Natalya U. Fedosova

2.3k total citations
72 papers, 1.8k citations indexed

About

Natalya U. Fedosova is a scholar working on Molecular Biology, Biomedical Engineering and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Natalya U. Fedosova has authored 72 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 13 papers in Biomedical Engineering and 9 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Natalya U. Fedosova's work include Ion Transport and Channel Regulation (47 papers), ATP Synthase and ATPases Research (18 papers) and Membrane-based Ion Separation Techniques (12 papers). Natalya U. Fedosova is often cited by papers focused on Ion Transport and Channel Regulation (47 papers), ATP Synthase and ATPases Research (18 papers) and Membrane-based Ion Separation Techniques (12 papers). Natalya U. Fedosova collaborates with scholars based in Denmark, Germany and United States. Natalya U. Fedosova's co-authors include Poul Nissen, Laure Yatime, Mette Laursen, Mikael Esmann, Sergey N. Fedosov, Torben E. Petersen, Ebba Nexø, J.L. Gregersen, Irena Kłodos and Jens Preben Morth and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Natalya U. Fedosova

70 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natalya U. Fedosova Denmark 22 1.4k 231 134 117 116 72 1.8k
Ángel L. Pey Spain 30 1.9k 1.4× 288 1.2× 34 0.3× 67 0.6× 113 1.0× 94 2.6k
Michael G. Gore United Kingdom 23 1.2k 0.9× 82 0.4× 84 0.6× 44 0.4× 115 1.0× 102 1.9k
Ludwig M.G. Heilmeyer Germany 33 2.4k 1.7× 313 1.4× 83 0.6× 98 0.8× 75 0.6× 88 3.4k
Juan C. Ferrer Spain 28 1.3k 0.9× 293 1.3× 38 0.3× 144 1.2× 69 0.6× 62 2.0k
Alessio Peracchi Italy 28 2.0k 1.4× 148 0.6× 96 0.7× 39 0.3× 57 0.5× 63 2.6k
Chad R. Borges United States 27 1.1k 0.8× 32 0.1× 247 1.8× 216 1.8× 125 1.1× 79 2.3k
Ross Shiman United States 24 1.1k 0.8× 80 0.3× 38 0.3× 117 1.0× 105 0.9× 39 2.1k
Kirk Beebe United States 21 1.9k 1.4× 48 0.2× 37 0.3× 112 1.0× 63 0.5× 31 2.5k
Klaus D. Schnackerz Germany 28 1.3k 1.0× 207 0.9× 41 0.3× 93 0.8× 35 0.3× 99 2.2k
Roberto Contestabile Italy 29 1.6k 1.2× 310 1.3× 44 0.3× 51 0.4× 48 0.4× 93 2.4k

Countries citing papers authored by Natalya U. Fedosova

Since Specialization
Citations

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

Fields of papers citing papers by Natalya U. Fedosova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natalya U. Fedosova. 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 Natalya U. Fedosova. The network helps show where Natalya U. Fedosova may publish in the future.

Co-authorship network of co-authors of Natalya U. Fedosova

This figure shows the co-authorship network connecting the top 25 collaborators of Natalya U. Fedosova. A scholar is included among the top collaborators of Natalya U. Fedosova 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 Natalya U. Fedosova. Natalya U. Fedosova 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.
Fedosova, Natalya U., et al.. (2024). How ligands modulate the gastric H,K-ATPase activity and its inhibition by tegoprazan. Journal of Biological Chemistry. 300(12). 107986–107986. 1 indexed citations
2.
3.
Middleton, David A., John M. Griffin, Mikael Esmann, & Natalya U. Fedosova. (2023). Solid-state NMR chemical shift analysis for determining the conformation of ATP bound to Na,K-ATPase in its native membrane. RSC Advances. 13(49). 34836–34846. 2 indexed citations
4.
Berg, Peder, et al.. (2023). Trimethoprim inhibits renal H+-K+-ATPase in states of K+ depletion. American Journal of Physiology-Renal Physiology. 326(1). F143–F151. 1 indexed citations
5.
Fedosova, Natalya U., et al.. (2022). Measurements of Na+-occluded intermediates during the catalytic cycle of the Na+/K+-ATPase provide novel insights into the mechanism of Na+ transport. Journal of Biological Chemistry. 299(2). 102811–102811. 4 indexed citations
6.
Fedosova, Natalya U., et al.. (2020). The interaction of Na+, K+, and phosphate with the gastric H,K-ATPase. Kinetics of E1–E2 conformational changes assessed by eosin fluorescence measurements. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1863(1). 183477–183477. 5 indexed citations
7.
Sehgal, Pankaj, Natalya U. Fedosova, Renato Murillo, et al.. (2015). Discovery of Tricyclic Clerodane Diterpenes as Sarco/Endoplasmic Reticulum Ca(2+)-ATPase Inhibitors and Structure-Activity Relationships.. 1 indexed citations
8.
Sehgal, Pankaj, Natalya U. Fedosova, Renato Murillo, et al.. (2015). Discovery of Tricyclic Clerodane Diterpenes as Sarco/Endoplasmic Reticulum Ca2+-ATPase Inhibitors and Structure–Activity Relationships. Journal of Natural Products. 78(6). 1262–1270. 13 indexed citations
9.
Reinhard, Linda, et al.. (2014). Crystals of Na+/K+-ATPase with bound cisplatin. Biochemical Pharmacology. 92(3). 494–498. 18 indexed citations
10.
Flygaard, Rasmus Kock, et al.. (2014). Structural analysis of the yeast exosome Rrp6p–Rrp47p complex by small-angle X-ray scattering. Biochemical and Biophysical Research Communications. 450(1). 634–640. 5 indexed citations
11.
Zhang, Rongrong, Hai‐Yan Tian, Tse‐Yu Chung, et al.. (2014). Structures, chemotaxonomic significance, cytotoxic and Na+,K+-ATPase inhibitory activities of new cardenolides from Asclepias curassavica. Organic & Biomolecular Chemistry. 12(44). 8919–8929. 30 indexed citations
12.
Yatime, Laure, Morten J. Buch-Pedersen, Maria Musgaard, et al.. (2009). P-type ATPases as drug targets: Tools for medicine and science. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1787(4). 207–220. 119 indexed citations
13.
Fodor, Elfrieda, et al.. (2008). Stabilization of Na,K–ATPase by ionic interactions. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1778(4). 835–843. 20 indexed citations
14.
Fedosov, Sergey N., Natalya U. Fedosova, Bernhard Kräutler, Ebba Nexø, & Torben E. Petersen. (2007). Mechanisms of Discrimination between Cobalamins and Their Natural Analogues during Their Binding to the Specific B 12 -Transporting Proteins. Biochemistry. 46(21). 6446–6458. 73 indexed citations
15.
Fedosov, Sergey N., Natalya U. Fedosova, Lars Berglund, et al.. (2004). Assembly of the Intrinsic Factor Domains and Oligomerization of the Protein in the Presence of Cobalamin. Biochemistry. 43(47). 15095–15102. 27 indexed citations
16.
Fedosova, Natalya U., Philippe Champeil, & Mikael Esmann. (2003). Characterization of the Electrostatic Component of the Nucleotide Binding to Na,K‐ATPase. Annals of the New York Academy of Sciences. 986(1). 263–264.
17.
Fedosova, Natalya U., Flemming Cornelius, Bliss Forbush, & Irena Kłodos. (1997). Diversity of the E2P Phosphoforms of Na, K‐ATPasea. Annals of the New York Academy of Sciences. 834(1). 386–389. 1 indexed citations
18.
Kłodos, Irena, Natalya U. Fedosova, & Liselotte Plesner. (1995). Influence of Intramembrane Electric Charge on Na,K-ATPase. Journal of Biological Chemistry. 270(9). 4244–4254. 11 indexed citations
19.
Fedosova, Natalya U., Flemming Cornelius, & Irena Kłodos. (1995). Fluorescent styryl dyes as probes for Na,K-ATPase reaction mechanism: significance of the charge of the hydrophilic moiety of RH dyes. Biochemistry. 34(51). 16806–16814. 29 indexed citations
20.
Boldyrev, A. A., Natalya U. Fedosova, & O. D. Lopina. (1991). The mechanism of the modifying effect of ATP on Na(+)-K+ ATPase.. PubMed. 2(5). 450–4. 7 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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