The time has come for next-generation sequencing in routine diagnostic workup in hematology von Haferlach, Torsten

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The Molecular Pathology of Myelodysplastic Syndrome von Haferlach, Torsten

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Advancing Leukemia Diagnostics: Role of Next Generation Sequencing (NGS) in Acute Myeloid Leukemia von Haferlach, Torsten

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Highly accurate differentiation of bone marrow cell morphologies using deep neural networks on a large image data set von Matek, Christian, Krappe, Sebastian, Münzenmayer, Christian, Haferlach, Torsten, Marr, Carsten

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Molecular Genetics of Adult Acute Myeloid Leukemia: Prognostic and Therapeutic Implications von Marcucci, Guido, Haferlach, Torsten, Döhner, Hartmut

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How artificial intelligence might disrupt diagnostics in hematology in the near future von Walter, Wencke, Haferlach, Claudia, Nadarajah, Niroshan, Schmidts, Ines, Kühn, Constanze, Kern, Wolfgang, Haferlach, Torsten

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The leukemic oncogene EVI1 hijacks a MYC super-enhancer by CTCF-facilitated loops von Ottema, Sophie, Mulet-Lazaro, Roger, Erpelinck-Verschueren, Claudia, van Herk, Stanley, Havermans, Marije, Arricibita Varea, Andrea, Vermeulen, Michael, Beverloo, H. Berna, Gröschel, Stefan, Haferlach, Torsten, Haferlach, Claudia, J. Wouters, Bas, Bindels, Eric, Smeenk, Leonie, Delwel, Ruud

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Molecular landscape and clonal architecture of adult myelodysplastic/myeloproliferative neoplasms von Palomo, Laura, Meggendorfer, Manja, Hutter, Stephan, Twardziok, Sven, Ademà, Vera, Fuhrmann, Irene, Fuster-Tormo, Francisco, Xicoy, Blanca, Zamora, Lurdes, Acha, Pamela, Kerr, Cassandra M., Kern, Wolfgang, Maciejewski, Jaroslaw P., Solé, Francesc, Haferlach, Claudia, Haferlach, Torsten

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TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups von Haase, Detlef, Stevenson, Kristen E., Neuberg, Donna, Maciejewski, Jaroslaw P., Nazha, Aziz, Sekeres, Mikkael A., Ebert, Benjamin L., Garcia-Manero, Guillermo, Haferlach, Claudia, Haferlach, Torsten, Kern, Wolfgang, Ogawa, Seishi, Nagata, Yasunobu, Yoshida, Kenichi, Graubert, Timothy A., Walter, Matthew J., List, Alan F., Komrokji, Rami S., Padron, Eric, Sallman, David, Papaemmanuil, Elli, Campbell, Peter J., Savona, Michael R., Seegmiller, Adam, Adès, Lionel, Fenaux, Pierre, Shih, Lee-Yung, Bowen, David, Groves, Michael J., Tauro, Sudhir, Fontenay, Michaela, Kosmider, Olivier, Bar-Natan, Michal, Steensma, David, Stone, Richard, Heuser, Michael, Thol, Felicitas, Cazzola, Mario, Malcovati, Luca, Karsan, Aly, Ganster, Christina, Hellström-Lindberg, Eva, Boultwood, Jacqueline, Pellagatti, Andrea, Santini, Valeria, Quek, Lynn, Vyas, Paresh, Tüchler, Heinz, Greenberg, Peter L., Bejar, Rafael

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Molecular analysis of myelodysplastic syndrome with isolated deletion of the long arm of chromosome 5 reveals a specific spectrum of molecular mutations with prognostic impact: a s... von Meggendorfer, Manja, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten

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Molecular genetic characterization of myeloid/lymphoid neoplasms associated with eosinophilia and rearrangement of PDGFRA, PDGFRB, FGFR1 or PCM1-JAK2 von Baer, Constance, Muehlbacher, Verena, Kern, Wolfgang, Haferlach, Claudia, Haferlach, Torsten

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Novel causative variants of VEXAS in UBA1 detected through whole genome transcriptome sequencing in a large cohort of hematological malignancies von Sakuma, Maki, Blombery, Piers, Meggendorfer, Manja, Haferlach, Claudia, Lindauer, Markus, Martens, Uwe M., Kern, Wolfgang, Haferlach, Torsten, Walter, Wencke

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Complex landscape of alternative splicing in myeloid neoplasms von Hershberger, Courtney E., Moyer, Devlin C., Adema, Vera, Kerr, Cassandra M., Walter, Wencke, Hutter, Stephan, Meggendorfer, Manja, Baer, Constance, Kern, Wolfgang, Nadarajah, Niroshan, Twardziok, Sven, Sekeres, Mikkael A., Haferlach, Claudia, Haferlach, Torsten, Maciejewski, Jaroslaw P., Padgett, Richard A.

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Prognostic relevance of FLT3-TKD mutations in AML: the combination matters—an analysis of 3082 patients von Bacher, Ulrike, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten, Schnittger, Susanne

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Dynamics of clonal evolution in myelodysplastic syndromes von Makishima, Hideki, Yoshizato, Tetsuichi, Yoshida, Kenichi, Sekeres, Mikkael A, Radivoyevitch, Tomas, Suzuki, Hiromichi, Przychodzen, Bartlomiej, Nagata, Yasunobu, Meggendorfer, Manja, Sanada, Masashi, Okuno, Yusuke, Hirsch, Cassandra, Kuzmanovic, Teodora, Sato, Yusuke, Sato-Otsubo, Aiko, LaFramboise, Thomas, Hosono, Naoko, Shiraishi, Yuichi, Chiba, Kenichi, Haferlach, Claudia, Kern, Wolfgang, Tanaka, Hiroko, Shiozawa, Yusuke, Gómez-Seguí, Inés, Husseinzadeh, Holleh D, Thota, Swapna, Guinta, Kathryn M, Dienes, Brittney, Nakamaki, Tsuyoshi, Miyawaki, Shuichi, Saunthararajah, Yogen, Chiba, Shigeru, Miyano, Satoru, Shih, Lee-Yung, Haferlach, Torsten, Ogawa, Seishi, Maciejewski, Jaroslaw P

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The mutational landscape of 18 investigated genes clearly separates four subtypes of myelodysplastic/myeloproliferative neoplasms von Meggendorfer, Manja, Jeromin, Sabine, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten

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Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation von Yoshizato, Tetsuichi, Nannya, Yasuhito, Atsuta, Yoshiko, Shiozawa, Yusuke, Iijima-Yamashita, Yuka, Yoshida, Kenichi, Shiraishi, Yuichi, Suzuki, Hiromichi, Nagata, Yasunobu, Sato, Yusuke, Kakiuchi, Nobuyuki, Matsuo, Keitaro, Onizuka, Makoto, Kataoka, Keisuke, Chiba, Kenichi, Tanaka, Hiroko, Ueno, Hiroo, Nakagawa, Masahiro M., Przychodzen, Bartlomiej, Haferlach, Claudia, Kern, Wolfgang, Aoki, Kosuke, Itonaga, Hidehiro, Kanda, Yoshinobu, Sekeres, Mikkael A., Maciejewski, Jaroslaw P., Haferlach, Torsten, Miyazaki, Yasushi, Horibe, Keizo, Sanada, Masashi, Miyano, Satoru, Makishima, Hideki, Ogawa, Seishi

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Minimal/measurable residual disease in AML: a consensus document from the European LeukemiaNet MRD Working Party von Schuurhuis, Gerrit J., Heuser, Michael, Freeman, Sylvie, Béné, Marie-Christine, Buccisano, Francesco, Cloos, Jacqueline, Grimwade, David, Haferlach, Torsten, Hills, Robert K., Hourigan, Christopher S., Jorgensen, Jeffrey L., Kern, Wolfgang, Lacombe, Francis, Maurillo, Luca, Preudhomme, Claude, van der Reijden, Bert A., Thiede, Christian, Venditti, Adriano, Vyas, Paresh, Wood, Brent L., Walter, Roland B., Döhner, Konstanze, Roboz, Gail J., Ossenkoppele, Gert J.

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Indeterminate and oncogenic potential: CHIP vs CHOP mutations in AML with NPM1 alteration von Cappelli, Luca Vincenzo, Meggendorfer, Manja, Baer, Constance, Nadarajah, Niroshan, Hutter, Stephan, Jeromin, Sabine, Dicker, Frank, Kern, Wolfgang, Haferlach, Torsten, Haferlach, Claudia, Höllein, Alexander

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Frequent pathway mutations of splicing machinery in myelodysplasia von Yoshida, Kenichi, Sanada, Masashi, Shiraishi, Yuichi, Nowak, Daniel, Nagata, Yasunobu, Yamamoto, Ryo, Sato, Yusuke, Sato-Otsubo, Aiko, Kon, Ayana, Nagasaki, Masao, Chalkidis, George, Suzuki, Yutaka, Shiosaka, Masashi, Kawahata, Ryoichiro, Yamaguchi, Tomoyuki, Otsu, Makoto, Obara, Naoshi, Sakata-Yanagimoto, Mamiko, Ishiyama, Ken, Mori, Hiraku, Nolte, Florian, Hofmann, Wolf-Karsten, Miyawaki, Shuichi, Sugano, Sumio, Haferlach, Claudia, Koeffler, H. Phillip, Shih, Lee-Yung, Haferlach, Torsten, Chiba, Shigeru, Nakauchi, Hiromitsu, Miyano, Satoru, Ogawa, Seishi

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