Steffen Uebe

6.7k total citations
58 papers, 1.3k citations indexed

About

Steffen Uebe is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Steffen Uebe has authored 58 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 27 papers in Genetics and 10 papers in Immunology. Recurrent topics in Steffen Uebe's work include Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Steffen Uebe is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Steffen Uebe collaborates with scholars based in Germany, Switzerland and Netherlands. Steffen Uebe's co-authors include Arif B. Ekici, André Reis, Heinrich Sticht, Juliane Hoyer, Georgia Vasileiou, Christiane Zweier, Rami Abou Jamra, Cornelia Kraus, Christian T. Thiel and Mandy Krumbiegel and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Experimental Medicine and PLoS ONE.

In The Last Decade

Steffen Uebe

57 papers receiving 1.3k citations

Peers

Steffen Uebe

GENET

IMMUN

Isabelle Thiffault United States

Tommaso Pippucci Italy

Carol Saunders United States

Julie Désir Belgium

Mohammed A. Aldahmesh Saudi Arabia

Eissa Faqeih Saudi Arabia

Christel Thauvin‐Robinet France

Claudio Graziano Italy

Jinmin Miao United States

Sharon Zeligson Israel

Isabelle Thiffault United States

Steffen Uebe

822 ×1.0

482 ×1.0

GENET

108 ×0.8

IMMUN

96 ×0.7

88 ×0.7

Citations per year, relative to Steffen Uebe Steffen Uebe (= 1×) peers Isabelle Thiffault

Countries citing papers authored by Steffen Uebe

Since Specialization

Citations

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

Fields of papers citing papers by Steffen Uebe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steffen Uebe

This figure shows the co-authorship network connecting the top 25 collaborators of Steffen Uebe. A scholar is included among the top collaborators of Steffen Uebe 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 Steffen Uebe. Steffen Uebe 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

Mühle, Christiane, Fabian Schumacher, Liubov S. Kalinichenko, et al.. (2025). Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia. Molecular Psychiatry. 30(7). 2891–2906. 1 indexed citations

Krumbiegel, Mandy, Thomas Rupprecht, Cornelia Kraus, et al.. (2024). Severe manifestation of Rauch‐Azzarello syndrome associated with biallelic deletion of CTNND2 . Clinical Genetics. 106(2). 180–186.

Frey, Benjamin, Ina Becker, Imke Atreya, et al.. (2021). Transcriptomes of MPO-Deficient Patients with Generalized Pustular Psoriasis Reveals Expansion of CD4+ Cytotoxic T Cells and an Involvement of the Complement System. Journal of Investigative Dermatology. 142(8). 2149–2158.e10. 10 indexed citations

Hüffmeier, Ulrike, Regina Trollmann, Ute Hehr, et al.. (2019). The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy. Orphanet Journal of Rare Diseases. 14(1). 38–38. 42 indexed citations

Hannemann, Nicole, Shan Cao, Daniel Eriksson, et al.. (2019). Transcription factor Fra-1 targets arginase-1 to enhance macrophage-mediated inflammation in arthritis. Journal of Clinical Investigation. 129(7). 2669–2684. 56 indexed citations

Díaz-Gallo, Lina-Marcela, Daniel Ramsköld, Klementy Shchetynsky, et al.. (2018). Systematic approach demonstrates enrichment of multiple interactions between non-HLA risk variants and HLA-DRB1 risk alleles in rheumatoid arthritis. Annals of the Rheumatic Diseases. 77(10). 1454–1462. 16 indexed citations

Graul‐Neumann, Luitgard, Martin A. Mensah, Eva Klopocki, et al.. (2018). Biallelic intragenic deletion in MASP1 in an adult female with 3MC syndrome. European Journal of Medical Genetics. 61(7). 363–368. 13 indexed citations

Leal, Alejandro, Arif B. Ekici, Steffen Uebe, et al.. (2018). The polynucleotide kinase 3′-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25. Neurogenetics. 19(4). 215–225. 27 indexed citations

Uebe, Steffen, et al.. (2018). Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability. BMC Medical Genomics. 11(1). 41–41. 5 indexed citations

10.

Grötsch, Bettina, Steffen Uebe, Georg F. Weber, et al.. (2017). Fra-2 regulates B cell development by enhancing IRF4 and Foxo1 transcription. The Journal of Experimental Medicine. 214(7). 2059–2071. 29 indexed citations

11.

Jiang, Xia, Chun Lai Too, Steffen Uebe, et al.. (2017). DNA methylation mediates genotype and smoking interaction in the development of anti-citrullinated peptide antibody-positive rheumatoid arthritis. Arthritis Research & Therapy. 19(1). 71–71. 40 indexed citations

12.

Zenkel, Matthias, Francesca Pasutto, Antonio Bergua, et al.. (2016). Expression of CACNA1A in Patients with Pseudoexfoliation Syndrome. Investigative Ophthalmology & Visual Science. 57(12). 5997–5997. 1 indexed citations

13.

Mauri, Lucia, Steffen Uebe, Heinrich Sticht, et al.. (2016). Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma. Orphanet Journal of Rare Diseases. 11(1). 108–108. 28 indexed citations

14.

Moosmann, Julia, Steffen Uebe, Sven Dittrich, et al.. (2015). Novel Loci for Non-Syndromic Coarctation of the Aorta in Sporadic and Familial Cases. PLoS ONE. 10(5). e0126873–e0126873. 9 indexed citations

15.

Vasileiou, Georgia, Arif B. Ekici, Steffen Uebe, et al.. (2015). Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling. The American Journal of Human Genetics. 97(3). 445–456. 64 indexed citations

16.

Kessler, Kristin, Steffen Uebe, Nathalie Falk, et al.. (2015). DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects. Scientific Reports. 5(1). 11649–11649. 26 indexed citations

17.

Zweier, Markus, Heinrich Sticht, Christiane Zweier, et al.. (2013). Biallelic SEMA3A defects cause a novel type of syndromic short stature. American Journal of Medical Genetics Part A. 161(11). 2880–2889. 9 indexed citations

18.

Gregor, Anne, Martin Oti, Evelyn N. Kouwenhoven, et al.. (2013). De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability. The American Journal of Human Genetics. 93(1). 124–131. 112 indexed citations

19.

Jamra, Rami Abou, Sigrun Wohlfart, Markus Zweier, et al.. (2011). Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity. European Journal of Human Genetics. 19(11). 1161–1166. 63 indexed citations

20.

Krumbiegel, Mandy, Francesca Pasutto, Ursula Schlötzer‐Schrehardt, et al.. (2010). Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. European Journal of Human Genetics. 19(2). 186–193. 45 indexed citations

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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