GRIONI, ANDREA
GRIONI, ANDREA
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
Recurrent genetic fusions redefine MLL germ line acute lymphoblastic leukemia in infants
2021 Fazio, G; Bardini, M; De Lorenzo, P; Grioni, A; Quadri, M; Pedace, L; Corral Abascal, L; Palamini, S; Palmi, C; Buldini, B; Vinti, L; Parasole, R; Barisone, E; Zecca, M; Favre, C; Locatelli, F; Conter, V; Rizzari, C; Valsecchi, M; Biondi, A; Cazzaniga, G
Application of modern data science to genomics and clinical research
2020 Grioni, A
High EVI1 Expression due to NRIP1/EVI1 Fusion in Therapy-related Acute Myeloid Leukemia: Description of the First Pediatric Case
2020 D’Angiò, M; Fazio, G; Grioni, A; Palamini, S; Sala, S; Galbiati, M; Biondi, A; Balduzzi, A; Rizzari, C; Cazzaniga, G
First evidence of a paediatric patient with Cornelia de Lange syndrome with acute lymphoblastic leukaemia
2019 Fazio, G; Massa, V; Grioni, A; Bystry, V; Rigamonti, S; Saitta, C; Galbiati, M; Rizzari, C; Consarino, C; Biondi, A; Selicorni, A; Cazzaniga, G
A simple RNA target capture NGS strategy for fusion genes assessment in the diagnostics of pediatric B-cell acute lymphoblastic leukemia
2019 Grioni, A; Fazio, G; Rigamonti, S; Bystry, V; Daniele, G; Dostalova, Z; Quadri, M; Saitta, C; Silvestri, D; Songia, S; Storlazzi, C; Biondi, A; Darzentas, N; Cazzaniga, G
Standardized next-generation sequencing of immunoglobulin and T-cell receptor gene recombinations for MRD marker identification in acute lymphoblastic leukaemia; a EuroClonality-NGS validation study
2019 Bruggemann, M; Kotrova, M; Knecht, H; Bartram, J; Boudjogrha, M; Bystry, V; Fazio, G; Fronkova, E; Giraud, M; Grioni, A; Hancock, J; Herrmann, D; Jimenez, C; Krejci, A; Moppett, J; Reigl, T; Salson, M; Scheijen, B; Schwarz, M; Songia, S; Svaton, M; van Dongen, J; Villarese, P; Wakeman, S; Wright, G; Cazzaniga, G; Davi, F; Garcia-Sanz, R; Gonzalez, D; Groenen, P; Hummel, M; Macintyre, E; Stamatopoulos, K; Pott, C; Trka, J; Darzentas, N; Langerak, A
Quality control and quantification in IG/TR next-generation sequencing marker identification: protocols and bioinformatic functionalities by EuroClonality-NGS
2019 Knecht, H; Reigl, T; Kotrova, M; Appelt, F; Stewart, P; Bystry, V; Krejci, A; Grioni, A; Pal, K; Stranska, K; Plevova, K; Rijntjes, J; Songia, S; Svaton, M; Fronkova, E; Bartram, J; Scheijen, B; Herrmann, D; Garcia-Sanz, R; Hancock, J; Moppett, J; van Dongen, J; Cazzaniga, G; Davi, F; Groenen, P; Hummel, M; Macintyre, E; Stamatopoulos, K; Trka, J; Langerak, A; Gonzalez, D; Pott, C; Bruggemann, M; Darzentas, N
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency
2018 Saettini, F; Moratto, D; Grioni, A; Maitz, S; Iascone, M; Rizzari, C; Pavan, F; Spinelli, M; Bettini, L; Biondi, A; Badolato, R