Estelle Chanudet
Publications by Year
Research Areas
Cancer Genomics and Diagnostics, Renal cell carcinoma treatment, Renal and related cancers, Genetic and Kidney Cyst Diseases, Lymphoma Diagnosis and Treatment
Most-Cited Works
- → Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS(2013)343 cited
- → Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence(2021)188 cited
- → A20 is targeted by promoter methylation, deletion and inactivating mutation in MALT lymphoma(2009)118 cited
- → Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome(2013)107 cited
- → ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies(2013)85 cited
- → Geographic variation of mutagenic exposures in kidney cancer genomes(2024)62 cited
- → Large‐scale genome‐wide screening of circulating microRNAs in clear cell renal cell carcinoma reveals specific signatures in late‐stage disease(2017)34 cited
- → Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt Signaling(2015)25 cited
- → Variable Phenotype of Severe Immunodeficiencies Associated with RMRP Gene Mutations(2015)25 cited
- → Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma(2023)17 cited