BONATTI, Francesco
BONATTI, Francesco
Dipartimento di Medicina e Chirurgia
Biological Role and Clinical Implications of microRNAs in BRCA Mutation Carriers
2021-01-01 Tommasi, Chiara; Pellegrino, Benedetta; Boggiani, Daniela; Sikokis, Angelica; Michiara, Maria; Uliana, Vera; Bortesi, Beatrice; Bonatti, Francesco; Mozzoni, Paola; Pinelli, Silvana; Squadrilli, Anna; Viani, Maria Vittoria; Cassi, Diana; Maglietta, Giuseppe; Meleti, Marco; Musolino, Antonino
Combination of ultrasound and molecular testing in malignancy risk estimate of Bethesda category IV thyroid nodules: results from a single-institution prospective study
2021-01-01 Marina, M; Zatelli, M C; Goldoni, M; Del Rio, P; Corcione, L; Martorana, D; Percesepe, A; Bonatti, F; Mozzoni, P; Crociara, A; Ceresini, G
Evidence fo Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias
2011-01-01 Vottero, Alessandra; Minari, Roberta; Viani, Isabella; F., Tassi; Bonatti, Francesco; Neri, Tauro Maria; Bertolini, Lorenzo; Bernasconi, Sergio; Ghizzoni, Lucia
Genetic Basis of Breast and Ovarian Cancer: Approaches and Lessons Learnt from Three Decades of Inherited Predisposition Testing
2024-01-01 Barili, Valeria; Ambrosini, Enrico; Bortesi, Beatrice; Minari, Roberta; De Sensi, Erika; Cannizzaro, Ilenia Rita; Taiani, Antonietta; Michiara, Maria; Sikokis, Angelica; Boggiani, Daniela; Tommasi, Chiara; Serra, Olga; Bonatti, Francesco; Adorni, Alessia; Luberto, Anita; Caggiati, Patrizia; Martorana, Davide; Uliana, Vera; Percesepe, Antonio; Musolino, Antonino; Pellegrino, Benedetta
Monogenic autoinflammatory diseases with mendelian inheritance: Genes, mutations, and genotype/phenotype correlations
2017-01-01 Martorana, Davide; Bonatti, Francesco; Mozzoni, Paola; Vaglio, Augusto; Percesepe, Antonio
PD-L1 SNPs as biomarkers to define benefit in patients with advanced NSCLC treated with immune checkpoint inhibitors
2021-01-01 Minari, R.; Bonatti, F.; Mazzaschi, G.; Dodi, A.; Facchinetti, F.; Gelsomino, F.; Cinquegrani, G.; Squadrilli, A.; Bordi, P.; Buti, S.; Bersanelli, M.; Leonetti, A.; Cosenza, A.; Ferri, L.; Rapacchi, E.; Quaini, F.; Ardizzoni, A.; Tiseo, M.
Role of ctDNA for the detection of minimal residual disease in resected non-small cell lung cancer: a systematic review
2022-01-01 Verze, M.; Pluchino, M.; Leonetti, A.; Coriano, M.; Bonatti, F.; Armillotta, M. P.; Perrone, F.; Casali, M.; Minari, R.; Tiseo, M.
Spectrum of X-linked intellectual disabilities and psychiatric symptoms in a family harbouring a Xp22.12 microduplication encompassing the RPS6KA3 gene
2019-01-01 Uliana, Vera; Bonatti, Francesco; Zanatta, Valentina; Mozzoni, Paola; Martorana, Davide; Percesepe, Antonio
The -2518 A/G polymorphism of the monocyte chemoattractant protein-1 as a candidate genetic predisposition factor for secondary myelofibrosis and biomarker of disease severity
2018-01-01 Masselli, Elena; Carubbi, Cecilia; Cambò, Benedetta; Pozzi, Giulia; Gobbi, Giuliana; Mirandola, Prisco; Follini, Elena; Pagliaro, Luca; Di Marcantonio, Daniela; Bonatti, Francesco; Percesepe, Antonio; Sykes, Stephen M.; Aversa, Franco; Vitale, Marco
Unmasking selective path integration deficits inAlzheimer’s disease risk carriers
2020-01-01 Lukaskunz, Annebierbrauer; Gomes, Carlos A.; Luhmann, Maike; Deuker, Lorena; Getzmann, Stephan; Wascher, Edmund; Gajewski, Patrick D.; Hengstler, Jan G.; Fernandez-Alvarez, Marina; Atienza, Mercedes; Cammisuli, Davide M.; Bonatti, Francesco; Pruneti, Carlo; Percesepe, Antonio; Bellaali, Youssef; Hanseeuw, Bernard; Strange, Bryan A.; Cantero, Jose L.; Axmacher, Nikolai
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Biological Role and Clinical Implications of microRNAs in BRCA Mutation Carriers | 1-gen-2021 | Tommasi, Chiara; Pellegrino, Benedetta; Boggiani, Daniela; Sikokis, Angelica; Michiara, Maria; Uliana, Vera; Bortesi, Beatrice; Bonatti, Francesco; Mozzoni, Paola; Pinelli, Silvana; Squadrilli, Anna; Viani, Maria Vittoria; Cassi, Diana; Maglietta, Giuseppe; Meleti, Marco; Musolino, Antonino | |
| Combination of ultrasound and molecular testing in malignancy risk estimate of Bethesda category IV thyroid nodules: results from a single-institution prospective study | 1-gen-2021 | Marina, M; Zatelli, M C; Goldoni, M; Del Rio, P; Corcione, L; Martorana, D; Percesepe, A; Bonatti, F; Mozzoni, P; Crociara, A; Ceresini, G | |
| Evidence fo Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias | 1-gen-2011 | Vottero, Alessandra; Minari, Roberta; Viani, Isabella; F., Tassi; Bonatti, Francesco; Neri, Tauro Maria; Bertolini, Lorenzo; Bernasconi, Sergio; Ghizzoni, Lucia | |
| Genetic Basis of Breast and Ovarian Cancer: Approaches and Lessons Learnt from Three Decades of Inherited Predisposition Testing | 1-gen-2024 | Barili, Valeria; Ambrosini, Enrico; Bortesi, Beatrice; Minari, Roberta; De Sensi, Erika; Cannizzaro, Ilenia Rita; Taiani, Antonietta; Michiara, Maria; Sikokis, Angelica; Boggiani, Daniela; Tommasi, Chiara; Serra, Olga; Bonatti, Francesco; Adorni, Alessia; Luberto, Anita; Caggiati, Patrizia; Martorana, Davide; Uliana, Vera; Percesepe, Antonio; Musolino, Antonino; Pellegrino, Benedetta | |
| Monogenic autoinflammatory diseases with mendelian inheritance: Genes, mutations, and genotype/phenotype correlations | 1-gen-2017 | Martorana, Davide; Bonatti, Francesco; Mozzoni, Paola; Vaglio, Augusto; Percesepe, Antonio | |
| PD-L1 SNPs as biomarkers to define benefit in patients with advanced NSCLC treated with immune checkpoint inhibitors | 1-gen-2021 | Minari, R.; Bonatti, F.; Mazzaschi, G.; Dodi, A.; Facchinetti, F.; Gelsomino, F.; Cinquegrani, G.; Squadrilli, A.; Bordi, P.; Buti, S.; Bersanelli, M.; Leonetti, A.; Cosenza, A.; Ferri, L.; Rapacchi, E.; Quaini, F.; Ardizzoni, A.; Tiseo, M. | |
| Role of ctDNA for the detection of minimal residual disease in resected non-small cell lung cancer: a systematic review | 1-gen-2022 | Verze, M.; Pluchino, M.; Leonetti, A.; Coriano, M.; Bonatti, F.; Armillotta, M. P.; Perrone, F.; Casali, M.; Minari, R.; Tiseo, M. | |
| Spectrum of X-linked intellectual disabilities and psychiatric symptoms in a family harbouring a Xp22.12 microduplication encompassing the RPS6KA3 gene | 1-gen-2019 | Uliana, Vera; Bonatti, Francesco; Zanatta, Valentina; Mozzoni, Paola; Martorana, Davide; Percesepe, Antonio | |
| The -2518 A/G polymorphism of the monocyte chemoattractant protein-1 as a candidate genetic predisposition factor for secondary myelofibrosis and biomarker of disease severity | 1-gen-2018 | Masselli, Elena; Carubbi, Cecilia; Cambò, Benedetta; Pozzi, Giulia; Gobbi, Giuliana; Mirandola, Prisco; Follini, Elena; Pagliaro, Luca; Di Marcantonio, Daniela; Bonatti, Francesco; Percesepe, Antonio; Sykes, Stephen M.; Aversa, Franco; Vitale, Marco | |
| Unmasking selective path integration deficits inAlzheimer’s disease risk carriers | 1-gen-2020 | Lukaskunz, Annebierbrauer; Gomes, Carlos A.; Luhmann, Maike; Deuker, Lorena; Getzmann, Stephan; Wascher, Edmund; Gajewski, Patrick D.; Hengstler, Jan G.; Fernandez-Alvarez, Marina; Atienza, Mercedes; Cammisuli, Davide M.; Bonatti, Francesco; Pruneti, Carlo; Percesepe, Antonio; Bellaali, Youssef; Hanseeuw, Bernard; Strange, Bryan A.; Cantero, Jose L.; Axmacher, Nikolai |