Jochen Harbott
Giessen, HE, Germany
Last Updated: 09/26/2026
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Found 14 publications
Next-generation-sequencing of recurrent childhood high hyperdiploid acute lymphoblastic leukemia reveals mutations typically associated with high risk patients.
Journal: Leukemia research
Published: April 14, 2015
Minimal residual disease-based treatment is adequate for relapse-prone childhood acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21: the experience of the ALL-BFM 2000 trial.
Journal: Klinische Padiatrie
Published: November 29, 2014
The impact of TEL-AML1 (ETV6-RUNX1) expression in precursor B cells and implications for leukaemia using three different genome-wide screening methods.
Journal: Blood cancer journal
Published: July 01, 2013
Key treatment questions in childhood acute lymphoblastic leukemia: results in 5 consecutive trials performed by the ALL-BFM study group from 1981 to 2000.
Journal: Klinische Padiatrie
Published: May 24, 2013
Next-generation-sequencing-based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemia.
Journal: Genes, chromosomes & cancer
Published: November 20, 2012
Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel.
Journal: Blood
Published: August 11, 2012
Last Updated: 09/26/2026