Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4

enthalten in: Genes, chromosomes & cancer | 2017

von Herold, T. | Metzeler, K. | Vosberg, S. | +19

Close correlation of copy number aberrations detected by next‐generation sequencing with results from routine cytogenetics in acute myeloid leukemia

enthalten in: Genes, chromosomes & cancer | 2016

von Vosberg, S. | Herold, T. | Hartmann, L. | +13

Spectrum and prognostic relevance of driver gene mutations in acute myeloid leukemia

enthalten in: Blood | 2016

von Metzeler, K. | Herold, T. | Rothenberg-Thurley, M. | +22

Detection of Clonal Evolution in Hematopoietic Malignancies by Combining Comparative Genomic Hybridization and Single Nucleotide Polymorphism Arrays

enthalten in: Clinical chemistry | 2014

von Hartmann, L. | Stephenson, C. | Verkamp, S. | +8

Isolated trisomy 13 defines a homogeneous AML subgroup with high frequency of mutations in spliceosome genes and poor prognosis

enthalten in: Blood | 2014

von Herold, T. | Metzeler, K. | Vosberg, S. | +25

Array-Based Karyotyping in Plasma Cell Neoplasia After Plasma Cell Enrichment Increases Detection of Genomic Aberrations

enthalten in: American journal of clinical pathology | 2012

von Zehentner, B. | Hartmann, L. | Johnson, K. | +8

Array-Based Karyotyping Post Plasma Cell Enrichment for the Detection of Genomic Abnormalities in Multiple Myeloma

enthalten in: Cancer genetics | 2012

von Zehentner, B. | Hartmann, L. | Johnson, K. | +8

Detection of Genomic Abnormalities in Multiple Myeloma: The Application of FISH Analysis in Combination With Various Plasma Cell Enrichment Techniques

enthalten in: American journal of clinical pathology | 2011

von Hartmann, L. | Biggerstaff, J. | Chapman, D. | +10