Literature DB >> 11409410

Search for multifactorial disease susceptibility genes in founder populations.

C Bourgain1, E Genin, H Quesneville, F Clerget-Darpoux.   

Abstract

The current challenge in biomedical research is to detect genetic risk factors involved in common complex diseases. The power to detect their role is generally poor in populations that have been large for a long time. It has been suggested that the power may be increased by taking advantage of the specificity of founder populations: linkage disequilibrium spanning larger regions and kinship coefficients being stronger than in large populations. A new method is proposed here, the Maximum Identity Length Contrast (MILC) which, in contrast with other existing methods, does not make the assumption of unique ancestry for the genetic risk factors. It is thus appropriate for a search for common genetic risk factors for complex diseases. Statistical properties of the method are discussed in realistic contexts.

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Year:  2000        PMID: 11409410     DOI: 10.1046/j.1469-1809.2000.6430255.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  24 in total

1.  Use of closely related affected individuals for the genetic study of complex diseases in founder populations.

Authors:  C Bourgain; E Génin; P Holopainen; K Mustalahti; M Mäki; J Partanen; F Clerget-Darpoux
Journal:  Am J Hum Genet       Date:  2000-11-30       Impact factor: 11.025

2.  On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.

Authors:  Jung-Ying Tzeng; B Devlin; Larry Wasserman; Kathryn Roeder
Journal:  Am J Hum Genet       Date:  2003-02-27       Impact factor: 11.025

3.  Transmission/disequilibrium test based on haplotype sharing for tightly linked markers.

Authors:  Shuanglin Zhang; Qiuying Sha; Huann-Sheng Chen; Jianping Dong; Renfang Jiang
Journal:  Am J Hum Genet       Date:  2003-08-15       Impact factor: 11.025

4.  Fast and robust association tests for untyped SNPs in case-control studies.

Authors:  Andrew S Allen; Glen A Satten; Sarah L Bray; Frank Dudbridge; Michael P Epstein
Journal:  Hum Hered       Date:  2010-07-30       Impact factor: 0.444

Review 5.  Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations.

Authors:  Daniel J Schaid
Journal:  Hum Hered       Date:  2010-07-03       Impact factor: 0.444

6.  Regression-based association analysis with clustered haplotypes through use of genotypes.

Authors:  Jung-Ying Tzeng; Chih-Hao Wang; Jau-Tsuen Kao; Chuhsing Kate Hsiao
Journal:  Am J Hum Genet       Date:  2005-12-19       Impact factor: 11.025

7.  An entropy-based statistic for genomewide association studies.

Authors:  Jinying Zhao; Eric Boerwinkle; Momiao Xiong
Journal:  Am J Hum Genet       Date:  2005-05-09       Impact factor: 11.025

8.  Association mapping via regularized regression analysis of single-nucleotide-polymorphism haplotypes in variable-sized sliding windows.

Authors:  Yi Li; Wing-Kin Sung; Jian Jun Liu
Journal:  Am J Hum Genet       Date:  2007-02-19       Impact factor: 11.025

9.  Linkage analysis with dense SNP maps in isolated populations.

Authors:  Céline Bellenguez; Carole Ober; Catherine Bourgain
Journal:  Hum Hered       Date:  2009-04-09       Impact factor: 0.444

10.  Association mapping by generalized linear regression with density-based haplotype clustering.

Authors:  Robert P Igo; Jing Li; Katrina A B Goddard
Journal:  Genet Epidemiol       Date:  2009-01       Impact factor: 2.135

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