S Schnittger

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The role of different genetic subtypes of CEBPA mutated AML

C Haferlach, A Kohlmann, T Haferlach, 2014, Leukemia.

Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia.

G. Behre, S. Schnittger, T. Pabst, 2001, Nature genetics.

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations

C Haferlach, T Haferlach, T. Haferlach, 2013, Leukemia.

Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH).

P Gruss, R. Balling, P. Gruss, 1992, Genomics.

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

C Haferlach, H Aburatani, S Miyano, 2013, Leukemia.

Pediatric acute lymphoblastic leukemia (ALL) gene expression signatures classify an independent cohort of adult ALL patients

W Hiddemann, M Dugas, A Kohlmann, 2004, Leukemia.

The MLL recombinome of acute leukemias

M. D. Boer, R. Pieters, R. Pieters, 2006, Leukemia.

Age, not therapy intensity, determines outcomes of adults with acute myeloid leukemia

C Haferlach, W Hiddemann, T Haferlach, 2016, Leukemia.

New insights to the MLL recombinome of acute leukemias

M. Krzywinski, E. Clappier, B. Schäfer, 2009, Leukemia.

Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure

C Haferlach, M Dugas, A Kohlmann, 2011, Leukemia.

Genetic classification of acute myeloid leukemia (AML).

W Hiddemann, T Haferlach, W. Hiddemann, 2004, Annals of hematology.