Ghent University Academic Bibliography

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Spontaneous remission and loss of monosomy 7 : a window of opportunity for young children with SAMD9L syndrome

Miriam Erlacher, Felicia Andresen, Martina Sukova, Jan Stary, Barbara De Moerloose (UGent) , Jutte van der Werff Ten Bosch, Michael Dworzak, Markus G. Seidel, Sophia Polychronopoulou, Rita Beier, et al.

(2024) HAEMATOLOGICA. 109(2). p.422-430
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Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome

Rachel Bortnick, Marcin Wlodarski, Valerie de Haas, Barbara De Moerloose (UGent) , Michael Dworzak, Henrik Hasle, Riccardo Masetti, Jan Starý, Dominik Turkiewicz, Marek Ussowicz, et al.

(2021) BONE MARROW TRANSPLANTATION. 56(11). p.2732-2741
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Association of unbalanced translocation der(1;7) with germline GATA2 mutations

Emilia J. Kozyra, Gudrun Goehring, Dennis D. Hickstein, Katherine R. Calvo, Courtney D. DiNardo, Michael Dworzak, Valerie de Haas, Jan Stary, Henrik Hasle, Akiko Shimamura, et al.

(2021) BLOOD. 138(23). p.2441-2445
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Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

Sushree S. Sahoo, Victor B. Pastor, Charnise Goodings, Rebecca K. Voss, Emilia J. Kozyra, Amina Szvetnik, Peter Noellke, Michael Dworzak, Jan Stary, Franco Locatelli, et al.

(2021) NATURE MEDICINE. 27(10). p.1806-1817
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Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

Emilia J. Kozyra, Victor B. Pastor, Stylianos Lefkopoulos, Sushree S. Sahoo, Hauke Busch, Rebecca K. Voss, Miriam Erlacher, Dirk Lebrecht, Enikoe A. Szvetnik, Shinsuke Hirabayashi, et al.

(2020) LEUKEMIA. 34(10). p.2673-2687
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RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia

Daniel B Lipka, Tania Witte, Reka Toth, Jing Yang, Manuel Wiesenfarth, Peter Noellke, Alexandra Fischer, David Brocks, Zuguang Gu, Jeongbin Park, et al.

(2017) NATURE COMMUNICATIONS. 8.
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Therapy with low-dose azacitidine for MDS in children and young adults: a retrospective analysis of the EWOG-MDS study group

Annamaria M Cseh, Charlotte M Niemeyer, Ayami Yoshimi, Albert Catala, Michael C Frühwald, Henrik Hasle, Mary M van den Heuvel-Eibrink, Melchior Lauten, Barbara De Moerloose (UGent) , Owen P Smith, et al.

(2016) BRITISH JOURNAL OF HAEMATOLOGY. 172(6). p.930-936
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- Conference Paper
- C3
Impact of somatic mutations on the outcome of children and adolescents with therapy-related myelodysplastic syndrome

Brigitte Strahm, Marcin W Wlodarski, Victor B Pastor, Bart Przychodzien, Albert Catala, Michael Dworzak, Oksana Fabri, Henrik Hasle, Kristian Kallay, Riccardo Masetti, et al.

(2016) BLOOD. 128(22).
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Prevalence, clinical characteristics and prognosis of GATA2-related myelodysplastic syndromes (MDS) in children and adolescents

Marcin W Wlodarski, Shinsuke Hirabayashi, Victor Pastor, Jan Starý, Henrik Hasle, Riccardo Masetti, Michael Dworzak, Markus Schmugge, Marry van den Heuvel-Eibrink, Marek Ussowicz, et al.

(2016) BLOOD. 127(11). p.1387-1397
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Clonal mutational landscape of childhood myelodysplastic syndromes

Emilia J Kozyra, Shinsuke Hirabayashi, Victor Bengt Pastor Loyola, Bartlomiej Przychodzen, Axel Karow, Albert Catala, Barbara De Moerloose (UGent) , Michael Dworzak, Henrik Hasle, Riccardo Masetti, et al.

(2015) BLOOD. 126(23).
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Somatic genetic and epigenetic architecture of myelodysplastic syndromes arising from GATA2 deficiency

Victor Bengt Pastor Loyola, Shinsuke Hirabayashi, Sandra Pohl, Emilia J Kozyra, Albert Catala, Barbara De Moerloose (UGent) , Marek Dworzak, Henrik Hasle, Riccardo Masetti, Markus Schmugge, et al.

(2015) BLOOD. 126(23).
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Reduced intensity conditioning for children with refractory cytopenia of childhood : results of the EWOG-MDS study SCT RX RIC 06

Brigitte Strahm, Peter Bader, Albert Catala, Michael Dworzak, Marry Vandenheuvel, Barbara De Moerloose (UGent) , Markus Schmugge, Owen Smith, Petr Sedlacek, Franco Locatelli, et al.

(2014) Childhood Leukemia, 9th Biennial symposium, Abstracts.
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- Conference Paper
- C3
Juvenile myelomonocytic leukemia : five genes, how many subtypes?

Charlotte M Niemeyer, Brigitte Strahm, Michael Dworzak, Barbara De Moerloose (UGent) , Henrik Hasle, Jan Stary, Markus Schmugge, Marek Ussowics, Marry Van Den Heuvel-Eibrink, Marco Zecca, et al.

(2014) Childhood Leukemia, 9th Biennial symposium, Abstracts.
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Comparison of horse and rabbit antithymocyte globulin in immunosuppressive therapy for refractory cytopenia of childhood

Ayami Yoshimi, Marry M van den Heuvel-Eibrink, Irith Baumann, Stephan Schwarz, Ingrid Simonitsch-Klupp, Pascale De Paepe, Vit Campr, Gitte Birk Kerndrup, Maureen O'Sullivan, Rita Devito, et al.

(2014) HAEMATOLOGICA. 99(4). p.656-663
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Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML

Shinsuke Hirabayashi, Christian Flotho, Jessica Moetter, Michael Heuser, Henrik Hasle, Bernd Gruhn, Thomas Klingebiel, Felicitas Thol, Brigitte Schlegelberger, Irith Baumann, et al.

(2012) BLOOD. 119(11). p.e96-e99
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- C3
Therapy-related myelodysplastic syndrome following treatment for childhood acute lymphoblastic leukemia: outcome of patients registered in the EWOG-MDS 98/06 studies

Brigitte Strahm, Roland Amann, Barbara De Moerloose (UGent) , Michael Dworzak, Henrik Hasle, Markus Schmugge, Jan Stary, Marry M Van den Heuvel-Eibrik, Marco Zecca, Brigitte Schlegelberger, et al.

(2011) 53rd ASH annual meeting and exposition : abstracts, program and personal scheduler.
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Aberrant DNA methylation characterizes juvenile myelomonocytic leukemia with poor outcome

Christiane Olk-Batz, Anna R Poetsch, Peter Nöllke, Rainer Claus, Manuela Zucknick, Inga Sandrock, Tania Witte, Brigitte Strahm, Henrik Hasle, Marco Zecca, et al.

(2011) BLOOD. 117(18). p.4871-4880
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- Conference Paper
- C3
Mutations of the spliceosome complex genes occur in adult patients but are very rare in children with myeloid neoplasia

Shinsuke Hirabayashi, Jessica Moetter, Kenichi Yoshida, Michael Heuser, Henrik Hasle, Alexandra Fischer, Brigitte Strahm, Brigitte Schlegelberger, Irith Baumann, Felicitas Thol, et al.

(2011) 53rd ASH annual meeting and exposition : abstracts, program and personal scheduler.
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- Conference Paper
- C3
Refractory Cytopenia in Childhood (RCC) with normal karyotype is unlikely to progress to advanced MDS under a watch and wait strategy

Shinsuke Hirabayashi, Brigitte Strahm, Stephan Schwarz, Marco Zecca, Markus Schmugge, Michael Dworzak, Marry Van Den Heuvel-Eibrink, Henrik Hasle, Barbara De Moerloose (UGent) , Jan Stary, et al.

(2010) BLOOD. 116(21). p.1633-1634
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Myelodysplastic syndromes in adolescents: characteristics and clinical outcome

Marco Zecca, Peter Noellke, Eva Bergsträßer, Barbara De Moerloose (UGent) , Henrik Hasle, Susanne Matthes-Martin, Laura Sainati, Jan Stary, Brigitte Strahm, Marry M. Van Den Heuvel-Eibrink, et al.

(2009) BONE MARROW TRANSPLANTATION. 43(Suppl. 1). p.S57-S57

Academic Bibliography

Spontaneous remission and loss of monosomy 7 : a window of opportunity for young children with SAMD9L syndrome

Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome

Association of unbalanced translocation der(1;7) with germline GATA2 mutations

Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia

Therapy with low-dose azacitidine for MDS in children and young adults: a retrospective analysis of the EWOG-MDS study group

Impact of somatic mutations on the outcome of children and adolescents with therapy-related myelodysplastic syndrome

Prevalence, clinical characteristics and prognosis of GATA2-related myelodysplastic syndromes (MDS) in children and adolescents

Clonal mutational landscape of childhood myelodysplastic syndromes

Somatic genetic and epigenetic architecture of myelodysplastic syndromes arising from GATA2 deficiency

Reduced intensity conditioning for children with refractory cytopenia of childhood : results of the EWOG-MDS study SCT RX RIC 06

Juvenile myelomonocytic leukemia : five genes, how many subtypes?

Comparison of horse and rabbit antithymocyte globulin in immunosuppressive therapy for refractory cytopenia of childhood

Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML

Therapy-related myelodysplastic syndrome following treatment for childhood acute lymphoblastic leukemia: outcome of patients registered in the EWOG-MDS 98/06 studies

Aberrant DNA methylation characterizes juvenile myelomonocytic leukemia with poor outcome

Mutations of the spliceosome complex genes occur in adult patients but are very rare in children with myeloid neoplasia

Refractory Cytopenia in Childhood (RCC) with normal karyotype is unlikely to progress to advanced MDS under a watch and wait strategy

Myelodysplastic syndromes in adolescents: characteristics and clinical outcome

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