Carbon Nanotube FET Technology for Radio-Frequency Electronics: State-of-the-Art Overview von Schroter, M., Claus, M., Sakalas, P., Haferlach, M., Dawei Wang

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Complete remission and early death after intensive chemotherapy in patients aged 60 years or older with acute myeloid leukaemia: a web-based application for prediction of outcomes von Krug, Utz, Dr, Röllig, Christoph, MD, Koschmieder, Anja, Heinecke, Achim, PhD, Sauerland, Maria Cristina, MSc, Schaich, Markus, Prof, Thiede, Christian, Prof, Kramer, Michael, Braess, Jan, Prof, Spiekermann, Karsten, MD, Haferlach, Torsten, Prof, Haferlach, Claudia, MD, Koschmieder, Steffen, MD, Rohde, Christian, PhD, Serve, Hubert, Prof, Wörmann, Bernhard, Prof, Hiddemann, Wolfgang, Prof, Ehninger, Gerhard, Prof, Berdel, Wolfgang E, Prof, Büchner, Thomas, Prof, Müller-Tidow, Carsten, Prof

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Contemporary consensus proposal on criteria and classification of eosinophilic disorders and related syndromes von Valent, Peter, MD, Klion, Amy D., MD, Horny, Hans-Peter, MD, Roufosse, Florence, MD, PhD, Gotlib, Jason, MD, Weller, Peter F., MD, Hellmann, Andrzej, MD, Metzgeroth, Georgia, MD, Leiferman, Kristin M., MD, Arock, Michel, PharmD, PhD, Butterfield, Joseph H., MD, Sperr, Wolfgang R., MD, Sotlar, Karl, MD, Vandenberghe, Peter, MD, PhD, Haferlach, Torsten, MD, Simon, Hans-Uwe, MD, PhD, Reiter, Andreas, MD, Gleich, Gerald J., MD

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Gene expression profiling in acute myeloid leukaemia (AML) von Bacher, Ulrike, MD, Kohlmann, Alexander, PhD, Haferlach, Claudia, MD, Haferlach, Torsten, MD

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A semi-empirical large-signal compact model for RF carbon nanotube field-effect transistors von Schroter, M., Haferlach, M., Sakalas, P., Claus, M.

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An overview on the state-of-the-art of Carbon-based radio-frequency electronics von Schroter, M., Claus, M., Sakalas, P., Wang, D., Haferlach, M.

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Mutational profiling in patients with MDS: Ready for every-day use in the clinic? von Bacher, Ulrike, MD, Kohlmann, Alexander, PhD, Haferlach, Torsten, MD

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Comparison Of Mutation Patterns Between Diagnosis and Relapse In 556 Adult Patients With AML Shows High Variability Of Stability von Schnittger, Susanne, Nadarajah, Niroshan, Alpermann, Tamara, Eder, Christiane, Kohlmann, Alexander, Kuznia, Sabrina, Weissmann, Sandra, Fasan, Annette, Weber, Simone, Albuquerque, Andreia, Jeromin, Sabine, Meggendorfer, Manja, Dicker, Frank, Kern, Wolfgang, Haferlach, Claudia, Haferlach, MD, Torsten

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The impact of TP53 mutations and TP53 deletions on survival varies between AML, ALL, MDS and CLL: an analysis of 3307 cases von Stengel, A, Kern, W, Haferlach, T, Meggendorfer, M, Fasan, A, Haferlach, C

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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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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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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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Landscape of genetic lesions in 944 patients with myelodysplastic syndromes von Haferlach, T, Nagata, Y, Grossmann, V, Okuno, Y, Bacher, U, Nagae, G, Schnittger, S, Sanada, M, Kon, A, Alpermann, T, Yoshida, K, Roller, A, Nadarajah, N, Shiraishi, Y, Shiozawa, Y, Chiba, K, Tanaka, H, Koeffler, H P, Klein, H-U, Dugas, M, Aburatani, H, Kohlmann, A, Miyano, S, Haferlach, C, Kern, W, Ogawa, S

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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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Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML von Stengel, A, Kern, W, Meggendorfer, M, Nadarajah, N, Perglerovà, K, Haferlach, T, Haferlach, C

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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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Additional mutations in SRSF2, ASXL1 and/or RUNX1 identify a high-risk group of patients with KIT D816V+ advanced systemic mastocytosis von Jawhar, M, Schwaab, J, Schnittger, S, Meggendorfer, M, Pfirrmann, M, Sotlar, K, Horny, H-P, Metzgeroth, G, Kluger, S, Naumann, N, Haferlach, C, Haferlach, T, Valent, P, Hofmann, W-K, Fabarius, A, Cross, N C P, Reiter, A

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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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Prognostic impact and landscape of NOTCH1 mutations in chronic lymphocytic leukemia (CLL): a study on 852 patients von Weissmann, S, Roller, A, Jeromin, S, Hernández, M, Abáigar, M, Hernández-Rivas, J M, Grossmann, V, Haferlach, C, Kern, W, Haferlach, T, Schnittger, S, Kohlmann, A

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