FAZIO, GRAZIA
FAZIO, GRAZIA
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
Biallelic PI4KA Mutations Disrupt B-Cell Metabolism and Cause B-Cell Lymphopenia and Hypogammaglobulinemia
2025 Saettini, F; Guerra, F; Mauri, M; Salter, C; Adam, M; Adams, D; Baple, E; Barredo, E; Bhatia, S; Borkhardt, A; Brusco, A; Bugarin, C; Chinello, C; Crosby, A; D'Souza, P; Denti, V; Fazio, G; Giuliani, S; Kuehn, H; Amel, H; Elmi, A; Lo, B; Malighetti, F; Mandrile, G; Martín-Nalda, A; Mefford, H; Moratto, D; Emam Mousavi, F; Nelson, Z; Gutiérrez-Solana, L; Macnamara, E; Michaud, V; O'Leary, M; Pagani, L; Pavinato, L; Santamaria, P; Planas-Serra, L; Quadri, M; Raspall-Chaure, M; Rebellato, S; Rosenzweig, S; Roubertie, A; Holzinger, D; Deal, C; Vockley, C; Savino, A; L. Stoddard, J; Uhlig, H; Pujol, A; Magni, F; Paglia, G; Cazzaniga, G; Piazza, R; Barberis, M; Biondi, A
Case report: An intriguing case of Philadelphia chromosome–positive acute lymphoblastic leukemia recurrence
2024 Peccatori, N; Chiocca, E; Conter, V; Tondo, A; Marzorati, M; Casini, T; Veltroni, M; Biondi, A; Fazio, G
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies
2024 Di Fede, E; Lettieri, A; Taci, E; Castiglioni, S; Rebellato, S; Parodi, C; Colombo, E; Grazioli, P; Natacci, F; Marchisio, P; Pezzani, L; Fazio, G; Milani, D; Massa, V; Gervasini, C
Diverse mechanisms of leukemogenesis associated with PAX5 germline mutation
2024 Bettini, L; Fazio, G; Saitta, C; Piazza, R; Palamini, S; Buracchi, C; Rebellato, S; Santoro, N; Simone, C; Biondi, A; Cazzaniga, G
Modeling skeletal dysplasia in Hurler syndrome using patient-derived bone marrow osteoprogenitor cells
2024 Donsante, S; Pievani, A; Palmisano, B; Finamore, M; Fazio, G; Corsi, A; Biondi, A; Tomatsu, S; Piazza, R; Serafini, M; Riminucci, M
Antibody Deficiency in Patients with Biallelic KARS1 Mutations
2023 Saettini, F; Guerra, F; Fazio, G; Bugarin, C; Mcmillan, H; Ohtake, A; Ardissone, A; Itoh, M; Giglio, S; Cappuccio, G; Giardino, G; Romano, R; Quadri, M; Gasperini, S; Moratto, D; Chiarini, M; Akira, I; Fukuhara, Y; Hayakawa, I; Okazaki, Y; Mauri, M; Piazza, R; Cazzaniga, G; Biondi, A
Correction to: Antibody Deficiency in Patients with Biallelic KARS1 Mutations (Journal of Clinical Immunology, (2023), 43, 8, (2115-2125), 10.1007/s10875-023-01584-7)
2023 Saettini, F; Guerra, F; Fazio, G; Bugarin, C; Mcmillan, H; Ohtake, A; Ardissone, A; Itoh, M; Giglio, S; Cappuccio, G; Giardino, G; Romano, R; Quadri, M; Gasperini, S; Moratto, D; Chiarini, M; Ishiguro, A; Fukuhara, Y; Hayakawa, I; Okazaki, Y; Mauri, M; Piazza, R; Cazzaniga, G; Biondi, A
miR-126 identifies a quiescent and chemo-resistant human B-ALL cell subset that correlates with minimal residual disease
2023 Caserta, C; Nucera, S; Barcella, M; Fazio, G; Naldini, M; Pagani, R; Pavesi, F; Desantis, G; Zonari, E; D'Angio, M; Capasso, P; Lombardo, A; Merelli, I; Spinelli, O; Rambaldi, A; Ciceri, F; Silvestri, D; Valsecchi, M; Biondi, A; Cazzaniga, G; Gentner, B
The chemerin/CMKLR1 axis regulates intestinal graft-versus-host disease
2023 Dander, E; Vinci, P; Vetrano, S; Recordati, C; Piazza, R; Fazio, G; Bardelli, D; Bugatti, M; Sozio, F; Piontini, A; Bonanomi, S; Bertola, L; Tassistro, E; Valsecchi, M; Calza, S; Vermi, W; Biondi, A; Del Prete, A; Sozzani, S; D'Amico, G
The recombinome of IKZF1 deletions in B-cell precursor ALL
2023 Lopes, B; Meyer, C; Bouzada, H; Kulp, M; Maciel, A; Larghero, P; Barbosa, T; Poubel, C; Barbieri, C; Venn, N; Pozza, L; Barbaric, D; Palmi, C; Fazio, G; Saitta, C; Aguiar, T; Lins, M; Ikoma-Colturato, M; Schramm, M; Chapchap, E; Cazzaniga, G; Sutton, R; Marschalek, R; Emerenciano, M
Conjoined Genes as Common Events in Childhood Acute Lymphoblastic Leukemia
2022 Severgnini, M; D'Angiò, M; Bungaro, S; Cazzaniga, G; Cifola, I; Fazio, G
HDAC6 inhibition decreases leukemic stem cell expansion driven by Hedgehog hyperactivation by restoring primary ciliogenesis
2022 Pezzotta, A; Gentile, I; Genovese, D; Totaro, M; Battaglia, C; Leung, A; Fumagalli, M; Parma, M; Cazzaniga, G; Fazio, G; Alcalay, M; Marozzi, A; Pistocchi, A
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype
2022 Saettini, F; Fazio, G; Bonati, M; Moratto, D; Massa, V; Di Fede, E; Castiglioni, S; Marchetti, D; Chiarini, M; Sottini, A; Iascone, M; Cazzaniga, G; Imberti, L; Biondi, A; Gervasini, C; Badolato, R
PAX5 fusion genes are frequent in poor risk childhood acute lymphoblastic leukaemia and can be targeted with BIBF1120
2022 Fazio, G; Bresolin, S; Silvestri, D; Quadri, M; Saitta, C; Vendramini, E; Buldini, B; Palmi, C; Bardini, M; Grioni, A; Rigamonti, S; Galbiati, M; Mecca, S; Savino, A; Peloso, A; Tu, J; Bhatia, S; Borkhardt, A; Micalizzi, C; Lo Nigro, L; Locatelli, F; Conter, V; Rizzari, C; Valsecchi, M; Te Kronnie, G; Biondi, A; Cazzaniga, G
Potential role of STAG1 mutations in genetic predisposition to childhood hematological malignancies
2022 Saitta, C; Rebellato, S; Bettini, L; Giudici, G; Panini, N; Erba, E; Massa, V; Auer, F; Friedrich, U; Hauer, J; Biondi, A; Fazio, G; Cazzaniga, G
Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma
2022 Schedel, A; Friedrich, U; Morcos, M; Wagener, R; Mehtonen, J; Watrin, T; Saitta, C; Brozou, T; Michler, P; Walter, C; Forsti, A; Baksi, A; Menzel, M; Horak, P; Paramasivam, N; Fazio, G; Autry, R; Frohling, S; Suttorp, M; Gertzen, C; Gohlke, H; Bhatia, S; Wadt, K; Schmiegelow, K; Dugas, M; Richter, D; Glimm, H; Heinaniemi, M; Jessberger, R; Cazzaniga, G; Borkhardt, A; Hauer, J; Auer, F
A novel homozygous disruptive PRF1 variant (K285Sfs*4) causes very early-onset of familial hemophagocytic lymphohystiocytosis type 2
2021 Saettini, F; Castelli, I; Provenzi, M; Fazio, G; Quadri, M; Cazzaniga, G; Sala, S; Dell'Acqua, F; Sieni, E; Coniglio, M; Pezzoli, L; Iascone, M; Vendemini, F; Balduzzi, A; Biondi, A; Rizzari, C; Bonanomi, S
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency
2021 Saettini, F; Poli, C; Vengoechea, J; Bonanomi, S; Orellana, J; Fazio, G; Rodriguez III, F; Noguera, L; Booth, C; Jarur-Chamy, V; Shams, M; Iascone, M; Vukic, M; Gasperini, S; Quadri, M; Seijas, A; Rivers, E; Mauri, M; Badolato, R; Cazzaniga, G; Bugarin, C; Gaipa, G; Kroes, W; Moratto, D; van Oostaijen-Ten Dam, M; Baas, F; van der Maarel, S; Piazza, R; Coban-Akdemir, Z; Lupski, J; Yuan, B; Chinn, I; Daxinger, L; Biondi, A
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis
2021 Saettini, F; Fazio, G; Moratto, D; Galbiati, M; Zucchini, N; Ippolito, D; Dinelli, M; Imberti, L; Mauri, M; Melzi, M; Bonanomi, S; Gerussi, A; Pinelli, M; Barisani, C; Bugarin, C; Chiarini, M; Giacomelli, M; Piazza, R; Cazzaniga, G; Invernizzi, P; Giliani, S; Badolato, R; Biondi, A
Potential and pitfalls of whole transcriptome-based immunogenetic marker identification in acute lymphoblastic leukemia; a EuroMRD and EuroClonality-NGS Working Group study
2021 van der Velden, V; Bruggemann, M; Cazzaniga, G; Scheijen, B; Tops, B; Trka, J; Pal, K; Hanzelmann, S; Fazio, G; Songia, S; Langerak, A; Darzentas, N; van der Velden, V