Klaudia Brix

4.9k total citations
108 papers, 3.8k citations indexed

About

Klaudia Brix is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Cancer Research. According to data from OpenAlex, Klaudia Brix has authored 108 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 30 papers in Endocrinology, Diabetes and Metabolism and 26 papers in Cancer Research. Recurrent topics in Klaudia Brix's work include Thyroid Disorders and Treatments (28 papers), Protease and Inhibitor Mechanisms (24 papers) and Erythrocyte Function and Pathophysiology (11 papers). Klaudia Brix is often cited by papers focused on Thyroid Disorders and Treatments (28 papers), Protease and Inhibitor Mechanisms (24 papers) and Erythrocyte Function and Pathophysiology (11 papers). Klaudia Brix collaborates with scholars based in Germany, United States and Norway. Klaudia Brix's co-authors include Volker Herzog, Silvia Jordans, Kristina Mayer, Werner M. Nau, Anthony I. Day, Carleen Cullinane, Vanya D. Uzunova, Martin Linke, Maren Rehders and Peter Lemansky and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Klaudia Brix

106 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Klaudia Brix Germany 33 1.7k 859 487 467 457 108 3.8k
Penelope E. Stein United Kingdom 27 2.2k 1.3× 1.4k 1.6× 620 1.3× 287 0.6× 346 0.8× 48 4.5k
Luc Camoin France 35 1.9k 1.1× 335 0.4× 366 0.8× 200 0.4× 789 1.7× 143 4.8k
Takayuki Nemoto Japan 34 1.9k 1.1× 346 0.4× 307 0.6× 260 0.6× 243 0.5× 196 3.9k
Yves A. Muller Germany 39 2.7k 1.6× 286 0.3× 355 0.7× 648 1.4× 204 0.4× 114 4.9k
C.A. Stein United States 45 5.7k 3.4× 816 0.9× 390 0.8× 322 0.7× 186 0.4× 98 7.9k
George Posthuma Netherlands 32 2.0k 1.2× 348 0.4× 509 1.0× 188 0.4× 446 1.0× 64 3.7k
Jason G. Williams United States 45 3.7k 2.2× 368 0.4× 1.9k 3.8× 267 0.6× 489 1.1× 144 6.4k
Renato Longhi Italy 52 3.9k 2.3× 307 0.4× 761 1.6× 280 0.6× 524 1.1× 210 8.2k
Keith K. Stanley Australia 43 3.4k 2.0× 753 0.9× 1.5k 3.1× 640 1.4× 821 1.8× 103 7.4k
Lewis Joel Greene Brazil 38 2.3k 1.4× 232 0.3× 331 0.7× 349 0.7× 309 0.7× 119 4.8k

Countries citing papers authored by Klaudia Brix

Since Specialization
Citations

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

Fields of papers citing papers by Klaudia Brix

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Klaudia Brix

This figure shows the co-authorship network connecting the top 25 collaborators of Klaudia Brix. A scholar is included among the top collaborators of Klaudia Brix 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 Klaudia Brix. Klaudia Brix 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.
Bielecka, Ewa, Grzegorz Bereta, Joanna Kozieł, et al.. (2025). Human tissue kallikrein 14 induces the expression of IL ‐6, IL ‐8, and CXCL1 in skin fibroblasts through protease‐activated receptor 1 signaling. FEBS Journal. 292(21). 5659–5675.
2.
Rehders, Maren, et al.. (2023). Investigations on Primary Cilia of Nthy-ori 3-1 Cells upon Cysteine Cathepsin Inhibition or Thyrotropin Stimulation. International Journal of Molecular Sciences. 24(11). 9292–9292. 3 indexed citations
3.
Kunath, Anne, Juliane Weiner, Kerstin Krause, et al.. (2021). Role of Kallikrein 7 in Body Weight and Fat Mass Regulation. Biomedicines. 9(2). 131–131. 9 indexed citations
4.
Ziros, Panos G., Dionysios V. Chartoumpekis, Massimo Bongiovanni, et al.. (2020). Mice Hypomorphic for Keap1 , a Negative Regulator of the Nrf2 Antioxidant Response, Show Age-Dependent Diffuse Goiter with Elevated Thyrotropin Levels. Thyroid. 31(1). 23–35. 17 indexed citations
5.
Tedelind, Sofia, Alexandra M. Pinzaru, Zeynep Hein, et al.. (2020). Significance of nuclear cathepsin V in normal thyroid epithelial and carcinoma cells. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1867(12). 118846–118846. 21 indexed citations
6.
Dauth, Stephanie, Ruxandra F. Sîrbulescu, Iulian Ilieş, et al.. (2019). Function of Cathepsin K in the Central Nervous System of Male Mice is Independent of Its Role in the Thyroid Gland. Cellular and Molecular Neurobiology. 40(5). 695–710. 9 indexed citations
7.
8.
Rijntjes, Eddy, et al.. (2018). Canonical TSH Regulation of Cathepsin-Mediated Thyroglobulin Processing in the Thyroid Gland of Male Mice Requires Taar1 Expression. Frontiers in Pharmacology. 9. 221–221. 22 indexed citations
9.
Brix, Klaudia, et al.. (2017). Physarum polycephalum—a new take on a classic model system. Journal of Physics D Applied Physics. 50(41). 413001–413001. 33 indexed citations
10.
11.
Fischer, Jana, Gunnar Kleinau, Claudia Rutz, et al.. (2017). Evidence of G-protein-coupled receptor and substrate transporter heteromerization at a single molecule level. Cellular and Molecular Life Sciences. 75(12). 2227–2239. 17 indexed citations
12.
Brix, Klaudia, et al.. (2015). Understanding the Healthy Thyroid State in 2015. European Thyroid Journal. 4(1). 1–8. 12 indexed citations
13.
Haugen, Mads H., Harald Thidemann Johansen, Solveig Pettersen, et al.. (2013). Nuclear Legumain Activity in Colorectal Cancer. PLoS ONE. 8(1). e52980–e52980. 71 indexed citations
14.
Tedelind, Sofia, Silvia Jordans, Henrike K. Resemann, et al.. (2011). Cathepsin B trafficking in thyroid carcinoma cells. Thyroid Research. 4(Suppl 1). S2–S2. 16 indexed citations
15.
McGowan, Sheena, Mary C. Pearce, James A. Irving, et al.. (2007). DNA Accelerates the Inhibition of Human Cathepsin V by Serpins. Journal of Biological Chemistry. 282(51). 36980–36986. 40 indexed citations
16.
Brix, Klaudia, et al.. (2001). Cysteine Proteinases Mediate Extracellular Prohormone Processing in the Thyroid. Biological Chemistry. 382(5). 717–25. 70 indexed citations
17.
Kanzler, Holger, et al.. (2000). Thyroglobulin type‐I‐like domains in invariant chain fusion proteins mediate resistance to cathepsin L digestion. FEBS Letters. 485(1). 67–70. 7 indexed citations
18.
Brix, Klaudia. (1997). Paracrine interaction between hepatocytes and macrophages after extrathyroidal proteolysis of thyroglobulin.. Hepatology. 26(5). 1232–1240. 3 indexed citations
19.
Fitzgerald, Ella, et al.. (1995). Fish PCB concentrations and consumption patterns among Mohawk women at Akwesasne.. PubMed. 5(1). 1–19. 45 indexed citations
20.
Christofidou‐Solomidou, Melpo, Klaudia Brix, & W. Stockem. (1989). Induced pinocytosis and cytoskeletal organization in Amoeba proteus — a combined fluorescence and electron microscopic study. European Journal of Protistology. 24(4). 336–345. 3 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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