Literature DB >> 29716745

Replicability and Prediction: Lessons and Challenges from GWAS.

Urko M Marigorta1, Juan Antonio Rodríguez2, Greg Gibson3, Arcadi Navarro4.   

Abstract

Since the publication of the Wellcome Trust Case Control Consortium (WTCCC) landmark study a decade ago, genome-wide association studies (GWAS) have led to the discovery of thousands of risk variants involved in disease etiology. This success story has two angles that are often overlooked. First, GWAS findings are highly replicable. This is an unprecedented phenomenon in complex trait genetics, and indeed in many areas of science, which in past decades have been plagued by false positives. At a time of increasing concerns about the lack of reproducibility, we examine the biological and methodological reasons that account for the replicability of GWAS and identify the challenges ahead. In contrast to the exemplary success of disease gene discovery, at present GWAS findings are not useful for predicting phenotypes. We close with an overview of the prospects for individualized prediction of disease risk and its foreseeable impact in clinical practice.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  GWAS; genetic architecture; genetic risk score; prediction; replicability

Mesh:

Year:  2018        PMID: 29716745      PMCID: PMC6003860          DOI: 10.1016/j.tig.2018.03.005

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


  64 in total

1.  Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease.

Authors:  Kirk E Lohmueller; Celeste L Pearce; Malcolm Pike; Eric S Lander; Joel N Hirschhorn
Journal:  Nat Genet       Date:  2003-01-13       Impact factor: 38.330

Review 2.  Five years of GWAS discovery.

Authors:  Peter M Visscher; Matthew A Brown; Mark I McCarthy; Jian Yang
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

3.  Complement factor H polymorphism in age-related macular degeneration.

Authors:  Robert J Klein; Caroline Zeiss; Emily Y Chew; Jen-Yue Tsai; Richard S Sackler; Chad Haynes; Alice K Henning; John Paul SanGiovanni; Shrikant M Mane; Susan T Mayne; Michael B Bracken; Frederick L Ferris; Jurg Ott; Colin Barnstable; Josephine Hoh
Journal:  Science       Date:  2005-03-10       Impact factor: 47.728

4.  Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases.

Authors:  John P A Ioannidis; Thomas A Trikalinos; Muin J Khoury
Journal:  Am J Epidemiol       Date:  2006-08-07       Impact factor: 4.897

5.  Additive genetic variation in schizophrenia risk is shared by populations of African and European descent.

Authors:  Teresa R de Candia; S Hong Lee; Jian Yang; Brian L Browning; Pablo V Gejman; Douglas F Levinson; Bryan J Mowry; John K Hewitt; Michael E Goddard; Michael C O'Donovan; Shaun M Purcell; Danielle Posthuma; Peter M Visscher; Naomi R Wray; Matthew C Keller
Journal:  Am J Hum Genet       Date:  2013-08-15       Impact factor: 11.025

6.  Integrative approaches for large-scale transcriptome-wide association studies.

Authors:  Alexander Gusev; Arthur Ko; Huwenbo Shi; Gaurav Bhatia; Wonil Chung; Brenda W J H Penninx; Rick Jansen; Eco J C de Geus; Dorret I Boomsma; Fred A Wright; Patrick F Sullivan; Elina Nikkola; Marcus Alvarez; Mete Civelek; Aldons J Lusis; Terho Lehtimäki; Emma Raitoharju; Mika Kähönen; Ilkka Seppälä; Olli T Raitakari; Johanna Kuusisto; Markku Laakso; Alkes L Price; Päivi Pajukanta; Bogdan Pasaniuc
Journal:  Nat Genet       Date:  2016-02-08       Impact factor: 38.330

Review 7.  Pitfalls of predicting complex traits from SNPs.

Authors:  Naomi R Wray; Jian Yang; Ben J Hayes; Alkes L Price; Michael E Goddard; Peter M Visscher
Journal:  Nat Rev Genet       Date:  2013-07       Impact factor: 53.242

8.  Empirical assessment of published effect sizes and power in the recent cognitive neuroscience and psychology literature.

Authors:  Denes Szucs; John P A Ioannidis
Journal:  PLoS Biol       Date:  2017-03-02       Impact factor: 8.029

9.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Authors: 
Journal:  Nature       Date:  2007-06-07       Impact factor: 49.962

10.  Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study.

Authors:  Christopher S Carlson; Tara C Matise; Kari E North; Christopher A Haiman; Megan D Fesinmeyer; Steven Buyske; Fredrick R Schumacher; Ulrike Peters; Nora Franceschini; Marylyn D Ritchie; David J Duggan; Kylee L Spencer; Logan Dumitrescu; Charles B Eaton; Fridtjof Thomas; Alicia Young; Cara Carty; Gerardo Heiss; Loic Le Marchand; Dana C Crawford; Lucia A Hindorff; Charles L Kooperberg
Journal:  PLoS Biol       Date:  2013-09-17       Impact factor: 8.029

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  42 in total

1.  Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2.

Authors:  Ana I Hernandez Cordero; Natalia M Gonzales; Clarissa C Parker; Greta Sokolof; David J Vandenbergh; Riyan Cheng; Mark Abney; Andrew Sko; Alex Douglas; Abraham A Palmer; Jennifer S Gregory; Arimantas Lionikas
Journal:  Am J Hum Genet       Date:  2019-11-21       Impact factor: 11.025

2.  Quantitative and Qualitative Role of Antagonistic Heterogeneity in Genetics of Blood Lipids.

Authors:  Alexander M Kulminski; Yury Loika; Alireza Nazarian; Irina Culminskaya
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2020-09-25       Impact factor: 6.053

Review 3.  Why is Disease Penetration So Variable? Role of Genetic Modifiers of Lung Function in Alpha-1 Antitrypsin Deficiency.

Authors:  Brian D Hobbs; Michael H Cho
Journal:  Chronic Obstr Pulm Dis       Date:  2020-07

4.  Genetic risks and clinical rewards.

Authors:  Andrew J Schork; M Anthony Schork; Nicholas J Schork
Journal:  Nat Genet       Date:  2018-09       Impact factor: 38.330

5.  DeepCOMBI: explainable artificial intelligence for the analysis and discovery in genome-wide association studies.

Authors:  Bettina Mieth; Alexandre Rozier; Juan Antonio Rodriguez; Marina M C Höhne; Nico Görnitz; Klaus-Robert Müller
Journal:  NAR Genom Bioinform       Date:  2021-07-20

6.  Phosphoproteomics reveals conserved exercise-stimulated signaling and AMPK regulation of store-operated calcium entry.

Authors:  Marin E Nelson; Benjamin L Parker; James G Burchfield; Nolan J Hoffman; Elise J Needham; Kristen C Cooke; Timur Naim; Lykke Sylow; Naomi Xy Ling; Deanne Francis; Dougall M Norris; Rima Chaudhuri; Jonathan S Oakhill; Erik A Richter; Gordon S Lynch; Jacqueline Stöckli; David E James
Journal:  EMBO J       Date:  2019-08-05       Impact factor: 11.598

Review 7.  Omics in Neurodegenerative Disease: Hope or Hype?

Authors:  Maria E Diaz-Ortiz; Alice S Chen-Plotkin
Journal:  Trends Genet       Date:  2020-01-10       Impact factor: 11.639

Review 8.  Results of the Seventh Scientific Workshop of ECCO: Precision Medicine in IBD-Disease Outcome and Response to Therapy.

Authors:  Bram Verstockt; Nurulamin M Noor; Urko M Marigorta; Polychronis Pavlidis; Parakkal Deepak; Ryan C Ungaro
Journal:  J Crohns Colitis       Date:  2021-09-25       Impact factor: 9.071

9.  Protective association of the ε2/ε3 heterozygote with Alzheimer's disease is strengthened by TOMM40-APOE variants in men.

Authors:  Alexander M Kulminski; Ian Philipp; Yury Loika; Liang He; Irina Culminskaya
Journal:  Alzheimers Dement       Date:  2021-07-26       Impact factor: 21.566

10.  Genetic Variation and Hot Flashes: A Systematic Review.

Authors:  Carolyn J Crandall; Allison L Diamant; Margaret Maglione; Rebecca C Thurston; Janet Sinsheimer
Journal:  J Clin Endocrinol Metab       Date:  2020-12-01       Impact factor: 5.958

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