Thomas Volz

2.8k total citations
62 papers, 1.8k citations indexed

About

Thomas Volz is a scholar working on Dermatology, Immunology and Surgery. According to data from OpenAlex, Thomas Volz has authored 62 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Dermatology, 20 papers in Immunology and 15 papers in Surgery. Recurrent topics in Thomas Volz's work include Dermatology and Skin Diseases (18 papers), Asthma and respiratory diseases (10 papers) and Hidradenitis Suppurativa and Treatments (9 papers). Thomas Volz is often cited by papers focused on Dermatology and Skin Diseases (18 papers), Asthma and respiratory diseases (10 papers) and Hidradenitis Suppurativa and Treatments (9 papers). Thomas Volz collaborates with scholars based in Germany, Switzerland and United States. Thomas Volz's co-authors include Tilo Biedermann, Susanne Kaesler, Yuliya Skabytska, Martin Röcken, Emmanuella Guenova, Florian Wölbing, Juliane Wannemacher, Dongsheng Jiang, Donovan Correa‐Gallegos and Haifeng Ye and has published in prestigious journals such as Nature, Nature Communications and Immunity.

In The Last Decade

Thomas Volz

53 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Volz Germany 22 844 436 390 276 240 62 1.8k
Tetsuro Kobayashi Japan 22 1.0k 1.2× 877 2.0× 318 0.8× 468 1.7× 198 0.8× 52 2.5k
Jung U Shin South Korea 22 1.2k 1.4× 262 0.6× 522 1.3× 273 1.0× 352 1.5× 81 2.0k
Zhikun Zhang China 15 504 0.6× 304 0.7× 255 0.7× 209 0.8× 226 0.9× 48 1.4k
Tiffany C. Scharschmidt United States 21 1.3k 1.6× 696 1.6× 515 1.3× 552 2.0× 261 1.1× 37 2.6k
Amanda S. MacLeod United States 26 628 0.7× 672 1.5× 125 0.3× 339 1.2× 129 0.5× 37 1.8k
Yvonne Marquardt Germany 23 819 1.0× 340 0.8× 243 0.6× 301 1.1× 163 0.7× 57 1.5k
Seung Hun Lee South Korea 23 979 1.2× 206 0.5× 321 0.8× 449 1.6× 191 0.8× 93 2.1k
Susanne Kaesler Germany 26 555 0.7× 732 1.7× 404 1.0× 671 2.4× 285 1.2× 42 2.0k
Anne-Marie Schmitt France 21 914 1.1× 200 0.5× 404 1.0× 259 0.9× 152 0.6× 46 1.7k
Anna De Benedetto United States 22 1.6k 1.9× 380 0.9× 1.0k 2.6× 247 0.9× 466 1.9× 70 2.2k

Countries citing papers authored by Thomas Volz

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Volz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Volz

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Volz. A scholar is included among the top collaborators of Thomas Volz 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 Thomas Volz. Thomas Volz 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.
Köberle, Martin, et al.. (2024). Bifidobacterium breve DSM 32583 and Limosilactobacillus fermentum CECT5716 postbiotics attenuate S. aureus and IL-33-induced Th2 responses. Microbiological Research. 289. 127913–127913. 1 indexed citations
2.
Kofler, Lukas, et al.. (2024). Positionspapier der Deutschen Gesellschaft für Dermatochirurgie – Dermatochirurgische Tätigkeiten in Schwangerschaft und Stillzeit. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 22(7). 1056–1059.
3.
Balakirski, Galina, Sören L. Becker, Daniela Hartmann, et al.. (2023). Perioperative Antibiotikaprophylaxe in der Dermatochirurgie – Positionspapier der Arbeitsgruppe Antibiotic Stewardship der Deutschen Gesellschaft für Dermatochirurgie (DGDC), Teil 2: Spezielle Indikationen und Situationen. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 21(10). 1109–1119.
4.
Correa‐Gallegos, Donovan, Haifeng Ye, Safwen Kadri, et al.. (2023). CD201+ fascia progenitors choreograph injury repair. Nature. 623(7988). 792–802. 46 indexed citations
5.
Kurgyis, Zsuzsanna, Larsen Vornholz, Konstanze Pechloff, et al.. (2021). Keratinocyte-intrinsic BCL10/MALT1 activity initiates and amplifies psoriasiform skin inflammation. Science Immunology. 6(65). eabi4425–eabi4425. 10 indexed citations
6.
Scala, Emanuele, Sara Cacciapuoti, Natalie Garzorz‐Stark, et al.. (2021). Hidradenitis Suppurativa: Where We Are and Where We Are Going. Cells. 10(8). 2094–2094. 74 indexed citations
7.
Wan, Li, Dongsheng Jiang, Donovan Correa‐Gallegos, et al.. (2021). Connexin43 gap junction drives fascia mobilization and repair of deep skin wounds. Matrix Biology. 97. 58–71. 37 indexed citations
8.
Häusermann, Peter, et al.. (2020). Two‐stage pedicled interpolation flap with wings for reconstruction of combined nasal tip/columella defects. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 18(6). 644–647. 1 indexed citations
9.
Kaesler, Susanne, Florian Wölbing, W. Kempf, et al.. (2019). Targeting tumor-resident mast cells for effective anti-melanoma immune responses. JCI Insight. 4(19). 41 indexed citations
10.
Böhner, Alexander, et al.. (2019). Perioperative Antibiose in der Dermatochirurgie – Stand 2019. Der Hautarzt. 70(11). 842–849.
11.
Fischer, Tatjana, et al.. (2019). Chronische Wunden richtig behandeln. MMW - Fortschritte der Medizin. 161(5). 48–56. 2 indexed citations
12.
Fischer, Tatjana, et al.. (2019). Die Versorgung akuter Wunden. MMW - Fortschritte der Medizin. 161(4). 46–53. 3 indexed citations
13.
Volz, Thomas, Susanne Kaesler, Christian Draing, et al.. (2017). 349 Induction of IL-10-balanced immune profiles following exposure to LTA from Staphylococcus epidermidis. Journal of Investigative Dermatology. 137(10). S252–S252. 2 indexed citations
14.
Kaesler, Susanne, Yuliya Skabytska, W. Kempf, et al.. (2016). Staphylococcus aureus–derived lipoteichoic acid induces temporary T-cell paralysis independent of Toll-like receptor 2. Journal of Allergy and Clinical Immunology. 138(3). 780–790.e6. 11 indexed citations
15.
Volz, Thomas, et al.. (2016). 232 NOD2 signaling critically influences sensitization to orally ingested allergens and severity of anaphylaxis. Journal of Investigative Dermatology. 136(9). S201–S201. 1 indexed citations
16.
Volz, Thomas, Susanne Kaesler, Yuliya Skabytska, & Tilo Biedermann. (2015). Zur Rolle des angeborenen Immunsystems bei atopischer Dermatitis. Der Hautarzt. 66(2). 90–95. 5 indexed citations
17.
Volz, Thomas & Tilo Biedermann. (2012). Welche Rolle spielt das natürliche Immunsystem bei atopischer Dermatitis? Bestandsaufnahme und Ausblick.. Allergo Journal. 21(8). 470–478. 3 indexed citations
18.
Guenova, Emmanuella, Thomas Volz, Karin Sauer, et al.. (2008). IL‐4‐mediated fine tuning of IL‐12p70 production by human DC. European Journal of Immunology. 38(11). 3138–3149. 40 indexed citations
19.
Volz, Thomas. (2008). Neuropharmacological Mechanisms Underlying the Neuroprotective Effects of Methylphenidate. Current Neuropharmacology. 6(4). 379–385. 34 indexed citations
20.
Kretschmer, B. D., et al.. (1992). The contribution of the different binding sites of the N-methyl-D-aspartate (NMDA) receptor to the expression of behavior. Journal of Neural Transmission. 87(1). 23–35. 53 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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