Tobias Rothoeft

1.6k total citations
21 papers, 513 citations indexed

About

Tobias Rothoeft is a scholar working on Immunology, Infectious Diseases and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Tobias Rothoeft has authored 21 papers receiving a total of 513 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Immunology, 4 papers in Infectious Diseases and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Tobias Rothoeft's work include Immune Cell Function and Interaction (6 papers), T-cell and B-cell Immunology (6 papers) and Immunotherapy and Immune Responses (5 papers). Tobias Rothoeft is often cited by papers focused on Immune Cell Function and Interaction (6 papers), T-cell and B-cell Immunology (6 papers) and Immunotherapy and Immune Responses (5 papers). Tobias Rothoeft collaborates with scholars based in Germany, Italy and France. Tobias Rothoeft's co-authors include U. Schauer, Holger Bartz, Sabine Hoffjan, Mathias Krummen, Stephan Grabbe, Sandra Balkow, Stefan Beissert, Georg Varga, Tetsuya Higuchi and Dietmar Vestweber and has published in prestigious journals such as New England Journal of Medicine, Blood and European Journal of Immunology.

In The Last Decade

Tobias Rothoeft

21 papers receiving 506 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tobias Rothoeft Germany 13 242 115 103 75 70 21 513
G Berger France 10 167 0.7× 76 0.7× 139 1.3× 38 0.5× 21 0.3× 15 505
Chan Sun China 11 269 1.1× 84 0.7× 106 1.0× 19 0.3× 30 0.4× 17 499
Levi B. Watkin United States 11 400 1.7× 112 1.0× 133 1.3× 43 0.6× 16 0.2× 15 574
Günter Hans‐Filho Brazil 20 134 0.6× 117 1.0× 98 1.0× 17 0.2× 52 0.7× 49 1.2k
Ian T. Lamborn United States 4 484 2.0× 68 0.6× 75 0.7× 46 0.6× 29 0.4× 7 619
Osamu Tatsuzawa Japan 12 415 1.7× 83 0.7× 142 1.4× 32 0.4× 30 0.4× 21 618
Gezahegn Gorfu United States 10 180 0.7× 89 0.8× 273 2.7× 17 0.2× 31 0.4× 11 551
Leslie S. Fujikawa United States 18 231 1.0× 283 2.5× 95 0.9× 65 0.9× 78 1.1× 25 1.2k
Kristina Kligys United States 11 79 0.3× 167 1.5× 129 1.3× 32 0.4× 136 1.9× 53 549
Mickaël Ménager France 9 437 1.8× 69 0.6× 155 1.5× 13 0.2× 143 2.0× 17 681

Countries citing papers authored by Tobias Rothoeft

Since Specialization
Citations

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

Fields of papers citing papers by Tobias Rothoeft

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tobias Rothoeft

This figure shows the co-authorship network connecting the top 25 collaborators of Tobias Rothoeft. A scholar is included among the top collaborators of Tobias Rothoeft 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 Tobias Rothoeft. Tobias Rothoeft is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Rothoeft, Tobias, Claudia S. Maier, Armin Hoffmann, et al.. (2024). Natural and hybrid immunity after SARS-CoV-2 infection in children and adolescents. Infection. 52(4). 1449–1458. 1 indexed citations
2.
Dings, Christiane, Dominik Selzer, Nicola Luigi Bragazzi, et al.. (2024). Effect of vaccinations and school restrictions on the spread of COVID-19 in different age groups in Germany. Infectious Disease Modelling. 9(4). 1250–1264. 1 indexed citations
3.
Thiels, Charlotte, Thomas Lücke, Tobias Rothoeft, et al.. (2023). ACOX1 Gain-of-Function Variant in Two German Pediatric Patients, in One Case Mimicking Autoimmune Inflammatory Disease. Neuropediatrics. 55(2). 140–145. 4 indexed citations
4.
Fuchs, Hans, Jörg Große-Onnebrink, Christina Keßler, et al.. (2023). Tracheostomy decannulation in children: a proposal for a structured approach on behalf of the working group chronic respiratory insufficiency within the German-speaking society of pediatric pulmonology. European Journal of Pediatrics. 182(7). 2999–3006. 3 indexed citations
5.
Rothoeft, Tobias, Folke Brinkmann, Christoph Maier, et al.. (2023). Motivations for Adolescent COVID-19 Vaccination: A Comparative Study of Adolescent and Caregiver Perspectives in Germany. Children. 10(12). 1890–1890. 2 indexed citations
6.
Kühn, Anna Luisa, Markus Wenning, Michael Zemlin, et al.. (2022). Mental Health and Health-Related Quality of Life in German Adolescents after the Third Wave of the COVID-19 Pandemic. Children. 9(6). 780–780. 13 indexed citations
7.
Paulus, Frank W., Anna Luisa Kühn, Markus Wenning, et al.. (2022). Problematic Internet Use among Adolescents 18 Months after the Onset of the COVID-19 Pandemic. Children. 9(11). 1724–1724. 31 indexed citations
8.
Kueckelhaus, Maximilian, Tobias Rothoeft, Laura De Rosa, et al.. (2021). Transgenic Epidermal Cultures for Junctional Epidermolysis Bullosa — 5-Year Outcomes. New England Journal of Medicine. 385(24). 2264–2270. 32 indexed citations
9.
Rosa, Laura De, Giorgio De Santis, Giovanni Pellacani, et al.. (2019). Laminin 332-Dependent YAP Dysregulation Depletes Epidermal Stem Cells in Junctional Epidermolysis Bullosa. Cell Reports. 27(7). 2036–2049.e6. 59 indexed citations
10.
Posovszky, Carsten, E. Jacobsen, Myriam Ricarda Lorenz, et al.. (2019). Persisting enteropathy and disturbed adaptive mucosal immunity due to MHC class II deficiency. Clinical Immunology. 203. 125–133. 9 indexed citations
11.
Dohna‐Schwake, Christian, Florian Stehling, Tobias Rothoeft, et al.. (2018). Differences of Medical Care for Acute Severe Viral Bronchiolitis in Two Urban Areas in Europe. Klinische Pädiatrie. 230(5). 245–250. 3 indexed citations
12.
Thiels, Charlotte, Cornelia Köhler, Matthias Vorgerd, et al.. (2014). Long Survival in Leigh Syndrome: New Cases and Review of Literature. Neuropediatrics. 45(6). 346–353. 18 indexed citations
13.
Rothoeft, Tobias, et al.. (2011). Ultrasound and colour Doppler in infantile subglottic haemangioma. Pediatric Radiology. 41(11). 1421–1428. 15 indexed citations
14.
Balkow, Sandra, Karin Loser, Mathias Krummen, et al.. (2008). Dendritic cell activation by combined exposure to anti‐CD40 plus interleukin (IL)‐12 and IL‐18 efficiently stimulates anti‐tumor immunity. Experimental Dermatology. 18(1). 78–87. 16 indexed citations
15.
Rothoeft, Tobias, et al.. (2007). Differential response of human naive and memory/effector T cells to dendritic cells infected by respiratory syncytial virus. Clinical & Experimental Immunology. 150(2). 263–273. 20 indexed citations
16.
Rothoeft, Tobias, Sandra Balkow, Mathias Krummen, et al.. (2006). Structure and duration of contact between dendritic cells and T cells are controlled by T cell activation state. European Journal of Immunology. 36(12). 3105–3117. 45 indexed citations
17.
Varga, Georg, Sandra Balkow, Martin K. Wild, et al.. (2006). Active MAC-1 (CD11b/CD18) on DCs inhibits full T-cell activation. Blood. 109(2). 661–669. 112 indexed citations
18.
Bartz, Holger, et al.. (2003). Respiratory syncytial virus decreases the capacity of myeloid dendritic cells to induce interferon‐γ in naïve T cells. Immunology. 109(1). 49–57. 72 indexed citations
19.
20.

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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