Mariya Y. Radeva

1.1k total citations
31 papers, 805 citations indexed

About

Mariya Y. Radeva is a scholar working on Molecular Biology, Cell Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Mariya Y. Radeva has authored 31 papers receiving a total of 805 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Cell Biology and 9 papers in Pathology and Forensic Medicine. Recurrent topics in Mariya Y. Radeva's work include Autoimmune Bullous Skin Diseases (9 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (8 papers) and Barrier Structure and Function Studies (7 papers). Mariya Y. Radeva is often cited by papers focused on Autoimmune Bullous Skin Diseases (9 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (8 papers) and Barrier Structure and Function Studies (7 papers). Mariya Y. Radeva collaborates with scholars based in Germany, Switzerland and United States. Mariya Y. Radeva's co-authors include Jens Waschke, Volker Spindler, Daniela Kugelmann, Franziska Vielmuth, Eva Hartlieb, Vera Rötzer, Elias Walter, Alexander García‐Ponce, F. E. Curry and Azadeh Kheirolomoom and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Mariya Y. Radeva

29 papers receiving 797 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mariya Y. Radeva Germany 15 279 211 171 148 107 31 805
Pia Svendsen Denmark 16 263 0.9× 115 0.5× 82 0.5× 108 0.7× 69 0.6× 30 1.1k
César Sanz-Rodrı́guez Spain 19 417 1.5× 186 0.9× 108 0.6× 70 0.5× 73 0.7× 30 1.2k
John Chapin United States 14 260 0.9× 83 0.4× 152 0.9× 37 0.3× 21 0.2× 26 1.2k
Siân Lax United Kingdom 19 450 1.6× 77 0.4× 75 0.4× 120 0.8× 35 0.3× 31 1.2k
Robert A. Matthijsen Netherlands 13 432 1.5× 128 0.6× 46 0.3× 161 1.1× 25 0.2× 23 1.2k
Marin Sekosan United States 19 181 0.6× 91 0.4× 54 0.3× 49 0.3× 48 0.4× 49 971
Y. Barbier France 13 219 0.8× 214 1.0× 63 0.4× 39 0.3× 29 0.3× 26 847
David A. Wilcox United States 24 478 1.7× 45 0.2× 137 0.8× 76 0.5× 20 0.2× 48 1.8k
Betsy Evans United Kingdom 8 213 0.8× 33 0.2× 58 0.3× 99 0.7× 40 0.4× 18 657
Chia Chi Sun United States 12 369 1.3× 172 0.8× 427 2.5× 37 0.3× 84 0.8× 13 1.7k

Countries citing papers authored by Mariya Y. Radeva

Since Specialization
Citations

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

Fields of papers citing papers by Mariya Y. Radeva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mariya Y. Radeva. 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 Mariya Y. Radeva. The network helps show where Mariya Y. Radeva may publish in the future.

Co-authorship network of co-authors of Mariya Y. Radeva

This figure shows the co-authorship network connecting the top 25 collaborators of Mariya Y. Radeva. A scholar is included among the top collaborators of Mariya Y. Radeva 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 Mariya Y. Radeva. Mariya Y. Radeva 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.
Hamad, Ibrahim, et al.. (2025). Plakoglobin does not participate in endothelial barrier stabilization mediated by cAMP. Scientific Reports. 15(1). 9043–9043.
2.
Sigmund, Anna M., Daniela Kugelmann, Elisabeth Butz, et al.. (2025). Epac1 contributes to apremilast-mediated rescue of pemphigus autoantibody-induced loss of keratinocyte adhesion. JCI Insight. 10(10). 1 indexed citations
3.
Hamad, Ibrahim, et al.. (2024). Cortactin is in a complex with VE-cadherin and is required for endothelial adherens junction stability through Rap1/Rac1 activation. Scientific Reports. 14(1). 1218–1218. 6 indexed citations
4.
Vielmuth, Franziska, Mariya Y. Radeva, Sunil Yeruva, Anna M. Sigmund, & Jens Waschke. (2023). cAMP: A master regulator of cadherin‐mediated binding in endothelium, epithelium and myocardium. Acta Physiologica. 238(4). e14006–e14006. 12 indexed citations
5.
Radeva, Mariya Y., et al.. (2023). Cytoskeletal anchorage of different Dsg3 pools revealed by combination of hybrid STED/SMFS-AFM. Cellular and Molecular Life Sciences. 80(1). 25–25. 9 indexed citations
6.
Sigmund, Anna M., Daniela Kugelmann, Desalegn Tadesse Egu, et al.. (2023). Apremilast prevents blistering in human epidermis and stabilizes keratinocyte adhesion in pemphigus. Nature Communications. 14(1). 116–116. 22 indexed citations
7.
8.
Kugelmann, Daniela, Mariya Y. Radeva, Dario Didona, et al.. (2022). Pemphigus Foliaceus Autoantibodies Induce Redistribution Primarily of Extradesmosomal Desmoglein 1 in the Cell Membrane. Frontiers in Immunology. 13. 882116–882116. 5 indexed citations
9.
Radeva, Mariya Y., Elias Walter, Amir S. Yazdi, et al.. (2019). ST18 Enhances PV-IgG-Induced Loss of Keratinocyte Cohesion in Parallel to Increased ERK Activation. Frontiers in Immunology. 10. 770–770. 20 indexed citations
10.
Radeva, Mariya Y., Daniela Kugelmann, René Keil, et al.. (2019). Plakophilin 1 but not plakophilin 3 regulates desmoglein clustering. Cellular and Molecular Life Sciences. 76(17). 3465–3476. 26 indexed citations
11.
Kugelmann, Daniela, Lukas T. Rotkopf, Mariya Y. Radeva, et al.. (2018). Histamine causes endothelial barrier disruption via Ca2+-mediated RhoA activation and tension at adherens junctions. Scientific Reports. 8(1). 13229–13229. 45 indexed citations
12.
Radeva, Mariya Y., et al.. (2018). Keratin Retraction and Desmoglein3 Internalization Independently Contribute to Autoantibody-Induced Cell Dissociation in Pemphigus Vulgaris. Frontiers in Immunology. 9. 858–858. 12 indexed citations
13.
Vielmuth, Franziska, Elias Walter, Mariya Y. Radeva, et al.. (2018). Keratins Regulate p38MAPK-Dependent Desmoglein Binding Properties in Pemphigus. Frontiers in Immunology. 9. 528–528. 28 indexed citations
14.
Vielmuth, Franziska, Mariya Y. Radeva, Daniela Kugelmann, et al.. (2017). Keratins Regulate the Adhesive Properties of Desmosomal Cadherins through Signaling. Journal of Investigative Dermatology. 138(1). 121–131. 43 indexed citations
15.
Kugelmann, Daniela, Jens Waschke, & Mariya Y. Radeva. (2015). Adducin Is Involved in Endothelial Barrier Stabilization. PLoS ONE. 10(5). e0126213–e0126213. 20 indexed citations
16.
Adamson, R. H., et al.. (2014). Albumin modulates S1P delivery from red blood cells in perfused microvessels: mechanism of the protein effect. American Journal of Physiology-Heart and Circulatory Physiology. 306(7). H1011–H1017. 57 indexed citations
17.
Spindler, Volker, Vera Rötzer, Carina Dehner, et al.. (2013). Peptide-mediated desmoglein 3 crosslinking prevents pemphigus vulgaris autoantibody-induced skin blistering. Journal of Clinical Investigation. 123(2). 800–11. 79 indexed citations
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Kirova, Elisaveta, et al.. (1986). Sensory aroma and taste profiles of raw-dried sausages manufactured with a lipolytically active yeast culture. 12 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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