Literature DB >> 16096108

Prospects and pitfalls in whole genome association studies.

Robert W Lawrence1, David M Evans, Lon R Cardon.   

Abstract

Recent large-scale studies of common genetic variation throughout the human genome are making it feasible to conduct whole genome studies of genotype-phenotype associations. Such studies have the potential to uncover novel contributors to common complex traits and thus lead to insights into the aetiology of multifactorial phenotypes. Despite this promise, it is important to recognize that the availability of genetic markers and the ability to assay them at realistic cost does not guarantee success of this approach. There are a number of practical issues that require close attention, some forms of allelic architecture are not readily amenable to the association approach with even the most rigorous design, and doubtless new hurdles will emerge as the studies begin. Here we discuss the promise and current challenges of the whole genome approach, and raise some issues to consider in interpreting the results of the first whole genome studies.

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Year:  2005        PMID: 16096108      PMCID: PMC1569530          DOI: 10.1098/rstb.2005.1689

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  53 in total

1.  Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

Authors:  N Patil; A J Berno; D A Hinds; W A Barrett; J M Doshi; C R Hacker; C R Kautzer; D H Lee; C Marjoribanks; D P McDonough; B T Nguyen; M C Norris; J B Sheehan; N Shen; D Stern; R P Stokowski; D J Thomas; M O Trulson; K R Vyas; K A Frazer; S P Fodor; D R Cox
Journal:  Science       Date:  2001-11-23       Impact factor: 47.728

2.  Estimating recombination rates from population genetic data.

Authors:  P Fearnhead; P Donnelly
Journal:  Genetics       Date:  2001-11       Impact factor: 4.562

3.  A coalescent-based method for detecting and estimating recombination from gene sequences.

Authors:  Gil McVean; Philip Awadalla; Paul Fearnhead
Journal:  Genetics       Date:  2002-03       Impact factor: 4.562

4.  High-resolution haplotype structure in the human genome.

Authors:  M J Daly; J D Rioux; S F Schaffner; T J Hudson; E S Lander
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

5.  The structure of haplotype blocks in the human genome.

Authors:  Stacey B Gabriel; Stephen F Schaffner; Huy Nguyen; Jamie M Moore; Jessica Roy; Brendan Blumenstiel; John Higgins; Matthew DeFelice; Amy Lochner; Maura Faggart; Shau Neen Liu-Cordero; Charles Rotimi; Adebowale Adeyemo; Richard Cooper; Ryk Ward; Eric S Lander; Mark J Daly; David Altshuler
Journal:  Science       Date:  2002-05-23       Impact factor: 47.728

Review 6.  A bias-ed assessment of the use of SNPs in human complex traits.

Authors:  Joseph D Terwilliger; Fatemeh Haghighi; Tero S Hiekkalinna; Harald H H Göring
Journal:  Curr Opin Genet Dev       Date:  2002-12       Impact factor: 5.578

7.  A first-generation linkage disequilibrium map of human chromosome 22.

Authors:  Elisabeth Dawson; Gonçalo R Abecasis; Suzannah Bumpstead; Yuan Chen; Sarah Hunt; David M Beare; Jagjit Pabial; Thomas Dibling; Emma Tinsley; Susan Kirby; David Carter; Marianna Papaspyridonos; Simon Livingstone; Rocky Ganske; Elin Lõhmussaar; Jana Zernant; Neeme Tõnisson; Maido Remm; Reedik Mägi; Tarmo Puurand; Jaak Vilo; Ants Kurg; Kate Rice; Panos Deloukas; Richard Mott; Andres Metspalu; David R Bentley; Lon R Cardon; Ian Dunham
Journal:  Nature       Date:  2002-07-10       Impact factor: 49.962

8.  Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants.

Authors:  Robert Lawrence; David M Evans; Andrew P Morris; Xiayi Ke; Sarah Hunt; Marta Paolucci; Jiannis Ragoussis; Panos Deloukas; David Bentley; Lon R Cardon
Journal:  Genome Res       Date:  2005-11       Impact factor: 9.043

9.  Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly.

Authors:  Laura A Lettice; Taizo Horikoshi; Simon J H Heaney; Marijke J van Baren; Herma C van der Linde; Guido J Breedveld; Marijke Joosse; Nurten Akarsu; Ben A Oostra; Naoto Endo; Minoru Shibata; Mikio Suzuki; Eiichi Takahashi; Toshikatsu Shinka; Yutaka Nakahori; Dai Ayusawa; Kazuhiko Nakabayashi; Stephen W Scherer; Peter Heutink; Robert E Hill; Sumihare Noji
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-28       Impact factor: 11.205

Review 10.  Patterns of linkage disequilibrium in the human genome.

Authors:  Kristin G Ardlie; Leonid Kruglyak; Mark Seielstad
Journal:  Nat Rev Genet       Date:  2002-04       Impact factor: 53.242

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  14 in total

1.  Sporadic, Global Linkage Disequilibrium Between Unlinked Segregating Sites.

Authors:  Daniel A Skelly; Paul M Magwene; Eric A Stone
Journal:  Genetics       Date:  2015-12-29       Impact factor: 4.562

2.  Introduction: genetic variation and human health.

Authors:  M P H Stumpf; D B Goldstein; N W Wood
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2005-08-29       Impact factor: 6.237

3.  Bayesian graphical models for genomewide association studies.

Authors:  Claudio J Verzilli; Nigel Stallard; John C Whittaker
Journal:  Am J Hum Genet       Date:  2006-05-30       Impact factor: 11.025

4.  Use of stochastic simulations to investigate the power and design of a whole genome association study using single nucleotide polymorphism arrays in farm animals.

Authors:  Benoît Auvray; Ken G Dodds
Journal:  J Zhejiang Univ Sci B       Date:  2007-11       Impact factor: 3.066

Review 5.  Neuroimaging endophenotypes: strategies for finding genes influencing brain structure and function.

Authors:  David C Glahn; Paul M Thompson; John Blangero
Journal:  Hum Brain Mapp       Date:  2007-06       Impact factor: 5.038

6.  Assessment of systematic effects of methodological characteristics on candidate genetic associations.

Authors:  Badr Aljasir; John P A Ioannidis; Alex Yurkiewich; David Moher; Julian P T Higgins; Paul Arora; Julian Little
Journal:  Hum Genet       Date:  2012-10-25       Impact factor: 4.132

7.  Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE Statement.

Authors:  Julian Little; Julian P T Higgins; John P A Ioannidis; David Moher; France Gagnon; Erik von Elm; Muin J Khoury; Barbara Cohen; George Davey-Smith; Jeremy Grimshaw; Paul Scheet; Marta Gwinn; Robin E Williamson; Guang Yong Zou; Kim Hutchings; Candice Y Johnson; Valerie Tait; Miriam Wiens; Jean Golding; Cornelia van Duijn; John McLaughlin; Andrew Paterson; George Wells; Isabel Fortier; Matthew Freedman; Maja Zecevic; Richard King; Claire Infante-Rivard; Alex Stewart; Nick Birkett
Journal:  Hum Genet       Date:  2009-02-01       Impact factor: 4.132

8.  STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement.

Authors:  Julian Little; Julian P T Higgins; John P A Ioannidis; David Moher; France Gagnon; Erik von Elm; Muin J Khoury; Barbara Cohen; George Davey-Smith; Jeremy Grimshaw; Paul Scheet; Marta Gwinn; Robin E Williamson; Guang Yong Zou; Kim Hutchings; Candice Y Johnson; Valerie Tait; Miriam Wiens; Jean Golding; Cornelia van Duijn; John McLaughlin; Andrew Paterson; George Wells; Isabel Fortier; Matthew Freedman; Maja Zecevic; Richard King; Claire Infante-Rivard; Alex Stewart; Nick Birkett
Journal:  PLoS Med       Date:  2009-02-03       Impact factor: 11.069

9.  STrengthening the REporting of Genetic Association studies (STREGA)--an extension of the STROBE statement.

Authors:  Julian Little; Julian P T Higgins; John P A Ioannidis; David Moher; France Gagnon; Erik von Elm; Muin J Khoury; Barbara Cohen; George Davey-Smith; Jeremy Grimshaw; Paul Scheet; Marta Gwinn; Robin E Williamson; Guang Yong Zou; Kim Hutchings; Candice Y Johnson; Valerie Tait; Miriam Wiens; Jean Golding; Cornelia van Duijn; John McLaughlin; Andrew Paterson; George Wells; Isabel Fortier; Matthew Freedman; Maja Zecevic; Richard King; Claire Infante-Rivard; Alex Stewart; Nick Birkett
Journal:  Eur J Clin Invest       Date:  2009-04       Impact factor: 4.686

Review 10.  Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement.

Authors:  Julian Little; Julian P T Higgins; John P A Ioannidis; David Moher; France Gagnon; Erik von Elm; Muin J Khoury; Barbara Cohen; George Davey-Smith; Jeremy Grimshaw; Paul Scheet; Marta Gwinn; Robin E Williamson; Guang Yong Zou; Kim Hutchings; Candice Y Johnson; Valerie Tait; Miriam Wiens; Jean Golding; Cornelia van Duijn; John McLaughlin; Andrew Paterson; George Wells; Isabel Fortier; Matthew Freedman; Maja Zecevic; Richard King; Claire Infante-Rivard; Alex Stewart; Nick Birkett
Journal:  Eur J Epidemiol       Date:  2009-02-03       Impact factor: 8.082

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