GENTILINI, DAVIDE
GENTILINI, DAVIDE
Universita' degli Studi di MILANO
Clinical relevance of the thyroid differentiation score (TDS) in benign and malignant thyroid tumors
2025 M. Muzza, C. Colombo, G. Pogliaghi, E. Carbone, L. Ermellino, M. Succi, C. Moneta, G. Dionigi, D. Gentilini, G. Vannucchi, G. Gazzano, L. Persani, L. Fugazzola
KIF5Ap.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral Sclerosis
2025 A. Manini, R. Vasta, A. Brusati, F. Scheveger, S. Peverelli, A. Maranzano, A. Doretti, F. Gentile, E. Colombo, M. Brunetti, C. Moglia, A. Canosa, U. Manera, M. Grassano, D. Gentilini, S. Messina, F. Verde, C. Morelli, J.E. Landers, B.J. Traynor, A. Chiò, V. Silani, A. Calvo, A. Ratti, N. Ticozzi
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genes
2025 A. Manini, A. Brusati, M. Grassano, G. Scacciatella, S. Peverelli, J. Spagliardi, V. Pensato, A. Doretti, R. Vasta, U. Manera, A. Canosa, M. Brunetti, D. Gentilini, S. Messina, F. Verde, C. Moglia, C. Morelli, E. Dalla Bella, P.J. Keagle, J.E. Landers, C. Gellera, G. Lauria Pinter, A. Chio, A. Ratti, A. Calvo, V. Silani, N. Ticozzi
Bridging the Gap of ALS Missing Heritability: Are Neurogenes Being Overlooked?
2025 A. Manini, A. Brusati, J. Spagliardi, S. Leoni, V. Pensato, S. Peverelli, P.J. Keagle, S. Magri, G. Scacciatella, A. Maranzano, B. Poletti, D. Gentilini, A. Doretti, S. Messina, C. Morelli, F. Verde, C. Gellera, V. Silani, A. Ratti, J.E. Landers, N. Ticozzi
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism
2023 D. Gentilini, M. Muzza, T. de Filippis, M.C. Vigone, G. Weber, L. Calzari, A. Cassio, M. Di Frenna, M. Bartolucci, E.S. Grassi, E. Carbone, A. Olivieri, L. Persani
Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study
2023 A. Brusati, S. Peverelli, L. Calzari, C. Tiloca, V. Casiraghi, M.N. Sorce, S. Invernizzi, E. Carbone, R. Cavagnola, F. Verde, V. Silani, N. Ticozzi, A. Ratti, D. Gentilini
Role of epigenetic therapy in the modulation of tumor growth and migration in human castration-resistant prostate cancer cells with neuroendocrine differentiation
2022 A. Dicitore, M.G. Bacalini, D. Saronni, G. Gaudenzi, M.C. Cantone, G. Gelmini, E.S. Grassi, D. Gentilini, M.O. Borghi, A.M. Di Blasio, L. Persani, P. Garagnani, C. Franceschi, G. Vitale
Molecular Characterization of Cancer Associated Fibroblasts in Prostate Cancer
2022 G. Vitale, M. Caraglia, V. Jung, J. Kamradt, D. Gentilini, M.T. Di Martino, A. Dicitore, M. Abate, P. Tagliaferri, A. Itro, M. Ferro, R. Balsamo, M. De Sio, G. Facchini, L. Persani, K. Schmitt, M. Saar, M. Stöckle, G. Unteregger, S. Zappavigna
Oxidative Stress Correlates with More Aggressive Features in Thyroid Cancer
2022 M. Muzza, G. Pogliaghi, C. Colombo, E. Carbone, V. Cirello, S. Palazzo, F. Frattini, D. Gentilini, G. Gazzano, L. Persani, L. Fugazzola
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects
2022 A. Brusati, A. Ratti, V. Pensato, S. Peverelli, D. Gentilini, E. Dalla Bella, M.N. Sorce, M. Meneri, D. Gagliardi, S. Corti, C. Gellera, G. Lauria Pinter, N. Ticozzi, V. Silani
TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis
2022 A. Manini, A. Ratti, A. Brusati, A. Maranzano, I. Fogh, S. Peverelli, S. Messina, D. Gentilini, F. Verde, B. Poletti, C. Morelli, V. Silani, N. Ticozzi
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency
2021 I. Bestetti, C. Barbieri, A. Sironi, V. Specchia, S.A. Yatsenko, M.D. De Donno, C. Caslini, D. Gentilini, M. Crippa, L. Larizza, A. Marozzi, A. Rajkovic, D. Toniolo, M.P. Bozzetti, P. Finelli
Soluble EMMPRIN levels discriminate aortic ectasia in marfan syndrome patients
2019 E. Rurali, G.L. Perrucci, R. Gaetano, A. Pini, D. Moschetta, D. Gentilini, P. Nigro, G. Pompilio
Pathogenic variants in STXBP1 and in genes for GABAa receptor subunities cause atypical rett/rett-like phenotypes
2019 F. Cogliati, V. Giorgini, M. Masciadri, M.T. Bonati, M. Marchi, I. Cracco, D. Gentilini, A. Peron, M.N. Savini, L. Spaccini, B. Scelsa, S. Maitz, E. Veneselli, G. Prato, M. Pintaudi, I. Moroni, A. Vignoli, L. Larizza, S. Russo
Multifactorial analysis of the stochastic epigenetic variability in cord blood confirmed an impact of common behavioral and environmental factors but not of in vitro conception.
2018 D. Gentilini, E. Somigliana, L. Pagliardini, E. Rabellotti, P. Garagnani, L. Bernardinelli, E. Papaleo, M. Candiani, A. Di Blasio, P. Viganò
Synergistic activity of everolimus and 5-aza-2'-deoxycytidine in medullary thyroid carcinoma cell lines
2017 G. Vitale, A. Dicitore, D. Pepe, D. Gentilini, E.S. Grassi, M.O. Borghi, G. Gelmini, M.C. Cantone, G. Gaudenzi, G. Misso, A.M. Di Blasio, L.J. Hofland, M. Caraglia, L. Persani
Epigenome-wide association study in hepatocellular carcinoma : Identification of stochastic epigenetic mutations through an innovative statistical approach
2017 D. Gentilini, S. Scala, G. Gaudenzi, P. Garagnani, M. Capri, M. Cescon, G.L. Grazi, M.G. Bacalini, S. Pisoni, A. Dicitore, L. Circelli, S. Santagata, F. Izzo, A.M. Di Blasio, L. Persani, C. Franceschi, G. Vitale
Antiphospholipid Antibodies and Infertility : A Gene Expression Study in Decidual Stromal Cells
2016 C.B. Chighizola, F. Pregnolato, E. Raschi, C. Grossi, D. Gentilini, M.O. Borghi, P. Chen, P.L. Meroni
Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in females
2015 D. Gentilini, P. Garagnani, S. Pisoni, M.G. Bacalini, L. Calzari, D. Mari, G. Vitale, C. Franceschi, A.M. Di Blasio
Decreased epigenetic age of PBMCs from Italian semi-supercentenarians and their offspring
2015 S. Horvath, C. Pirazzini, M.G. Bacalini, D. Gentilini, A.M. Di Blasio, M. Delledonne, D. Mari, B. Arosio, D. Monti, G. Passarino, F. De Rango, P. D'Aquila, C. Giuliani, M. Elena, S. Collino, P. Descombes, P. Garagnani, C. Franceschi