Literature DB >> 2018040

Testing for association between disease and linked marker loci: a log-linear-model analysis.

L Tiret1, P Amouyel, R Rakotovao, F Cambien, P Ducimetière.   

Abstract

One approach frequently used for identifying genetic factors involved in the process of a complex disease is the comparison of patients and controls for a number of genetic markers near a candidate gene. The analysis of such association studies raises some specific problems because of the fact that genotypic and not gametic data are generally available. We present a log-linear-model analysis providing a valid method for analyzing such studies. When studying the association of disease with one marker locus, the log-linear model allows one to test for the difference between allelic frequencies among affected and unaffected individuals, Hardy-Weinberg (H-W) equilibrium in both groups, and interaction between the association of alleles at the marker locus and disease. This interaction provides information about the dominance of the disease susceptibility locus, with dominance defined using the epidemiological notion of odds ratio. The degree of dominance measured at the marker locus depends on the strength of linkage disequilibrium between the marker locus and the disease locus. When studying the association of disease with several linked markers, the model becomes rapidly complex and uninterpretable unless it is assumed that affected and unaffected populations are in H-W equilibrium at each locus. This hypothesis must be tested before going ahead in the analysis. If it is not rejected, the log-linear model offers a stepwise method of identification of the parameters causing the difference between populations. This model can be extended to any number of loci, alleles, or populations.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 2018040      PMCID: PMC1683048     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  6 in total

1.  Tests for association of gene frequencies at several loci in random mating diploid populations.

Authors:  W G Hill
Journal:  Biometrics       Date:  1975-12       Impact factor: 2.571

2.  Measures of association between disease and genotype.

Authors:  P K Norwood; K Hinkelmann
Journal:  Biometrics       Date:  1978-12       Impact factor: 2.571

3.  Log-linear models for linked loci.

Authors:  B S Weir; S R Wilson
Journal:  Biometrics       Date:  1986-09       Impact factor: 2.571

4.  The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes.

Authors:  E A Thompson; S Deeb; D Walker; A G Motulsky
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

5.  Inferences about linkage disequilibrium.

Authors:  B S Weir
Journal:  Biometrics       Date:  1979-03       Impact factor: 2.571

6.  DNA polymorphisms of the apolipoprotein B gene in patients with premature coronary artery disease.

Authors:  J J Genest; J M Ordovas; J R McNamara; A M Robbins; T Meade; S D Cohn; D N Salem; P W Wilson; U Masharani; P M Frossard
Journal:  Atherosclerosis       Date:  1990-05       Impact factor: 5.162

  6 in total
  9 in total

1.  Identification of new polymorphisms of the angiotensin I-converting enzyme (ACE) gene, and study of their relationship to plasma ACE levels by two-QTL segregation-linkage analysis.

Authors:  E Villard; L Tiret; S Visvikis; R Rakotovao; F Cambien; F Soubrier
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.

Authors:  L Gouas; V Nicaud; S Chaouch; M Berthet; A Forhan; J Tichet; L Tiret; B Balkau; P Guicheney
Journal:  Eur J Hum Genet       Date:  2007-05-30       Impact factor: 4.246

3.  Sequence diversity in 36 candidate genes for cardiovascular disorders.

Authors:  F Cambien; O Poirier; V Nicaud; S M Herrmann; C Mallet; S Ricard; I Behague; V Hallet; H Blanc; V Loukaci; J Thillet; A Evans; J B Ruidavets; D Arveiler; G Luc; L Tiret
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

4.  Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.

Authors:  S Mead; S P Mahal; J Beck; T Campbell; M Farrall; E Fisher; J Collinge
Journal:  Am J Hum Genet       Date:  2001-11-05       Impact factor: 11.025

5.  Thrombomodulin gene polymorphisms in brain infarction and mortality after stroke.

Authors:  Jean-Marc Olivot; Julien Labreuche; Thomas De Broucker; Odette Poirier; François Cambien; Martine Aiach; Pierre Amarenco
Journal:  J Neurol       Date:  2008-01-23       Impact factor: 4.849

6.  Promoter variants in tissue inhibitor of metalloproteinase-3 (TIMP-3) protect against susceptibility in pigeon breeders' disease.

Authors:  M R Hill; L Briggs; M M Montaño; A Estrada; G J Laurent; M Selman; A Pardo
Journal:  Thorax       Date:  2004-07       Impact factor: 9.139

7.  The plasminogen activator inhibitor-1 (PAI-1) gene -844 A/G and -675 4G/5G promoter polymorphism significantly influences plasma PAI-1 levels in women with polycystic ovary syndrome.

Authors:  Sun Lin; Zhang Huiya; Liu Bo; Wei Wei; Guan Yongmei
Journal:  Endocrine       Date:  2009-10-24       Impact factor: 3.633

8.  Meta-analysis of haplotype-association studies: comparison of methods and empirical evaluation of the literature.

Authors:  Pantelis G Bagos
Journal:  BMC Genet       Date:  2011-01-19       Impact factor: 2.797

9.  On the use of haplotype phylogeny to detect disease susceptibility loci.

Authors:  Claire Bardel; Vincent Danjean; Jean-Pierre Hugot; Pierre Darlu; Emmanuelle Génin
Journal:  BMC Genet       Date:  2005-05-18       Impact factor: 2.797

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.