Massimi, Luca
Università Cattolica del Sacro Cuore · Agostino Gemelli University Polyclinic
9 papers on CoChatORCID 0000-0003-3088-0822
Most cited papers
- Verified
Intertumoral Heterogeneity within Medulloblastoma Subgroups
Cavalli, F. M. G., Remke, M., Rampasek, L., Peacock, J., Shih, D. J. H., Luu, B., Garzia, L., Torchia, J., Nor, C., Morrissy, A. S., et al. (2017) · Cancer Cell
Glioma Diagnosis and TreatmentCancer Genomics and Diagnostics
Cited by 1,219
- Verified
Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations
Rausch, T., Jones, D. T. W., Zapatka, M., Stütz, A. M., Zichner, T., Weischenfeldt, J., Jäger, N., Remke, M., Shih, D., Northcott, P. A., et al. (2012) · Cell
Cancer Genomics and DiagnosticsGenomic variations and chromosomal abnormalities
Cited by 865
- Verified
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Mack, S. C., Witt, H., Piro, R. M., Gu, L., Zuyderduyn, S., Stütz, A. M., Wang, X., Gallo, M., Garzia, L., Zayne, K., et al. (2014) · Nature
Glioma Diagnosis and TreatmentEpigenetics and DNA Methylation
Cited by 607
- Verified
Intracranial pressure monitoring in children with single suture and complex craniosynostosis: a review
Tamburrini, G., Caldarelli, M., Massimi, L., Santini, P., & Di Rocco, C. (2005) · Child's Nervous System
Craniofacial Disorders and TreatmentsTraumatic Brain Injury and Neurovascular Disturbances
Cited by 261
- Verified
TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma
Remke, M., Ramaswamy, V., Peacock, J., Shih, D. J. H., Koelsche, C., Northcott, P. A., Hill, N., Cavalli, F. M. G., Kool, M., Wang, X., et al. (2013) · Acta Neuropathologica
Glioma Diagnosis and TreatmentCancer Genomics and Diagnostics
Cited by 164
- Verified
Isolated sagittal craniosynostosis: definition, classification, and surgical indications
Massimi, L., Caldarelli, M., Tamburrini, G., Paternoster, G., & Di Rocco, C. (2012) · Child s Nervous System
Craniofacial Disorders and TreatmentsPectus Deformity Diagnosis and Treatment
Cited by 76
- Verified
BBS9 gene in nonsyndromic craniosynostosis: Role of the primary cilium in the aberrant ossification of the suture osteogenic niche
Barba, M., Di Pietro, L., Massimi, L., Geloso, M. C., Frassanito, P., Caldarelli, M., Michetti, F., Della Longa, S., Romitti, P. A., Di Rocco, C., et al. (2018) · Bone
Craniofacial Disorders and TreatmentsBone Metabolism and Diseases
Cited by 19
- Verified
A systematic quantitative morpho-volumetric analysis in infants with sagittal craniosynostosis and relationship with the severity of scaphocephalic deformity
Calandrelli, R., Pilato, F., Massimi, L., Panfili, M., & Colosimo, C. (2020) · La radiologia medica
Craniofacial Disorders and TreatmentsPectus Deformity Diagnosis and Treatment
Cited by 9
- Verified
Genetics versus environment in the pathophysiology of sagittal synostosis
De Gregorio, V., Tosi, D. D., Vita, A., Salvati, M., Massimi, L., Tamburrini, G., Tiberio, F., & Lattanzi, W. (2026) · Child's Nervous System
Craniofacial Disorders and TreatmentsPectus Deformity Diagnosis and Treatment
Cited by 2
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