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J. Skokowa · SciRah

Researcher profile · Semantic Scholar

J. Skokowa

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J. Skokowa — researcher profile on SciRah

h-index: 30
Works: 197
Citations: 4,264

Most-cited papers

Severe congenital neutropenias
J. Skokowa, D. Dale, I. Touw, C. Zeidler +1 more
2017Nature Reviews Disease Primers268 citations Open access
Semantic Scholar
NAMPT signaling is critical for the proangiogenic activity of tumor‐associated neutrophils
E. Pylaeva, M. Harati, I. Spyra, S. Bordbari +11 more
2018International Journal of Cancer90 citations Open access
Semantic Scholar
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action
F. Fioredda, J. Skokowa, H. Tamary, M. Spanoudakis +13 more
2023HemaSphere81 citations Open access
Semantic Scholar
CRISPR/Cas9-mediated ELANE knockout enables neutrophilic maturation of primary hematopoietic stem and progenitor cells and induced pluripotent stem cells of severe congenital neutropenia patients
M. Nasri, M. Ritter, P. Mir, B. Dannenmann +18 more
2019Haematologica55 citations Open access
Semantic Scholar
The chemokine CXCL14 mediates platelet function and migration via direct interaction with CXCR4.
A. Witte, A. Rohlfing, B. Dannenmann, Valerie Dicenta +8 more
2020Cardiovascular Research46 citations
Semantic Scholar
Development of a First-in-Class Small-Molecule Inhibitor of the C-Terminal Hsp90 Dimerization
S. Bhatia, Lukas V Spanier, David Bickel, N. Dienstbier +22 more
2021ACS Central Science31 citations Open access
Semantic Scholar
SRP54 mutations induce Congenital Neutropenia via dominant-negative effects on XBP1 splicing.
Christoph Schürch, T. Schaefer, Joëlle S. Müller, Pauline Hanns +11 more
2020Blood27 citations Open access
Semantic Scholar
iPSC modeling of stage-specific leukemogenesis reveals BAALC as a key oncogene in severe congenital neutropenia.
B. Dannenmann, M. Klimiankou, B. Oswald, A. Solovyeva +20 more
2021Cell Stem Cell24 citations Open access
Semantic Scholar
LMO2 activation by deacetylation is indispensable for hematopoiesis and T-ALL leukemogenesis.
T. Morishima, Ann-Christin Krahl, M. Nasri, Yun Xu +20 more
2019Blood24 citations Open access
Semantic Scholar
Fluorescent labeling of CRISPR/Cas9 RNP for gene knockout in HSPCs and iPSCs reveals an essential role for GADD45b in stress response.
M. Nasri, P. Mir, B. Dannenmann, D. Amend +6 more
2019Blood Advances22 citations Open access
Semantic Scholar
CRISPR/Cas9n-mediated ELANE promoter editing for gene therapy of severe congenital neutropenia.
M. Nasri, M. Ritter, P. Mir, B. Dannenmann +10 more
2024Molecular Therapy20 citations Open access
Semantic Scholar
Ultra-Sensitive CSF3R Deep Sequencing in Patients With Severe Congenital Neutropenia
M. Klimiankou, Murat Uenalan, Siarhei Kandabarau, R. Nustede +5 more
2019Frontiers in Immunology20 citations Open access
Semantic Scholar
Human iPSC-based model of severe congenital neutropenia reveals elevated UPR and DNA damage in CD34+ cells preceding leukemic transformation.
B. Dannenmann, Azadeh Zahabi, P. Mir, B. Oswald +10 more
2019Experimental Hematology19 citations Open access
Semantic Scholar
New insights into the pathomechanism of cyclic neutropenia
P. Mir, M. Klimiankou, B. Findik, Karin Hähnel +4 more
2020Annals of the New York Academy of Sciences18 citations Open access
Semantic Scholar
NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells
Yun Xu, M. Nasri, B. Dannenmann, P. Mir +4 more
2020Stem cell research & therapeutics17 citations Open access
Semantic Scholar
Nicotinamide (vitamin B3) treatment improves response to G‐CSF in severe congenital neutropenia patients
E. Deordieva, O. Shvets, K. Voronin, A. Maschan +4 more
2021British Journal of Haematology15 citations Open access
Semantic Scholar
GM-CSF treatment is not effective in congenital neutropenia patients due to its inability to activate NAMPT signaling
Corinna Koch, Bardia Samareh, T. Morishima, P. Mir +4 more
2017Annals of Hematology15 citations
Semantic Scholar
A unique role of p53 haploinsufficiency or loss in the development of acute myeloid leukemia with FLT3-ITD mutation
Min Yang, Zeng-Kai Pan, Ke-Zhi Huang, G. Büsche +15 more
2021Leukemia14 citations Open access
Semantic Scholar
A zebrafish model for HAX1-associated congenital neutropenia
L. Doll, N. Aghaallaei, Advaita M. Dick, K. Welte +2 more
2020Haematologica13 citations Open access
Semantic Scholar
A topological refactoring design strategy yields highly stable granulopoietic proteins
J. Skokowa, Birte Hernandez Alvarez, M. Coles, M. Ritter +13 more
2022Nature Communications12 citations Open access
Semantic Scholar
CRISPR/Cas9 Genome Editing of Human-Induced Pluripotent Stem Cells Followed by Granulocytic Differentiation.
B. Dannenmann, M. Nasri, K. Welte, J. Skokowa
2020Methods in molecular biology12 citations
Semantic Scholar
Old drug revisited: disulfiram, NETs, and sepsis.
M. Klimiankou, J. Skokowa
2021Blood11 citations
Semantic Scholar
Design of novel granulopoietic proteins by topological rescaffolding
Birte Hernandez Alvarez, J. Skokowa, M. Coles, P. Mir +8 more
2020PLoS Biology11 citations Open access
Semantic Scholar
Lentiviral gene therapy and vitamin B3 treatment enable granulocytic differentiation of G6PC3-deficient induced pluripotent stem cells
D. Hoffmann, J. Kuehle, Daniela Lenz, F. Philipp +8 more
2020Gene Therapy10 citations
Semantic Scholar
European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet‐INNOCHRON COST Action based on a systematic evidence review
F. Fioredda, M. Spanoudakis, J. Skokowa, H. Tamary +17 more
2025HemaSphere9 citations Open access
Semantic Scholar
Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients
C. Schroeder, U. Faust, Luisa Krauße, Alexandra Liebmann +24 more
2023European Journal of Human Genetics8 citations Open access
Semantic Scholar
Cooperating, congenital neutropenia–associated Csf3r and Runx1 mutations activate pro-inflammatory signaling and inhibit myeloid differentiation of mouse HSPCs
M. Ritter, M. Klimiankou, O. Klimenkova, A. Schambach +6 more
2020Annals of Hematology8 citations Open access
Semantic Scholar
A JAGN1-associated severe congenital neutropenia zebrafish model revealed an altered G-CSFR signaling and UPR activation
L. Doll, Karl Welte, J. Skokowa, B. Bajoghli
2024Blood Advances7 citations Open access
Semantic Scholar
Regenerative medicine meets translational oncology: Modeling leukemic bone marrow niche
Natalia Borbarán-Bravo, P. Arreba-Tutusaus, M. Ritter, M. Nasri +2 more
2022Cell Reports Medicine6 citations Open access
Semantic Scholar
The design of functional proteins using tensorized energy calculations
Kateryna Maksymenko, Andreas Maurer, N. Aghaallaei, Caroline Barry +8 more
2023Cell Reports Methods5 citations Open access
Semantic Scholar
HAX1‐related congenital neutropenia: Long‐term observation in paediatric and adult patients enrolled in the European branch of the Severe Chronic Neutropenia International Registry (SCNIR)
D. Pogozhykh, Deniz Yılmaz Karapınar, M. Klimiankou, N. Gerschmann +10 more
2023British Journal of Haematology5 citations Open access
Semantic Scholar
Differential transcriptional control of hematopoiesis in congenital and cyclic neutropenia patients harboring ELANE mutations
Alexander Zeidler, Natalia Borbarán-Bravo, B. Dannenmann, M. Ritter +8 more
2023Haematologica4 citations Open access
Semantic Scholar
Generation, expansion, and drug treatment of hematopoietic progenitor cells derived from human iPSCs
B. Dannenmann, J. Skokowa
2022STAR Protocols4 citations Open access
Semantic Scholar
Circumventing Mutation to Nix Neutropenia.
J. Skokowa
2021New England Journal of Medicine4 citations
Semantic Scholar
Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON Action
H. Papadaki, I. Mavroudi, Antonio M. Almeida, J. Bux +14 more
2020HemaSphere4 citations Open access
Semantic Scholar
Tuning of granulopoietic signaling by de novo designed agonists
Timo Ullrich, Christoph Pollmann, M. Ritter, Jérémy Haaf +15 more
2024bioRxiv3 citations Open access
Semantic Scholar
Chronic neutropenic colitis with complete colonic obstruction in a patient with severe congenital neutropenia associated with G6PC3 mutations
T. Nikolouzakis, K. Spyridakis, M. Tzardi, G. Tsaknakis +5 more
2022Annals of Hematology3 citations
Semantic Scholar
CLPB in neutropenia: 1 gene with many faces.
C. Lengerke, J. Skokowa
2022Blood3 citations Open access
Semantic Scholar
102 Patients with Primary Autoimmune Neutropenia : An Analysis of the European Severe Chronic Neutropenia International Registry (SCNIR)
Fabian Frömling, S. Mellor-Heineke, N. Gerschmann, Lena Röbbel +3 more
2019Blood3 citations Open access
Semantic Scholar
Efficient Correction of ELANE mutations in Primary HSPCs of Severe Congenital Neutropenia Patients Using CRISPR/Cas9 and rAVV6 HDR Repair Templates
M. Ritter, Benjamin Secker, M. Klimiankou, M. Nasri +9 more
2019Blood3 citations Open access
Semantic Scholar
Genotype-Phenotype Correlations in Patients with Severe Chronic Neutropenia Harboring ELANE Mutations: A Long-Term Study of the Severe Chronic Neutropenia International Registry
Ivan Tesakov, V. Makaryan, A. Bolyard, M. Klimiankou +10 more
2024Blood2 citations Open access
Semantic Scholar
Gene Knockout in Hematopoietic Stem and Progenitor Cells Followed by Granulocytic Differentiation.
P. Mir, M. Ritter, K. Welte, J. Skokowa +1 more
2020Methods in molecular biology2 citations
Semantic Scholar
Efficient Correction of HAX1 Mutations in Primary HSPCs of Severe Congenital Neutropenia Patients Using CRISPR/CAS9 GENE-Editing
M. Ritter, Benjamin Secker, M. Nasri, M. Klimiankou +9 more
20202 citations
Semantic Scholar
Response to High Dose G-CSF Treatment (20µg/kg/d or Higher) of Patients with Congenital Neutropenia: An Analysis By the Scnir in Europe
C. Zeidler, N. Gerschmann, S. Mellor-Heineke, Fabian Frömling +2 more
2019Blood2 citations
Semantic Scholar
Identification of GFI1 mutations in adult patients with congenital neutropenia
E. Boutakoglou, M. Klimiankou, G. Tsaknakis, Elias Drakos +2 more
2022Annals of Hematology1 citations
Semantic Scholar
Accumulation of Specific Somatic Leukemia-Associated Mutations in Congenital Neutropenia Precedes Malignant Transformation - New Preconditions for Treatment Decisions
M. Klimiankou, Sergey Kandabarau, C. Zeidler, I. Steiert +4 more
2022Blood1 citations Open access
Semantic Scholar
A Zebrafish Model for Severe Congenital Neutropenia with Jagn1b-Deficiency
L. Doll, N. Aghaallaei, J. Skokowa, K. Welte +1 more
20201 citations Open access
Semantic Scholar
Heterozygous Mutations of Clpb As a Newly Identified and Frequent Cause of Severe Congenital Neutropenia
J. Warren, Peeradol Wattanasirakul, David H. Spencer, A. Locke +6 more
2019Blood1 citations Open access
Semantic Scholar
Mechanism of BAALC-Mediated Leukemogenesis Downstream of RUNX1-Mutations in Severe Congenital Neutropenia
B. Dannenmann, M. Klimiankou, B. Oswald, M. Ritter +6 more
2018Blood1 citations Open access
Semantic Scholar
Chronische Neutropenien im Kindesalter
J. Skokowa, C. Zeidler, Karl Welte
2018Monatsschrift Kinderheilkunde1 citations Open access
Semantic Scholar

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M. Klimiankou×22
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