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Stefan Mundlos
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Journal Articles

Integration of Hi-C and Nanopore Sequencing for Structural Variant Analysis in AML with a Complex Karyotype: (Chromothripsis)²

Marius-Konstantin Klever, Eric Sträng, PhD, Julius Jungnitsch, Uirá Souto Melo, Sara Hetzel, Anna Dolnik, Robert Schöpflin, Jens F. Schrezenmeier, Olga Blau, Jörg Westermann, Konstanze Döhner, Hubert Schrezenmeier, Malte Spielmann, Alexander Meissner, PhD, Stefan Mundlos, Lars Bullinger, MD
Journal: Blood
Blood (2020) 136 (Supplement 1): 28.
https://doi.org/10.1182/blood-2020-133787
Published: 2020
Journal Articles

A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT

Brief Report
Peter M. Krawitz, Britta Höchsmann, Yoshiko Murakami, Britta Teubner, Ulrike Krüger, Eva Klopocki, Heidemarie Neitzel, Alexander Hoellein, Christina Schneider, Dmitri Parkhomchuk, Jochen Hecht, Peter N. Robinson, Stefan Mundlos, Taroh Kinoshita, Hubert Schrezenmeier
Journal: Blood
Blood (2013) 122 (7): 1312–1315.
https://doi.org/10.1182/blood-2013-01-481499
Published: 2013
Includes: Supplemental data
Journal Articles

G6PC3 Deficiency Associated with Congenital Neutropenia and Enterocolitis

Jana Diestelhorst, Daniel Kotlarz, Giridharan Appaswamy, PhD, Rita Beier, MD, Peter M Krawitz, MD, PhD, Peter N Robinson, MD, PhD, Jochen Hecht, PhD, Jacek Puchalka, PhD, Alejandro A. Schäffer, PhD, Dietmar Pfeifer, PhD, Ulrich Baumann, MD, Eva-Doreen Pfister, MD, Gudrun Brandes, PhD, Gabriella Palla, MD, Roland Jacobs, PhD, Hans H. Kreipe, MD, Stefan Mundlos, MD, Christoph Klein, MD, PhD
Journal: Blood
Blood (2011) 118 (21): 2170.
https://doi.org/10.1182/blood.V118.21.2170.2170
Published: 2011
Journal Articles

Mesenchymal stromal cells of myelodysplastic syndrome and acute myeloid leukemia patients have distinct genetic abnormalities compared with leukemic blasts

Olga Blau, Claudia Dorothea Baldus, Wolf-Karsten Hofmann, Gundula Thiel, Florian Nolte, Thomas Burmeister, Seval Türkmen, Ouidad Benlasfer, Elke Schümann, Annette Sindram, Mara Molkentin, Stefan Mundlos, Ulrich Keilholz, Eckhard Thiel, Igor Wolfgang Blau
Journal: Blood
Blood (2011) 118 (20): 5583–5592.
https://doi.org/10.1182/blood-2011-03-343467
Published: 2011
Journal Articles

Release of Alkaline Phosphatase Caused by PIGV Mutations In Patients with Hyperphosphatasia-Mental Retardation Syndrome (HPMR), a Recently Found Second Inherited GPI Anchor Deficiency.

Yoshiko Murakami, MD, PhD, Peter M Krawitz, MD, PhD, Peter N Robinson, MD, PhD, Stefan Mundlos, MD, PhD, Yusuke Maeda, MD, PhD, Taroh Kinoshita, PhD
Journal: Blood
Blood (2010) 116 (21): 2031.
https://doi.org/10.1182/blood.V116.21.2031.2031
Published: 2010
Journal Articles

The Abrogated Thrombopoietin (TPO) Signal Transduction In Pediatric Patients Suffering From Thrombocytopenia-Absent Radii Syndrome Is Restored In Adult Patients, Suggesting An Additional, c-Mpl-Jak2-Independent Mechanism for Platelet Biogenesis.

Janine Fiedler, Gabriele Strauss, Martin Wannack, Silke Fleischhauer, Kerstin Seidel, Eva Klopocki, Stefan Mundlos, Markus Schmugge, MD, Harald Schulze, PhD
Journal: Blood
Blood (2010) 116 (21): 1561.
https://doi.org/10.1182/blood.V116.21.1561.1561
Published: 2010
Journal Articles

A Novel BACH2 - BCL2L1 Fusion Gene in the Burkitt’s Lymphoma Derived Cell Line BLUE - 1

Seval Türkmen, Mathias Riehn, Stefan Mundlos, Eckhard Thiel, Thomas Burmeister
Journal: Blood
Blood (2008) 112 (11): 4146.
https://doi.org/10.1182/blood.V112.11.4146.4146
Published: 2008
Journal Articles

Acute Lymphoblastic Leukemia in a Case of Ring Chromosome

Seval Türkmen, Sebastian Muller, Stefan Mundlos, Günter Henze, Holger Lode
Journal: Blood
Blood (2008) 112 (11): 4151.
https://doi.org/10.1182/blood.V112.11.4151.4151
Published: 2008