Pellegrini, Cristina
University of L'Aquila
2 papers on CoChatORCID 0000-0003-2168-8097
Most cited papers
- Verified
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma
NCI DCEG Cancer Sequencing Working Group, Shi, J., Laboratory, N. D. C. G. R., French Familial Melanoma Study Group, Yang, X. R., Ballew, B., Rotunno, M., Calista, D., Fargnoli, M. C., Ghiorzo, P., et al. (2014) · Nature Genetics
Cutaneous Melanoma Detection and ManagementTelomeres, Telomerase, and Senescence
Cited by 331
- Verified
Understanding the Molecular Genetics of Basal Cell Carcinoma
Pellegrini, C., Maturo, M., Di Nardo, L., Ciciarelli, V., Gutiérrez García-Rodrigo, C., & Fargnoli, M. (2017) · International Journal of Molecular Sciences
Nonmelanoma Skin Cancer StudiesHedgehog Signaling Pathway Studies
Cited by 242
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