Molecular Genetics of Adult Acute Myeloid Leukemia: Prognostic and Therapeutic Implications
Marcucci, Guido, Haferlach, Torsten, Döhner, Hartmut
Published in Journal of clinical oncology (10.02.2011)
Published in Journal of clinical oncology (10.02.2011)
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Journal Article
Minimal/measurable residual disease in AML: a consensus document from the European LeukemiaNet MRD Working Party
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.
Published in Blood (22.03.2018)
Published in Blood (22.03.2018)
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Journal Article
How artificial intelligence might disrupt diagnostics in hematology in the near future
Walter, Wencke, Haferlach, Claudia, Nadarajah, Niroshan, Schmidts, Ines, Kühn, Constanze, Kern, Wolfgang, Haferlach, Torsten
Published in Oncogene (24.06.2021)
Published in Oncogene (24.06.2021)
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Journal Article
Molecular genetic characterization of myeloid/lymphoid neoplasms associated with eosinophilia and rearrangement of PDGFRA, PDGFRB, FGFR1 or PCM1-JAK2
Baer, Constance, Muehlbacher, Verena, Kern, Wolfgang, Haferlach, Claudia, Haferlach, Torsten
Published in Haematologica (Roma) (01.08.2018)
Published in Haematologica (Roma) (01.08.2018)
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Journal Article
Molecular landscape and clonal architecture of adult myelodysplastic/myeloproliferative neoplasms
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
Published in Blood (15.10.2020)
Published in Blood (15.10.2020)
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Journal Article
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 study on 123 patients and 27 genes
Meggendorfer, Manja, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten
Published in Haematologica (Roma) (01.09.2017)
Published in Haematologica (Roma) (01.09.2017)
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Journal Article
Novel causative variants of VEXAS in UBA1 detected through whole genome transcriptome sequencing in a large cohort of hematological malignancies
Sakuma, Maki, Blombery, Piers, Meggendorfer, Manja, Haferlach, Claudia, Lindauer, Markus, Martens, Uwe M., Kern, Wolfgang, Haferlach, Torsten, Walter, Wencke
Published in Leukemia (01.05.2023)
Published in Leukemia (01.05.2023)
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Journal Article
The leukemic oncogene EVI1 hijacks a MYC super-enhancer by CTCF-facilitated loops
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
Published in Nature communications (28.09.2021)
Published in Nature communications (28.09.2021)
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Journal Article
Prognostic relevance of FLT3-TKD mutations in AML: the combination matters—an analysis of 3082 patients
Bacher, Ulrike, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten, Schnittger, Susanne
Published in Blood (01.03.2008)
Published in Blood (01.03.2008)
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Journal Article
Complex landscape of alternative splicing in myeloid neoplasms
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.
Published in Leukemia (01.04.2021)
Published in Leukemia (01.04.2021)
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Journal Article
Classification and Personalized Prognostic Assessment on the Basis of Clinical and Genomic Features in Myelodysplastic Syndromes
Bersanelli, Matteo, Travaglino, Erica, Meggendorfer, Manja, Matteuzzi, Tommaso, Sala, Claudia, Mosca, Ettore, Chiereghin, Chiara, Di Nanni, Noemi, Gnocchi, Matteo, Zampini, Matteo, Rossi, Marianna, Maggioni, Giulia, Termanini, Alberto, Angelucci, Emanuele, Bernardi, Massimo, Borin, Lorenza, Bruno, Benedetto, Bonifazi, Francesca, Santini, Valeria, Bacigalupo, Andrea, Voso, Maria Teresa, Oliva, Esther, Riva, Marta, Ubezio, Marta, Morabito, Lucio, Campagna, Alessia, Saitta, Claudia, Savevski, Victor, Giampieri, Enrico, Remondini, Daniel, Passamonti, Francesco, Ciceri, Fabio, Bolli, Niccolò, Rambaldi, Alessandro, Kern, Wolfgang, Kordasti, Shahram, Sole, Francesc, Palomo, Laura, Sanz, Guillermo, Santoro, Armando, Platzbecker, Uwe, Fenaux, Pierre, Milanesi, Luciano, Haferlach, Torsten, Castellani, Gastone, Della Porta, Matteo G
Published in Journal of clinical oncology (10.04.2021)
Published in Journal of clinical oncology (10.04.2021)
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Journal Article
TP53 mutations in myelodysplastic syndromes and secondary AML confer an immunosuppressive phenotype
Sallman, David A., McLemore, Amy F., Aldrich, Amy L., Komrokji, Rami S., McGraw, Kathy L., Dhawan, Abhishek, Geyer, Susan, Hou, Hsin-An, Eksioglu, Erika A., Sullivan, Amy, Warren, Sarah, MacBeth, Kyle J., Meggendorfer, Manja, Haferlach, Torsten, Boettcher, Steffen, Ebert, Benjamin L., Al Ali, Najla H., Lancet, Jeffrey E., Cleveland, John L., Padron, Eric, List, Alan F.
Published in Blood (10.12.2020)
Published in Blood (10.12.2020)
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Journal Article
Unraveling the germline inheritance of the JAK2F556V gene mutation in familial thrombocythemia: a comprehensive analysis of 11 family members and potential implications for surveillance
Meggendorfer, Manja, Haferlach, Torsten, Beykirch, Maria K., Petrides, Petro E.
Published in Haematologica (Roma) (26.09.2024)
Published in Haematologica (Roma) (26.09.2024)
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Journal Article
Circulating microbial content in myeloid malignancy patients is associated with disease subtypes and patient outcomes
Woerner, Jakob, Huang, Yidi, Hutter, Stephan, Gurnari, Carmelo, Sánchez, Jesús María Hernández, Wang, Janet, Huang, Yimin, Schnabel, Daniel, Aaby, Michael, Xu, Wanying, Thorat, Vedant, Jiang, Dongxu, Jha, Babal K., Koyuturk, Mehmet, Maciejewski, Jaroslaw P., Haferlach, Torsten, LaFramboise, Thomas
Published in Nature communications (24.02.2022)
Published in Nature communications (24.02.2022)
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