Mazza, Tommaso

Biological and clinical manifestations of juvenile Huntington’s disease: A retrospective analysis

Fusilli, C., Migliore, S., Mazza, T., Consoli, F., De Luca, A., Barbagallo, G., Ciammola, A., Gatto, E. M., Cesarini, M., Etcheverry, J. L., et al. (2018) · The Lancet Neurology

Genetic Neurodegenerative DiseasesDeep Brain Stimulation and Movement Disorders

Cited by 148

Dysregulation of EGFR Pathway in EphA2 Cell Subpopulation Significantly Associates with Poor Prognosis in Colorectal Cancer

De Robertis, M., Loiacono, L., Fusilli, C., Poeta, M. L., Mazza, T., Sanchez, M., Marchionni, L., Signori, E., Lamorte, G., Vescovi, A. L., et al. (2017) · Clinical Cancer Research

Colorectal Cancer Treatments and StudiesHER2/EGFR in Cancer Research

Cited by 78

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

Bianco, S. D., Parca, L., Petrizzelli, F., Biagini, T., Giovannetti, A., Liorni, N., Napoli, A., Carella, M., Procaccio, V., Lott, M., et al. (2023) · Nature Communications

Genomics and Rare DiseasesMitochondrial Function and Pathology

Cited by 44

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

Bianco, S. D., Parca, L., Petrizzelli, F., Biagini, T., Giovannetti, A., Liorni, N., Napoli, A., Carella, M., Procaccio, V., Lott, M. T., et al. (2023) · Nature Communications

Genomics and Rare DiseasesMitochondrial Function and Pathology

Cited by 44

Expanding the clinical and molecular Spectrum of PSMD12-related neurodevelopmental syndrome: an additional patient and review

Palumbo, P., Palumbo, O., Di Muro, E., Pia Leone, M., Castellana, S., Biagini, T., Mazza, T., Leotta, V., Carella, M., & Bukvic, N. (2019) · Archives of Clinical and Medical Case Reports

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 5