Publications by authors named "Luise Hartmann"

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Engineering an inducible leukemia-associated fusion protein enables large-scale ex vivo production of functional human phagocytes.
Roland Windisch, Sarah Soliman, Adrian Hoffmann, Linping Chen-Wichmann, Anna Danese, Luise Hartmann

Proc Natl Acad Sci U S A· June 2024

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Integrated analysis of genotype and phenotype reveals clonal evolution and cytogenetically driven disruption of myeloid cell maturation in myelodysplastic syndromes.
Jevon A Cutler, Haley R Pugsley, Richard Bennington, Wayne Fritschle, Luise Hartmann

Cytometry B Clin Cytom· March 2023

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Compartment-specific mutational landscape of clonal hematopoiesis.
Luise Hartmann, Judith S Hecker, Maja Rothenberg-Thurley, Jennifer Rivière, Madlen Jentzsch

Leukemia· November 2022

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Adaptive Cellular Immunity against African Swine Fever Virus Infections.
Alexander Schäfer, Giulia Franzoni, Christopher L Netherton, Luise Hartmann, Sandra Blome

Pathogens· February 2022

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CHIP and hips: clonal hematopoiesis is common in patients undergoing hip arthroplasty and is associated with autoimmune disease.
Judith S Hecker, Luise Hartmann, Jennifer Rivière, Michèle C Buck, Mark van der Garde

Blood· November 2021

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Comparison of the Proteomes of Porcine Macrophages and a Stable Porcine Cell Line after Infection with African Swine Fever Virus.
Elisabeth Wöhnke, Walter Fuchs, Luise Hartmann, Ulrike Blohm, Sandra Blome

Viruses· November 2021

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The clinical mutatome of core binding factor leukemia.
Sabrina Opatz, Stefanos A Bamopoulos, Klaus H Metzeler, Tobias Herold, Bianka Ksienzyk, Luise Hartmann

Leukemia· June 2020

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Molecular characterization of acute myeloid leukemia patients who relapse more than 3 years after diagnosis: an exome sequencing study of 31 patients.
Luise Hartmann, Claudia Haferlach, Manja Meggendorfer, Niroshan Nadarajah, Wolfgang Kern

Haematologica· April 2020

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ZBTB7A prevents RUNX1-RUNX1T1-dependent clonal expansion of human hematopoietic stem and progenitor cells.
Enric Redondo Monte, Anja Wilding, Georg Leubolt, Paul Kerbs, Johannes W Bagnoli, Luise Hartmann

Oncogene· April 2020

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Molecular characterization of a second myeloid neoplasm developing after treatment for acute myeloid leukemia.
Luise Hartmann, Niroshan Nadarajah, Manja Meggendorfer, Alexander Höllein, Calogero Vetro

Leukemia· March 2020

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Clonal hematopoiesis and preleukemia-Genetics, biology, and clinical implications.
Luise Hartmann, Klaus H Metzeler

Genes Chromosomes Cancer· December 2019

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Comprehensive molecular characterization of myeloid malignancies with 9q deletion.
Luise Hartmann, Torsten Haferlach, Manja Meggendorfer, Wolfgang Kern, Claudia Haferlach

Leuk Lymphoma· October 2019

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Myeloid malignancies with isolated 7q deletion can be further characterized by their accompanying molecular mutations.
Luise Hartmann, Claudia Haferlach, Manja Meggendorfer, Wolfgang Kern, Torsten Haferlach

Genes Chromosomes Cancer· October 2019

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Relapse of acute myeloid leukemia after allogeneic stem cell transplantation is associated with gain of alterations and high mutation load.
Sebastian Vosberg, Luise Hartmann, Klaus H Metzeler, Nikola P Konstandin, Stephanie Schneider

Haematologica· December 2018

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Evolution of Cytogenetically Normal Acute Myeloid Leukemia During Therapy and Relapse: An Exome Sequencing Study of 50 Patients.
Philipp A Greif, Luise Hartmann, Sebastian Vosberg, Sophie M Stief, Raphael Mattes

Clin Cancer Res· April 2018

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A 29-gene and cytogenetic score for the prediction of resistance to induction treatment in acute myeloid leukemia.
Tobias Herold, Vindi Jurinovic, Aarif M N Batcha, Stefanos A Bamopoulos, Maja Rothenberg-Thurley, Luise Hartmann

Haematologica· March 2018

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Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosis.
Tobias Herold, Stephanie Schneider, Klaus H Metzeler, Martin Neumann, Luise Hartmann

Haematologica· January 2017

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Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4.
Tobias Herold, Klaus H Metzeler, Sebastian Vosberg, Luise Hartmann, Vindi Jurinovic

Genes Chromosomes Cancer· January 2017

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Spectrum and prognostic relevance of driver gene mutations in acute myeloid leukemia.
Klaus H Metzeler, Tobias Herold, Maja Rothenberg-Thurley, Susanne Amler, Maria C Sauerland, Luise Hartmann

Blood· August 2016

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Close correlation of copy number aberrations detected by next-generation sequencing with results from routine cytogenetics in acute myeloid leukemia.
Sebastian Vosberg, Tobias Herold, Luise Hartmann, Martin Neumann, Sabrina Opatz

Genes Chromosomes Cancer· July 2016

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ZBTB7A mutations in acute myeloid leukaemia with t(8;21) translocation.
Luise Hartmann, Sayantanee Dutta, Sabrina Opatz, Sebastian Vosberg, Katrin Reiter

Nat Commun· June 2016

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Detection of clonal evolution in hematopoietic malignancies by combining comparative genomic hybridization and single nucleotide polymorphism arrays.
Luise Hartmann, Christine F Stephenson, Stephanie R Verkamp, Krystal R Johnson, Bettina Burnworth

Clin Chem· December 2014

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Isolated trisomy 13 defines a homogeneous AML subgroup with high frequency of mutations in spliceosome genes and poor prognosis.
Tobias Herold, Klaus H Metzeler, Sebastian Vosberg, Luise Hartmann, Christoph Röllig

Blood· August 2014

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Array-based karyotyping in plasma cell neoplasia after plasma cell enrichment increases detection of genomic aberrations.
Barbara K Zehentner, Luise Hartmann, Krystal R Johnson, Christine F Stephenson, Douglas B Chapman

Am J Clin Pathol· October 2012

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Detection of genomic abnormalities in multiple myeloma: the application of FISH analysis in combination with various plasma cell enrichment techniques.
Luise Hartmann, Julie Sanford Biggerstaff, Douglas B Chapman, Janice M Scott, Krystal R Johnson

Am J Clin Pathol· November 2011

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