  | Sohier, P., Legrand, L., Aktary, Z., Grill, C., Delmas, V., Bernex, F., Reyes-Gomez, E., Larue, L., & Vergier, B. (May 2018). A histopathological classification system of Tyr::NRASQ61K murine melanocytic lesions: A reproducible simplified classification. Pigment Cell and Melanoma Research, 31 (3), 423 - 431. doi:10.1111/pcmr.12677  Peer Reviewed verified by ORBi |
 | Grill, C., Benzekri, L., Rubod, A., Aktary, Z., Ezzedine, K., Taïeb, A., Gauthier, Y., Larue, L., & Delmas, V. (May 2018). Epidermal melanocytes in segmental vitiligo show altered expression of E-cadherin, but not P-cadherin. British Journal of Dermatology, 178 (5), 1204 - 1206. doi:10.1111/bjd.16352 Peer Reviewed verified by ORBi |
 | Grill, C., & Larue, L. (2016). NRAS, NRAS, Which Mutation Is Fairest of Them All? Journal of Investigative Dermatology, 136 (10), 1936-1938. doi:10.1016/j.jid.2016.06.011 Peer Reviewed verified by ORBi |
 | Grill, C., & Larue, L. (January 2016). What's up NF1? Pigment Cell and Melanoma Research, 29 (1), 4-5. doi:10.1111/pcmr.12423 Peer Reviewed verified by ORBi |
 | Praetorius, C., Grill, C., Stacey, S. N., Metcalf, A. M., Gorkin, D. U., Robinson, K. C., Van Otterloo, E., Kim, R. S. Q., Bergsteinsdottir, K., Ogmundsdottir, M. H., Magnusdottir, E., Mishra, P. J., Davis, S. R., Guo, T., Zaidi, M. R., Helgason, A. S., Sigurdsson, M. I., Meltzer, P. S., Merlino, G., ... Steingrimsson, E. (21 November 2013). A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway. Cell, 155 (5), 1022-33. doi:10.1016/j.cell.2013.10.022 Peer Reviewed verified by ORBi |
 | Grill, C., Bergsteinsdóttir, K., Ogmundsdóttir, M. H., Pogenberg, V., Schepsky, A., Wilmanns, M., Pingault, V., & Steingrímsson, E. (01 November 2013). MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein function. Human Molecular Genetics, 22 (21), 4357-67. doi:10.1093/hmg/ddt285 Peer Reviewed verified by ORBi |
 | Grill, C., Sunitsch, S., Hatz, M., Hauser-Kronberger, C., Leuschner, I., Hoefler, G., & Guertl, B. (December 2011). Activation of beta-catenin is a late event in the pathogenesis of nephroblastomas and rarely correlated with genetic changes of the APC gene. Pathology, 43 (7), 702-6. doi:10.1097/PAT.0b013e32834bf65c Peer Reviewed verified by ORBi |
 | Grill, C., Guelly, C., Ebner, B., Leuschner, I., Hauser-Kronberger, C., Hoefler, G., & Guertl, B. (August 2010). Loss of PTEN/MMAC1 activity is a rare and late event in the pathogenesis of nephroblastomas. Human Pathology, 41 (8), 1172-7. doi:10.1016/j.humpath.2009.10.024 Peer Reviewed verified by ORBi |
