Literature DB >> 19851339

Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse.

Hirofumi Nakaoka1, Ituro Inoue.   

Abstract

Meta-analysis is a useful tool to increase the statistical power to detect gene-disease associations by combining results from the original and subsequent replication studies. Recently, consortium-based meta-analyses of several genome-wide association (GWA) data sets have discovered new susceptibility genes of common diseases. We reviewed the process and the methods of meta-analysis of genetic association studies. To conduct and report a transparent meta-analysis, the search strategy, the inclusion or exclusion criteria of studies and the statistical procedures should be fully described. Assessing consistency or heterogeneity of the associations across studies is an important aim of meta-analysis. Random effects model (REM) meta-analysis can incorporate between-study heterogeneity. We illustrated properties of test for and measures of between-study heterogeneity and the effect of between-study heterogeneity on conclusions of meta-analyses through simulations. Our simulation shows that the power of REM meta-analysis of GWA data sets (total case-control sample size: 5000-20,000) to detect a small genetic effect (odds ratio (OR)=1.4 under dominant model) decreases as between-study heterogeneity increases and then the mean of OR of the simulated meta-analyses passing the genome-wide significance threshold would be upwardly biased (winner's curse phenomenon). Addressing observed between-study heterogeneity may be challenging but give a new insight into the gene-disease association.

Mesh:

Year:  2009        PMID: 19851339     DOI: 10.1038/jhg.2009.95

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  41 in total

1.  Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement.

Authors:  George R Uhl; Tomas Drgon; Catherine Johnson; Marco F Ramoni; Frederique M Behm; Jed E Rose
Journal:  Mol Med       Date:  2010-08-24       Impact factor: 6.354

2.  Methods to increase reproducibility in differential gene expression via meta-analysis.

Authors:  Timothy E Sweeney; Winston A Haynes; Francesco Vallania; John P Ioannidis; Purvesh Khatri
Journal:  Nucleic Acids Res       Date:  2016-09-14       Impact factor: 16.971

3.  Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.

Authors:  Alexander Gusev; S Hong Lee; Gosia Trynka; Hilary Finucane; Bjarni J Vilhjálmsson; Han Xu; Chongzhi Zang; Stephan Ripke; Brendan Bulik-Sullivan; Eli Stahl; Anna K Kähler; Christina M Hultman; Shaun M Purcell; Steven A McCarroll; Mark Daly; Bogdan Pasaniuc; Patrick F Sullivan; Benjamin M Neale; Naomi R Wray; Soumya Raychaudhuri; Alkes L Price
Journal:  Am J Hum Genet       Date:  2014-11-06       Impact factor: 11.025

Review 4.  Genetic factors contributing to skeletal class III malocclusion: a systematic review and meta-analysis.

Authors:  Alexandra Dehesa-Santos; Paula Iber-Diaz; Alejandro Iglesias-Linares
Journal:  Clin Oral Investig       Date:  2021-02-07       Impact factor: 3.573

5.  Adjustment for covariates using summary statistics of genome-wide association studies.

Authors:  Tao Wang; Xiaonan Xue; Xianhong Xie; Kenny Ye; Xiaofeng Zhu; Robert C Elston
Journal:  Genet Epidemiol       Date:  2018-09-20       Impact factor: 2.135

Review 6.  Clinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed.

Authors:  Yi-Hsiang Hsu; Douglas P Kiel
Journal:  J Clin Endocrinol Metab       Date:  2012-09-10       Impact factor: 5.958

7.  Replication study of genome-wide associated SNPs with late-onset Alzheimer's disease.

Authors:  L C Burns; R L Minster; F Y Demirci; M M Barmada; M Ganguli; O L Lopez; S T DeKosky; M I Kamboh
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2011-04-07       Impact factor: 3.568

8.  "Does replication groups scoring reduce false positive rate in SNP interaction discovery? Response".

Authors:  Javier Gayán; Antonio González-Pérez; Agustín Ruiz
Journal:  BMC Genomics       Date:  2010-06-24       Impact factor: 3.969

9.  Independent susceptibility markers for atrial fibrillation on chromosome 4q25.

Authors:  Steven A Lubitz; Moritz F Sinner; Kathryn L Lunetta; Seiko Makino; Arne Pfeufer; Rosanna Rahman; Caroline E Veltman; John Barnard; Joshua C Bis; Stephan P Danik; Akshata Sonni; Marisa A Shea; Federica Del Monte; Siegfried Perz; Martina Müller; Annette Peters; Steven M Greenberg; Karen L Furie; Charlotte van Noord; Eric Boerwinkle; Bruno H C Stricker; Jacqueline Witteman; Jonathan D Smith; Mina K Chung; Susan R Heckbert; Emelia J Benjamin; Jonathan Rosand; Dan E Arking; Alvaro Alonso; Stefan Kääb; Patrick T Ellinor
Journal:  Circulation       Date:  2010-08-23       Impact factor: 29.690

10.  The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions.

Authors:  Marilyn C Cornelis; Arpana Agrawal; John W Cole; Nadia N Hansel; Kathleen C Barnes; Terri H Beaty; Siiri N Bennett; Laura J Bierut; Eric Boerwinkle; Kimberly F Doheny; Bjarke Feenstra; Eleanor Feingold; Myriam Fornage; Christopher A Haiman; Emily L Harris; M Geoffrey Hayes; John A Heit; Frank B Hu; Jae H Kang; Cathy C Laurie; Hua Ling; Teri A Manolio; Mary L Marazita; Rasika A Mathias; Daniel B Mirel; Justin Paschall; Louis R Pasquale; Elizabeth W Pugh; John P Rice; Jenna Udren; Rob M van Dam; Xiaojing Wang; Janey L Wiggs; Kayleen Williams; Kai Yu
Journal:  Genet Epidemiol       Date:  2010-05       Impact factor: 2.135

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