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The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms
Joseph David Khoury et al. · Leukemia
Open access |
22 Jun 2022 |
4,204 |
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Frequent pathway mutations of splicing machinery in myelodysplasia
Kenichi Yoshida et al. · Nature
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9 Sep 2011 |
2,089 |
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Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
Torsten Haferlach et al. · Leukemia
Open access |
13 Nov 2013 |
1,550 |
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Minimal/measurable residual disease in AML: a consensus document from the European LeukemiaNet MRD Working Party
Gerrit Jan Schuurhuis et al. · Blood
Open access |
12 Jan 2018 |
1,054 |
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BRAF Mutations in Hairy-Cell Leukemia
Enrico Tiacci et al. · New England Journal of Medicine
Open access |
11 Jun 2011 |
1,029 |
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Contemporary consensus proposal on criteria and classification of eosinophilic disorders and related syndromes
Peter Valent, Amy D. Klion, Hans‐Peter Horny et al. · Journal of Allergy and Clinical Immunology
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28 Mar 2012 |
774 |
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2021 Update on MRD in acute myeloid leukemia: a consensus document from the European LeukemiaNet MRD Working Party
Michael Heuser et al. · Blood
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Nov 2021 |
772 |
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Selective BCL-2 Inhibition by ABT-199 Causes On-Target Cell Death in Acute Myeloid Leukemia
Rongqing Aaron Pan et al. · Cancer Discovery
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17 Dec 2013 |
751 |
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Integration of gene mutations in risk prognostication for patients receiving first-line immunochemotherapy for follicular lymphoma: a retrospective analysis of a prospective clinical trial and validation in a population-based registry
Alessandro Pastore et al. · The Lancet Oncology
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7 Aug 2015 |
621 |
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Sorafenib Maintenance After Allogeneic Hematopoietic Stem Cell Transplantation for Acute Myeloid Leukemia With FLT3 –Internal Tandem Duplication Mutation (SORMAIN)
Andreas Burchert et al. · Journal of Clinical Oncology
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16 Jul 2020 |
578 |
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Definitions and standards in the diagnosis and treatment of the myelodysplastic syndromes: Consensus statements and report from a working conference
Peter Valent, Hans‐Peter Horny, John M. Bennett et al. · Leukemia Research
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26 Jan 2007 |
511 |
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Distinctive microRNA signature of acute myeloid leukemia bearing cytoplasmic mutated nucleophosmin
Ramiro Garzon, Michela Garofalo, Maria Paola Martelli et al. · Proceedings of the National Academy of Sciences
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28 Feb 2008 |
504 |
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Deregulated expression of cytokine receptor gene, CRLF2, is involved in lymphoid transformation in B-cell precursor acute lymphoblastic leukemia
Lisa Jane Russell et al. · Blood
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29 Jul 2009 |
502 |
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Cardiopulmonary recovery after COVID-19: an observational prospective multicentre trial
Thomas Sonnweber et al. · European Respiratory Journal
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10 Dec 2020 |
452 |
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Landscape Of Genetic Lesions In 944 Patients With Myelodysplastic Syndromes
Yasunobu Nagata et al. · Blood
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15 Nov 2013 |
431 |
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Dynamics of clonal evolution in myelodysplastic syndromes
Hideki Makishima et al. · Nature Genetics
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19 Dec 2016 |
428 |
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Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
Rocco Piazza et al. · Nature Genetics
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9 Dec 2012 |
428 |
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Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML)
Benjamin Hanfstein et al. · Leukemia
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26 Mar 2012 |
420 |
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Prognostic relevance of FLT3-TKD mutations in AML: the combination matters—an analysis of 3082 patients
Ulrike Bacher, Claudia Haferlach, Wolfgang Kern et al. · Blood
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26 Oct 2007 |
417 |
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New insights to the MLL recombinome of acute leukemias
Claus Meyer et al. · Leukemia
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5 Mar 2009 |
412 |
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Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms
Ayana Kon et al. · Nature Genetics
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18 Aug 2013 |
406 |
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Myelodysplastic Cells in Patients Reprogram Mesenchymal Stromal Cells to Establish a Transplantable Stem Cell Niche Disease Unit
Hind Medyouf et al. · Cell stem cell
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3 Apr 2014 |
386 |
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KIT-D816 mutations in AML1-ETO-positive AML are associated with impaired event-free and overall survival
Susanne Schnittger, Tobias M. Kohl, Torsten Haferlach et al. · Blood
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28 Oct 2005 |
381 |
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Integrating clinical features and genetic lesions in the risk assessment of patients with chronic myelomonocytic leukemia
Chiara Elena et al. · Blood
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6 Jul 2016 |
367 |
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Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation
Tetsuichi Yoshizato et al. · Blood
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21 Feb 2017 |
359 |
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Mechanisms of antigen escape from BCMA- or GPRC5D-targeted immunotherapies in multiple myeloma
Holly Lee et al. · Nature Medicine
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31 Aug 2023 |
354 |
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Comprehensive genetic characterization of CLL: a study on 506 cases analysed with chromosome banding analysis, interphase FISH, IgVH status and immunophenotyping
Claudia Haferlach, Frank Dicker, Susanne Schnittger et al. · Leukemia
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6 Sep 2007 |
347 |
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Assessment of imatinib as first-line treatment of chronic myeloid leukemia: 10-year survival results of the randomized CML study IV and impact of non-CML determinants
for the SAKK and the German CML Study Group et al. · Leukemia
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14 Aug 2017 |
342 |
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Homozygous BCMA gene deletion in response to anti-BCMA CAR T cells in a patient with multiple myeloma
Matteo Da Vià et al. · Nature Medicine
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22 Feb 2021 |
341 |
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Minimal residual disease levels assessed by NPM1 mutation–specific RQ-PCR provide important prognostic information in AML
Susanne Schnittger, Wolfgang Kern, Claudia Tschulik et al. · Blood
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8 Jul 2009 |
332 |
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EZH2 mutations are frequent and represent an early event in follicular lymphoma
Csaba Bödör et al. · Blood
Open access |
20 Sep 2013 |
329 |
| 32 |
Early human cytomegalovirus replication after transplantation is associated with a decreased relapse risk: evidence for a putative virus-versus-leukemia effect in acute myeloid leukemia patients
Ahmet H Elmaagacli, Nina K. Steckel, Michael Koldehoff et al. · Blood
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3 May 2011 |
317 |
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Updated Diagnostic Criteria and Classification of Mast Cell Disorders: A Consensus Proposal
Peter Valent et al. · HemaSphere
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13 Oct 2021 |
308 |
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SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)
Manja Meggendorfer, Andreas Roller, Torsten Haferlach et al. · Blood
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24 Aug 2012 |
308 |
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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
Utz O. Krug et al. · The Lancet
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Dec 2010 |
307 |
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Implications of NRAS mutations in AML: a study of 2502 patients
Ulrike Bacher, Torsten Haferlach, Claudia Schoch et al. · Blood
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25 Jan 2006 |
305 |
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SF3B1-mutant MDS as a distinct disease subtype: a proposal from the International Working Group for the Prognosis of MDS
Luca Malcovati et al. · Blood
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29 Apr 2020 |
302 |
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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, CBL, RAS, and RUNX1
Alexander Kohlmann, Vera Großmann, Hans‐Ulrich Klein et al. · Journal of Clinical Oncology
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20 Jul 2010 |
294 |
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KIT mutation analysis in mast cell neoplasms: recommendations of the European Competence Network on Mastocytosis
Michel Arock et al. · Leukemia
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4 Feb 2015 |
292 |
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Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia
Yilong Li et al. · Nature
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23 Mar 2014 |
291 |
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Impact of additional cytogenetic aberrations at diagnosis on prognosis of CML: long-term observation of 1151 patients from the randomized CML Study IV
Alice Charlotte Fabarius et al. · Blood
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29 Oct 2011 |
291 |
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Human-level recognition of blast cells in acute myeloid leukaemia with convolutional neural networks
Christian Matek, Simone Schwarz, Karsten Spiekermann et al. · Nature Machine Intelligence
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12 Nov 2019 |
283 |
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T-cell exhaustion induced by continuous bispecific molecule exposure is ameliorated by treatment-free intervals
Nora Philipp et al. · Blood
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25 Jul 2022 |
282 |
| 44 |
Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype
Vera Großmann et al. · Blood
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20 Oct 2011 |
270 |
| 45 |
Determination of relapse risk based on assessment of minimal residual disease during complete remission by multiparameter flow cytometry in unselected patients with acute myeloid leukemia
Wolfgang Kern, Daniela Voskova, Claudia Schoch et al. · Blood
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30 Jul 2004 |
269 |
| 46 |
RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis
Susanne Schnittger, Frank Dicker, Wolfgang Kern et al. · Blood
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10 Dec 2010 |
266 |
| 47 |
TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups
Detlef Haase et al. · Leukemia
Open access |
11 Jan 2019 |
264 |
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Comprehensive mutational profiling in advanced systemic mastocytosis
Juliana Schwaab et al. · Blood
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19 Aug 2013 |
263 |
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Landscape of TET2 mutations in acute myeloid leukemia
Sandra Weißmann, Tamara Alpermann, Vera Grossmann et al. · Leukemia
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25 Nov 2011 |
261 |
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Aberrant splicing of U12-type introns is the hallmark of ZRSR2 mutant myelodysplastic syndrome
Vikas Madan, Deepika Kanojia, Jia Li et al. · Nature Communications
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14 Jan 2015 |
253 |