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RICCIO, Andrea

RICCIO, Andrea  

Dipartimento di Scienze e Tecnologie Ambientali Biologiche e Farmaceutiche (DISTABiF)  

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Adult‐Onset β‐Thalassemia Major as Acquired Imprinting Disorder 1-gen-2026 D'Angelo, Emilia; Mandrile, Giorgia; Tesio, Nicolò; Cecere, Francesco; Ceglie, Teresa; De Maria, Rosa Maria; Mellone, Simona; Giordano, Mara; Kargutar, Neha Sanjay; Cerrato, Flavia; Riccio, Andrea; Ferrero, Giovanni Battista
A Maternal Loss‐of‐Function Variant in KHDC3L Gene Causes a Range of Adverse Pregnancy Outcomes: A Case Report 1-gen-2025 Anvar, Zahra; Jafarpour, Farnoosh; Jahromi, Bahia Namavar; Riccio, Andrea; Nasr‐esfahani, Mohammad Hossein; Cubellis, Maria Vittoria
Beckwith-Wiedemann spectrum (BWSp): an update on diagnosis, management, and follow-up from the scientific committee of the Italian BWSp association 1-gen-2025 Russo, Silvia; Milani, Donatella; Meossi, Camilla; Marcucci, Lorenzo; Pajno, Roberta; Butti, Niccolò; Cocchi, Guido; Tannorella, Pierpaola; Bertoletti, Monica; Carli, Diana; Meazzini, Maria Costanza; Tortora, Chiara; Ferrari, Mario; Zampino, Giuseppe; Massuras, Stefania; Ferrero, Giovanni Battista; Quarello, Paola; Rossetti, Giulia; Montirosso, Rosario; De Pellegrin, Maurizio; Riccio, Andrea; Mussa, Alessandro
Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances 1-gen-2025 Cecere, Francesco; Pignata, Laura; D'Angelo, Emilia; Giaccari, Carlo; Saadat, Abu; Sparago, Angela; Angelini, Claudia; Hay Mele, Bruno; Mussa, Alessandro; Ferrero, Giovanni Battista; Scarano, Gioacchino; Gori, Giulia; Di Maria, Emilio; Romano, Corrado; Tarani, Luigi; Piscopo, Carmelo; Scala, Iris; Tenorio, Jair Antonio; Lapunzina, Pablo; Cerrato, Flavia; Riccio, Andrea
Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome 1-gen-2025 D'Angelo, Emilia; Pignata, Laura; Cecere, Francesco; Vimercati, Alessandro; Cubellis, Maria Vittoria; Saadat, Abu; Giaccari, Carlo; Thibaud, Nathalie; Eggermann, Thomas; Fernández-Fructuoso, Jose Ramon; Russo, Silvia; Netchine, Irène; Cerrato, Flavia; Riccio, Andrea; Brioude, Frédéric
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans 1-gen-2025 Cecere, Francesco; Relator, Raissa; Levy, Michael; Verma, Ankit; Mcconkey, Haley; Mele, Bruno Hay; Pignata, Laura; Giaccari, Carlo; D'Angelo, Emilia; Saha, Subham; Saadat, Abu; Sparago, Angela; Angelini, Claudia; Cerrato, Flavia; Sadikovic, Bekim; Riccio, Andrea
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 1-gen-2024 Giaccari, Carlo; Cecere, Francesco; Argenziano, Lucia; Pagano, Angela; Galvao, Antonio; Acampora, Dario; Rossi, Gianna; Hay Mele, Bruno; Acurzio, Basilia; Coonrod, Scott; Cubellis, Maria Vittoria; Cerrato, Flavia; Andrews, Simon; Cecconi, Sandra; Kelsey, Gavin; Riccio, Andrea
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 1-gen-2024 Lullo, Vincenzo; Cecere, Francesco; Batti, Saveria; Allegretti, Sara; Morone, Barbara; Fioriniello, Salvatore; Pisapia, Laura; Genesio, Rita; Della Ragione, Floriana; Giardino, Giuliana; Pignata, Claudio; Riccio, Andrea; Matarazzo, Maria R.; Strazzullo, Maria
A novel missense variant in PNLDC1 associated with nonobstructive azoospermia 1-gen-2024 Rahimian, Mouness; Askari, Masomeh; Salehi, Najmeh; Jaafarinia, Mojtaba; Forouzanfar, Mohsen; Almadani, Navid; Riccio, Andrea; Totonchi, Mehdi
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis 1-gen-2024 G Mackay, Deborah J; Gazdagh, Gabriella; Monk, David; Brioude, Frederic; Giabicani, Eloise; M Krzyzewska, Izabela; M Kalish, Jennifer; M Maas, Saskia; Kagami, Masayo; Beygo, Jasmin; Kahre, Tiina; Tenorio-Castano, Jair; Ambrozaitytė, Laima; Burnytė, Birutė; Cerrato, Flavia; H Davies, Justin; Battista Ferrero, Giovanni; Fjodorova, Olga; Manero-Azua, Africa; Pereda, Arrate; Russo, Silvia; Tannorella, Pierpaola; I Temple, Karen; Õunap, Katrin; Riccio, Andrea; Perez de Nanclares, Guiomar; R Maher, Eamonn; Lapunzina, Pablo; Netchine, Irène; Eggermann, Thomas; Bliek, Jet; Tümer, Zeynep
New insights into oocyte cytoplasmic lattice-associated proteins 1-gen-2024 Giaccari, Carlo; Cecere, Francesco; Argenziano, Lucia; Pagano, Angela; Riccio, Andrea
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors 1-gen-2024 Cillo, F.; Coppola, E.; Habetswallner, F.; Cecere, F.; Pignata, L.; Toriello, E.; De Rosa, A.; Grilli, L.; Ammendola, A.; Salerno, P.; Romano, R.; Cirillo, E.; Merla, G.; Riccio, A.; Pignata, C.; Giardino, G.
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 1-gen-2023 Elefante, Pierandrea; Spedicati, Beatrice; Faletra, Flavio; Pignata, Laura; Cerrato, Flavia; Riccio, Andrea; Barbi, Egidio; Memo, Luigi; Travan, Laura
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? 1-gen-2023 Pignata, Laura; Cecere, Francesco; Acquaviva, Fabio; D'Angelo, Emilia; Cioffi, Daniela; Pellino, Valeria; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Sparago, Angela; De Brasi, Daniele; Cerrato, Flavia; Riccio, Andrea
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer 1-gen-2023 Cecere, F.; Pignata, L.; Hay Mele, B.; Saadat, A.; D'Angelo, E.; Palumbo, O.; Palumbo, P.; Carella, M.; Scarano, G.; Rossi, G. B.; Angelini, C.; Sparago, A.; Cerrato, F.; Riccio, A.
Current trends and future prospects of drug repositioning in gastrointestinal oncology 1-gen-2023 Fatemi, Nayeralsadat; Karimpour, Mina; Bahrami, Hoda; Zali, Mohammad Reza; Chaleshi, Vahid; Riccio, Andrea; Nazemalhosseini-Mojarad, Ehsan; Totonchi, Mehdi
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming 1-gen-2023 Verma, A.; Poondi Krishnan, V.; Cecere, F.; D'Angelo, E.; Lullo, V.; Strazzullo, M.; Selig, S.; Angelini, C.; Matarazzo, M. R.; Riccio, A.
Imprinting disorders 1-gen-2023 Eggermann, Thomas; Monk, David; Perez de Nanclares, Guiomar; Kagami, Masayo; Giabicani, Eloïse; Riccio, Andrea; Tümer, Zeynep; Kalish, Jennifer M.; Tauber, Maithé; Duis, Jessica; Weksberg, Rosanna; Maher, Eamonn R.; Begemann, Matthias; Elbracht, Miriam
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development 1-gen-2023 Luca, Maria; Carli, Diana; Cardaropoli, Simona; Milani, Donatella; Cocchi, Guido; Leoni, Chiara; Macchiaiolo, Marina; Bartuli, Andrea; Tarani, Luigi; Melis, Daniela; Bontempo, Piera; D'Elia, Gemma; Prada, Elisabetta; Vitale, Raffaele; Grammegna, Angelina; Tannorella, Pierpaola; Sparago, Angela; Pignata, Laura; Riccio, Andrea; Russo, Silvia; Ferrero, Giovanni Battista; Mussa, Alessandro
Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques 1-gen-2022 Carli, Diana; Operti, Matteo; Russo, Silvia; Cocchi, Guido; Milani, Donatella; Leoni, Chiara; Prada, Elisabetta; Melis, Daniela; Falco, Mariateresa; Spina, Jennifer; Uliana, Vera; Sara, Osimani; Sirchia, Fabio; Tarani, Luigi; Macchiaiolo, Marina; Cerrato, Flavia; Sparago, Angela; Pignata, Laura; Tannorella, Pierpaola; Cardaropoli, Simona; Bartuli, Andrea; Riccio, Andrea; Ferrero, Giovanni Battista; Mussa, Alessandro