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Integrating Case‐control and TDT Studies
Open accessAbstract
Summary: Genetic‐association studies are widely expected to unravel the genetic basis of complex diseases. The population‐based case‐control study, a commonly used approach for association studies, is subject to the problem of population admixture. Consequently, evidence of disease‐marker associations obtained from such studies is ideally confirmed by alternative methods. The Transmission/Disequilibrium Test (TDT) is suitable to assess evidence of association obtained from case‐control studies. Since data are increasingly available from both case‐control and TDT studies of the same disease‐marker association, it is useful to obtain a combined estimate of disease‐marker association. The odds ratio is a commonly used measure of the magnitude of a disease‐marker association that can be easily obtained in case‐control studies. Here we show how an odds ratio estimate and its' associated standard error can be obtained from TDT results. Furthermore, we suggest a method for integrating results from case‐control studies and the TDT to provide a combined estimate of disease‐marker association. Such combined estimates can be used to contrast the results of the two studies and provides an overall picture of the effect size attributable to such polymorphism. An illustrative application is made to a published data set on type 2 diabetes.
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Cites
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Cited by
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
the NIDDK IBD Genetics Consortium, Barrett, J. C., the Belgian-French IBD Consortium, the Wellcome Trust Case Control Consortium, Hansoul, S., Nicolae, D. L., Cho, J. H., Duerr, R. H., Rioux, J. D., Brant, S. R., et al. (2008) · Nature Genetics · doi:10.1038/ng.175 · Cited by 2,593
Candidate gene studies of ADHD: a meta-analytic review
Gizer, I. R., Ficks, C., & Waldman, I. D. (2009) · Human Genetics · doi:10.1007/s00439-009-0694-x · Cited by 1,020
Robertson, C. C., Inshaw, J. R. J., Onengut-Gumuscu, S., Chen, W.-M., Santa Cruz, D. F., Yang, H., Cutler, A. J., Crouch, D. J. M., Farber, E., Bridges, S. L., et al. (2021) · Nature Genetics · doi:10.1038/s41588-021-00880-5 · Cited by 302
Justice, C. M., Yagnik, G., Kim, Y., Peter, I., Jabs, E. W., Erazo, M., Ye, X., Ainehsazan, E., Shi, L., Cunningham, M. L., et al. (2012) · Nature Genetics · doi:10.1038/ng.2463 · Cited by 140
Bloch, M. H., Landeros‐Weisenberger, A., Sen, S., Dombrowski, P., Kelmendi, B., Coric, V., Pittenger, C., & Leckman, J. F. (2008) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30699 · Cited by 108
Metadata
- Authors
- Kazeem, G. R., & Farrall, M.
- Venue
- Annals of Human Genetics
- Publisher
- Wiley
- Published
- 2005-05
- Volume
- 69
- Issue
- 3
- Pages
- 329-335
- ISSN
- 0003-4800 (ISSN-L)
- 1469-1809
- OpenAlex
- W2019571281
- Cited by
- 159
- References
- 3
- FWCI
- 5.88
- Type
- journal article
- Language
- en
- Open access
- bronze
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