Julia Skokowa

5.6k total citations · 2 hit papers
107 papers, 3.5k citations indexed

About

Julia Skokowa is a scholar working on Genetics, Oncology and Immunology. According to data from OpenAlex, Julia Skokowa has authored 107 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Genetics, 48 papers in Oncology and 41 papers in Immunology. Recurrent topics in Julia Skokowa's work include Blood disorders and treatments (68 papers), Neutropenia and Cancer Infections (40 papers) and Immunodeficiency and Autoimmune Disorders (25 papers). Julia Skokowa is often cited by papers focused on Blood disorders and treatments (68 papers), Neutropenia and Cancer Infections (40 papers) and Immunodeficiency and Autoimmune Disorders (25 papers). Julia Skokowa collaborates with scholars based in Germany, United States and Netherlands. Julia Skokowa's co-authors include Karl Welte, Cornelia Zeidler, Martin Stanulla, Axel Schambach, Manuela Germeshausen, Gunnar Cario, Rudolf Grosschedl, Murat Uenalan, Matthias Eder and Michaela Scherr and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Julia Skokowa

97 papers receiving 3.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia

2006 964 citations Julia Skokowa, Gunnar Cario et al. profile →
Neutrophils: Between Host Defence, Immune Modulation, and Tissue Injury

2015 495 citations Julia Skokowa et al. profile →

Peers

Countries citing papers authored by Julia Skokowa

Since Specialization

Citations

This map shows the geographic impact of Julia Skokowa's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Julia Skokowa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julia Skokowa more than expected).

Fields of papers citing papers by Julia Skokowa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julia Skokowa. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Julia Skokowa. The network helps show where Julia Skokowa may publish in the future.

Co-authorship network of co-authors of Julia Skokowa

This figure shows the co-authorship network connecting the top 25 collaborators of Julia Skokowa. A scholar is included among the top collaborators of Julia Skokowa based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Julia Skokowa. Julia Skokowa is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A Complementarity‐Based Approach to De Novo Binder Design 2025 ·Advanced Science ·(unknown), (unknown), M.P. Coles, Narges Aghaallaei, (unknown), (unknown), (unknown), Philip Bucher, (unknown), Joana Pereira, Marcus D. Hartmann, Ghazaleh Tabatabai, Judith Feucht, Stefan Liebau, Patrick Müller, Andrei N. Lupas, Julia Skokowa, (unknown)	0
2	Expanding the genetic landscape of congenital neutropenia: <i>CXCR2</i> mutations in three families revealed through whole exome sequencing 2024 ·Haematologica ·Maksim Klimiankou, (unknown), Grigorios Tsaknakis, (unknown), Irene Mavroudi, (unknown), Marc Sturm, Julia Skokowa, Helen Α. Papadaki	1
3	Genotype-Phenotype Correlations in Patients with Severe Chronic Neutropenia Harboring ELANE Mutations: A Long-Term Study of the Severe Chronic Neutropenia International Registry 2024 ·Blood ·(unknown), Vahagn Makaryan, Audrey Anna Bolyard, Maksim Klimiankou, (unknown), (unknown), (unknown), (unknown), Akiko Shimamura, Peter E. Newburger, Julia Skokowa, Karl Welte, David C. Dale, Cornelia Zeidler	0
4	Comparison of Gene-Editing Approaches for Severe Congenital Neutropenia-Causing Mutations in the ELANE Gene 2024 ·The CRISPR Journal ·(unknown), (unknown), Benjamin Dannenmann, (unknown), (unknown), (unknown), Maksim Klimiankou, Karl Welte, Julia Skokowa	3
5	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 2023 ·HemaSphere ·Francesca Fioredda, Julia Skokowa, Hannah Tamary, (unknown), Piero Farruggia, António Almeida, (unknown), Petter Höglund, Peter E. Newburger, Jan Palmblad, Ivo P. Touw, Cornelia Zeidler, Alan J. Warren, David C. Dale, Karl Welte, Carlo Dufour, Helen Α. Papadaki	22
6	A topological refactoring design strategy yields highly stable granulopoietic proteins 2022 ·Nature Communications ·Julia Skokowa, Birte Hernandez Alvarez, M.P. Coles, (unknown), (unknown), (unknown), Narges Aghaallaei, Yun Xu, (unknown), (unknown), Katherine W. Rogers, (unknown), Baubak Bajoghli, Karl Welte, Andrei N. Lupas, Patrick Müller, (unknown)	9
7	SRP54mutations induce congenital neutropenia via dominant-negative effects onXBP1splicing 2020 ·Blood ·(unknown), Thorsten Schaefer, (unknown), Pauline Hanns, (unknown), (unknown), (unknown), Irmgard Sinning, Klemens Wild, Julia Skokowa, Karl Welte, Raphaël Carapito, Seiamak Bahram, Martina Konantz, Claudia Lengerke	15
8	Lentiviral gene therapy and vitamin B3 treatment enable granulocytic differentiation of G6PC3-deficient induced pluripotent stem cells 2020 ·Gene Therapy ·Dirk Hoffmann, Johannes Kuehle, (unknown), (unknown), Daniela Zychlinski, Nico Lachmann, Thomas Moritz, Doris Steinemann, Michael Morgan, Julia Skokowa, Christoph Klein, Axel Schambach	10
9	A zebrafish model for HAX1-associated congenital neutropenia 2020 ·Haematologica ·(unknown), Narges Aghaallaei, (unknown), Karl Welte, Julia Skokowa, Baubak Bajoghli	10
10	CBX7 a Regulator of Self-Renewal of Human Hscs and Novel Non-Canonical Interactions and Potential Therapeutic Opportunities in AML 2018 ·Experimental Hematology ·(unknown), Johannes Jung, Ellen Weersing, (unknown), Hein Schepers, Julia Skokowa, Raymond A. Poot, Leonid Bystrykh, Gerald de Haan	1
11	HAX1 Associated Congenital Neutropenia: A 25 Year Long-Term Analysis of the European Scnir Cohort 2017 ·Blood ·Cornelia Zeidler, (unknown), Maksim Klimiankou, Julia Skokowa, Karl Welte	1
12	BAALC Is a Key Mediator of Leukemia Development in Congenital Neutropenia 2017 ·Blood ·Benjamin Dannenmann, Maksim Klimiankou, (unknown), (unknown), (unknown), (unknown), (unknown), Christian Lindner, Tatsuya Morishima, Doris Steinemann, Cornelia Zeidler, Lothar Kanz, Karl Welte, Julia Skokowa	1
13	Effects of CSF3R mutations on Myeloid Differentiation and Proliferation of Hematopoietic Cells of Congenital Neutropenia Patients 2017 ·Blood ·Maksim Klimiankou, Benjamin Dannenmann, (unknown), (unknown), (unknown), Cornelia Zeidler, (unknown), Lothar Kanz, Julia Skokowa, Karl Welte	1
14	Large-Scale Hematopoietic Differentiation of Human Induced Pluripotent Stem Cells Provides Granulocytes or Macrophages for Cell Replacement Therapies 2015 ·Stem Cell Reports ·Nico Lachmann, Mania Ackermann, Eileen Frenzel, (unknown), Sebastian Brennig, Christine Happle, Dirk Hoffmann, Olga Klimenkova, (unknown), (unknown), Mark Kühnel, Axel Schambach, Sabina Janciauskiene, Constança Figueiredo, Gesine Hansen, Julia Skokowa, Thomas Moritz	145
15	TCIRG1-Associated Congenital Neutropenia 2014 ·Human Mutation ·Vahagn Makaryan, Elisabeth A. Rosenthal, Audrey Anna Bolyard, Merideth L. Kelley, Jennifer E. Below, Michael J. Bamshad, (unknown), Joshua D. Smith, Kati J. Buckingham, Laurence A. Boxer, Julia Skokowa, Karl Welte, Deborah A. Nickerson, Gail P. Jarvik, David C. Dale	30
16	NAMPT pathway is involved in the FOXO3a-mediated regulation of GADD45A expression 2012 ·Biochemical and Biophysical Research Communications ·Basant Kumar Thakur, (unknown), (unknown), Chandra Prakash, Julia Skokowa, Karl Welte	19
17	Dysregulation of Myeloid‐specific Transcription Factors in Congenital Neutropenia 2009 ·Annals of the New York Academy of Sciences ·Julia Skokowa, Karl Welte	25
18	Thrombopoietin Regulates Differentiation of Rhesus Monkey Embryonic Stem Cells to Hematopoietic Cells 2005 ·Annals of the New York Academy of Sciences ·Zheng Wang, Julia Skokowa, (unknown), Matthias Ballmaier, Karl Welte	10
19	Heterogeneous expression pattern of pro‐ and anti‐apoptotic factors in myeloid progenitor cells of patients with severe congenital neutropenia treated with granulocyte colony‐stimulating factor 2005 ·British Journal of Haematology ·Gunnar Cario, Julia Skokowa, Zheng Wang, Vesna Bucan, Cornelia Zeidler, Martin Stanulla, Martin Schrappe, Karl Welte	15
20	FcγRIII-Mediated Production of TNF-α Induces Immune Complex Alveolitis Independently of CXC Chemokine Generation 2001 ·The Journal of Immunology ·(unknown), Julia Skokowa, Ulrich Baumann, Thomas Tschernig, (unknown), Bernhard Nieswandt, Reinhold Schmidt, J. Engelbert Gessner	44

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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