Sfoglia per Autore
Lack of Viral Load Within Chronic Lymphoproliferative Disorder of Natural Killer Cells: What Is Outside the Leukemic Clone?
2021 Giussani, Edoardo; Binatti, Andrea; Calabretto, Giulia; Gasparini, Vanessa Rebecca; Teramo, Antonella; Vicenzetto, Cristina; Barilà, Gregorio; Facco, Monica; Coppe, Alessandro; Semenzato, Gianpietro; Bortoluzzi, Stefania; Zambello, Renato
A high definition picture of somatic mutations in chronic lymphoproliferative disorder of natural killer cells
2020 Gasparini, V. R.; Binatti, A.; Coppe, A.; Teramo, A.; Vicenzetto, C.; Calabretto, G.; Barila, G.; Barizza, A.; Giussani, E.; Facco, M.; Mustjoki, S.; Semenzato, G.; Zambello, R.; Bortoluzzi, S.
iWhale: a computational pipeline based on Docker and SCons for detection and annotation of somatic variants in cancer WES data
2020 Binatti, Andrea; Bresolin, Silvia; Bortoluzzi, Stefania; Coppe, Alessandro
A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell Acute Lymphoblastic Leukemia
2020 Marzollo, Antonio; Maestrini, Giacomo; La Starza, Roberta; Elia, Loredana; Malfona, Francesco; Pierini, Tiziana; TRETTI PARENZAN, Caterina; Coppe, Alessandro; Bortoluzzi, Stefania; Biffi, Alessandra; Mecucci, Cristina; Bresolin, Silvia; Maria Testi, Anna
A high definition picture of key genes and pathways mutated in pediatric follicular lymphoma
2019 Lovisa, Federica; Binatti, Andrea; Coppe, Alessandro; Primerano, Simona; Carraro, Elisa; Pillon, Marta; Pizzi, Marco; Guzzardo, Vincenza; Buffardi, Salvatore; Porta, Fulvio; Farruggia, Piero; De Santis, Raffaela; Bulian, Pietro; Basso, Giuseppe; Lazzari, Elena; D'Amore, Emanuele S G; Bortoluzzi, Stefania; Mussolin, Lara
Somatic mutations activating Wiskott-Aldrich syndrome protein concomitant with RAS pathway mutations in Juvenile myelomonocytic leukemia patients
2018 Coppe, A; Nogara, L; Pizzuto, M. S; Cani, A; Cesaro, S; Masetti, R; Locatelli, F; Te Kronnie, G; Basso, G; Bortoluzzi, S; Bresolin, S.
Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder
2018 Salvoro, C.; Bortoluzzi, S.; Coppe, A.; Valle, G.; Feltrin, E.; Mostacciuolo, M. L.; Vazza, G.
Somatic mutations in specific and connected sub-pathways are associated to short neuroblastoma patients' survival and indicate proteins targetable at onset of disease
2018 Esposito, MARIA ROSARIA; Binatti, Andrea; Pantile, Marcella; Coppe, Alessandro; Mazzocco, Katia; Longo, Luca; Capasso, Mario; Lasorsa, Vito Alessandro; Luksch, Roberto; Bortoluzzi, Stefania; Tonini, Gian Paolo
Genomic landscape characterization of large granular lymphocyte leukemia with a systems genetics approach
2017 Coppe, A; Andersson, E I; Binatti, A; Gasparini, V R; Bortoluzzi, S; Clemente, M; Herling, M; Maciejewski, J; Mustjoki, S; Bortoluzzi, S
Nuovi meccanismi molecolari e marcatori diagnostici nel linfoma follicolare pediatrico.
2017 Lovisa, F; Coppe, A; Pomari, E; Primerano, S; Carraro, E; Lazzari, E; Smith, A; Buffardi, S; La Porta, Filippo; Farruggia, P; de SANTIS, Riccardo; Basso, G; Bortoluzzi, S; D’Amore, Esg; Pillon, M; Mussolin, L
A guilt-by-association mutation network in LGL leukemia
2017 Andersson, Emma I.; Coppe, Alessandro; Bortoluzzi, Stefania
High incidence of activating STAT5B mutations in CD4-positive T-cell large granular lymphocyte leukemia
2016 Andersson, Emma; Tanahashi, Takahiro; Sekiguchi, Nodoka; Gasparini, VANESSA REBECCA; Bortoluzzi, Sabrina; Kawakami, Toru; Matsuda, Kazuyuki; Mitsui, Takeki; Eldfors, Samuli; Bortoluzzi, Stefania; Coppe, Alessandro; Binatti, Andrea; Lagström, Sonja; Ellonen, Pekka; Fukushima, Noriyasu; Nishina, Sayaka; Senoo, Noriko; Sakai, Hitoshi; Nakazawa, Hideyuki; Kwong, Yok Lam; Loughran, Thomas P; Maciejewski, Jaroslaw P; Mustjoki, Satu; Ishida, Fumihiro
A data-driven network model of primary myelofibrosis: transcriptional and post-transcriptional alterations in CD34+ cells
2016 Calura, Enrica; Pizzini, Silvia; Bisognin, Andrea; Coppe, Alessandro; Sales, Gabriele; Gaffo, Enrico; Fanelli, T; Mannarelli, C; Zini, R; Norfo, R; Pennucci, V; Manfredini, R; Romualdi, Chiara; Guglielmelli, P; Vannucchi, A. M; Bortoluzzi, Stefania
Subset-Specific Recurrence of Mutations and Identification of Functional Modules Provides New Clues about the Pathogenesis of Large Granular Lymphocyte Leukemia
2016 Coppe, Alessandro; Andersson, Ei; Binatti, Andrea; Gasparini, VANESSA REBECCA; Bortoluzzi, Stefania; Clemente, M; Herling, M; Maciejewski, J; Mustjoki, S; Bortoluzzi, Sabrina
Small RNA Sequencing Uncovers New miRNAs and moRNAs Differentially Expressed in Normal and Primary Myelofibrosis CD34+ Cells
2015 Guglielmelli, Paola; Bisognin, Andrea; Saccoman, Claudia; Mannarelli, Carmela; Coppe, Alessandro; Vannucchi, Alessandro M; Bortoluzzi, Stefania
Abnormal expression patterns of WT1-as, MEG3 and ANRIL long non-coding RNAs in CD34+ cells from patients with primary myelofibrosis and their clinical correlations.
2014 Pennucci, V; Zini, R; Norfo, R; Guglielmelli, P; Bianchi, E; Salati, S; Sacchi, G; Prudente, Z; Tenedini, E; Ruberti, S; Paoli, C; Fanelli, T; Mannarelli, C; Tagliafico, E; Ferrari, S; Vannucchi, Am; Manfredini, R; on behalf of Associazione Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie Mieloproliferative Investigators Collaborators Vannucchi, Am; Balliu, M; Bartalucci, N; Bogani, C; Bosi, A; Fanelli, T; Fjerza, R; Guglielmelli, P; Mannarelli, C; Martinelli, S; Pancrazzi, A; Paoli, C; Pieri, L; Bisognin, Andrea; Bortoluzzi, Stefania; Coppe, Alessandro; Saccoman, Claudia; Masciulli, A; Giovani, B; Azzan, C; Badalucco, S; Balduini, A; Bonetti, E; Campanelli, R; Catarsi, P; Isgrò, Ma; Lupo, Ml; Magrini, U; Massa, M; Poletto, V; Rosti, V; Villani, L; Cazzola, M; Ambaglio, I; Bernasconi, P; Casetti, Ic; Catricalà, S; Elena, C; Fugazza, E; Gallì, A; Malcovati, L; Milanesi, C; Pascutto, C; Pietra, D; Ripamonti, F; Rossi, M; Rumi, E; Dejana, E; Breviario, F; Corada, M; Erba, Bg; Rambaldi, A; Barbui, T; Ferrari, Ml; Finazzi, G; Finazzi, Mc; Gritti, G; Belotti, C; Boroni, C; Salmoiraghi, S; Amaru, A; Golay, J; Cilloni, D; Campia, V; Carturan, S; Guerrasio, A; Manfredini, R; Bianchi, E; Montanari, M; Salati, S; Tagliafico, E; Tenedini, E; Zini, R.
mRNA-Seq and microarray development for the Grooved carpet shell clam, Ruditapes decussatus: a functional approach to unravel host -parasite interaction
2013 Ricardo B., Leite; Milan, Massimo; Coppe, Alessandro; Bortoluzzi, Stefania; António dos, Anjos; Richard, Reinhardt; M., Leonor Cancela; Carlos, Saavedra; Patarnello, Tomaso; Bargelloni, Luca
Genome Evolution in the Cold: Antarctic Icefish Muscle Transcriptome Reveals Selective Duplications Increasing Mitochondrial Function
2013 Coppe, Alessandro; Agostini, Cecilia; Marino, ILARIA ANNA MARIA; Zane, Lorenzo; Bargelloni, Luca; Bortoluzzi, Stefania; Patarnello, Tomaso
Transcriptome sequencing and de novo annotation of the critically endangered Adriatic sturgeon
2013 Michele, Vidotto; Grapputo, Alessandro; Boscari, Elisa; Federica, Barbisan; Coppe, Alessandro; Gilberto, Grandi; Abhishek, Kumar; Congiu, Leonardo
MAGIA2: from miRNA and genes expression data integrative analysis to microRNA-transcription factor mixed regulatory circuits (2012 update).
2012 Bisognin, Andrea; Sales, Gabriele; Coppe, Alessandro; Bortoluzzi, Stefania; Romualdi, Chiara
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