Martin Morales, L.* , Manzano, S.* , Rodrigo-Faus, M.* , Vicente-Barrueco, A., Lorca, V., Núñez-Moreno, G., Bragado, P., Porras, A., Caldes, T., Garre, P., & Gutierrez-Uzquiza, A. (January 2023). Germline gain-of-function MMP11 variant results in an aggressive form of colorectal cancer. International Journal of Cancer, 152 (2), 283-297. doi:10.1002/ijc.34289 * These authors have contributed equally to this work. |
Martin Morales, L., Garre, P., Lorca, V., Cazorla, M., Llovet, P., Bando, I., Garcia-Barberan, V., Gonzalez-Morales, M. L., Esteban-Jurado, C., de la Hoya, M., Castellvi-Bel, S., & Caldes, T. (February 2021). BRIP1, a Gene Potentially Implicated in Familial Colorectal Cancer Type X. Cancer Prevention Research, 14 (2), 185-194. doi:10.1158/1940-6207.CAPR-20-0316 |
Lorca, V., Rueda, D., Martin Morales, L., Fernandez-Aceñero, M. J., Grolleman, J., Poves, C., Llovet, P., Tapial, S., Garcia-Barberan, V., Sanz, J., Perez-Segura, P., de Voer, R. M., Diaz-Rubio, E., de la Hoya, M., Caldes, T., & Garre, P. (July 2019). Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing. Scientific Reports, 9 (1), 9814. doi:10.1038/s41598-019-46403-5 |
Martin Morales, L.* , Rofes, P.* , Diaz-Rubio, E., Llovet, P., Lorca, V., Bando, I., Perez-Segura, P., de la Hoya, M., Garre, P., Garcia-Barberan, V., & Caldes, T. (September 2018). Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predisposition. PLoS ONE, 13 (9), 0203885. doi:10.1371/journal.pone.0203885 * These authors have contributed equally to this work. |
Lorca, V., Rueda, D., Martin Morales, L., Poves, C., Fernandez-Aceñero, M. J., Ruiz-Ponte, C., Llovet, P., Marrupe, D., Garcia-Barberan, V., Garcia-Paredes, B., Perez-Segura, P., de la Hoya, M., Diaz-Rubio, Caldes, T., & Garre, P. (November 2017). Role of GALNT12 in the genetic predisposition to attenuated adenomatous polyposis syndrome. PLoS ONE, 12 (11), 0187312. doi:10.1371/journal.pone.0187312 |
Martin Morales, L., Feldman, M., Vershinin, Z., Garre, P., Caldes, T., & Levy, D. (November 2017). SETD6 dominant negative mutation in familial colorectal cancer type X. Human Molecular Genetics, 26 (22), 4481-4493. doi:10.1093/hmg/ddx336 |
Llovet, P., Illana, F., Martin Morales, L., de la Hoya, M., Garre, P., Ibañez-Royo, M. D., Perez-Segura, P., Caldes, T., & Garcia-Barberan, V. (October 2017). A novel TP53 germline inframe deletion identified in a Spanish series of Li-fraumeni syndrome suspected families. Familial Cancer, 16 (4), 567-575. doi:10.1007/s10689-017-9990-0 |
Garre, P., Martin Morales, L., Bando, I., Tosar, A., Llovet, P., Sanz, J., Romero, A., de la Hoya, M., Diaz-Rubio, E., & Caldes, T. (March 2014). Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer. Familial Cancer, 13 (1), 109-19. doi:10.1007/s10689-013-9683-2 |