Gemma Tell‐Martí
Centre for Biomedical Network Research on Rare Diseases(ES)
Publications by Year
Research Areas
Cutaneous Melanoma Detection and Management, melanin and skin pigmentation, Skin Protection and Aging, Melanoma and MAPK Pathways, Immunotherapy and Immune Responses
Most-Cited Works
- → Genetic Abnormalities in Large to Giant Congenital Nevi: Beyond NRAS Mutations(2018)102 cited
- → AURKA Overexpression Is Driven by FOXM1 and MAPK/ERK Activation in Melanoma Cells Harboring BRAF or NRAS Mutations: Impact on Melanoma Prognosis and Therapy(2017)59 cited
- → The MC1R melanoma risk variant p.R160W is associated with Parkinson disease(2015)55 cited
- → Capturing the biological impact of CDKN2A and MC1R genes as an early predisposing event in melanoma and non melanoma skin cancer(2013)48 cited
- → Prevalence ofMITFp.E318K in Patients With Melanoma Independent of the Presence ofCDKN2ACausative Mutations(2015)47 cited
- → Mutational status of naevus-associated melanomas(2015)45 cited
- → Melanocortin 1 receptor (MC1R) polymorphisms’ influence on size and dermoscopic features of nevi(2017)30 cited
- → Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases(2022)29 cited
- → Prognostic role of tumoral PDL1 expression and peritumoral FoxP3+ lymphocytes in vulvar melanomas(2018)24 cited
- → KIT mutations and CD 117 overexpression are markers of better progression‐free survival in vulvar melanomas(2017)23 cited