6 September 2017

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Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

6 September 2017

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Sustained attention deficits as markers of genetic susceptibility to schizophrenia

6 September 2017

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dbSNP-database for single nucleotide polymorphisms and other classes of minor genetic variation

6 September 2017

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The effect of family structure on linkage tests using allelic association.

6 September 2017

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Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

6 September 2017

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Functional analysis of the human D2 dopamine receptor missense variants

6 September 2017

1 reference

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Implementing a unified approach to family-based tests of association.

28 September 2017

1 reference

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A structural polymorphism of human dopamine D2 receptor, D2(Ser311-->Cys).

26 June 2018

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Genome-wide linkage scan of schizophrenia: a cross-isolate study.

26 June 2018

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PBAT: tools for family-based association studies

2 September 2018

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Meta-analysis identifies an association between the dopamine D2 receptor gene and schizophrenia

2 September 2018

1 reference

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The family based association test method: strategies for studying general genotype--phenotype associations.

2 September 2018

1 reference

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No association of the Ser/Cys311 DRD2 molecular variant with schizophrenia using a classical case control study and the haplotype relative risk

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FMP.2008.30

Hardy–Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations and power

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FMP.2008.30

Association of dopamine D2 receptor molecular variant with schizophrenia

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18332877

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/MP.2008.30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18332877%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18332877%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

PubMed publication ID

18332877

1 reference