BAGNULO, ROSANNA
BAGNULO, ROSANNA
DIPARTIMENTO DI MEDICINA DI PRECISIONE E RIGENERATIVA E AREA JONICA DiMePRe-J
636 Genotoxic damage and dna repair gene polymorphisms in workers exposed to low doses of ionising radiation
2018-01-01 Lovreglio, P; Rotondi, R; Chiarappa, P; Resta, N; Bagnulo, R; Drago, I; Fracasso, Me; D'Oria, Domenico; Soleo, L
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1
2018-01-01 Stella, Alessandro; Lastella, Patrizia; Loconte, Daria Carmela; Bukvic, Nenad; Varvara, Dora; Patruno, Margherita; Bagnulo, Rosanna; Lovaglio, Rosaura; Bartolomeo, Nicola; Serio, Gabriella; Resta, Nicoletta
Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation
2017-01-01 Guaraldi, Federica; Di Nardo, Giovanni; Tarani, Luigi; Bertelli, Luca; Susca, Francesco Claudio; Bagnulo, Rosanna; Resta, Nicoletta
Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers
2022-01-01 Turchiano, Antonella; Loconte, Daria Carmela; De Nola, Rosalba; Arezzo, Francesca; Chiarello, Giulia; Pantaleo, Antonino; Iacoviello, Matteo; Bagnulo, Rosanna; De Luisi, Annunziata; Perrelli, Sonia; Martino, Stefania; Ranieri, Carlotta; Garganese, Antonella; Stella, Alessandro; Forleo, Cinzia; Loizzi, Vera; Marinaccio, Marco; Cicinelli, Ettore; Cormio, Gennaro; Resta, Nicoletta
Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes
2014-01-01 Forte, Giovanna; Grossi, Valentina; Celestini, Valentina; Lucisano, Giuseppe; Scardapane, Marco; Varvara, Dora; Patruno, Margherita; Bagnulo, Rosanna; Loconte, DARIA CARMELA; Giunti, Laura; Petracca, Antonio; Giglio, Sabrina; Genuardi, Maurizio; Pellegrini, Fabio; Resta, Nicoletta; Simone, Cristiano
Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene
2022-01-01 Stella, Alessandro; Lastella, Patrizia; Viggiano, Luigi; Bagnulo, Rosanna; Resta, Nicoletta
Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes
2023-01-01 Forte, Giovanna; Cariola, Filomena; Buonadonna, Antonia Lucia; Guglielmi, Anna Filomena; Manghisi, Andrea; De Marco, Katia; Grossi, Valentina; Fasano, Candida; Lepore Signorile, Martina; Sanese, Paola; Bagnulo, Rosanna; Resta, Nicoletta; Disciglio, Vittoria; Simone, Cristiano
Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency
2024-01-01 Martino, Stefania; D'Addabbo, Pietro; Turchiano, Antonella; Fc, Radio; Bruselles, Alessandro; Cordeddu, Viviana; Mancini, Cecilia; Stella, Alessandro; Laforgia, Nicola; Capodiferro, Donatella; Simonetti, Simonetta; Bagnulo, Rosanna; Palumbo, Orazio; Marzano, Flaviana; Tabaku, Ornella; Garganese, Antonella; Stasi, Michele; Tartaglia, Marco; Pesole, Graziano; Resta, Nicoletta
Epidemiology of the disorders of the Pik3ca-related overgrowth spectrum (Pros)
2023-01-01 Reynolds, Giuseppe; Cardaropoli, Simona; Carli, Diana; Luca, Maria; Gazzin, Andrea; Coppo, Paola; La Selva, Roberta; Piglionica, Marilidia; Bagnulo, Rosanna; Turchiano, Antonella; Ranieri, Carlotta; Resta, Nicoletta; Mussa, Alessandro
Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy
2023-01-01 Di Ciaula, A; Iacoviello, M; Bonfrate, L; Khalil, M; Shanmugam, H; Lopalco, G; Bagnulo, R; Garganese, A; Iannone, F; Resta, N; Portincasa, P; Stella, A.
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants
2022-01-01 Mussa, Alessandro; Leoni, Chiara; Iacoviello, Matteo; Carli, Diana; Ranieri, Carlotta; Pantaleo, Antonino; Buonuomo, Paola Sabrina; Bagnulo, Rosanna; Ferrero, Giovanni Battista; Bartuli, Andrea; Melis, Daniela; Maitz, Silvia; Loconte, Daria Carmela; Turchiano, Antonella; Piglionica, Marilidia; De Luisi, Annunziata; Susca, Francesco Claudio; Bukvic, Nenad; Forleo, Cinzia; Selicorni, Angelo; Zampino, Giuseppe; Onesimo, Roberta; Cappuccio, Gerarda; Garavelli, Livia; Novelli, Chiara; Memo, Luigi; Morando, Carla; Della Monica, Matteo; Accadia, Maria; Capurso, Martina; Piscopo, Carmelo; Cereda, Anna; Di Giacomo, Marilena Carmela; Saletti, Veronica; Spinelli, Alessandro Mauro; Lastella, Patrizia; Tenconi, Romano; Dvorakova, Veronika; Irvine, Alan D; Resta, Nicoletta
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer
2023-01-01 Turchiano, Antonella; Piglionica, Marilidia; Martino, Stefania; Bagnulo, Rosanna; Garganese, Antonella; De Luisi, Annunziata; Chirulli, Stefania; Iacoviello, Matteo; Stasi, Michele; Tabaku, Ornella; Meneleo, Eleonora; Capurso, Martina; Crocetta, Silvia; Lattarulo, Simone; Krylovska, Yevheniia; Lastella, Patrizia; Forleo, Cinzia; Stella, Alessandro; Bukvic, Nenad; Simone, Cristiano; Resta, Nicoletta
In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS)
2018-01-01 Ranieri, C; Di Tommaso, S; Loconte, D C; Grossi, V; Sanese, P; Bagnulo, R; Susca, F C; Forte, G; Peserico, A; De Luisi, A; Bartuli, A; Selicorni, A; Melis, D; Lerone, M; Praticò, A D; Abbadessa, G; Yu, Y; Schwartz, B; Ruggieri, Martino; Simone, Cristiano; Resta, Nicoletta
Influence of polymorphisms of DNA repair and GST genes on genotoxic damage and mutagen sensitivity in workers occupationally exposed to very low doses of ionizing radiation
2019-01-01 Stufano, A.; Chiarappa, P.; Bagnulo, R.; Drago, I.; Rapisarda, V.; Ledda, C.; Vimercati, L.; De Benedictis, L.; Resta, N.; Soleo, L.; Lovreglio, P.
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies
2022-01-01 Mussa, Alessandro; Turchiano, Antonella; Cardaropoli, Simona; Coppo, Paola; Pantaleo, Antonino; Bagnulo, Rosanna; Ranieri, Carlotta; Iacoviello, Matteo; Garganese, Antonella; Stella, Alessandro; Gabriele Vallero, Stefano; Bertin, Daniele; Santoro, Federica; Carli, Diana; Battista Ferrero, Giovanni; Resta, Nicoletta
Loss of STK11 expression is an early event in prostate carcinogenesis and predicts therapeutic response to targeted therapy against MAPK/p38.
2015-01-01 Grossi, Valentina; Lucarelli, Giuseppe; Forte, Giovanna; Peserico, Alessia; Matrone, Antonio; Germani, Aldo; Rutigliano, Monica; Stella, Alessandro; Bagnulo, Rosanna; Loconte, DARIA CARMELA; Galleggiante, Vanessa; Sanguedolce, Francesca; Cagiano, Simona; Bufo, Pantaleo; Trabucco, Senia; Maiorano, Eugenio; Ditonno, Pasquale; Battaglia, Michele; Resta, Nicoletta; Simone, Cristiano
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience
2024-01-01 Forleo, Cinzia; Carella, Maria Cristina; Basile, Paolo; Carulli, Eugenio; Dadamo, Michele Luca; Amati, Francesca; Loizzi, Francesco; Sorrentino, Sandro; Dentamaro, Ilaria; Dicorato, Marco Maria; Ricci, Stefano; Bagnulo, Rosanna; Iacoviello, Matteo; Santobuono, Vincenzo Ezio; Caiati, Carlo; Pepe, Martino; Desaphy, Jean-Francois; Ciccone, Marco Matteo; Resta, Nicoletta; Guaricci, Andrea Igoren
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience
2024-01-01 Forleo, Cinzia; Carella, Maria Cristina; Basile, Paolo; Carulli, Eugenio; Dadamo, Michele Luca; Amati, Francesca; Loizzi, Francesco; Sorrentino, Sandro; Dentamaro, Ilaria; Dicorato, Marco Maria; Ricci, Stefano; Bagnulo, Rosanna; Iacoviello, Matteo; Santobuono, Vincenzo Ezio; Caiati, Carlo; Pepe, Martino; Desaphy, Jean-Francois; Ciccone, Marco Matteo; Resta, Nicoletta; Guaricci, Andrea Igoren
Novel scn5a p.W697x nonsense mutation segregation in a family with brugada syndrome
2019-01-01 Micaglio, E.; Monasky, M. M.; Resta, N.; Bagnulo, R.; Ciconte, G.; Gianelli, L.; Locati, E. T.; Vicedomini, G.; Borrelli, V.; Ghiroldi, A.; Anastasia, L.; Benedetti, S.; Di Resta, C.; Ferrari, M.; Pappone, C.
Old treatments for new genetic conditions: Sirolimus therapy in a child affected by mosaic overgrowth with fibroadipose hyperplasia
2019-01-01 Leoni, C.; Onesimo, R.; Resta, N.; Patti, M. L.; De Santis, R.; Bagnulo, R.; Russo, L.; Manfredi, R.; Genuardi, M.; Zampino, G.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 636 Genotoxic damage and dna repair gene polymorphisms in workers exposed to low doses of ionising radiation | 1-gen-2018 | Lovreglio, P; Rotondi, R; Chiarappa, P; Resta, N; Bagnulo, R; Drago, I; Fracasso, Me; D'Oria, Domenico; Soleo, L | |
| Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 | 1-gen-2018 | Stella, Alessandro; Lastella, Patrizia; Loconte, Daria Carmela; Bukvic, Nenad; Varvara, Dora; Patruno, Margherita; Bagnulo, Rosanna; Lovaglio, Rosaura; Bartolomeo, Nicola; Serio, Gabriella; Resta, Nicoletta | |
| Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulation | 1-gen-2017 | Guaraldi, Federica; Di Nardo, Giovanni; Tarani, Luigi; Bertelli, Luca; Susca, Francesco Claudio; Bagnulo, Rosanna; Resta, Nicoletta | |
| Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers | 1-gen-2022 | Turchiano, Antonella; Loconte, Daria Carmela; De Nola, Rosalba; Arezzo, Francesca; Chiarello, Giulia; Pantaleo, Antonino; Iacoviello, Matteo; Bagnulo, Rosanna; De Luisi, Annunziata; Perrelli, Sonia; Martino, Stefania; Ranieri, Carlotta; Garganese, Antonella; Stella, Alessandro; Forleo, Cinzia; Loizzi, Vera; Marinaccio, Marco; Cicinelli, Ettore; Cormio, Gennaro; Resta, Nicoletta | |
| Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes | 1-gen-2014 | Forte, Giovanna; Grossi, Valentina; Celestini, Valentina; Lucisano, Giuseppe; Scardapane, Marco; Varvara, Dora; Patruno, Margherita; Bagnulo, Rosanna; Loconte, DARIA CARMELA; Giunti, Laura; Petracca, Antonio; Giglio, Sabrina; Genuardi, Maurizio; Pellegrini, Fabio; Resta, Nicoletta; Simone, Cristiano | |
| Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene | 1-gen-2022 | Stella, Alessandro; Lastella, Patrizia; Viggiano, Luigi; Bagnulo, Rosanna; Resta, Nicoletta | |
| Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes | 1-gen-2023 | Forte, Giovanna; Cariola, Filomena; Buonadonna, Antonia Lucia; Guglielmi, Anna Filomena; Manghisi, Andrea; De Marco, Katia; Grossi, Valentina; Fasano, Candida; Lepore Signorile, Martina; Sanese, Paola; Bagnulo, Rosanna; Resta, Nicoletta; Disciglio, Vittoria; Simone, Cristiano | |
| Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency | 1-gen-2024 | Martino, Stefania; D'Addabbo, Pietro; Turchiano, Antonella; Fc, Radio; Bruselles, Alessandro; Cordeddu, Viviana; Mancini, Cecilia; Stella, Alessandro; Laforgia, Nicola; Capodiferro, Donatella; Simonetti, Simonetta; Bagnulo, Rosanna; Palumbo, Orazio; Marzano, Flaviana; Tabaku, Ornella; Garganese, Antonella; Stasi, Michele; Tartaglia, Marco; Pesole, Graziano; Resta, Nicoletta | |
| Epidemiology of the disorders of the Pik3ca-related overgrowth spectrum (Pros) | 1-gen-2023 | Reynolds, Giuseppe; Cardaropoli, Simona; Carli, Diana; Luca, Maria; Gazzin, Andrea; Coppo, Paola; La Selva, Roberta; Piglionica, Marilidia; Bagnulo, Rosanna; Turchiano, Antonella; Ranieri, Carlotta; Resta, Nicoletta; Mussa, Alessandro | |
| Genetic and clinical features of Familial Mediterranean Fever (FMF) in a homogeneous cohort of patients from south-eastern Italy | 1-gen-2023 | Di Ciaula, A; Iacoviello, M; Bonfrate, L; Khalil, M; Shanmugam, H; Lopalco, G; Bagnulo, R; Garganese, A; Iannone, F; Resta, N; Portincasa, P; Stella, A. | |
| Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants | 1-gen-2022 | Mussa, Alessandro; Leoni, Chiara; Iacoviello, Matteo; Carli, Diana; Ranieri, Carlotta; Pantaleo, Antonino; Buonuomo, Paola Sabrina; Bagnulo, Rosanna; Ferrero, Giovanni Battista; Bartuli, Andrea; Melis, Daniela; Maitz, Silvia; Loconte, Daria Carmela; Turchiano, Antonella; Piglionica, Marilidia; De Luisi, Annunziata; Susca, Francesco Claudio; Bukvic, Nenad; Forleo, Cinzia; Selicorni, Angelo; Zampino, Giuseppe; Onesimo, Roberta; Cappuccio, Gerarda; Garavelli, Livia; Novelli, Chiara; Memo, Luigi; Morando, Carla; Della Monica, Matteo; Accadia, Maria; Capurso, Martina; Piscopo, Carmelo; Cereda, Anna; Di Giacomo, Marilena Carmela; Saletti, Veronica; Spinelli, Alessandro Mauro; Lastella, Patrizia; Tenconi, Romano; Dvorakova, Veronika; Irvine, Alan D; Resta, Nicoletta | |
| Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer | 1-gen-2023 | Turchiano, Antonella; Piglionica, Marilidia; Martino, Stefania; Bagnulo, Rosanna; Garganese, Antonella; De Luisi, Annunziata; Chirulli, Stefania; Iacoviello, Matteo; Stasi, Michele; Tabaku, Ornella; Meneleo, Eleonora; Capurso, Martina; Crocetta, Silvia; Lattarulo, Simone; Krylovska, Yevheniia; Lastella, Patrizia; Forleo, Cinzia; Stella, Alessandro; Bukvic, Nenad; Simone, Cristiano; Resta, Nicoletta | |
| In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) | 1-gen-2018 | Ranieri, C; Di Tommaso, S; Loconte, D C; Grossi, V; Sanese, P; Bagnulo, R; Susca, F C; Forte, G; Peserico, A; De Luisi, A; Bartuli, A; Selicorni, A; Melis, D; Lerone, M; Praticò, A D; Abbadessa, G; Yu, Y; Schwartz, B; Ruggieri, Martino; Simone, Cristiano; Resta, Nicoletta | |
| Influence of polymorphisms of DNA repair and GST genes on genotoxic damage and mutagen sensitivity in workers occupationally exposed to very low doses of ionizing radiation | 1-gen-2019 | Stufano, A.; Chiarappa, P.; Bagnulo, R.; Drago, I.; Rapisarda, V.; Ledda, C.; Vimercati, L.; De Benedictis, L.; Resta, N.; Soleo, L.; Lovreglio, P. | |
| Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: another piece added to the puzzle of mosaic RASopathies | 1-gen-2022 | Mussa, Alessandro; Turchiano, Antonella; Cardaropoli, Simona; Coppo, Paola; Pantaleo, Antonino; Bagnulo, Rosanna; Ranieri, Carlotta; Iacoviello, Matteo; Garganese, Antonella; Stella, Alessandro; Gabriele Vallero, Stefano; Bertin, Daniele; Santoro, Federica; Carli, Diana; Battista Ferrero, Giovanni; Resta, Nicoletta | |
| Loss of STK11 expression is an early event in prostate carcinogenesis and predicts therapeutic response to targeted therapy against MAPK/p38. | 1-gen-2015 | Grossi, Valentina; Lucarelli, Giuseppe; Forte, Giovanna; Peserico, Alessia; Matrone, Antonio; Germani, Aldo; Rutigliano, Monica; Stella, Alessandro; Bagnulo, Rosanna; Loconte, DARIA CARMELA; Galleggiante, Vanessa; Sanguedolce, Francesca; Cagiano, Simona; Bufo, Pantaleo; Trabucco, Senia; Maiorano, Eugenio; Ditonno, Pasquale; Battaglia, Michele; Resta, Nicoletta; Simone, Cristiano | |
| Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience | 1-gen-2024 | Forleo, Cinzia; Carella, Maria Cristina; Basile, Paolo; Carulli, Eugenio; Dadamo, Michele Luca; Amati, Francesca; Loizzi, Francesco; Sorrentino, Sandro; Dentamaro, Ilaria; Dicorato, Marco Maria; Ricci, Stefano; Bagnulo, Rosanna; Iacoviello, Matteo; Santobuono, Vincenzo Ezio; Caiati, Carlo; Pepe, Martino; Desaphy, Jean-Francois; Ciccone, Marco Matteo; Resta, Nicoletta; Guaricci, Andrea Igoren | |
| Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience | 1-gen-2024 | Forleo, Cinzia; Carella, Maria Cristina; Basile, Paolo; Carulli, Eugenio; Dadamo, Michele Luca; Amati, Francesca; Loizzi, Francesco; Sorrentino, Sandro; Dentamaro, Ilaria; Dicorato, Marco Maria; Ricci, Stefano; Bagnulo, Rosanna; Iacoviello, Matteo; Santobuono, Vincenzo Ezio; Caiati, Carlo; Pepe, Martino; Desaphy, Jean-Francois; Ciccone, Marco Matteo; Resta, Nicoletta; Guaricci, Andrea Igoren | |
| Novel scn5a p.W697x nonsense mutation segregation in a family with brugada syndrome | 1-gen-2019 | Micaglio, E.; Monasky, M. M.; Resta, N.; Bagnulo, R.; Ciconte, G.; Gianelli, L.; Locati, E. T.; Vicedomini, G.; Borrelli, V.; Ghiroldi, A.; Anastasia, L.; Benedetti, S.; Di Resta, C.; Ferrari, M.; Pappone, C. | |
| Old treatments for new genetic conditions: Sirolimus therapy in a child affected by mosaic overgrowth with fibroadipose hyperplasia | 1-gen-2019 | Leoni, C.; Onesimo, R.; Resta, N.; Patti, M. L.; De Santis, R.; Bagnulo, R.; Russo, L.; Manfredi, R.; Genuardi, M.; Zampino, G. |