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2022 Book Chapter Integrating family-based and Mendelian randomization designsHwang, Liang-Dar, Davies, Neil M., Warrington, Nicole M. and Evans, David M. (2022). Integrating family-based and Mendelian randomization designs. Combining human genetics and causal inference to understand human disease and development. (pp. 137-150) edited by George Davey Smith, Rebecca Richmond and Jean-Baptiste Pingault. Cold Spring Harbor, NY, United States: Cold Spring Harbor Laboratory Press. |
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2012 Book Chapter Detailing patient specific modeling to aid clinical decision-makingRichmond, S., Al Ali, A. M., Beldie, L., Chong, Y. T., Cronin, A., Djordjevic, J., Drage, N. A., Evans, D. M., Jones, D., Lu, Y., Marshall, D., Middleton, J., Parker, G., Paternoster, L., Playle, R. A., Popat, H., Rosin, P. L., Sidorov, K., Toma, A. M., Walker, B., Wilson, C. and Zhurov, A. I. (2012). Detailing patient specific modeling to aid clinical decision-making. Patient-Specific Computational Modeling. (pp. 105-131) Dordrecht, Netherlands: Springer . doi: 10.1007/978-94-007-4552-0_5 |
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2011 Book Chapter Mapping complex disease genes using linkage disequilibrium and genomewide association scansPalmer, Lyle J., Timpson, Nicholas J., Evans, David M., Smith, George Davey and Cardon, Lon R. (2011). Mapping complex disease genes using linkage disequilibrium and genomewide association scans. An Introduction to Genetic Epidemiology. (pp. 91-130) Bristol, United Kingdom: Policy Press. |
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2011 Book Chapter Gene-gene interaction and epistasisEvans, David M. (2011). Gene-gene interaction and epistasis. Analysis of complex disease association studies. (pp. 197-213) edited by Eleftheria Zeggini and Andrew Morris. Amsterdam, Netherlands: Elsevier. doi: 10.1016/B978-0-12-375142-3.10012-4 |
