Fernando Gianfrancesco (F Gianfrancesco)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 14

Top Venues

Communications biology

Bone research

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Clinical genetics

University of Campania Luigi Vanvitelli

University of Bologna (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Campania Luigi Vanvitelli

Italy

Professor of Human Genetics :: Department of Environmental, Biological and Pharmaceutical Sciences and Technologies

National Research Council of Italy

Italy

Researcher :: Department of Biomedical Sciences

Education History

University of Bologna

Italy

PHD

Publications

Federica Scotto di Carlo, Sharon Russo, Francesc Muyas, Maria Mangini, Lorenza Garribba, Laura Pazzaglia, Rita Genesio, Flavia Biamonte, Anna Chiara De Luca, Stefano Santaguida, Katia Scotlandi, Isidro Cortes-Ciriano, Fernando Gianfrancesco
Profilin 1 deficiency drives mitotic defects and reduces genome stability. Communications biology 6 (1) (2023)
Sharon Russo, Federica Scotto di Carlo, Antonio Maurizi, Giorgio Fortunato, Anna Teti, Danilo Licastro, Carmine Settembre, Tommaso Mello, Fernando Gianfrancesco
A mutation in the ZNF687 gene that is responsible for the severe form of Paget's disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset in a knock-in mouse model. Bone research 11 (1) (2023)
Federica Scotto di Carlo, Sharon Russo, Francesc Muyas, Maria Mangini, Lorenza Garribba, Laura Pazzaglia, Rita Genesio, Flavia Biamonte, Anna Chiara De Luca, Stefano Santaguida, Katia Scotlandi, Isidro Cortes-Ciriano, Fernando Gianfrancesco
Profilin 1 deficiency drives mitotic defects and reduces genome stability. Communications biology 6 (1) (2023)
Federica Scotto di Carlo, Sharon Russo, Francesc Muyas, Maria Mangini, Lorenza Garribba, Laura Pazzaglia, Rita Genesio, Flavia Biamonte, Anna Chiara De Luca, Stefano Santaguida, Katia Scotlandi, Isidro Cortes-Ciriano, Fernando Gianfrancesco
Profilin 1 deficiency drives mitotic defects and reduces genome stability. Communications biology 6 (1) (2023)
Federica Scotto di Carlo, Sharon Russo, Francesc Muyas, Maria Mangini, Lorenza Garribba, Laura Pazzaglia, Rita Genesio, Flavia Biamonte, Anna Chiara De Luca, Stefano Santaguida, Katia Scotlandi, Isidro Cortes-Ciriano, Fernando Gianfrancesco
Profilin 1 deficiency drives mitotic defects and reduces genome stability. Communications biology 6 (1) (2023)
Federica Scotto di Carlo, Sharon Russo, Francesc Muyas, Maria Mangini, Lorenza Garribba, Laura Pazzaglia, Rita Genesio, Flavia Biamonte, Anna Chiara De Luca, Stefano Santaguida, Katia Scotlandi, Isidro Cortes-Ciriano, Fernando Gianfrancesco
Profilin 1 deficiency drives mitotic defects and reduces genome stability. Communications biology 6 (1) (2023)
Federica Scotto di Carlo, Sharon Russo, Francesc Muyas, Maria Mangini, Lorenza Garribba, Laura Pazzaglia, Rita Genesio, Flavia Biamonte, Anna Chiara De Luca, Stefano Santaguida, Katia Scotlandi, Isidro Cortes-Ciriano, Fernando Gianfrancesco
Profilin 1 deficiency drives mitotic defects and reduces genome stability. Communications biology 6 (1) (2023)
Sharon Russo, Federica Scotto di Carlo, Antonio Maurizi, Giorgio Fortunato, Anna Teti, Danilo Licastro, Carmine Settembre, Tommaso Mello, Fernando Gianfrancesco
A mutation in the ZNF687 gene that is responsible for the severe form of Paget's disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset in a knock-in mouse model. Bone research 11 (1) (2023)
Magdalena Kostrzewa, Ali Mokhtar Mahmoud, Roberta Verde, Federica Scotto di Carlo, Fernando Gianfrancesco, Fabiana Piscitelli, Alessia Ligresti
Modulation of Endocannabinoid Tone in Osteoblastic Differentiation of MC3T3-E1 Cells and in Mouse Bone Tissue over Time. Cells 10 (5) (2021)
Federica Scotto di Carlo, Laura Pazzaglia, Steven Mumm, Maria S Benassi, Annarosaria De Chiara, Alessandro Franchi, Antonina Parafioriti, Alberto Righi, Teresa Esposito, Michael P Whyte, Fernando Gianfrancesco
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 35 (10) (2020)
Federica Scotto di Carlo, Laura Pazzaglia, Teresa Esposito, Fernando Gianfrancesco
The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 35 (8) (2020)
Federica Scotto di Carlo, Giuseppina Divisato, Maurizio Iacoangeli, Teresa Esposito, Fernando Gianfrancesco
The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this location. BMC cancer 18 (1) (2018)
F Napolitano, V Di Iorio, F Testa, A Tirozzi, M G Reccia, L Lombardi, O Farina, F Simonelli, Fernando Gianfrancesco, G Di Iorio, M A B Melone, Teresa Esposito, S Sampaolo
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation. Clinical genetics 93 (5) (2018)
G Divisato, F Scotto di Carlo, N Petrillo, Teresa Esposito, Fernando Gianfrancesco
ZNF687 mutations are frequently found in pagetic patients from South Italy: implication in the pathogenesis of Paget's disease of bone. Clinical genetics 93 (6) (2018)

Fernando Gianfrancesco.css-eqlu8i{font-size:small;padding-left:4px;} (F Gianfrancesco)

Publication Activity (10 Years)

Top Topics

Top Venues

Fernando Gianfrancesco (F Gianfrancesco)