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The last 5 uploaded publications
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances
Laura Pignata, Francesco Cecere, Ankit Verma, Bruno Hay Mele, Maria Monticelli, Basilia Acurzio, Carlo Giaccari, Angela Sparago, José Ramón Hernández Mora, Ana Monteagudo, Manel Esteller, Arrate Pereda, Jair Tenorio, Orazio Palumbo, Massimo Carella, Paolo Prontera, Carmelo Piscopo, Maria Accadia, Pablo Lapunzina, Maria Vittoria Cubellis, Guiomar Pérez de Nanclares, David Monk, Andrea Riccio, Flavia Cerrato (2022). Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances. , 14(1), DOI: https://doi.org/10.1186/s13148-022-01292-w.
Article330 days agoNovel epigenetic signature, molecular subtypes and insights into IGF2/H19 dysregulation in Wilms tumour revealed by methylomic and transcriptomic profiling
Abu Saadat, Francesco Cecere, Federica Rossetti, Laura Pignata, Bruno Hay Mele, Emilia D’Angelo, Carlo Giaccari, Gaetano Verde, Paola Quarello, Franca Fagioli, Josep Roma, Manel Esteller, Enrique de Álava, Flavia Cerrato, Andrea Riccio, Angela Sparago (2025). Novel epigenetic signature, molecular subtypes and insights into IGF2/H19 dysregulation in Wilms tumour revealed by methylomic and transcriptomic profiling. , DOI: https://doi.org/10.21203/rs.3.rs-8030860/v1.
Preprint68 days ago