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Journal Articles

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

Ilenia Simeoni, Jonathan C. Stephens, Fengyuan Hu, Sri V. V. Deevi, Karyn Megy, Tadbir K. Bariana, Claire Lentaigne, Sol Schulman, Suthesh Sivapalaratnam, Minka J. A. Vries, Sarah K. Westbury, Daniel Greene, Sofia Papadia, Marie-Christine Alessi, Antony P. Attwood, Matthias Ballmaier, Gareth Baynam, Emilse Bermejo, Marta Bertoli, Paul F. Bray, Loredana Bury, Marco Cattaneo, Peter Collins, Louise C. Daugherty, Rémi Favier, Deborah L. French, Bruce Furie, Michael Gattens, Manuela Germeshausen, Cedric Ghevaert, Anne C. Goodeve, Jose A. Guerrero, Daniel J. Hampshire, Daniel P. Hart, Johan W. M. Heemskerk, Yvonne M. C. Henskens, Marian Hill, Nancy Hogg, Jennifer D. Jolley, Walter H. Kahr, Anne M. Kelly, Ron Kerr, Myrto Kostadima, Shinji Kunishima, Michele P. Lambert, Ri Liesner, José A. López, Rutendo P. Mapeta, Mary Mathias, Carolyn M. Millar, Amit Nathwani, Marguerite Neerman-Arbez, Alan T. Nurden, Paquita Nurden, Maha Othman, Kathelijne Peerlinck, David J. Perry, Pawan Poudel, Pieter Reitsma, Matthew T. Rondina, Peter A. Smethurst, William Stevenson, Artur Szkotak, Salih Tuna, Christel van Geet, Deborah Whitehorn, David A. Wilcox, Bin Zhang, Shoshana Revel-Vilk, Paolo Gresele, Daniel B. Bellissimo, Christopher J. Penkett, Michael A. Laffan, Andrew D. Mumford, Augusto Rendon, Keith Gomez, Kathleen Freson, Willem H. Ouwehand, Ernest Turro

Blood (2016) 127 (23): 2791–2803.

https://doi.org/10.1182/blood-2015-12-688267

Published: 2016

Includes: Supplemental data

Journal Articles

Lentiviral gene transfer regenerates hematopoietic stem cells in a mouse model for Mpl-deficient aplastic anemia

Dirk Heckl, Daniel C. Wicke, Martijn H. Brugman, Johann Meyer, Axel Schambach, Guntram Büsche, Matthias Ballmaier, Christopher Baum, Ute Modlich

Blood (2011) 117 (14): 3737–3747.

https://doi.org/10.1182/blood-2010-09-308262

Published: 2011

Includes: Supplemental data

Journal Articles

Multiple extrathymic precursors contribute to T-cell development with different kinetics

Namita Saran, Marcin Łyszkiewicz, Jens Pommerencke, Katrin Witzlau, Ramin Vakilzadeh, Matthias Ballmaier, Harald von Boehmer, Andreas Krueger

Blood (2010) 115 (6): 1137–1144.

https://doi.org/10.1182/blood-2009-07-230821

Published: 2010

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

Biclonal expansion and heterogeneous lineage involvement in a case of chronic myeloproliferative disease with concurrent MPL W515L /JAK2 V617F mutation

Kais Hussein, Oliver Bock, Katharina Theophile, Jerome Schlue, Matthias Ballmaier, Nicolaus Kröger, Gudrun Göhring, Guntram Büsche, Hans Kreipe

Blood (2009) 113 (6): 1391–1392.

https://doi.org/10.1182/blood-2008-01-136499

Published: 2009

Includes: Supplemental data

Journal Articles

In vivo expansion of cells expressing acquired CSF3R mutations in patients with severe congenital neutropenia

Manuela Germeshausen, Karl Welte, Matthias Ballmaier

Blood (2009) 113 (3): 668–670.

https://doi.org/10.1182/blood-2008-09-178087

Published: 2009

Includes: Supplemental data

Journal Articles

Ectopic Expression of the Extracellular Domain of Mpl Is Sufficient to Induce a Hematopoietic Population Crisis

Daniel C. Wicke, Johann Meyer, Guntram Büsche, MD, Hans Kreipe, MD, Zhixiong Li, MD, Karl Welte, Matthias Ballmaier, Christopher Baum, Ute Modlich

Blood (2008) 112 (11): 2886.

https://doi.org/10.1182/blood.V112.11.2886.2886

Published: 2008

Journal Articles

Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations

Manuela Germeshausen, Magda Grudzien, Cornelia Zeidler, Hengameh Abdollahpour, Sevgi Yetgin, Nima Rezaei, Matthias Ballmaier, Bodo Grimbacher, Karl Welte, Christoph Klein

Blood (2008) 111 (10): 4954–4957.

https://doi.org/10.1182/blood-2007-11-120667

Published: 2008

Journal Articles

Serial Analysis of Hematopoietic Progenitors in Mpl −/− Mice.

Janet Kaffanke, PhD, Manuela Germeshausen, PhD, Karl Welte, MD, Matthias Ballmaier, PhD

Blood (2007) 110 (11): 2100.

https://doi.org/10.1182/blood.V110.11.2100.2100

Published: 2007

Journal Articles

In Vivo Growth Advantage of Cells Expressing Acquired CSF3R Mutations in Patients with Severe Congenital Neutropenia.

Manuela Germeshausen, PhD, Matthias Ballmaier, PhD, Karl Welte, MD

Blood (2007) 110 (11): 3296.

https://doi.org/10.1182/blood.V110.11.3296.3296

Published: 2007

Journal Articles

The angiogenic factor CCN1 promotes adhesion and migration of circulating CD34 + progenitor cells: potential role in angiogenesis and endothelial regeneration

Karsten Grote, Gustavo Salguero, Matthias Ballmaier, Marc Dangers, Helmut Drexler, Bernhard Schieffer

Blood (2007) 110 (3): 877–885.

https://doi.org/10.1182/blood-2006-07-036202

Published: 2007

Includes: Supplemental data

Journal Articles

Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: results of a long-term survey

Manuela Germeshausen, Matthias Ballmaier, Karl Welte

Blood (2006) 109 (1): 93–99.

https://doi.org/10.1182/blood-2006-02-004275

Published: 2006

Includes: Supplemental data

Journal Articles

c-mpl Mutations in Congenital Amegakaryocytic Thrombocytopenia: Residual TPO Receptor Activity in Patients of Group CAMT II.

Matthias Ballmaier, PhD, Karl Welte, MD, Manuela Germeshausen, PhD

Blood (2005) 106 (11): 2157.

https://doi.org/10.1182/blood.V106.11.2157.2157

Published: 2005

Journal Articles

RAS and G-CSF Receptor Mutations Are Mutually Exclusive in Leukemogenesis in Severe Congenital Neutropenia.

Manuela Germeshausen, PhD, Chris Kratz, MD, Matthias Ballmaier, PhD, Kevin M. Shannon, MD, Karl Welte, MD

Blood (2005) 106 (11): 3073.

https://doi.org/10.1182/blood.V106.11.3073.3073

Published: 2005

Journal Articles

Congenital Amegakaryocytic Thrombocytopenia (CAMT): A Detailed Clinical Analysis of 21 Cases Reveals Different Types of CAMT.

Stephanie King, Manuela Germeshausen, Gabriele Strauss, Karl Welte, Matthias Ballmaier

Blood (2004) 104 (11): 740.

https://doi.org/10.1182/blood.V104.11.740.740

Published: 2004

Journal Articles

Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia

Manuela Germeshausen, Matthias Ballmaier, Harald Schulze, Karl Welte, Thomas Flohr, Klaus Beiske, Ingebjørg Storm-Mathisen, Tore G. Abrahamsen

Blood (2001) 97 (3): 829–830.

https://doi.org/10.1182/blood.V97.3.829

Published: 2001

Journal Articles

c- mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia

Matthias Ballmaier, Manuela Germeshausen, Harald Schulze, Klara Cherkaoui, Sabine Lang, Annika Gaudig, Stephanie Krukemeier, Martin Eilers, Gabriele Strauß, Karl Welte

Blood (2001) 97 (1): 139–146.

https://doi.org/10.1182/blood.V97.1.139

Published: 2001

Journal Articles

Thrombopoietin in Patients With Congenital Thrombocytopenia and Absent Radii: Elevated Serum Levels, Normal Receptor Expression, But Defective Reactivity to Thrombopoietin

Matthias Ballmaier, Harald Schulze, Gabriele Strauβ, Klara Cherkaoui, Nicole Wittner, Stefanie Lynen, Susanne Wolters, Jakob Bogenberger, Karl Welte

Blood (1997) 90 (2): 612–619.

https://doi.org/10.1182/blood.V90.2.612

Published: 1997

Journal Articles

Downregulation of c- kit Expression in Human Endothelial Cells by Inflammatory Stimuli

Andrea König, Selim Corbacioglu, Matthias Ballmaier, Karl Welte

Blood (1997) 90 (1): 148–155.

https://doi.org/10.1182/blood.V90.1.148

Published: 1997

NARROW

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

Lentiviral gene transfer regenerates hematopoietic stem cells in a mouse model for Mpl-deficient aplastic anemia

Multiple extrathymic precursors contribute to T-cell development with different kinetics

RAS and CSF3R mutations in severe congenital neutropenia

Biclonal expansion and heterogeneous lineage involvement in a case of chronic myeloproliferative disease with concurrent MPL W515L /JAK2 V617F mutation

In vivo expansion of cells expressing acquired CSF3R mutations in patients with severe congenital neutropenia

Ectopic Expression of the Extracellular Domain of Mpl Is Sufficient to Induce a Hematopoietic Population Crisis

Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations

Serial Analysis of Hematopoietic Progenitors in Mpl −/− Mice.

In Vivo Growth Advantage of Cells Expressing Acquired CSF3R Mutations in Patients with Severe Congenital Neutropenia.

The angiogenic factor CCN1 promotes adhesion and migration of circulating CD34 + progenitor cells: potential role in angiogenesis and endothelial regeneration

Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: results of a long-term survey

c-mpl Mutations in Congenital Amegakaryocytic Thrombocytopenia: Residual TPO Receptor Activity in Patients of Group CAMT II.

RAS and G-CSF Receptor Mutations Are Mutually Exclusive in Leukemogenesis in Severe Congenital Neutropenia.

Congenital Amegakaryocytic Thrombocytopenia (CAMT): A Detailed Clinical Analysis of 21 Cases Reveals Different Types of CAMT.

Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia

c- mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia

Thrombopoietin in Patients With Congenital Thrombocytopenia and Absent Radii: Elevated Serum Levels, Normal Receptor Expression, But Defective Reactivity to Thrombopoietin

Downregulation of c- kit Expression in Human Endothelial Cells by Inflammatory Stimuli

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American Society of Hematology

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ASH Publications

American Society of Hematology

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