Teresa Esposito (T Esposito)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 14

Top Venues

Molecular neurobiology

Clinical genetics

Neuropathology and applied neurobiology

Ophthalmic genetics

Istituto Neurologico Mediterraneo Neuromed

Azienda Ospedaliera Universitaria Policlinico di Modena (PHD)

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

Affiliation History

Istituto Neurologico Mediterraneo Neuromed Jan 19o 2016

Italy

Scientific Consultant

Education History

Azienda Ospedaliera Universitaria Policlinico di Modena

Italy

PHD :: Istologia, Embriologia e Genetica

Publications

Nicole Piera Palomba, Giorgio Fortunato, Giuseppe Pepe, Nicola Modugno, Sara Pietracupa, Immacolata Damiano, Giada Mascio, Federica Carrillo, Luca Giovanni Di Giovannantonio, Laura Ianiro, Katiuscia Martinello, Viola Volpato, Vincenzo Desiato, Riccardo Acri, Marianna Storto, Ferdinando Nicoletti, Caleb Webber, Antonio Simeone, Sergio Fucile, Vittorio Maglione, Teresa Esposito
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients. Molecular neurobiology 60 (4) (2023)
Nicole Piera Palomba, Giorgio Fortunato, Giuseppe Pepe, Nicola Modugno, Sara Pietracupa, Immacolata Damiano, Giada Mascio, Federica Carrillo, Luca Giovanni Di Giovannantonio, Laura Ianiro, Katiuscia Martinello, Viola Volpato, Vincenzo Desiato, Riccardo Acri, Marianna Storto, Ferdinando Nicoletti, Caleb Webber, Antonio Simeone, Sergio Fucile, Vittorio Maglione, Teresa Esposito
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients. Molecular neurobiology 60 (4) (2023)
Nicole Piera Palomba, Giorgio Fortunato, Giuseppe Pepe, Nicola Modugno, Sara Pietracupa, Immacolata Damiano, Giada Mascio, Federica Carrillo, Luca Giovanni Di Giovannantonio, Laura Ianiro, Katiuscia Martinello, Viola Volpato, Vincenzo Desiato, Riccardo Acri, Marianna Storto, Ferdinando Nicoletti, Caleb Webber, Antonio Simeone, Sergio Fucile, Vittorio Maglione, Teresa Esposito
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients. Molecular neurobiology 60 (4) (2023)
Nicole Piera Palomba, Giorgio Fortunato, Giuseppe Pepe, Nicola Modugno, Sara Pietracupa, Immacolata Damiano, Giada Mascio, Federica Carrillo, Luca Giovanni Di Giovannantonio, Laura Ianiro, Katiuscia Martinello, Viola Volpato, Vincenzo Desiato, Riccardo Acri, Marianna Storto, Ferdinando Nicoletti, Caleb Webber, Antonio Simeone, Sergio Fucile, Vittorio Maglione, Teresa Esposito
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients. Molecular neurobiology 60 (4) (2023)
Nicole Piera Palomba, Giorgio Fortunato, Giuseppe Pepe, Nicola Modugno, Sara Pietracupa, Immacolata Damiano, Giada Mascio, Federica Carrillo, Luca Giovanni Di Giovannantonio, Laura Ianiro, Katiuscia Martinello, Viola Volpato, Vincenzo Desiato, Riccardo Acri, Marianna Storto, Ferdinando Nicoletti, Caleb Webber, Antonio Simeone, Sergio Fucile, Vittorio Maglione, Teresa Esposito
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients. Molecular neurobiology 60 (4) (2023)
Nicole Piera Palomba, Giorgio Fortunato, Giuseppe Pepe, Nicola Modugno, Sara Pietracupa, Immacolata Damiano, Giada Mascio, Federica Carrillo, Luca Giovanni Di Giovannantonio, Laura Ianiro, Katiuscia Martinello, Viola Volpato, Vincenzo Desiato, Riccardo Acri, Marianna Storto, Ferdinando Nicoletti, Caleb Webber, Antonio Simeone, Sergio Fucile, Vittorio Maglione, Teresa Esposito
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients. Molecular neurobiology (2023)
Rosita Stanzione, Maria Cotugno, Maurizio Forte, Franca Bianchi, Simona Marchitti, Nicole Piera Palomba, Teresa Esposito, Bastianina Zanda, Alessandra Sanna, Speranza Rubattu
Role of Uncoupling Protein 2 Gene Polymorphisms on the Risk of Ischemic Stroke in a Sardinian Population. Life (Basel, Switzerland) 12 (5) (2022)
Alessandro Gialluisi, Mafalda Giovanna Reccia, Nicola Modugno, Teresa Nutile, Alessia Lombardi, Luca Giovanni Di Giovannantonio, Sara Pietracupa, Daniela Ruggiero, Simona Scala, Stefano Gambardella, null null, Licia Iacoviello, Fernando Gianfrancesco, Dario Acampora, Maurizio D'Esposito, Antonio Simeone, Marina Ciullo, Teresa Esposito
Identification of sixteen novel candidate genes for late onset Parkinson's disease. Molecular neurodegeneration 16 (1) (2021)
Filomena Napolitano, Chiara Terracciano, Giorgia Bruno, Paolo De Blasiis, Luca Lombardi, Alessandro Gialluisi, Fernando Gianfrancesco, Donatella De Giovanni, Albina Tummolo, Giuseppe Di Iorio, Giuseppe Limongelli, Teresa Esposito, Mariarosa Anna Beatrice Melone, Simone Sampaolo
Novel autophagic vacuolar myopathies: Phenotype and genotype features. Neuropathology and applied neurobiology 47 (5) (2021)
Filomena Napolitano, Giorgia Bruno, Chiara Terracciano, Giuseppina Franzese, Nicole Piera Palomba, Federica Scotto di Carlo, Elisabetta Signoriello, Paolo De Blasiis, Stefano Navarro, Alessandro Gialluisi, Mariarosa Anna Beatrice Melone, Silvio Peluso, Teresa Esposito
Rare Variants in Autophagy and Non-Autophagy Genes in Late-Onset Pompe Disease: Suggestions of Their Disease-Modifying Role in Two Italian Families. International journal of molecular sciences 22 (7) (2021)
Filomena Napolitano, Valentina Di Iorio, Giuseppe Di Iorio, Mariarosa Anna Beatrice Melone, Fernando Gianfrancesco, Francesca Simonelli, Teresa Esposito, Francesco Testa, Simone Sampaolo
Early posterior vitreous detachment is associated with LAMA5 dominant mutation. Ophthalmic genetics 40 (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)
Simone Sampaolo, Filomena Napolitano, Alfonsina Tirozzi, Mafalda Giovanna Reccia, Luca Lombardi, Olimpia Farina, Adriano Barra, Ferdinando Cirillo, Mariarosa Anna Beatrice Melone, Fernando Gianfrancesco, Giuseppe Di Iorio, Teresa Esposito
Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix. Journal of medical genetics 54 (10) (2017)

Teresa Esposito.css-eqlu8i{font-size:small;padding-left:4px;} (T Esposito)

Publication Activity (10 Years)

Top Topics

Top Venues

Teresa Esposito (T Esposito)