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Journal Articles

UBTF tandem Duplications Account for a Third of Advanced Pediatric MDS without Genetic Predisposition to Myeloid Neoplasia

Blood (2022) 140 (Supplement 1): 1355–1356.

https://doi.org/10.1182/blood-2022-159002

Published: 2022

Journal Articles

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

Blood (2021) 138 (23): 2441–2445.

https://doi.org/10.1182/blood.2021012781

Published: 2021

Includes: Supplemental data

Journal Articles

Hematological Presentation and Change in Clinical Phenotype during Follow-up in Pearson Syndrome

Ayami Yoshimi, MD PhD, Sarah C Grünert, MD, Holger Cario, MD PhD, Ute Gross-Wieltsch, MD, Udo Kontny, MD, Kyogo Suzuki, MD PhD, Stephan Lobitz, MD, Helen Wagner, MD, Irene Schmid, MD, Daniela Karall, MD, Arndt Borkhardt, MD, Miriam Erlacher, Peter Noellke, MPH, Charlotte M. Niemeyer, MD

Blood (2019) 134 (Supplement_1): 3746.

https://doi.org/10.1182/blood-2019-125199

Published: 2019

Journal Articles

Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Children and Adolescents with GATA2-Related Myelodysplastic Syndrome

Blood (2019) 134 (Supplement_1): 2033.

https://doi.org/10.1182/blood-2019-122403

Published: 2019

Journal Articles

SAMD9 and SAMD9L Germline Disorders in Patients Enrolled in Studies of the European Working Group of MDS in Childhood (EWOG-MDS): Prevalence, Outcome, Phenotype and Functional Characterisation

Blood (2018) 132 (Supplement 1): 643.

https://doi.org/10.1182/blood-2018-99-118389

Published: 2018

Journal Articles

Impact of Somatic Mutations on the Outcome of Children and Adolescents with Therapy-Related Myelodysplastic Syndrome

Blood (2016) 128 (22): 3162.

https://doi.org/10.1182/blood.V128.22.3162.3162

Published: 2016

Journal Articles

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

Blood (2016) 127 (11): 1387–1397.

https://doi.org/10.1182/blood-2015-09-669937

Published: 2016

Includes: Supplemental data

Journal Articles

LIN28B overexpression defines a novel fetal-like subgroup of juvenile myelomonocytic leukemia

Blood (2016) 127 (9): 1163–1172.

https://doi.org/10.1182/blood-2015-09-667808

Published: 2016

Includes: Supplemental data

Journal Articles

Somatic Genetic and Epigenetic Architecture of Myelodysplastic Syndromes Arising from GATA2 Deficiency

Victor Bengt Pastor Loyola, MSc, Shinsuke Hirabayashi, MD, Sandra Pohl, PhD, Emilia J Kozyra, MSc, Albert Catala, MD, Barbara De Moerloose, MD PhD, Michael Dworzak, MD, Henrik Hasle, MD, Riccardo Masetti, MD, Markus Schmugge, MD, Owen Smith, Jan Starý, MD, Marek Ussowicz, MD, Marry M. van den Heuvel-Eibrink, MD PhD, Ester Mejstrikova, MD PhD, Ulrich Salzer, MD, Michael Lübbert, MD, Daniel Heudobler, MD, David Betts, MD, Jose Cervera, MD, Gudrun Göhring, MD, Oskar A. Haas, Olga Haus, MD, Kyra Michalova, PhD DSc, Francesco Pasquali, MD, Joelle Tchinda, MD, Nadine van Roy, MD, Brigitte Schlegelberger, MD Prof., H. Berna Beverloo, PhD, Peter Noellke, MSc, Ayami Yoshimi, MD, Franco Locatelli, Prof, MD PhD, Brigitte Strahm, MD, Jaroslaw P. Maciejewski, MD PhD, Michael Rehli, PhD, Charlotte M Niemeyer, Prof, MD, Marcin W Wlodarski, MD

Blood (2015) 126 (23): 299.

https://doi.org/10.1182/blood.V126.23.299.299

Published: 2015

Journal Articles

Recurrent 6pLOH Is the Most Common Somatic Lesion in Refractory Cytopenia of Childhood and Occurs Very Infrequently in Severe Aplastic Anemia

Marcin W Wlodarski, Shinsuke Hirabayashi, Brigitte Strahm, Sandra Urbaniak, Brigitte Schlegelberger, Ingrid Furlan, Alexandra Fischer, Wilfried Truckenmüller, Ayami Yoshimi-Noellke, Peter Noellke, Irith Baumann, Charlotte M Niemeyer

Blood (2012) 120 (21): 644.

https://doi.org/10.1182/blood.V120.21.644.644

Published: 2012

Journal Articles

JMML Revisited: Role Und Outcome of Hematopoietic Stem Cell Transplantation in Subtypes of Juvenile Myelomonocytic Leukemia (JMML)

Blood (2012) 120 (21): 955.

https://doi.org/10.1182/blood.V120.21.955.955

Published: 2012

Journal Articles

Analysis of Ribosomal Protein Genes Associated with Diamond Blackfan Anemia (DBA) In German DBA Patients and Their Relatives

Jessica Moetter, Ph.D., Mutlu Kartal, M.D., Joerg Meerpohl, M.D., Alexandra Fischer, Thorsten Simon, Prof. Dr., Sandra Urbaniak, Shinsuke Hirabayashi, Friedrich Kapp, M.D., Peter Noellke, MPH, Christian Kratz, MD, Charlotte M Niemeyer, Marcin W. Wlodarski, M.D.

Blood (2011) 118 (21): 729.

https://doi.org/10.1182/blood.V118.21.729.729

Published: 2011

Journal Articles

Identification of Novel Mutations In Ribosomal Genes In Patients with Diamond Blackfan Anemia (DBA) In Germany and Genotype-Phenotype Correlation Analysis

Mihaela Pali, M.A., Jessica Moetter, Ph.D., Joerg Meerpohl, M.D., Mutlu Kartal, M.D., Alexandra Fischer, Sandra Urbaniak, Peter Noellke, MPH, Manfred Fliegauf, Ph.D., Lydie M. Da Costa, M.D., Ph.D., Charlotte M Niemeyer, M.D., Marcin W. Wlodarski, M.D.

Blood (2010) 116 (21): 2244.

https://doi.org/10.1182/blood.V116.21.2244.2244

Published: 2010

Journal Articles

Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome

Blood (2010) 116 (19): 3766–3769.

https://doi.org/10.1182/blood-2010-04-280313

Published: 2010

Includes: Supplemental data

Journal Articles

Development of an allele-specific minimal residual disease assay for patients with juvenile myelomonocytic leukemia

Sophie Archambeault, Nikki J. Flores, Ayami Yoshimi, Christian P. Kratz, Miriam Reising, Alexandra Fischer, Peter Noellke, Franco Locatelli, Petr Sedlacek, Christian Flotho, Marco Zecca, Peter D. Emanuel, Robert P. Castleberry, Charlotte M. Niemeyer, Peter Bader, Mignon L. Loh

Blood (2008) 111 (3): 1124–1127.

https://doi.org/10.1182/blood-2007-06-093302

Published: 2008

Includes: Supplemental data

Journal Articles

A Complex Karyotype but Not Monosomy 7 Is an Independent Prognostic Factor in Advanced Childhood MDS.

Gudrun Gohring, Kyra Michalova, Berna Beverloo, David Betts, Jochen Harbott, Oskar Haas, Gitte Kerndrup, Laura Sainati, Eva Bergstraesser, Henrik Hasle, Jan Starý, Monika Trebo, Marry van den Heuvel-Eibrink, Marco Zecca, Alexandra Fischer, Peter Noellke, Franco Locatelli, Brigitte Schlegelberger, Charlotte M. Niemeyer

Blood (2007) 110 (11): 2452.

https://doi.org/10.1182/blood.V110.11.2452.2452

Published: 2007

Journal Articles

Hematopoietic Stem Cell Transplantation (HSCT) after a Myeloablative Conditioning Regimen in Children with Refractory Cytopenia (RC): Results of a Retrospective Analysis from the EWOG-MDS Group.

Franco Locatelli, Peter Noellke, Alexandra Fisher, Peter Bader, Maria Ester Bernardo, Eva Bergstraesser, Henrik Hasle, Marry van den Heuvel-Eibrink, Elisabeth Korthof, Jan Stary, Brigitte Strahm, Felix Zintl, Petr Sedlacek, Marco Zecca, Charlotte M. Niemeyer

Blood (2007) 110 (11): 251.

https://doi.org/10.1182/blood.V110.11.251.251

Published: 2007

Journal Articles

Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study

Blood (2007) 109 (11): 4641–4647.

https://doi.org/10.1182/blood-2006-10-051342

Published: 2007

Includes: Supplemental data

Journal Articles

Development of an Allele-Specific Minimal Residual Disease Assay for Patients with Juvenile Myelomonocytic Leukemia-Moving beyond Clinical Assessment.

Sophie Archambeault, Ayami Yoshimi, MD, Christian Kratz, MD, Miriam Reising, Alexandra Fischer, Peter Noellke, PhD, Franco Locatelli, MD, Petr Sedlacek, MD, Christian Flotho, MD, Marco Zecca, MD, Peter Dean Emanuel, MD, Robert Castleberry, MD, Charlotte Marie Niemeyer, MD, Peter Bader, MD, Mignon Loh, MD

Blood (2006) 108 (11): 2681.

https://doi.org/10.1182/blood.V108.11.2681.2681

Published: 2006

Journal Articles

Allogeneic Stem Cell Transplantation for Children with Advanced Primary MDS: Results from the EWOG-MDS Study Group Employing a Pre-Transplant Preparative Regimen with Busulfan, Cyclophosphamide and Melphalan.

Charlotte Marie Niemeyer, Marco Zecca, Elisabeth Korthoff, Ulrich Duffner, Felix Zintl, Wolfram Ebell, Jan Starý, Dagmar Dilloo, Christina Peters, Markus Schmugge, Petr Sedlacek, Chiara Messina, Marry van Heuvel, Eva Bergstraesser, Monika Trebo, Peter Noellke, Franco Locatelli

Blood (2004) 104 (11): 2300.

https://doi.org/10.1182/blood.V104.11.2300.2300

Published: 2004

NARROW

UBTF tandem Duplications Account for a Third of Advanced Pediatric MDS without Genetic Predisposition to Myeloid Neoplasia

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

Hematological Presentation and Change in Clinical Phenotype during Follow-up in Pearson Syndrome

Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Children and Adolescents with GATA2-Related Myelodysplastic Syndrome

SAMD9 and SAMD9L Germline Disorders in Patients Enrolled in Studies of the European Working Group of MDS in Childhood (EWOG-MDS): Prevalence, Outcome, Phenotype and Functional Characterisation

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 in children and adolescents

LIN28B overexpression defines a novel fetal-like subgroup of juvenile myelomonocytic leukemia

Somatic Genetic and Epigenetic Architecture of Myelodysplastic Syndromes Arising from GATA2 Deficiency

Recurrent 6pLOH Is the Most Common Somatic Lesion in Refractory Cytopenia of Childhood and Occurs Very Infrequently in Severe Aplastic Anemia

JMML Revisited: Role Und Outcome of Hematopoietic Stem Cell Transplantation in Subtypes of Juvenile Myelomonocytic Leukemia (JMML)

Analysis of Ribosomal Protein Genes Associated with Diamond Blackfan Anemia (DBA) In German DBA Patients and Their Relatives

Identification of Novel Mutations In Ribosomal Genes In Patients with Diamond Blackfan Anemia (DBA) In Germany and Genotype-Phenotype Correlation Analysis

Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome

Development of an allele-specific minimal residual disease assay for patients with juvenile myelomonocytic leukemia

A Complex Karyotype but Not Monosomy 7 Is an Independent Prognostic Factor in Advanced Childhood MDS.

Hematopoietic Stem Cell Transplantation (HSCT) after a Myeloablative Conditioning Regimen in Children with Refractory Cytopenia (RC): Results of a Retrospective Analysis from the EWOG-MDS Group.

Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study

Development of an Allele-Specific Minimal Residual Disease Assay for Patients with Juvenile Myelomonocytic Leukemia-Moving beyond Clinical Assessment.

Allogeneic Stem Cell Transplantation for Children with Advanced Primary MDS: Results from the EWOG-MDS Study Group Employing a Pre-Transplant Preparative Regimen with Busulfan, Cyclophosphamide and Melphalan.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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