Célia Bádenas
Instituto de Salud Carlos III(ES)Centre for Biomedical Network Research on Rare Diseases(ES)Centro de Investigación Biomédica en Red(ES)Hospital Clínic de Barcelona(ES)Consorci Institut D'Investigacions Biomediques August Pi I Sunyer(ES)Instituto de Investigación de Enfermedades Raras(ES)Universitat de Barcelona(ES)
Publications by Year
Research Areas
Cutaneous Melanoma Detection and Management, Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, melanin and skin pigmentation, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides(1998)548 cited
- → A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma(2011)515 cited
- → Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families(2009)318 cited
- → TERT Promoter Mutation Status as an Independent Prognostic Factor in Cutaneous Melanoma(2014)254 cited
- → Benefits of total body photography and digital dermatoscopy (“two-step method of digital follow-up”) in the early diagnosis of melanoma in patients at high risk for melanoma(2011)225 cited
- → Update in genetic susceptibility in melanoma.(2015)199 cited