Published Works

• Degasperi, A., Zou, X., Amarante, T. D., Martinez-Martinez, A., Koh, G. C. C., Dias, J. M. L., Heskin, L., Chmelova, L., Rinaldi, G., Wang, V. Y. W., Nanda, A. S., Bernstein, A., Momen, S. E., Young, J., Perez-Gil, D., Memari, Y., Badja, C., Shooter, S., Czarnecki, J., Brown, M. A., … Nik-Zainal, S. (2022). Substitution mutational signatures in whole-genome-sequenced cancers in the UK population. Science (New York, N.Y.), 376(6591), science.abl9283. https://doi.org/10.1126/science.abl9283
• Steinthorsdottir, V., McGinnis, R., Williams, N. O., Stefansdottir, L., Thorleifsson, G., Shooter, S., Fadista, J., Sigurdsson, J. K., Auro, K. M., Berezina, G., Borges, M. C., Bumpstead, S., Bybjerg-Grauholm, J., Colgiu, I., Dolby, V. A., Dudbridge, F., Engel, S. M., Franklin, C. S., Frigge, M. L., Frisbaek, Y., … Morgan, L. (2020). Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Nature communications, 11(1), 5976. https://doi.org/10.1038/s41467-020-19733-6
• Degasperi, A., Amarante, T. D., Czarnecki, J., Shooter, S., Zou, X., Glodzik, D., Morganella, S., Nanda, A. S., Badja, C., Koh, G., Momen, S. E., Georgakopoulos-Soares, I., Dias, J. M. L., Young, J., Memari, Y., Davies, H., & Nik-Zainal, S. (2020). A practical framework and online tool for mutational signature analyses show inter-tissue variation and driver dependencies. Nature cancer, 1(2), 249–263. https://doi.org/10.1038/s43018-020-0027-5
• McGinnis, R., Steinthorsdottir, V., Williams, N. O., Thorleifsson, G., Shooter, S., Hjartardottir, S., Bumpstead, S., Stefansdottir, L., Hildyard, L., Sigurdsson, J. K., Kemp, J. P., Silva, G. B., Thomsen, L. C. V., Jääskeläinen, T., Kajantie, E., Chappell, S., Kalsheker, N., Moffett, A., Hiby, S., Lee, W. K., … Morgan, L. (2017). Variants in the fetal genome near FLT1 are associated with risk of preeclampsia. Nature genetics, 49(8), 1255–1260. https://doi.org/10.1038/ng.3895