Steffi Treitschke

1.1k total citations
7 papers, 427 citations indexed

About

Steffi Treitschke is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Steffi Treitschke has authored 7 papers receiving a total of 427 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Oncology and 4 papers in Cancer Research. Recurrent topics in Steffi Treitschke's work include Cancer Cells and Metastasis (4 papers), Cancer Genomics and Diagnostics (4 papers) and Fungal and yeast genetics research (3 papers). Steffi Treitschke is often cited by papers focused on Cancer Cells and Metastasis (4 papers), Cancer Genomics and Diagnostics (4 papers) and Fungal and yeast genetics research (3 papers). Steffi Treitschke collaborates with scholars based in Germany and United Kingdom. Steffi Treitschke's co-authors include Gunther Doehlemann, Assmann Daniela, André N. Mueller, Martin Schuster, Gero Steinberg, Justin E. Molloy, Nicholas J. Harmer, Sreedhar Kilaru, Bernhard Polzer and Sebastian Haferkamp and has published in prestigious journals such as Nature Communications, The EMBO Journal and The Plant Cell.

In The Last Decade

Steffi Treitschke

7 papers receiving 423 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steffi Treitschke Germany 4 282 248 120 45 26 7 427
Amber Sorenson United States 3 162 0.6× 252 1.0× 62 0.5× 38 0.8× 63 2.4× 3 411
Ruifang Li China 11 297 1.1× 151 0.6× 30 0.3× 34 0.8× 47 1.8× 27 441
Olga Rodríguez‐Galán Spain 13 150 0.5× 440 1.8× 128 1.1× 50 1.1× 8 0.3× 21 577
Takahiko Utsugi Japan 12 124 0.4× 382 1.5× 104 0.9× 69 1.5× 29 1.1× 15 458
Neta Agmon United States 13 185 0.7× 663 2.7× 44 0.4× 33 0.7× 41 1.6× 15 733
Anna Golovko Sweden 8 150 0.5× 286 1.2× 44 0.4× 40 0.9× 15 0.6× 12 431
Yuanyuan Shao China 9 534 1.9× 155 0.6× 112 0.9× 10 0.2× 18 0.7× 11 627
Yosr Z. Haffani Canada 10 147 0.5× 321 1.3× 129 1.1× 85 1.9× 17 0.7× 17 423
Natalya Kouprina United States 19 248 0.9× 897 3.6× 88 0.7× 39 0.9× 22 0.8× 26 955
Weidong Chen United States 11 193 0.7× 113 0.5× 180 1.5× 19 0.4× 12 0.5× 14 355

Countries citing papers authored by Steffi Treitschke

Since Specialization
Citations

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

Fields of papers citing papers by Steffi Treitschke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steffi Treitschke

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

All Works

7 of 7 papers shown
1.
Treitschke, Steffi, Kathrin Weidele, Adithi R. Varadarajan, et al.. (2023). Ex vivo expansion of lung cancer‐derived disseminated cancer cells from lymph nodes identifies cells associated with metastatic progression. International Journal of Cancer. 153(10). 1854–1867. 1 indexed citations
2.
Hoffmann, Martin, Zbigniew T. Czyż, Bernhard Polzer, et al.. (2022). Disseminated cancer cells detected by immunocytology in lymph nodes of NSCLC patients are highly prognostic and undergo parallel molecular evolution. The Journal of Pathology. 258(3). 250–263. 1 indexed citations
3.
Werner‐Klein, Melanie, Milan Obradović, Martin Hoffmann, et al.. (2019). Abstract LB-312: Interleukin 6 transsignaling is a candidate mechanism to drive progression of human DCCs during periods of clinical latency. Cancer Research. 79(13_Supplement). LB–312. 1 indexed citations
4.
Werner‐Klein, Melanie, Martin Hoffmann, Klaus Dietz, et al.. (2018). Genetic alterations driving metastatic colony formation are acquired outside of the primary tumour in melanoma. Nature Communications. 9(1). 595–595. 60 indexed citations
5.
Mueller, André N., et al.. (2013). Compatibility in the Ustilago maydis–Maize Interaction Requires Inhibition of Host Cysteine Proteases by the Fungal Effector Pit2. PLoS Pathogens. 9(2). e1003177–e1003177. 203 indexed citations
6.
Schuster, Martin, Steffi Treitschke, Sreedhar Kilaru, et al.. (2011). Myosin-5, kinesin-1 and myosin-17 cooperate in secretion of fungal chitin synthase. The EMBO Journal. 31(1). 214–227. 91 indexed citations
7.
Treitschke, Steffi, Gunther Doehlemann, Martin Schuster, & Gero Steinberg. (2010). The Myosin Motor Domain of Fungal Chitin Synthase V Is Dispensable for Vesicle Motility but Required for Virulence of the Maize PathogenUstilago maydis . The Plant Cell. 22(7). 2476–2494. 70 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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