Manuela Germeshausen

5.4k total citations · 1 hit paper
56 papers, 3.4k citations indexed

About

Manuela Germeshausen is a scholar working on Genetics, Immunology and Hematology. According to data from OpenAlex, Manuela Germeshausen has authored 56 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 26 papers in Immunology and 23 papers in Hematology. Recurrent topics in Manuela Germeshausen's work include Blood disorders and treatments (47 papers), Immunodeficiency and Autoimmune Disorders (24 papers) and Neutropenia and Cancer Infections (19 papers). Manuela Germeshausen is often cited by papers focused on Blood disorders and treatments (47 papers), Immunodeficiency and Autoimmune Disorders (24 papers) and Neutropenia and Cancer Infections (19 papers). Manuela Germeshausen collaborates with scholars based in Germany, Türkiye and United Kingdom. Manuela Germeshausen's co-authors include Karl Welte, Matthias Ballmaier, Cornelia Zeidler, Julia Skokowa, Christopher Baum, Matthias Eder, Michaela Scherr, Karin Battmer, Murat Uenalan and Martin Stanulla and has published in prestigious journals such as Nature Medicine, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Manuela Germeshausen

56 papers receiving 3.3k 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. Nature Medicine profile →

Peers

Countries citing papers authored by Manuela Germeshausen

Since Specialization

Citations

This map shows the geographic impact of Manuela Germeshausen'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 Manuela Germeshausen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manuela Germeshausen more than expected).

Fields of papers citing papers by Manuela Germeshausen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Manuela Germeshausen. 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 Manuela Germeshausen. The network helps show where Manuela Germeshausen may publish in the future.

Co-authorship network of co-authors of Manuela Germeshausen

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Germeshausen. A scholar is included among the top collaborators of Manuela Germeshausen 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 Manuela Germeshausen. Manuela Germeshausen 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	Congenital amegakaryocytic thrombocytopenia – Not a single disease 2021 ·Best Practice & Research Clinical Haematology ·Manuela Germeshausen, Matthias Ballmaier	12
2	CAMT-MPL: congenital amegakaryocytic thrombocytopenia caused by MPL mutations - heterogeneity of a monogenic disorder - a comprehensive analysis of 56 patients 2020 ·Haematologica ·Manuela Germeshausen, Matthias Ballmaier	26
3	Clinic, pathogenic mechanisms and drug testing of two inherited thrombocytopenias, ANKRD26-related Thrombocytopenia and MYH9-related diseases 2018 ·European Journal of Medical Genetics ·Alessandra Balduini, Hana Raslová, Christian A. Di Buduo, (unknown), Matthias Ballmaier, Manuela Germeshausen, Carlo L. Balduini	22
4	Granulocyte Colony-Stimulating Factor (G-CSF) Treatment of Childhood Acute Myeloid Leukemias That Overexpress the Differentiation-Defective G-CSF Receptor Isoform IV Is Associated With a Higher Incidence of Relapse 2010 ·Journal of Clinical Oncology ·(unknown), (unknown), Martin Zimmermann, (unknown), Manuela Germeshausen, Nils von Neuhoff, C. Michel Zwaan, Katarina Reinhardt, Iris H.I.M. Hollink, Jan‐Henning Klusmann, Thomas Lehrnbecher, (unknown), Jan Starý, Michael Dworzak, Karl Welte, Ursula Creutzig, Dirk Reinhardt	47
5	Digenic mutations in severe congenital neutropenia 2010 ·Haematologica ·Manuela Germeshausen, Cornelia Zeidler, Manfred Stuhrmann, Marina Lanciotti, Matthias Ballmaier, Karl Welte	41
6	Eponym 2010 ·European Journal of Pediatrics ·Caner Aytekin, Manuela Germeshausen, Nilden Tuygun, Gönül Tanır, Figen Doğu, Aydan İkincioğulları	8
7	Acute lymphoblastic leukemia following severe congenital neutropenia or de novo ALL? 2009 ·Leukemia Research ·Elvis Terci Valera, María Sol Brassesco, Manuela Germeshausen, Vanessa S. Silveira, Rosane Gomes de Paula Queiróz, Pérsio Roxo-Júnior, Carlos Alberto Scrideli, (unknown), Virgínia Paes Leme Ferriani, Luíz Gonzaga Tone	1
8	Multiple independent second‐site mutations in two siblings with somatic mosaicism for Wiskott–Aldrich syndrome 2008 ·Clinical Genetics ·Kaan Boztuǧ, Manuela Germeshausen, Inés Avedillo Díez, Vera Gulácsy, Jana Diestelhorst, Matthias Ballmaier, Karl Welte, László Maródi, Л.И. Чернышова, Christoph Klein	36
9	Unrelated cord blood transplantation in children with severe congenital neutropenia 2008 ·Pediatric Transplantation ·M. Akif Yeşilipek, (unknown), Manuela Germeshausen, Alphan Küpesiz, Vedat Uygun, Volkan Hazar	3
10	Clinical implications of ELA2‐, HAX1‐, and G‐CSF‐receptor (CSF3R) mutations in severe congenital neutropenia 2008 ·British Journal of Haematology ·Cornelia Zeidler, Manuela Germeshausen, Christoph Klein, Karl Welte	92
11	Severe congenital neutropenia: inheritance and pathophysiology 2007 ·Current Opinion in Hematology ·Julia Skokowa, Manuela Germeshausen, Cornelia Zeidler, Karl Welte	52
12	The Clinical, Immunohematological, and Molecular Study of Iranian Patients with Severe Congenital Neutropenia 2007 ·Journal of Clinical Immunology ·Nima Rezaei, Mostafa Moin, Zahra Pourpak, (unknown), (unknown), Zahra Chavoshzadeh, Roya Sherkat, Asghar Aghamohammadi, Mehdi Yeganeh, Maryam Mahmoudi, Fatemeh Mahjoub, Manuela Germeshausen, (unknown), Marshall S. Horwitz, Christoph Klein, Abolhassan Farhoudi	36
13	Congenital dysgranulopoietic neutropenia 2006 ·Pediatric Blood & Cancer ·Lale Olcay, Sevgi Yetgin, Esra Erdemlı, Manuela Germeshausen, Dilek Aktaş, Yahya Büyükaşık, Hamza Okur	5
14	LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia 2006 ·Nature Medicine ·Julia Skokowa, Gunnar Cario, Murat Uenalan, Axel Schambach, Manuela Germeshausen, Karin Battmer, Cornelia Zeidler, Ulrich Lehmann, Matthias Eder, Christopher Baum, Rudolf Grosschedl, Martin Stanulla, Michaela Scherr, Karl Welte	158
15	Congenital amegakaryocytic thrombocytopenia: a retrospective clinical analysis of 20 patients 2005 ·British Journal of Haematology ·Stephanie King, Manuela Germeshausen, Gabriele Strauß, Karl Welte, Matthias Ballmaier	88
16	An acquired G-CSF receptor mutation results in increased proliferation of CMML cells from a patient with severe congenital neutropenia 2005 ·Leukemia ·Manuela Germeshausen, Harald Schulze, Christian P. Kratz, Ludwig Wilkens, Roland Repp, Kevin Shannon, Karl Welte, Matthias Ballmaier	21
17	Reduced intensity hematopoietic stem-cell transplantation across human leukocyte antigen barriers in a patient with congenital amegakaryocytic thrombocytopenia and monosomy 7 2005 ·Pediatric Blood & Cancer ·MacGregor Steele, Johann Hitzler, John Doyle, Manuela Germeshausen, Conrad V. Fernandez, (unknown), Yigal Dror	15
18	Thrombopoietin Is Essential for the Maintenance of Normal Hematopoiesis in Humans 2003 ·Annals of the New York Academy of Sciences ·Matthias Ballmaier, Manuela Germeshausen, (unknown), Karl Welte	63
19	Mutations in the gene encoding neutrophil elastase (ELA2) are not sufficient to cause the phenotype of congenital neutropenia 2001 ·British Journal of Haematology ·Manuela Germeshausen, Harald Schulze, Matthias Ballmaier, Cornelia Zeidler, Karl Welte	49
20	Thrombopoietin induces the generation of distinct Stat1, Stat3, Stat5a and Stat5b homo- and heterodimeric complexes with different kinetics in human platelets 2000 ·Experimental Hematology ·Harald Schulze, Matthias Ballmaier, Karl Welte, Manuela Germeshausen	37

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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