Literature DB >> 17202285

Haplotype thinking in lung disease.

Edwin K Silverman1.   

Abstract

To identify the genetic etiology of a disease of interest, disease-related characteristics (phenotypes) are often tested for association with genetic variants (genotypes). Although genetic association studies of single genetic variants have been widely performed, there has been increasing interest in studies of multiple adjacent genetic variants on one chromosome, known as a haplotype. In this review, we will provide background about the origin of haplotypes and why they can be useful in genetic studies; we will discuss approaches to determining haplotypes and performing haplotype-based genetic association studies; and we will compare single variant and haplotype-based approaches.

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Year:  2007        PMID: 17202285      PMCID: PMC2647613          DOI: 10.1513/pats.200607-145JG

Source DB:  PubMed          Journal:  Proc Am Thorac Soc        ISSN: 1546-3222


  36 in total

1.  Use of unlinked genetic markers to detect population stratification in association studies.

Authors:  J K Pritchard; N A Rosenberg
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

2.  Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations.

Authors:  S K Service; D W Lang; N B Freimer; L A Sandkuijl
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

3.  PBAT: tools for family-based association studies.

Authors:  Christoph Lange; Dawn DeMeo; Edwin K Silverman; Scott T Weiss; Nan M Laird
Journal:  Am J Hum Genet       Date:  2004-02       Impact factor: 11.025

4.  Comparison of prospective and retrospective methods for haplotype inference in case-control studies.

Authors:  Glen A Satten; Michael P Epstein
Journal:  Genet Epidemiol       Date:  2004-11       Impact factor: 2.135

Review 5.  Single-molecule analysis for molecular haplotyping.

Authors:  Pui-Yan Kwok; Ming Xiao
Journal:  Hum Mutat       Date:  2004-05       Impact factor: 4.878

6.  Little loss of information due to unknown phase for fine-scale linkage-disequilibrium mapping with single-nucleotide-polymorphism genotype data.

Authors:  A P Morris; J C Whittaker; D J Balding
Journal:  Am J Hum Genet       Date:  2004-04-07       Impact factor: 11.025

Review 7.  Inference of haplotypes from PCR-amplified samples of diploid populations.

Authors:  A G Clark
Journal:  Mol Biol Evol       Date:  1990-03       Impact factor: 16.240

8.  Identification of the cystic fibrosis gene: genetic analysis.

Authors:  B Kerem; J M Rommens; J A Buchanan; D Markiewicz; T K Cox; A Chakravarti; M Buchwald; L C Tsui
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

9.  Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population.

Authors:  L Excoffier; M Slatkin
Journal:  Mol Biol Evol       Date:  1995-09       Impact factor: 16.240

10.  A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping or DNA sequencing. V. Analysis of case/control sampling designs: Alzheimer's disease and the apoprotein E locus.

Authors:  A R Templeton
Journal:  Genetics       Date:  1995-05       Impact factor: 4.562

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  2 in total

1.  Genetic diversity of Ophiocordyceps sinensis, a medicinal fungus endemic to the Tibetan Plateau: implications for its evolution and conservation.

Authors:  Yongjie Zhang; Lingling Xu; Shu Zhang; Xingzhong Liu; Zhiqiang An; Mu Wang; Yinglan Guo
Journal:  BMC Evol Biol       Date:  2009-12-16       Impact factor: 3.260

2.  Association of PDE11A global haplotype with major depression and antidepressant drug response.

Authors:  Huai-Rong Luo; Gui-Sheng Wu; Chuanhui Dong; Mauricio Arcos-Burgos; Luciana Ribeiro; Julio Licinio; Ma-Li Wong
Journal:  Neuropsychiatr Dis Treat       Date:  2009-04-08       Impact factor: 2.570

  2 in total

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