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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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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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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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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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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Male predominance in AML is associated with specific preleukemic mutations von De-Morgan, Aviv, Meggendorfer, Manja, Haferlach, Claudia, Shlush, Liran

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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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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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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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Minimal residual disease levels assessed by NPM1 mutation–specific RQ-PCR provide important prognostic information in AML von Schnittger, Susanne, Kern, Wolfgang, Tschulik, Claudia, Weiss, Tamara, Dicker, Frank, Falini, Brunangelo, Haferlach, Claudia, Haferlach, Torsten

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Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia von Meggendorfer, Manja, Haferlach, Torsten, Alpermann, Tamara, Jeromin, Sabine, Haferlach, Claudia, Kern, Wolfgang, Schnittger, Susanne

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Detection of ABL1 kinase domain mutations in therapy-naïve BCR-ABL1 -positive acute lymphoblastic leukemia von Baer, Constance, Meggendorfer, Manja, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten

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Cytogenetic complexity in chronic lymphocytic leukemia: definitions, associations, and clinical impact von Baliakas, Panagiotis, Jeromin, Sabine, Iskas, Michalis, Puiggros, Anna, Plevova, Karla, Nguyen-Khac, Florence, Davis, Zadie, Rigolin, Gian Matteo, Visentin, Andrea, Xochelli, Aliki, Delgado, Julio, Baran-Marszak, Fanny, Stalika, Evangelia, Abrisqueta, Pau, Durechova, Kristina, Papaioannou, George, Eclache, Virginie, Dimou, Maria, Iliakis, Theodoros, Collado, Rosa, Doubek, Michael, Calasanz, M. Jose, Ruiz-Xiville, Neus, Moreno, Carolina, Jarosova, Marie, Leeksma, Alexander C., Panayiotidis, Panayiotis, Podgornik, Helena, Cymbalista, Florence, Anagnostopoulos, Achilles, Trentin, Livio, Stavroyianni, Niki, Davi, Fred, Ghia, Paolo, Kater, Arnon P., Cuneo, Antonio, Pospisilova, Sarka, Espinet, Blanca, Athanasiadou, Anastasia, Oscier, David, Haferlach, Claudia, Stamatopoulos, Kostas

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A novel hierarchical prognostic model of AML solely based on molecular mutations von Grossmann, Vera, Schnittger, Susanne, Kohlmann, Alexander, Eder, Christiane, Roller, Andreas, Dicker, Frank, Schmid, Christoph, Wendtner, Clemens-Martin, Staib, Peter, Serve, Hubert, Kreuzer, Karl-Anton, Kern, Wolfgang, Haferlach, Torsten, Haferlach, Claudia

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Homozygous BCMA gene deletion in response to anti-BCMA CAR T cells in a patient with multiple myeloma von Da Vià, Matteo C., Dietrich, Oliver, Truger, Marietta, Arampatzi, Panagiota, Duell, Johannes, Heidemeier, Anke, Zhou, Xiang, Danhof, Sophia, Kraus, Sabrina, Chatterjee, Manik, Meggendorfer, Manja, Twardziok, Sven, Goebeler, Maria-Elisabeth, Topp, Max S., Hudecek, Michael, Prommersberger, Sabrina, Hege, Kristen, Kaiser, Shari, Fuhr, Viktoria, Weinhold, Niels, Rosenwald, Andreas, Erhard, Florian, Haferlach, Claudia, Einsele, Hermann, Kortüm, K. Martin, Saliba, Antoine-Emmanuel, Rasche, Leo

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Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms von Kon, Ayana, Shih, Lee-Yung, Minamino, Masashi, Sanada, Masashi, Shiraishi, Yuichi, Nagata, Yasunobu, Yoshida, Kenichi, Okuno, Yusuke, Bando, Masashige, Nakato, Ryuichiro, Ishikawa, Shumpei, Sato-Otsubo, Aiko, Nagae, Genta, Nishimoto, Aiko, Haferlach, Claudia, Nowak, Daniel, Sato, Yusuke, Alpermann, Tamara, Nagasaki, Masao, Shimamura, Teppei, Tanaka, Hiroko, Chiba, Kenichi, Yamamoto, Ryo, Yamaguchi, Tomoyuki, Otsu, Makoto, Obara, Naoshi, Sakata-Yanagimoto, Mamiko, Nakamaki, Tsuyoshi, Ishiyama, Ken, Nolte, Florian, Hofmann, Wolf-Karsten, Miyawaki, Shuichi, Chiba, Shigeru, Mori, Hiraku, Nakauchi, Hiromitsu, Koeffler, H Phillip, Aburatani, Hiroyuki, Haferlach, Torsten, Shirahige, Katsuhiko, Miyano, Satoru, Ogawa, Seishi

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Detection of recurrent and of novel fusion transcripts in myeloid malignancies by targeted RNA sequencing von Stengel, Anna, Nadarajah, Niroshan, Haferlach, Torsten, Dicker, Frank, Kern, Wolfgang, Meggendorfer, Manja, Haferlach, Claudia

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Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2,... von KOHLMANN, Alexander, GROSSMANN, Vera, HAFERLACH, Claudia, HAFERLACH, Torsten, KLEIN, Hans-Ulrich, SCHINDELA, Sonja, WEISS, Tamara, KAZAK, Beray, DICKER, Frank, SCHNITTGER, Susanne, DUGAS, Martin, KERN, Wolfgang

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Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups von Creutzig, Ursula, Zimmermann, Martin, Reinhardt, Dirk, Rasche, Mareike, Neuhoff, Christine, Alpermann, Tamara, Dworzak, Michael, Perglerová, Karolína, Zemanova, Zuzana, Tchinda, Joelle, Bradtke, Jutta, Thiede, Christian, Haferlach, Claudia

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Refractory anemia with ring sideroblasts and marked thrombocytosis cases harbor mutations in SF3B1 or other spliceosome genes accompanied by JAK2V617F and ASXL1 mutations von Jeromin, Sabine, Haferlach, Torsten, Weissmann, Sandra, Meggendorfer, Manja, Eder, Christiane, Nadarajah, Niroshan, Alpermann, Tamara, Kohlmann, Alexander, Kern, Wolfgang, Haferlach, Claudia, Schnittger, Susanne

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