Literature DB >> 17627801

Design and analysis of genetic association studies to finely map a locus identified by linkage analysis: assessment of the extent to which an association can account for the linkage.

R L Hanson1, W C Knowler.   

Abstract

Association studies are often used to finely map quantitative trait loci identified by linkage analysis. Once a polymorphism associated with the trait has been identified, it may be useful to conduct linkage analyses which adjust for this polymorphism to determine the extent to which the association accounts for the linkage signal. However, methods for conducting statistical significance tests for an observed reduction in the linkage signal are not well developed. In the present study we develop methods for assessment of the statistical significance of an observed reduction in the variance due to the linked locus, with variance components or with Haseman-Elston linkage methods. Simulations indicate that these methods have appropriate levels of type I error and that, like other association statistics, their power depends on the magnitude of linkage disequilibrium between functional and marker alleles and on the extent of similarity between the frequency of the functional allele and the frequency of the associated marker allele. These methods can help determine which association results are likely due to strong linkage disequilibrium with functional alleles and, thus, can facilitate the selection of small chromosomal regions for more extensive study.

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Year:  2007        PMID: 17627801     DOI: 10.1111/j.1469-1809.2007.00382.x

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


  4 in total

1.  Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees.

Authors:  Alejandro A Schäffer; Mathieu Lemire; Jürg Ott; G Mark Lathrop; Daniel E Weeks
Journal:  Hum Hered       Date:  2011-07-06       Impact factor: 0.444

2.  Association of variants in the carnosine peptidase 1 gene (CNDP1) with diabetic nephropathy in American Indians.

Authors:  Harini A Chakkera; Robert L Hanson; Sayuko Kobes; Meredith P Millis; Robert G Nelson; William C Knowler; Johanna K Distefano
Journal:  Mol Genet Metab       Date:  2011-02-19       Impact factor: 4.797

3.  Identification of genetic variation that determines human trehalase activity and its association with type 2 diabetes.

Authors:  Yunhua L Muller; Robert L Hanson; William C Knowler; Jamie Fleming; Jayita Goswami; Ke Huang; Michael Traurig; Jeff Sutherland; Chris Wiedrich; Kim Wiedrich; Darin Mahkee; Vicky Ossowski; Sayuko Kobes; Clifton Bogardus; Leslie J Baier
Journal:  Hum Genet       Date:  2013-03-07       Impact factor: 4.132

4.  A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes.

Authors:  Robert L Hanson; Yunhua L Muller; Sayuko Kobes; Tingwei Guo; Li Bian; Victoria Ossowski; Kim Wiedrich; Jeffrey Sutherland; Christopher Wiedrich; Darin Mahkee; Ke Huang; Maryam Abdussamad; Michael Traurig; E Jennifer Weil; Robert G Nelson; Peter H Bennett; William C Knowler; Clifton Bogardus; Leslie J Baier
Journal:  Diabetes       Date:  2013-10-07       Impact factor: 9.461

  4 in total

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