Literature DB >> 18450062

Association methods in human genetics.

Carl D Langefeld1, Tasha E Fingerlin.   

Abstract

Genetic association studies are increasingly used in the search for susceptibility variants for human traits. While many of the statistical tools available for such studies are well established, the field is advancing rapidly, as biological and technological developments allow investigators to generate vast amounts of detailed genetic data. This chapter gives an overview of the statistical evaluation of genetic data in both unrelated individuals and families. A brief introduction to fundamental population genetics concepts is followed by detailed examinations of measures of linkage disequilibrium and single-marker and haplotype association tests. Emphasis is given to the historical development of family-based tests to provide the context for more recent advancements. The chapter concludes with a discussion of design strategies for genetic association studies with dense genotyping of hundreds or thousands of markers, such as those planned for follow up of a linkage-candidate region or genome-wide association studies.

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Mesh:

Year:  2007        PMID: 18450062     DOI: 10.1007/978-1-59745-530-5_21

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  6 in total

1.  A new permutation strategy of pathway-based approach for genome-wide association study.

Authors:  Yan-Fang Guo; Jian Li; Yuan Chen; Li-Shu Zhang; Hong-Wen Deng
Journal:  BMC Bioinformatics       Date:  2009-12-18       Impact factor: 3.169

Review 2.  The Alpha Project: a model system for systems biology research.

Authors:  R C Yu; O Resnekov; A P Abola; S S Andrews; K R Benjamin; J Bruck; I E Burbulis; A Colman-Lerner; D Endy; A Gordon; M Holl; L Lok; C G Pesce; E Serra; R D Smith; T M Thomson; A E Tsong; R Brent
Journal:  IET Syst Biol       Date:  2008-09       Impact factor: 1.615

3.  Impact of the AHI1 gene on the vulnerability to schizophrenia: a case-control association study.

Authors:  Olga Rivero; Andreas Reif; Julio Sanjuán; María D Moltó; Sarah Kittel-Schneider; Carmen Nájera; Theresia Töpner; Klaus-Peter Lesch
Journal:  PLoS One       Date:  2010-08-18       Impact factor: 3.240

4.  Whole-genome haplotyping approaches and genomic medicine.

Authors:  Gustavo Glusman; Hannah C Cox; Jared C Roach
Journal:  Genome Med       Date:  2014-09-25       Impact factor: 11.117

5.  Association of DTNBP1 With Schizophrenia: Findings From Two Independent Samples of Han Chinese Population.

Authors:  Yongfeng Yang; Luwen Zhang; Dong Guo; Lin Zhang; Hongyan Yu; Qing Liu; Xi Su; Minglong Shao; Men Song; Yan Zhang; Minli Ding; Yanli Lu; Bing Liu; Wenqiang Li; Weihua Yue; Xiaoduo Fan; Ge Yang; Luxian Lv
Journal:  Front Psychiatry       Date:  2020-05-25       Impact factor: 4.157

6.  Working memory deficits in schizophrenia are associated with the rs34884856 variant and expression levels of the NR4A2 gene in a sample Mexican population: a case control study.

Authors:  Elizabeth Ruiz-Sánchez; Janet Jiménez-Genchi; Yessica M Alcántara-Flores; Carlos J Castañeda-González; Carlos L Aviña-Cervantes; Petra Yescas; María Del Socorro González-Valadez; Nancy Martínez-Rodríguez; Antonio Ríos-Ortiz; Martha González-González; María E López-Navarro; Patricia Rojas
Journal:  BMC Psychiatry       Date:  2021-02-09       Impact factor: 3.630

  6 in total

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