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Journal Articles

Transient Monosomy 7 Is a Rare Event in Young Children with SAMD9L Syndrome

Blood (2022) 140 (Supplement 1): 8678–8679.

https://doi.org/10.1182/blood-2022-159221

Published: 2022

Journal Articles

Inherited Disorders of the Ras-MAPK Pathway

Christian P. Kratz, MD, Martin Zenker, MD

Blood (2018) 132 (Supplement 1): SCI-41.

https://doi.org/10.1182/blood-2018-99-109379

Published: 2018

Journal Articles

Genome-Wide Association Study (GWAS) of High-Risk Minimal Residual Disease and Relapse in B-Cell Acute Lymphoblastic Leukemia on Trial AIEOP-BFM ALL 2000

Laura Hinze, Stefanie V. Junk, PhD, Norman Klein, Anja Moricke, MD, Gunnar Cario, MD, Christian P. Kratz, MD, Richard S Houlston, MD PhD, Claus R Bartam, MD, Rolf Koehler, PhD, Martin Zimmermann, PhD, Martin Schrappe, MD PhD, Martin Stanulla, MD PhD

Blood (2017) 130 (Supplement 1): 3981.

https://doi.org/10.1182/blood.V130.Suppl_1.3981.3981

Published: 2017

Journal Articles

TP53 , ETV6 and RUNX1 Germline Variants in Patients Developing Secondary Neoplasms after Treatment for Childhood Acute Lymphoblastic Leukemia

Stefanie V. Junk, PhD, Norman Klein, Sabine Schreek, Martin Zimmermann, PhD, Anja Möricke, MD, Kirsten Bleckmann, Gunnar Cario, MD, Martin Schrappe, MD PhD, Christian P. Kratz, MD, Martin Stanulla, MD PhD

Blood (2017) 130 (Supplement 1): 884.

https://doi.org/10.1182/blood.V130.Suppl_1.884.884

Published: 2017

Journal Articles

SCT for Secondary AML in a Patient with Glycogen Storage Disease Type 1b

Cornelia Zeidler, MD, Kinan Kafa, Martin G. Sauer, MD, Britta Maecker-Kolhoff, Johann Greil, MD, Karl Welte, MD, Christian P Kratz, MD, Karl-Walter Sykora

Blood (2012) 120 (21): 4402.

https://doi.org/10.1182/blood.V120.21.4402.4402

Published: 2012

Journal Articles

RAS and CSF3R mutations in severe congenital neutropenia

Manuela Germeshausen, Christian P. Kratz, Matthias Ballmaier, Karl Welte

Blood (2009) 114 (16): 3504–3505.

https://doi.org/10.1182/blood-2009-07-232512

Published: 2009

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

Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations

Christian Flotho, Christian P. Kratz, Eva Bergsträsser, Henrik Hasle, Jan Starý, Monika Trebo, Marry M. van den Heuvel-Eibrink, Dorota Wójcik, Marco Zecca, Franco Locatelli, Charlotte M. Niemeyer

Blood (2008) 111 (2): 966–967.

https://doi.org/10.1182/blood-2007-09-111831

Published: 2008

Journal Articles

Novel Germ Line Mutations in the KRAS2 Gene Cause Noonan Syndrome and Deregulate Hematopoietic Cell Growth.

Suzanne Schubbert, Martin Zenker, MD, Sara L. Rowe, Silke Böll, Cornelia Klein, Ineke van der Burgt, MD, Luciana Musante, PhD, Hoa Nguyen, Brian West, PhD, Gideon Bollag, PhD, Charlotte M. Niemeyer, MD, Kevin M. Shannon, MD, Christian P. Kratz, MD

Blood (2005) 106 (11): 1602.

https://doi.org/10.1182/blood.V106.11.1602.1602

Published: 2005

Journal Articles

The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease

Christian P. Kratz, Charlotte M. Niemeyer, Robert P. Castleberry, Mualla Cetin, Eva Bergsträsser, Peter D. Emanuel, Henrik Hasle, Gabriela Kardos, Cornelia Klein, Seiji Kojima, Jan Stary, Monika Trebo, Marco Zecca, Bruce D. Gelb, Marco Tartaglia, Mignon L. Loh

Blood (2005) 106 (6): 2183–2185.

https://doi.org/10.1182/blood-2005-02-0531

Published: 2005

Journal Articles

PTPN11 Mutational Spectrum in Juvenile Myelomonocytic Leukemia and Noonan Syndrome.

Christian P. Kratz, MD, Charlotte M. Niemeyer, MD, Bruce D. Gelb, MD, Marco Tartaglia, PhD, Mignon L. Loh, MD

Blood (2004) 104 (11): 3417.

https://doi.org/10.1182/blood.V104.11.3417.3417

Published: 2004

Journal Articles

Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor

Christian P. Kratz, Brooke M. Emerling, Jeannette Bonifas, Winfred Wang, Eric D. Green, Michelle M. Le Beau, Kevin M. Shannon

Blood (2002) 99 (1): 372–374.

https://doi.org/10.1182/blood.V99.1.372

Published: 2002

NARROW

Transient Monosomy 7 Is a Rare Event in Young Children with SAMD9L Syndrome

Inherited Disorders of the Ras-MAPK Pathway

Genome-Wide Association Study (GWAS) of High-Risk Minimal Residual Disease and Relapse in B-Cell Acute Lymphoblastic Leukemia on Trial AIEOP-BFM ALL 2000

TP53 , ETV6 and RUNX1 Germline Variants in Patients Developing Secondary Neoplasms after Treatment for Childhood Acute Lymphoblastic Leukemia

SCT for Secondary AML in a Patient with Glycogen Storage Disease Type 1b

RAS and CSF3R mutations in severe congenital neutropenia

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

Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations

Novel Germ Line Mutations in the KRAS2 Gene Cause Noonan Syndrome and Deregulate Hematopoietic Cell Growth.

The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease

PTPN11 Mutational Spectrum in Juvenile Myelomonocytic Leukemia and Noonan Syndrome.

Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor

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American Society of Hematology

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American Society of Hematology

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