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Journal Articles

HAX1 Associated Congenital Neutropenia: A 25 Year Long-Term Analysis of the European Scnir Cohort

Cornelia Zeidler, Sabine Mellor-Heineke, MD, Maksim Klimiankou, Julia Skokowa, Karl Welte, MD PhD

Blood (2017) 130 (Supplement 1): 3566.

https://doi.org/10.1182/blood.V130.Suppl_1.3566.3566

Published: 2017

Journal Articles

BAALC Is a Key Mediator of Leukemia Development in Congenital Neutropenia

Benjamin Dannenmann, Maksim Klimiankou, Anna Solovyeva, Azadeh Zahabi, MSc, Perihan Mir, Masoud Nasri, MSc, Regine Bernhard, Christian Lindner, Tatsuya Morishima, MD PhD, Doris Steinemann, PhD, Cornelia Zeidler, Lothar Kanz, Karl Welte, MD PhD, Julia Skokowa

Blood (2017) 130 (Supplement 1): 541.

https://doi.org/10.1182/blood.V130.Suppl_1.541.541

Published: 2017

Journal Articles

Effects of CSF3R mutations on Myeloid Differentiation and Proliferation of Hematopoietic Cells of Congenital Neutropenia Patients

Maksim Klimiankou, Benjamin Dannenmann, Anna Solovyeva, Regine Bernhard, Diana Amend, Cornelia Zeidler, Sabine Mellor-Heineke, MD, Lothar Kanz, Julia Skokowa, Karl Welte, MD PhD

Blood (2017) 130 (Supplement 1): 2278.

https://doi.org/10.1182/blood.V130.Suppl_1.2278.2278

Published: 2017

Journal Articles

Analysis of Leukemogenic Effects of RUNX1 and CSF3R Mutations Using Congenital Neutropenia (CN)/AML Patient-Derived Induced Pluripotent Stem Cells (iPSCs)

Benjamin Dannenmann, M.Sc., Maksim Klimiankou, PhD, Christian Lindner, B.Sc., Azadeh Zahabi, M.Sc., Regine Bernhard, Tatsuya Morishima, MD PhD, Cornelia Zeidler, MD, Lothar Kanz, MD, Karl Welte, MD, Julia Skokowa, MD PhD

Blood (2016) 128 (22): 404.

https://doi.org/10.1182/blood.V128.22.404.404

Published: 2016

Journal Articles

Evaluation of Genetic Mutations in Plasma Exosomes As a Biomarker Tool for Detecting the Clonal Evolution of Leukemic Cells in Pediatric AML

Fabienne Kunz, Katarina Reinhardt, PhD, Nils Von Neuhoff, PhD, Karl Welte, MD, Dirk Reinhardt, MD PhD, Basant Kumar Thakur, PhD

Blood (2016) 128 (22): 1711.

https://doi.org/10.1182/blood.V128.22.1711.1711

Published: 2016

Journal Articles

Impaired DNA Damage Repair in Severe Congenital Neutropenia Patients

Perihan Mir, Maksim Klimiankou, PhD, Benjamin Dannenmann, Cornelia Zeidler, MD, Klaus Schulze-Osthoff, PhD, Lothar Kanz, MD, Karl Welte, MD, Julia Skokowa, MD PhD

Blood (2016) 128 (22): 1334.

https://doi.org/10.1182/blood.V128.22.1334.1334

Published: 2016

Journal Articles

Termination and Frameshift Mutations in ELANE Are Associated with Adverse Outcomes in Patients with Severe Chronic Neutropenia

David C. Dale, MD, Vahagn Makaryan, MD, Merideth L. Kelley, MS, Audrey Anna Bolyard, RN, BS, Laurence A. Boxer, MD, Peter E. Newburger, MD, Mary Ann Bonilla, MD, Maksim Klimiankou, PhD, Julia Skokowa, MD PhD, Cornelia Zeidler, MD MPH, Karl Welte, MD

Blood (2016) 128 (22): 1326.

https://doi.org/10.1182/blood.V128.22.1326.1326

Published: 2016

Journal Articles

Optimization of CSF3R Mutation Detection in Severe Congenital Neutropenia and Cyclic Neutropenia Patients for Routine Diagnostics Using Next Generation Sequencing

Maksim Klimiankou, PhD, Cornelia Zeidler, MD, Sabine Mellor-Heineke, Ingeborg Steiert, Karin Haehnel, Karl Welte, MD PhD, Julia Skokowa, MD PhD

Blood (2016) 128 (22): 3685.

https://doi.org/10.1182/blood.V128.22.3685.3685

Published: 2016

Journal Articles

Thrombopoietin (TPO) Induces Hematopoietic Differentiation of Mouse ES Cells Via HIF-1 Alpha-Dependent Activation of a BMP4 Autoregulatory Loop

Azadeh Zahabi, Tatsuya Morishima, MD PhD, Andri Pramono, Dan Lan, Lothar Kanz, MD, Karl Welte, MD, Julia Skokowa, Prof. Dr.

Blood (2015) 126 (23): 1186.

https://doi.org/10.1182/blood.V126.23.1186.1186

Published: 2015

Journal Articles

SIRT2 Plays Essential Role in Early Hematopoiesis through Deacetylation of LMO2 Protein

Tatsuya Morishima, MD PhD, Regine Bernhard, Azadeh Zahabi, Benjamin Dannenmann, Masoud Nasri, M.Sc, Bardia Samareh, PhD, Lothar Kanz, Prof. Dr. MD, Karl Welte, MD, Julia Skokowa, Prof. Dr.

Blood (2015) 126 (23): 3574.

https://doi.org/10.1182/blood.V126.23.3574.3574

Published: 2015

Journal Articles

Differential Expression of Neutrophil Granule Protein Genes in Bone Marrow Myeloid Cells at the Peak and Nadir of Neutrophil Counts in Cyclic Neutropenia

Olga Klimenkova, PhD, Maksim Klimiankou, PhD, Lothar Kanz, MD, Cornelia Zeidler, MD, Karl Welte, MD, Julia Skokowa, Prof. Dr.

Blood (2015) 126 (23): 2194.

https://doi.org/10.1182/blood.V126.23.2194.2194

Published: 2015

Journal Articles

The Mechanism of Type I Interferon-Mediated Polarization of Tumor-Associated Neutrophils in Mice and Human

Lisa Andzinski, PhD, Mozhgan Dehghan Harati, Edyta Zyla, Nadine Kasnitz, Stephanie Stahnke, Ching-Fang Wu, MD PhD, Marcus Gereke, PhD, Maren von Köckritz-Blickwede, PhD, Bastian Schilling, MD, Sven Brandau, PhD, Lothar Kanz, MD, Karl Welte, MD, Siegfried Weiss, PhD, Julia Skokowa, Prof. Dr., Jadwiga Jablonska, PhD

Blood (2015) 126 (23): 644.

https://doi.org/10.1182/blood.V126.23.644.644

Published: 2015

Journal Articles

Understanding Neutropenia: The 20 Year Experience of the Severe Chronic Neutropenia International Registry (SCNIR)

David C. Dale, MD, Audrey Anna Bolyard, RN, BS, Cornelia Zeidler, MDMPH, Tracy M. Marrero, Laurence A. Boxer, MD, Peter E. Newburger, MD, Blanche P. Alter, MD MPH, PK Morrow, MD, Mary Ann Bonilla, MD, Yigal Dror, MD FRCP(C), Frank Firkin, MBBS PhDFRACP FRCPA, Sally Kinsey, MD, John E. Levine, MD MS, Daniel C. Link, MD, Lee Reeves, Philip S. Rosenberg, PhD, Akiko Shimamura, MD PhD, Karl Welte, MD

Blood (2014) 124 (21): 2730.

https://doi.org/10.1182/blood.V124.21.2730.2730

Published: 2014

Journal Articles

Mutations in the TNFRSF1A, CEBPE and ELANE genes in a Congenital Cyclic Neutropenia Patient: A New Syndrome?

Julia Skokowa, MD, PhD, Olga Klimenkova, Maksim Klimiankou, Siarhei Kandabarau, Marlene Reuter, Anna-Lena Hagemann, Karl Welte, MD

Blood (2012) 120 (21): 11.

https://doi.org/10.1182/blood.V120.21.11.11

Published: 2012

Journal Articles

Identification of New Leukemia Associated Gene Mutations by Whole Genome Sequencing of DNA From Two Siblings with Congenital Neutropenia and Secondary AML

Maksim Klimiankou, Siarhei Kandabarau, Marlene Reuter, Anna-Lena Hagemann, Cornelia Zeidler, MD, Karl Welte, MD, Julia Skokowa, MD, PhD

Blood (2012) 120 (21): 12.

https://doi.org/10.1182/blood.V120.21.12.12

Published: 2012

Journal Articles

Clinical Outcomes for Patients with Severe Chronic Neutropenia Due to Mutations in the Gene for Neutrophil Elastase, ELANE

Vahagn Makaryan, MD, Cornelia Zeidler, MD, Audrey Anna Bolyard, RN, BS, Julia Skokowa, MD, PhD, Merideth L. Kelley, BS, Laurence A. Boxer, MD, Mary Ann Bonilla, MD, Peter E. Newburger, MD, Akiko Shimamura, MD, PhD, Karl Welte, MD, David C. Dale, MD, for The Severe Chronic Neutropenia International Registry and Repository

Blood (2012) 120 (21): 3275.

https://doi.org/10.1182/blood.V120.21.3275.3275

Published: 2012

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

A Lack of Secretory Leukocyte Protease Inhibitor (SLPI) Causes Defects in Myeloid Differentiation

Olga Klimenkova, Wienke Ellerbeck, Ana Gigina, Karl Welte, MD, Julia Skokowa, MD, PhD

Blood (2012) 120 (21): 10.

https://doi.org/10.1182/blood.V120.21.10.10

Published: 2012

Journal Articles

RUNX1 Mutations Are the Most Frequent Leukemia Associated Mutations in Congenital Neutropenia Patients

Julia Skokowa, MD, PhD, Doris Steinemann, PhD, Vahagn Makaryan, MD, Maksim Klimiankou, Susanne Schnittger, PhD, Alexander Kohlmann, PhD, Brigitte Schlegelberger, Cornelia Zeidler, MD, David C. Dale, MD, Karl Welte, MD

Blood (2012) 120 (21): 7.

https://doi.org/10.1182/blood.V120.21.7.7

Published: 2012

Journal Articles

mRNA and Protein Expression Levels of Secretory Leukocyte Protease Inhibitor (SLPI) Are Severely Reduced in Patients with Severe Congenital Neutropenia (CN)

Wienke Ellerbeck, Olga Klimenkova, Julia Skokowa, MD, PhD, Karl Welte, MD

Blood (2011) 118 (21): 2165.

https://doi.org/10.1182/blood.V118.21.2165.2165

Published: 2011

NARROW

HAX1 Associated Congenital Neutropenia: A 25 Year Long-Term Analysis of the European Scnir Cohort

BAALC Is a Key Mediator of Leukemia Development in Congenital Neutropenia

Effects of CSF3R mutations on Myeloid Differentiation and Proliferation of Hematopoietic Cells of Congenital Neutropenia Patients

Analysis of Leukemogenic Effects of RUNX1 and CSF3R Mutations Using Congenital Neutropenia (CN)/AML Patient-Derived Induced Pluripotent Stem Cells (iPSCs)

Evaluation of Genetic Mutations in Plasma Exosomes As a Biomarker Tool for Detecting the Clonal Evolution of Leukemic Cells in Pediatric AML

Impaired DNA Damage Repair in Severe Congenital Neutropenia Patients

Termination and Frameshift Mutations in ELANE Are Associated with Adverse Outcomes in Patients with Severe Chronic Neutropenia

Optimization of CSF3R Mutation Detection in Severe Congenital Neutropenia and Cyclic Neutropenia Patients for Routine Diagnostics Using Next Generation Sequencing

Thrombopoietin (TPO) Induces Hematopoietic Differentiation of Mouse ES Cells Via HIF-1 Alpha-Dependent Activation of a BMP4 Autoregulatory Loop

SIRT2 Plays Essential Role in Early Hematopoiesis through Deacetylation of LMO2 Protein

Differential Expression of Neutrophil Granule Protein Genes in Bone Marrow Myeloid Cells at the Peak and Nadir of Neutrophil Counts in Cyclic Neutropenia

The Mechanism of Type I Interferon-Mediated Polarization of Tumor-Associated Neutrophils in Mice and Human

Understanding Neutropenia: The 20 Year Experience of the Severe Chronic Neutropenia International Registry (SCNIR)

Mutations in the TNFRSF1A, CEBPE and ELANE genes in a Congenital Cyclic Neutropenia Patient: A New Syndrome?

Identification of New Leukemia Associated Gene Mutations by Whole Genome Sequencing of DNA From Two Siblings with Congenital Neutropenia and Secondary AML

Clinical Outcomes for Patients with Severe Chronic Neutropenia Due to Mutations in the Gene for Neutrophil Elastase, ELANE

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

A Lack of Secretory Leukocyte Protease Inhibitor (SLPI) Causes Defects in Myeloid Differentiation

RUNX1 Mutations Are the Most Frequent Leukemia Associated Mutations in Congenital Neutropenia Patients

mRNA and Protein Expression Levels of Secretory Leukocyte Protease Inhibitor (SLPI) Are Severely Reduced in Patients with Severe Congenital Neutropenia (CN)

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American Society of Hematology

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ASH Publications

American Society of Hematology

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