D. Hardekopf

Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome

V. Trifonov, K. Mrasek, T. Liehr, 2015, Cytogenetic and Genome Research.

A new human natural killer leukemia cell line, IMC-1. A complex chromosomal rearrangement defined by spectral karyotyping: functional and cytogenetic characterization.

C. Willman, M. Whalen, I. Chen, 2004, Leukemia research.

Microdeletion and Microduplication Syndromes

S. Bhatt, K. Mrasek, T. Liehr, 2012, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient

K. Kreuzer, A. Rothe, M. Othman, 2014, Molecular Cytogenetics.

Candidatus Neoehrlichia mikurensis infection identified in 2 hematooncologic patients: benefit of molecular techniques for rare pathogen detection.

R. Cmejla, J. Vydra, T. Kozák, 2011, Diagnostic microbiology and infectious disease.

Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report

N. Rao, K. Mrasek, T. Liehr, 2012, Molecular Cytogenetics.

Emerging Numbers of MMSs

S. Bhatt, K. Mrasek, T. Liehr, 2012 .

Myeloid antigen positive acute lymphoblastic leukemia with the Philadelphia translocation and a jumping translocation of 1q in a child

K. Foucar, D. Hardekopf, S. Winter, 2004, Leukemia.

A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients.

T. Liehr, M. Karas, R. Cmejla, 2013, Leukemia research.

How to narrow down chromosomal breakpoints in small and large derivative chromosomes – a new probe set

K. Mrasek, T. Liehr, T. Karamysheva, 2012, Journal of Applied Genetics.

A comprehensive study of TP53 mutations in chronic lymphocytic leukemia: Analysis of 1287 diagnostic and 1148 follow-up CLL samples.

M. Karas, R. Cmejla, L. Smolej, 2011, Leukemia research.