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1.
Herold, T. et al.: Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4. Genes Chromosomes Cancer 56, 75-86 (2017)
2.
Vosberg, S. et al.: Close correlation of copy number aberrations detected by next-generation sequencing with results from routine cytogenetics in acute myeloid leukemia. Genes Chromosomes Cancer 55, 553-567 (2016)
3.
Herold, T. et al.: Expression analysis of genes located in the minimally deleted regions of 13q14 and 11q22-23 in chronic lymphocytic leukemia - unexpected expression pattern of the RHO GTPase activator ARHGAP20. Genes Chromosomes Cancer 50, 546-558 (2011)
4.
Popp, H.D. & Bohlander, S.K.: Genetic instability in inherited and sporadic leukemias. Genes Chromosomes Cancer 49, 1071-1081 (2010)
5.
Salaverria, I.* et al.: Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques. Genes Chromosomes Cancer 47, 1086-1097 (2008)
6.
Hutter, G.* et al.: Differential effect of epigenetic alterations and genomic deletions of CDK inhibitors [p16(INK4a), p15(INK4b), p14(ARF)] in Mantle cell lymphoma. Genes Chromosomes Cancer 45, 203-210 (2006)
7.
Schnittger, S.* et al.: D324N single-nucleotide polymorphism in the FLT3 gene is associated with higher risk of myeloid leukemias. Genes Chromosomes Cancer 45, 332-337 (2006)
8.
Griesinger, F.* et al.: A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;qII.2) translocation in a patient with a clinically typical chronic myeloid leukemia. Genes Chromosomes Cancer 44, 329-333 (2005)
9.
Fauth, C. ; O'Hare, M.J.* ; Lederer, G.* ; Jat, P.S.* & Speicher, M.R.: Order of genetic events is critical determinant of aberrations in chromosome count and structure. Genes Chromosomes Cancer 40, 298-306 (2004)
10.
Müller, S.* ; Eder, S.* & Wienberg, J.: A nonredundant multicolor bar code as a screening tool for rearrangements in neoplasia. Genes Chromosomes Cancer 39, 59-70 (2004)
11.
Zitzelsberger, H. et al.: Gene amplification of analytical PKC-binding PARD3 in radiation-transformed neoplastic retinal pigment epithelial cell lines. Genes Chromosomes Cancer 40, 55-59 (2004)
12.
Kraus, J. ; Pantel, K.* ; Pinkel, D.* ; Albertson, D.G.* & Speicher, M.R.: High-resolution genomic profiling of occult micrometastatic tumor cells. Genes Chromosomes Cancer 36, 159-166 (2003)
13.
Zeidler, R.* et al.: Breakpoints of Burkitt's lymphoma t(8;22) translocations map within a distance of 300 kb downstream of MYC. Genes Chromosomes Cancer 9, 282-287 (1994)
14.
Bock, S. et al.: Detection of Somatic Changes in Human Renal Cell Carcinomas with Oligonucleotide Probes Specific for Simple Repeat Motifs. Genes Chromosomes Cancer 6, 113-117 (1993)
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