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 (Q40722387)

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scientific article published on 9 December 2002

Language	Label	Description	Also known as
English	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	scientific article published on 9 December 2002

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

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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 (English)

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

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genetic variation

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inferred from title

Marcella Rietschel

8

object named as

Marcella Rietschel

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Europe PubMed Central

PMC publication ID

23 September 2017

author name string

Sibylle G Schwab

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23 September 2017

Michael Knapp

2

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23 September 2017

Stephanie Mondabon

3

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23 September 2017

Joachim Hallmayer

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23 September 2017

Margitta Borrmann-Hassenbach

5

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23 September 2017

Margot Albus

6

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23 September 2017

Bernard Lerer

7

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23 September 2017

Matyas Trixler

9

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23 September 2017

Wolfgang Maier

10

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23 September 2017

Dieter B Wildenauer

11

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23 September 2017

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publication date

9 December 2002

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23 September 2017

American Journal of Human Genetics

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23 September 2017

72

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23 September 2017

1

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23 September 2017

185-190

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23 September 2017

Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness

1 reference

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25 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378624

25 September 2017

Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain

1 reference

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The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

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Transmission/disequilibrium tests using multiple tightly linked markers

1 reference

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Fluorescence polarization in homogeneous nucleic acid analysis

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25 September 2017

Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378624

25 September 2017

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

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25 September 2017

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

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25 September 2017

Haplotype studies in Wilson disease

1 reference

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25 September 2017

Haplotypes and mutations in Wilson disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378624

25 September 2017

On measures of gametic disequilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378624

25 September 2017

Schizophrenia and chromosome 6p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378624

25 September 2017

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

1 reference

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17 June 2018

Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population

1 reference

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Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12474144

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based on heuristic

inferred from PubMed ID database lookup

Evidence for a susceptibility locus for schizophrenia on chromosome 6pter–p22

1 reference

https://pubmed.ncbi.nlm.nih.gov/12474144

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An international two–stage genome–wide search for schizophrenia susceptibility genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12474144

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib–pair linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12474144

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8

1 reference

https://pubmed.ncbi.nlm.nih.gov/12474144

12 December 2020

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Chromosome 6 workshop report

1 reference

https://pubmed.ncbi.nlm.nih.gov/12474144

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Evaluation of linkage of markers on chromosome 6p with schizophrenia in Taiwanese families

1 reference

https://pubmed.ncbi.nlm.nih.gov/12474144

12 December 2020

based on heuristic

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Identifiers

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

ResearchGate publication ID

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