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Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41 Homan, Claire C.; Drazer, Michael W.; Yu, Kai; Lawrence, David M.; Feng, Jinghua; Arriola-Martinez, Luis; Pozsgai, Matthew J.; Mcneely, Kelsey E.; Ha, Thuong; Venugopal, Parvathy; Arts, Peer; King-Smith, Sarah L.; Cheah, Jesse; Armstrong, Mark; Wang, Paul; Bodor, Csaba; Cantor, Alan B.; Cazzola, Mario; Degelman, Erin; Dinardo, Courtney D.; Duployez, Nicolas; Favier, Remi; Froehling, Stefan; Rio-Machin, Ana; Klco, Jeffery M.; Kraemer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil, V; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P.; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Kim, Erika; NISC Comparative Sequencing Program, Amy P.; Hsu, Amy P.; Holland, Steven M.; Phillips, Kerry; Poplawski, Nicola K.; Babic, Milena; Wei, Andrew H.; Forsyth, Cecily; Fan, Helen Mar; Lewis, Ian D.; Cooney, Julian; Susman, Rachel; Fox, Lucy C.; Blombery, Piers; Singhal, Deepak; Hiwase, Devendra; Phipson, Belinda; Schreiber, Andreas W.; Hahn, Christopher N.; Scott, Hamish S.; Liu, Paul; Godley, Lucy A.; Brown, Anna L. Share Save
Implementation and adoption of a web tool to support precision diagnostic and treatment decisions for patient with myelodysplastic syndromes Bernard, Elsa; Ossa, Juan E. Arango; Tuechler, Heinz; Greenberg, Peter L.; Hasserjian, Robert P.; Nannya, Yasuhito; Devlin, Sean M.; Creignou, Maria; Pinel, Philippe; Monier, Lily; Medina-Martinez, Juan S.; Domenico, Dylan; Jadersten, Martin; Germing, Ulrich; Sanz, Guillermo; van de Loosdrecht, Arjan A.; Kosmider, Olivier; Follo, Matilde Y.; Thol, Felicitas; Zamora, Lurdes; Pinheiro, Ronald F.; Pellagatti, Andrea; Haase, Detlef; Fenaux, Pierre; Belickova, Monika; Savona, Michael R.; Klimek, Virginia M.; Santos, Fabio P.; Boultwood, Jacqueline; Kotsianidis, Ioannis; Santini, Valeria; Sole, Francesc; Platzbecker, Uwe; Heuser, Michael; Valent, Peter; Ohyashiki, Kazuma; Finelli, Carlo; Voso, Maria Teresa; Shih, Lee-Yung; Fontenay, Michaela; Jansen, Joop H.; Cervera, Jose; Gattermann, Norbert; Ebert, Benjamin L.; Bejar, Rafael; Malcovati, Luca; Cazzola, Mario; Ogawa, Seishi; Hellstrom-Lindberg, Eva; Papaemmanuil, Elli Share Save
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Response to The WHO classification of haematolymphoid tumours (Editorial) Swerdlow, Steven H.; Campo, Elias; Arber, Daniel A.; Cazzola, Mario; Cook, James R.; Doehner, Hartmut; Dreyling, Martin; Hasserjian, Robert P.; Jaffe, Elaine S.; Orazi, Attilio; Quintanilla-Martinez, Leticia; Scott, David W.; Tefferi, Ayalew; Winter, Jane N.; Zelenetz, Andrew D. Share Save
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Pseudouridine-modified tRNA fragments repress aberrant protein synthesis and predict leukaemic progression in myelodysplastic syndrome Guzzi, Nicola; Muthukumar, Sowndarya; Ciesla, Maciej; Todisco, Gabriele; Ngoc, Phuong Cao Thi; Madej, Magdalena; Munita, Roberto; Fazio, Serena; Ekstrom, Simon; Mortera-Blanco, Teresa; Jansson, Monika; Nannya, Yasuhito; Cazzola, Mario; Ogawa, Seishi; Malcovati, Luca; Hellstrom-Lindberg, Eva; Dimitriou, Marios; Bellodi, Cristian Share Save
Classification of myeloid neoplasms/acute leukemia: Global perspectives and the international consensus classification approach COMMENT Arber, Daniel A.; Hasserjian, Robert P.; Orazi, Attilio; Mathews, Vikram; Roberts, Andrew W.; Schiffer, Charles A.; Roug, Anne Stidsholt; Cazzola, Mario; Doehner, Hartmut; Tefferi, Ayalew Share Save
PD-L1 overexpression correlates with JAK2-V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms Milosevic Feenstra, Jelena D.; Jaeger, Roland; Schischlik, Fiorella; Ivanov, Daniel; Eisenwort, Gregor; Rumi, Elisa; Schuster, Michael; Gisslinger, Bettina; Machherndl-Spandl, Sigrid; Bettelheim, Peter; Krauth, Maria-Theresa; Keil, Felix; Bock, Christoph; Cazzola, Mario; Gisslinger, Heinz; Kralovics, Robert; Valent, Peter Share Save
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy Homan, Claire C.; King-Smith, Sarah L.; Lawrence, David M.; Arts, Peer; Feng, Jinghua; Andrews, James; Armstrong, Mark; Ha, Thuong; Dobbins, Julia; Drazer, Michael W.; Yu, Kai; Bodor, Csaba; Cantor, Alan; Cazzola, Mario; Degelman, Erin; DiNardo, Courtney D.; Duployez, Nicolas; Favier, Remi; Frohling, Stefan; Fitzgibbon, Jude; Klco, Jeffery M.; Kramer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil V.; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P.; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Liu, Paul; Godley, Lucy A.; Schreiber, Andreas W.; Hahn, Christopher N.; Scott, Hamish S.; Brown, Anna L. Share Save
Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (vol 26, pg 1549, 2020) Bernard, Elsa; Nannya, Yasuhito; Hasserjian, Robert P.; Devlin, Sean M.; Tuechler, Heinz; Medina-Martinez, Juan S.; Yoshizato, Tetsuichi; Shiozawa, Yusuke; Saiki, Ryunosuke; Malcovati, Luca; Levine, Max F.; Arango, Juan E.; Zhou, Yangyu; Sole, Francesc; Cargo, Catherine A.; Haase, Detlef; Creignou, Maria; Germing, Ulrich; Zhang, Yanming; Gundem, Gunes; Sarian, Araxe; van de Loosdrecht, Arjan A.; Jadersten, Martin; Tobiasson, Magnus; Kosmider, Olivier; Follo, Matilde Y.; Thol, Felicitas; Pinheiro, Ronald F.; Santini, Valeria; Kotsianidis, Ioannis; Boultwood, Jacqueline; Santos, Fabio P. S.; Schanz, Julie; Kasahara, Senji; Ishikawa, Takayuki; Tsurumi, Hisashi; Takaori-Kondo, Akifumi; Kiguchi, Toru; Polprasert, Chantana; Bennett, John M.; Klimek, Virginia M.; Savona, Michael R.; Belickova, Monika; Ganster, Christina; Palomo, Laura; Sanz, Guillermo; Ades, Lionel; Della Porta, Matteo Giovanni; Smith, Alexandra G.; Werner, Yesenia; Patel, Minal; Viale, Agnes; Vanness, Katelynd; Neuberg, Donna S.; Stevenson, Kristen E.; Menghrajani, Kamal; Bolton, Kelly L.; Fenaux, Pierre; Pellagatti, Andrea; Platzbecker, Uwe; Heuser, Michael; Valent, Peter; Chiba, Shigeru; Miyazaki, Yasushi; Finelli, Carlo; Voso, Maria Teresa; Shih, Lee-Yung; Fontenay, Michaela; Jansen, Joop H.; Cervera, Jose; Atsuta, Yoshiko; Gattermann, Norbert; Ebert, Benjamin L.; Bejar, Rafael; Greenberg, Peter L.; Cazzola, Mario; Hellstrom-Lindberg, Eva; Ogawa, Seishi; Papaemmanuil, Elli Share Save
Gene expression profile correlates with molecular and clinical features in patients with myelofibrosis Rontauroli, Sebastiano; Castellano, Sara; Guglielmelli, Paola; Zini, Roberta; Bianchi, Elisa; Genovese, Elena; Carretta, Chiara; Parenti, Sandra; Fantini, Sebastian; Mallia, Selene; Tavernari, Lara; Sartini, Stefano; Mirabile, Margherita; Mannarelli, Carmela; Gesullo, Francesca; Pacilli, Annalisa; Pietra, Daniela; Rumi, Elisa; Salmoiraghi, Silvia; Mora, Barbara; Villani, Laura; Grilli, Andrea; Rosti, Vittorio; Barosi, Giovanni; Passamonti, Francesco; Rambaldi, Alessandro; Malcovati, Luca; Cazzola, Mario; Bicciato, Silvio; Tagliafico, Enrico; Vannucchi, Alessandro M.; Manfredini, Rossella Share Save
Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (vol 26, pg 1549, 2020) Bernard, Elsa; Nannya, Yasuhito; Hasserjian, Robert P.; Devlin, Sean M.; Tuechler, Heinz; Medina-Martinez, Juan S.; Yoshizato, Tetsuichi; Shiozawa, Yusuke; Saiki, Ryunosuke; Malcovati, Luca; Levine, Max F.; Arango, Juan E.; Zhou, Yangyu; Sole, Francesc; Cargo, Catherine A.; Haase, Detlef; Creignou, Maria; Germing, Ulrich; Zhang, Yanming; Gundem, Gunes; Sarian, Araxe; van de Loosdrecht, Arjan A.; Jadersten, Martin; Tobiasson, Magnus; Kosmider, Olivier; Follo, Matilde Y.; Thol, Felicitas; Pinheiro, Ronald F.; Santini, Valeria; Kotsianidis, Ioannis; Boultwood, Jacqueline; Santos, Fabio P. S.; Schanz, Julie; Kasahara, Senji; Ishikawa, Takayuki; Tsurumi, Hisashi; Takaori-Kondo, Akifumi; Kiguchi, Toru; Polprasert, Chantana; Bennett, John M.; Klimek, Virginia M.; Savona, Michael R.; Belickova, Monika; Ganster, Christina; Palomo, Laura; Sanz, Guillermo; Ades, Lionel; Della Porta, Matteo Giovanni; Smith, Alexandra G.; Werner, Yesenia; Patel, Minal; Viale, Agnes; Vanness, Katelynd; Neuberg, Donna S.; Stevenson, Kristen E.; Menghrajani, Kamal; Bolton, Kelly L.; Fenaux, Pierre; Pellagatti, Andrea; Platzbecker, Uwe; Heuser, Michael; Valent, Peter; Chiba, Shigeru; Miyazaki, Yasushi; Finelli, Carlo; Voso, Maria Teresa; Shih, Lee-Yung; Fontenay, Michaela; Jansen, Joop H.; Cervera, Jose; Atsuta, Yoshiko; Gattermann, Norbert; Ebert, Benjamin L.; Bejar, Rafael; Greenberg, Peter L.; Cazzola, Mario; Hellstrom-Lindberg, Eva; Ogawa, Seishi; Papaemmanuil, Elli Share Save
Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2P95-mutated neoplasms Todisco, Gabriele; Creignou, Maria; Gall, Anna; Guglielmelli, Paola; Rumi, Elisa; Roncador, Marco; Rizzo, Ettore; Nannya, Yasuhito; Pietra, Daniela; Elena, Chiara; Bono, Elisa; Molteni, Elisabetta; Rosti, Vittorio; Catrical, Silvia; Sarchi, Martina; Dimitriou, Marios; Ungerstedt, Johanna; Vannucchi, Alessandro Maria; Hellstrom-Lindberg, Eva; Ogawa, Seishi; Cazzola, Mario; Malcovati, Luca Share Save
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Implications ofTP53allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes Bernard, Elsa; Nannya, Yasuhito; Hasserjian, Robert P.; Devlin, Sean M.; Tuechler, Heinz; Medina-Martinez, Juan S.; Yoshizato, Tetsuichi; Shiozawa, Yusuke; Saiki, Ryunosuke; Malcovati, Luca; Levine, Max F.; Arango, Juan E.; Zhou, Yangyu; Sole, Francesc; Cargo, Catherine A.; Haase, Detlef; Creignou, Maria; Germing, Ulrich; Zhang, Yanming; Gundem, Gunes; Sarian, Araxe; van de Loosdrecht, Arjan A.; Jadersten, Martin; Tobiasson, Magnus; Kosmider, Olivier; Follo, Matilde Y.; Thol, Felicitas; Pinheiro, Ronald F.; Santini, Valeria; Kotsianidis, Ioannis; Boultwood, Jacqueline; Santos, Fabio P. S.; Schanz, Julie; Kasahara, Senji; Ishikawa, Takayuki; Tsurumi, Hisashi; Takaori-Kondo, Akifumi; Kiguchi, Toru; Polprasert, Chantana; Bennett, John M.; Klimek, Virginia M.; Savona, Michael R.; Belickova, Monika; Ganster, Christina; Palomo, Laura; Sanz, Guillermo; Ades, Lionel; Della Porta, Matteo Giovanni; Smith, Alexandra G.; Werner, Yesenia; Patel, Minal; Viale, Agnes; Vanness, Katelynd; Neuberg, Donna S.; Stevenson, Kristen E.; Menghrajani, Kamal; Bolton, Kelly L.; Fenaux, Pierre; Pellagatti, Andrea; Platzbecker, Uwe; Heuser, Michael; Valent, Peter; Chiba, Shigeru; Miyazaki, Yasushi; Finelli, Carlo; Voso, Maria Teresa; Shih, Lee-Yung; Fontenay, Michaela; Jansen, Joop H.; Cervera, Jose; Atsuta, Yoshiko; Gattermann, Norbert; Ebert, Benjamin L.; Bejar, Rafael; Greenberg, Peter L.; Cazzola, Mario; Hellstrom-Lindberg, Eva; Ogawa, Seishi; Papaemmanuil, Elli Share Save
Impaired virus-specific T cell responses in patients with myeloproliferative neoplasms treated with ruxolitinib Rumi, Elisa; Sant'Antonio, Emanuela; Cavalloni, Chiara; Comolli, Giuditta; Ferretti, Virginia Valeria; Cassaniti, Irene; Pietra, Daniela; Trotti, Chiara; Ciboddo, Michele; Furione, Milena; Vanni, Daniele; Casetti, Ilaria Carola; Favaron, Cristina; Baldanti, Fausto; Arcaini, Luca; Cazzola, Mario Share Save
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