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Genome-wide association studies
Open accessAbstract
Genome-wide association studies (GWAS) test hundreds of thousands of genetic variants across many genomes to find those statistically associated with a specific trait or disease. This methodology has generated a myriad of robust associations for a range of traits and diseases, and the number of associated variants is expected to grow steadily as GWAS sample sizes increase. GWAS results have a range of applications, such as gaining insight into a phenotype’s underlying biology, estimating its heritability, calculating genetic correlations, making clinical risk predictions, informing drug development programmes and inferring potential causal relationships between risk factors and health outcomes. In this Primer, we provide the reader with an introduction to GWAS, explaining their statistical basis and how they are conducted, describe state-of-the art approaches and discuss limitations and challenges, concluding with an overview of the current and future applications for GWAS results. Uffelmann et al. describe the key considerations and best practices for conducting genome-wide association studies (GWAS), techniques for deriving functional inferences from the results and applications of GWAS in understanding disease risk and trait architecture. The Primer also provides information on the best practices for data sharing and discusses important ethical considerations when considering GWAS populations and data.
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“Misinterpretation or oversights can lead to inaccurate biological conclusions, highlighting the importance of precision in WGA algorithms [80].”
From Whole-Genome Alignment: Methods, Challenges, and Future Directions (2024) · cites this paper as [80]
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“Beyond oncology, there has been a remarkable increase in the last 15 years in the availability and sharing of genetic data, which enabled genome-wide association studies 12 and characterization of the genetic architecture of complex human conditions and traits 13 .”
From Multimodal biomedical AI (2022) · cites this paper as [12]
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PLINK: a tool set for whole-genome association and population-based linkage analyses.
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., Maller, J., Sklar, P., de Bakker, P. I. W., Daly, M. J., et al. (2007) · The American Journal of Human Genetics · doi:10.1086/519795 · Cited by 34,089
The FAIR Guiding Principles for scientific data management and stewardship
Wilkinson, M. D., Dumontier, M., Aalbersberg, I. J., Appleton, G., Axton, M., Baak, A., Blomberg, N., Boiten, J.-W., da Silva Santos, L. B., Bourne, P. E., et al. (2016) · Scientific Data · doi:10.1038/sdata.2016.18 · Cited by 18,423
A global reference for human genetic variation
The 1000 Genomes Project Consortium, authors, C., Auton, A., Abecasis, G. R., Steering committee, Altshuler, D. M., Durbin, R. M., Abecasis, G. R., Bentley, D. R., Chakravarti, A., et al. (2015) · Nature · doi:10.1038/nature15393 · Cited by 18,247
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Wang, K., Li, M., & Hakonarson, H. H. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq603 · Cited by 14,724
Principal components analysis corrects for stratification in genome-wide association studies
Price, A. L., Patterson, N. J., Plenge, R. M., Weinblatt, M. E., Shadick, N. A., & Reich, D. (2006) · Nature Genetics · doi:10.1038/ng1847 · Cited by 10,248
The mutational constraint spectrum quantified from variation in 141,456 humans
Karczewski, K. J., Francioli, L. C., Tiao, G., Cummings, B. B., Alföldi, J., Wang, Q., Collins, R. L., Laricchia, K. M., Ganna, A., Birnbaum, D. P., et al. (2020) · Nature · doi:10.1038/s41586-020-2308-7 · Cited by 9,434
The UK Biobank resource with deep phenotyping and genomic data
Bycroft, C., Freeman, C., Petkova, D., Band, G., Elliott, L. T., Sharp, K., Motyer, A., Vukcevic, D., Delaneau, O., O’Connell, J., et al. (2018) · Nature · doi:10.1038/s41586-018-0579-z · Cited by 8,876
Verbanck, M., Chen, C.-Y., Neale, B., & Do, R. (2018) · Nature Genetics · doi:10.1038/s41588-018-0099-7 · Cited by 8,591
Finding the missing heritability of complex diseases
Manolio, T. A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., Hunter, D. J., McCarthy, M. I., Ramos, E. M., Cardon, L. R., Chakravarti, A., et al. (2009) · Nature · doi:10.1038/nature08494 · Cited by 8,336
GCTA: a tool for genome-wide complex trait analysis
Yang, J., Lee, S. H., Goddard, M. E., & Visscher, P. M. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2010.11.011 · Cited by 8,279
Research works printed but not linked: 7
- Morris, T. T., Davies, N. M., Hemani, G. & Smith, G. D. Population phenomena inflate genetic associations of complex social traits. Sci. Adv. 6, eaay0328 (2020). · DOI · Paper page
- Morris, J. A. et al. Discovery of target genes and pathways of blood trait loci using pooled CRISPR screens and single cell RNA sequencing. Preprint at bioRxiv https://doi.org/10.1101/2021.04.07.438882v1 (2021). · DOI
- Kerimov, N. et al. eQTL Catalogue: a compendium of uniformly processed human gene expression and splicing QTLs. Preprint at bioRxiv https://doi.org/10.1101/2020.01.29.924266v1 (2020). · DOI
- Márquez-Luna, C. et al. Modeling functional enrichment improves polygenic prediction accuracy in UK Biobank and 23andMe data sets. Preprint at bioRxiv https://doi.org/10.1101/375337v1 (2018). · DOI
- Falconer, D. S. & Mackay, T. F. C. Introduction to Quantitative Genetics (Pearson, Prentice Hall, 2009).
- Bernabeu, E. et al. Sexual differences in genetic architecture in UK Biobank. Preprint at bioRxiv https://doi.org/10.1101/2020.07.20.211813v1 (2020). · DOI
- Wellcome Trust. Sharing Data from Large-scale Biological Research Projects: A System of Tripartite Responsibility Vol. 6 (Wellcome Trust, 2003).
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Zhou, F., Tian, G., Cui, Y., He, S., & Yan, Y. (2023) · Pediatric Obesity · doi:10.1111/ijpo.13077 · Cited by 6
Papini, N. M., Presseller, E. K., Bulik, C. M., Holde, K. E. V., Larsen, J. T., Thornton, L. M., Albiñana, C., Vilhjálmsson, B. J., Mortensen, P. B., Yılmaz, Z., et al. (2024) · Psychological Medicine · doi:10.1017/s0033291724000175 · Cited by 8
Yang, C., Fredua‐Agyeman, R., Hwang, S., Gorim, L. Y., & Strelkov, S. E. (2024) · Frontiers in Plant Science · doi:10.3389/fpls.2024.1389082 · Cited by 6
Xiong, Z., Liu, S., Tan, J., Huang, Z., Li, X., Zhuang, G., Fang, Z., Chen, T., & Zhang, L. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158414 · Cited by 8
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Gardeux, V., Bevers, R. P. J., David, F. P. A., Rosschaert, E., Rochepeau, R., & Deplancke, B. (2023) · eLife · doi:10.7554/elife.88981.3 · Cited by 13
Ogweng, P., Bowden, C. F., Smyser, T. J., Muwanika, V. B., Piaggio, A. J., & Masembe, C. (2024) · Tropical Animal Health and Production · doi:10.1007/s11250-024-04195-5 · Cited by 6
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Nikolić, S., Ignatov, D. I., Khvorykh, G. V., Limborska, S. A., & Владимирович, Х. А. (2024) · PeerJ Computer Science · doi:10.7717/peerj-cs.2454 · Cited by 6
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Li, Y., Xiao, J., Ming, J., Zeng, Y., & Cai, M. (2024) · Bioinformatics · doi:10.1093/bioinformatics/btaf017 · Cited by 6
Gou, Y., Jing, Y., Wang, Y., Li, X., Yang, J., Wang, K., He, H., Yang, Y., Tang, Y., Wang, C., et al. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.108267 · Cited by 6
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Weekley, B. H., Ahmed, N. I., & Maze, I. S. (2025) · iScience · doi:10.1016/j.isci.2025.112092 · Cited by 7
Zhao, H., MacLeod, I. M., Keeble‐Gagnère, G., Barbulescu, D. M., Tibbits, J. F. G., Kaur, S., & Hayden, M. (2025) · BMC Genomics · doi:10.1186/s12864-025-11250-4 · Cited by 6
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Guan, H., Zhang, P., Park, R., & Ding, Y. (2025) · Molecular Plant Pathology · doi:10.1111/mpp.70082 · Cited by 5
Saras, M. A. M., Mitra, M. K., & Tyagi, S. (2025) · Biology Methods and Protocols · doi:10.1093/biomethods/bpaf028 · Cited by 6
Cozzoli, D., Daponte, A., Fazio, S. D., Ariano, V., Quaranta, M. R., Leone, V., Ostuni, A., Casanova, M., Catacchio, C. R., Ventura, M., et al. (2021) · Biomedicines · doi:10.3390/biomedicines9121799 · Cited by 8
Maranian, M. J., & Snead, M. P. (2022) · Genes · doi:10.3390/genes13101885 · Cited by 6
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Jo, K. R., Choi, J., Kwon, D.-H., Park, Y.-E., & Kim, S. (2023) · Agronomy · doi:10.3390/agronomy13030642 · Cited by 6
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Monti, R., & Ohler, U. (2023) · Annual Review of Biomedical Data Science · doi:10.1146/annurev-biodatasci-122120-110102 · Cited by 6
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Rossi, S., Richards, E., Orozco, G., & Eyre, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25137349 · Cited by 6
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Metadata
- Authors
- Uffelmann, E., Huang, Q. Q., Munung, N. S., de Vries, J., Okada, Y., Martin, A. R., Martin, H. C., Lappalainen, T., & Posthuma, D.
- Affiliations
- Amsterdam Neuroscience (NL)
- Wellcome Sanger Institute (GB)
- University of Cape Town (ZA)
- Immunology Frontier Research Center, The University of Osaka (JP)
- Broad Institute (US)
- Science for Life Laboratory (SE)
- ORCID
- Venue
- Nature Reviews Methods Primers
- Published
- 2021-08-26
- Volume
- 1
- Issue
- 1
- ISSN
- 2662-8449 (ISSN-L)
- OpenAlex
- W3195285310
- Cited by
- 1,849
- References
- 288
- Citations by year
- 2026: 292 · 2025: 512 · 2024: 546 · 2023: 304 · 2022: 163 · 2021: 22
- FWCI
- 38.81
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Nature Reviews Methods Primers (publishedVersion, public-domain)
- VU Research Portal (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Funders
- Japan Agency for Medical Research and Development (JP20ek0109413, JP20km0405217, JP20gm4010006, JP20ek0410075, JP20gm4010006, JP20ek0410075, JP20km0405211)
- Wellcome Trust (219600/Z/19/Z, 098051)
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (VICI 435-14-005, 024.004.012, 435-14-005)
- National Institutes of Health
- Japan Society for the Promotion of Science (19H01021 and 20K21834, 834057, 20K21834, 19H01021)
- National Heart, Lung, and Blood Institute (R01HL142028, U24HL135600)
- National Institute of Mental Health (R01MH106842)
- National Human Genome Research Institute (UM1HG008901, U54HG009790)
- National Institute of General Medical Sciences (R01GM122924)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and phenotypic traits in livestock
- Keywords
- genome-wide association study, genetic variants, disease risk, heritability, genetic correlation, clinical risk prediction, drug development, causal inference, data sharing, research ethics
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