Literature DB >> 8533170

Polygenic disease: methods for mapping complex disease traits.

D E Weeks1, G M Lathrop.   

Abstract

Improved genotyping technology has made it feasible to use a genetic approach to map genes involved in the etiology of common human diseases. We discuss here recent developments in several different statistical approaches to linkage analysis of these traits, including affected-sib-pair methods, the affected-pedigree-member method, regressive models and linkage-disequilibrium-based approaches. We discuss advantages and disadvantages of the various approaches, as well as factors influencing study design and the ability to detect loci. Statistical methodology in this area is advancing rapidly and will help enable the mapping and cloning of loci involved in susceptibility to common multifactorial diseases.

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Year:  1995        PMID: 8533170     DOI: 10.1016/s0168-9525(00)89163-5

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  43 in total

1.  Genetic and nongenetic bases for the L-shaped distribution of quantitative trait loci effects.

Authors:  B Bost; D de Vienne; F Hospital; L Moreau; C Dillmann
Journal:  Genetics       Date:  2001-04       Impact factor: 4.562

2.  Sampling strategies for model free linkage analyses of quantitative traits: implications for sib pair studies of reading and spelling disabilities to minimize the total study cost.

Authors:  A Ziegler
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

3.  Full flexibility genotyping of single nucleotide polymorphisms by the GOOD assay.

Authors:  S Sauer; D Lechner; K Berlin; C Plançon; A Heuermann; H Lehrach; I G Gut
Journal:  Nucleic Acids Res       Date:  2000-12-01       Impact factor: 16.971

4.  A tale of two genotypes: consistency between two high-throughput genotyping centers.

Authors:  Daniel E Weeks; Yvette P Conley; Robert E Ferrell; Tammy S Mah; Michael B Gorin
Journal:  Genome Res       Date:  2002-03       Impact factor: 9.043

5.  Genomewide scans of complex human diseases: true linkage is hard to find.

Authors:  J Altmüller; L J Palmer; G Fischer; H Scherb; M Wjst
Journal:  Am J Hum Genet       Date:  2001-09-14       Impact factor: 11.025

Review 6.  Defining the genetic contribution of type 2 diabetes mellitus.

Authors:  J van Tilburg; T W van Haeften; P Pearson; C Wijmenga
Journal:  J Med Genet       Date:  2001-09       Impact factor: 6.318

7.  Linkage and association studies of atopy and the chromosome 11q13 region.

Authors:  K A Deichmann; B Starke; S Schlenther; A Heinzmann; S H Sparholt; J Forster; J Kuehr
Journal:  J Med Genet       Date:  1999-05       Impact factor: 6.318

8.  MALDI mass spectrometry analysis of single nucleotide polymorphisms by photocleavage and charge-tagging.

Authors:  Sascha Sauer; Hans Lehrach; Richard Reinhardt
Journal:  Nucleic Acids Res       Date:  2003-06-01       Impact factor: 16.971

Review 9.  A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia).

Authors:  S E Fisher; J F Stein; A P Monaco
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

10.  The association of flowering time quantitative trait loci with duplicated regions and candidate loci in Brassica oleracea.

Authors:  E J Bohuon; L D Ramsay; J A Craft; A E Arthur; D F Marshall; D J Lydiate; M J Kearsey
Journal:  Genetics       Date:  1998-09       Impact factor: 4.562

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