Clonal myelopoiesis in the UK Biobank cohort: ASXL1 mutations are strongly associated with smoking von Dawoud, Ahmed A. Z., Tapper, William J., Cross, Nicholas C. P.

Volltext

The number of prognostically detrimental mutations and prognosis in primary myelofibrosis: an international study of 797 patients von Guglielmelli, P, Lasho, T L, Rotunno, G, Score, J, Mannarelli, C, Pancrazzi, A, Biamonte, F, Pardanani, A, Zoi, K, Reiter, A, Duncombe, A, Fanelli, T, Pietra, D, Rumi, E, Finke, C, Gangat, N, Ketterling, R P, Knudson, R A, Hanson, C A, Bosi, A, Pereira, A, Manfredini, R, Cervantes, F, Barosi, G, Cazzola, M, Cross, N C P, Vannucchi, A M, Tefferi, A

Volltext

Experimental evidence for the co-evolution of hominin tool-making teaching and language von Morgan, T. J. H., Uomini, N. T., Rendell, L. E., Chouinard-Thuly, L., Street, S. E., Lewis, H. M., Cross, C. P., Evans, C., Kearney, R., de la Torre, I., Whiten, A., Laland, K. N.

Volltext

KIT mutation analysis in mast cell neoplasms: recommendations of the European Competence Network on Mastocytosis von Arock, M, Sotlar, K, Akin, C, Broesby-Olsen, S, Hoermann, G, Escribano, L, Kristensen, T K, Kluin-Nelemans, H C, Hermine, O, Dubreuil, P, Sperr, W R, Hartmann, K, Gotlib, J, Cross, N C P, Haferlach, T, Garcia-Montero, A, Orfao, A, Schwaab, J, Triggiani, M, Horny, H-P, Metcalfe, D D, Reiter, A, Valent, P

Volltext

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders von Ernst, Thomas, Chase, Andrew J, Score, Joannah, Hidalgo-Curtis, Claire E, Bryant, Catherine, Jones, Amy V, Waghorn, Katherine, Zoi, Katerina, Ross, Fiona M, Reiter, Andreas, Hochhaus, Andreas, Drexler, Hans G, Duncombe, Andrew, Cervantes, Francisco, Oscier, David, Boultwood, Jacqueline, Grand, Francis H, Cross, Nicholas C P

Volltext

HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions von Bruford, Elspeth A., Antonescu, Cristina R., Carroll, Andrew J., Chinnaiyan, Arul, Cree, Ian A., Cross, Nicholas C. P., Dalgleish, Raymond, Gale, Robert Peter, Harrison, Christine J., Hastings, Rosalind J., Huret, Jean-Loup, Johansson, Bertil, Le Beau, Michelle, Mecucci, Cristina, Mertens, Fredrik, Verhaak, Roel, Mitelman, Felix

Volltext

Prognostic Score Including Gene Mutations in Chronic Myelomonocytic Leukemia von ITZYKSON, Raphaël, KOSMIDER, Olivier, VEY, Norbert, BRAUN, Thorsten, HAFERLACH, Torsten, DREYFUS, François, CROSS, Nicholas C. P, PREUDHOMME, Claude, BERNARD, Olivier A, FONTENAY, Michaela, VAINCHENKER, William, SCHNITTGER, Susanne, RENNEVILLE, Aline, BIRNBAUM, Daniel, DROIN, Nathalie, SOLARY, Eric, GELSI-BOYER, Véronique, MEGGENDORFER, Manja, MORABITO, Margot, BERTHON, Céline, ADES, Lionel, FENAUX, Pierre, BEYNE-RAUZY, Odile

Volltext

Desirable performance characteristics for BCR-ABL measurement on an international reporting scale to allow consistent interpretation of individual patient response and comparison o... von Branford, Susan, Fletcher, Linda, Cross, Nicholas C.P., Müller, Martin C., Hochhaus, Andreas, Kim, Dong-Wook, Radich, Jerald P., Saglio, Giuseppe, Pane, Fabrizio, Kamel-Reid, Suzanne, Wang, Y. Lynn, Press, Richard D., Lynch, Kevin, Rudzki, Zbigniew, Goldman, John M., Hughes, Timothy

Volltext

EZH2 mutational status predicts poor survival in myelofibrosis von Guglielmelli, Paola, Biamonte, Flavia, Score, Joannah, Hidalgo-Curtis, Claire, Cervantes, Francisco, Maffioli, Margherita, Fanelli, Tiziana, Ernst, Thomas, Winkelman, Nils, Jones, Amy V., Zoi, Katerina, Reiter, Andreas, Duncombe, Andrew, Villani, Laura, Bosi, Alberto, Barosi, Giovanni, Cross, Nicholas C.P., Vannucchi, Alessandro M.

Volltext

Harmonization of molecular monitoring of CML therapy in Europe von Müller, M C, Cross, N C P, Erben, P, Schenk, T, Hanfstein, B, Ernst, T, Hehlmann, R, Branford, S, Saglio, G, Hochhaus, A

Volltext

JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms von Jones, Amy V, Chase, Andrew, Silver, Richard T, Oscier, David, Zoi, Katerina, Wang, Y Lynn, Cario, Holger, Pahl, Heike L, Collins, Andrew, Reiter, Andreas, Grand, Francis, Cross, Nicholas C P

Volltext

Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms von Score, Joannah, Hidalgo-Curtis, Claire, Jones, Amy V., Winkelmann, Nils, Skinner, Alison, Ward, Daniel, Zoi, Katerina, Ernst, Thomas, Stegelmann, Frank, Döhner, Konstanze, Chase, Andrew, Cross, Nicholas C.P.

Volltext

Molecular pathogenesis of atypical CML, CMML and MDS/MPN-unclassifiable von Zoi, Katerina, Cross, Nicholas C. P.

Volltext

Social living mitigates the costs of a chronic illness in a cooperative carnivore von Almberg, E. S, Cross, P. C, Dobson, A. P, Smith, D. W, Metz, M. C, Stahler, D. R, Hudson, P. J, Festa‐Bianchet, Marco

Volltext

Mutations and prognosis in primary myelofibrosis von Vannucchi, A M, Lasho, T L, Guglielmelli, P, Biamonte, F, Pardanani, A, Pereira, A, Finke, C, Score, J, Gangat, N, Mannarelli, C, Ketterling, R P, Rotunno, G, Knudson, R A, Susini, M C, Laborde, R R, Spolverini, A, Pancrazzi, A, Pieri, L, Manfredini, R, Tagliafico, E, Zini, R, Jones, A, Zoi, K, Reiter, A, Duncombe, A, Pietra, D, Rumi, E, Cervantes, F, Barosi, G, Cazzola, M, Cross, N C P, Tefferi, A

Volltext

Is cancer latency an outdated concept? Lessons from chronic myeloid leukemia von Abecasis, Manuel, Cross, Nicholas C. P., Brito, Manuel, Ferreira, Isabelina, Sakamoto, Kathleen M., Hijiya, Nobuko, Score, Joannah, Gale, Robert Peter

Volltext

Analysis of chronic myeloid leukaemia during deep molecular response by genomic PCR: a traffic light stratification model with impact on treatment-free remission von Machova Polakova, Katerina, Zizkova, Hana, Zuna, Jan, Motlova, Eliska, Hovorkova, Lenka, Gottschalk, Andrea, Glauche, Ingmar, Koblihova, Jitka, Pecherkova, Pavla, Klamova, Hana, Stastna Markova, Marketa, Srbova, Dana, Benesova, Adela, Polivkova, Vaclava, Jurcek, Tomas, Zackova, Daniela, Mayer, Jiri, Ernst, Thomas, Mahon, Francois X., Saussele, Susanne, Roeder, Ingo, Cross, Nicholas C. P., Hochhaus, Andreas

Volltext

Clinical and biological implications of driver mutations in myelodysplastic syndromes von Papaemmanuil, Elli, Gerstung, Moritz, Malcovati, Luca, Tauro, Sudhir, Gundem, Gunes, Van Loo, Peter, Yoon, Chris J., Ellis, Peter, Wedge, David C., Pellagatti, Andrea, Shlien, Adam, Groves, Michael John, Forbes, Simon A., Raine, Keiran, Hinton, Jon, Mudie, Laura J., McLaren, Stuart, Hardy, Claire, Latimer, Calli, Della Porta, Matteo G., O'Meara, Sarah, Ambaglio, Ilaria, Galli, Anna, Butler, Adam P., Walldin, Gunilla, Teague, Jon W., Quek, Lynn, Sternberg, Alex, Gambacorti-Passerini, Carlo, Cross, Nicholas C.P., Green, Anthony R., Boultwood, Jacqueline, Vyas, Paresh, Hellstrom-Lindberg, Eva, Bowen, David, Cazzola, Mario, Stratton, Michael R., Campbell, Peter J.

Volltext

The ABNL-MARRO 001 study: a phase 1-2 study of randomly allocated active myeloid target compound combinations in MDS/MPN overlap syndromes von Moyo, Tamara K, Mendler, Jason H, Itzykson, Raphael, Kishtagari, Ashwin, Solary, Eric, Seegmiller, Adam C, Gerds, Aaron T, Ayers, Gregory D, Dezern, Amy E, Nazha, Aziz, Valent, Peter, van de Loosdrecht, Arjan A, Onida, Francesco, Pleyer, Lisa, Cirici, Blanca Xicoy, Tibes, Raoul, Geissler, Klaus, Komrokji, Rami S, Zhang, Jing, Germing, Ulrich, Steensma, David P, Wiseman, Daniel H, Pfeilstöecker, Michael, Elena, Chiara, Cross, Nicholas C P, Kiladjian, Jean-Jacques, Luebbert, Michael, Mesa, Ruben A, Montalban-Bravo, Guillermo, Sanz, Guillermo F, Platzbecker, Uwe, Patnaik, Mrinal M, Padron, Eric, Santini, Valeria, Fenaux, Pierre, Savona, Michael R

Volltext

Molecular diagnosis of the myeloproliferative neoplasms: UK guidelines for the detection of JAK2 V617F and other relevant mutations von Bench, Anthony J., White, Helen E., Foroni, Letizia, Godfrey, Anna L., Gerrard, Gareth, Akiki, Susanna, Awan, Abida, Carter, Ian, Goday‐Fernandez, Andrea, Langabeer, Stephen E., Clench, Tim, Clark, Jordan, Evans, Paul A., Grimwade, David, Schuh, Anna, McMullin, Mary F., Green, Anthony R., Harrison, Claire N., Cross, Nicholas C. P.

Volltext