Marina Bayeva

2.3k total citations · 1 hit paper
18 papers, 1.8k citations indexed

About

Marina Bayeva is a scholar working on Molecular Biology, Hematology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Marina Bayeva has authored 18 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Hematology and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Marina Bayeva's work include Iron Metabolism and Disorders (5 papers), Trace Elements in Health (4 papers) and Mitochondrial Function and Pathology (3 papers). Marina Bayeva is often cited by papers focused on Iron Metabolism and Disorders (5 papers), Trace Elements in Health (4 papers) and Mitochondrial Function and Pathology (3 papers). Marina Bayeva collaborates with scholars based in United States, Spain and Canada. Marina Bayeva's co-authors include Hossein Ardehali, Arineh Khechaduri, Rongxue Wu, Mihai Gheorghiade, Mohsen Ghanefar, Tejaswitha Jairaj Naik, R. Kannan Mutharasan, Yoshihiko Ichikawa, Sathyamangla V. Naga Prasad and Hsiang‐Chun Chang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and Journal of Clinical Investigation.

In The Last Decade

Marina Bayeva

18 papers receiving 1.8k citations

Hit Papers

Cardiotoxicity of doxorub... 2014 2026 2018 2022 2014 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marina Bayeva United States 16 830 664 292 257 228 18 1.8k
Rongxue Wu United States 21 1.0k 1.3× 720 1.1× 334 1.1× 275 1.1× 182 0.8× 48 2.4k
Bruno Baudin France 24 647 0.8× 408 0.6× 110 0.4× 132 0.5× 113 0.5× 80 1.9k
Tejaswitha Jairaj Naik United States 6 561 0.7× 546 0.8× 416 1.4× 174 0.7× 76 0.3× 6 1.4k
Philippe Ratajczak France 20 777 0.9× 652 1.0× 229 0.8× 136 0.5× 119 0.5× 37 1.9k
Reheman Adili United States 28 509 0.6× 453 0.7× 124 0.4× 253 1.0× 897 3.9× 61 2.4k
Shengfu Piao United States 13 1.3k 1.6× 360 0.5× 188 0.6× 94 0.4× 85 0.4× 15 2.5k
Louise Dunn Australia 20 729 0.9× 130 0.2× 135 0.5× 194 0.8× 237 1.0× 44 1.7k
Patrizia Nigro Italy 23 1.5k 1.9× 426 0.6× 233 0.8× 343 1.3× 108 0.5× 44 2.4k
Mohsen Ghanefar United States 6 442 0.5× 476 0.7× 267 0.9× 173 0.7× 73 0.3× 8 1.1k

Countries citing papers authored by Marina Bayeva

Since Specialization
Citations

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

Fields of papers citing papers by Marina Bayeva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Bayeva

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

All Works

18 of 18 papers shown
1.
Sawicki, Konrad Teodor, Hsiang‐Chun Chang, Jason Shapiro, et al.. (2018). Hepatic tristetraprolin promotes insulin resistance through RNA destabilization of FGF21. JCI Insight. 3(13). 25 indexed citations
2.
Sato, Tatsuya, Hsiang‐Chun Chang, Marina Bayeva, et al.. (2018). mRNA-binding protein tristetraprolin is essential for cardiac response to iron deficiency by regulating mitochondrial function. Proceedings of the National Academy of Sciences. 115(27). E6291–E6300. 65 indexed citations
3.
Chang, Hsiang‐Chun, Marina Bayeva, Babafemi Taiwo, et al.. (2014). Short Communication: High Cellular Iron Levels Are Associated with Increased HIV Infection and Replication. AIDS Research and Human Retroviruses. 31(3). 305–312. 42 indexed citations
4.
Ichikawa, Yoshihiko, Mohsen Ghanefar, Marina Bayeva, et al.. (2014). Cardiotoxicity of doxorubicin is mediated through mitochondrial iron accumulation. Journal of Clinical Investigation. 124(2). 617–630. 704 indexed citations breakdown →
5.
Wu, Rongxue, Hsiang‐Chun Chang, Arineh Khechaduri, et al.. (2014). Cardiac-specific ablation of ARNT leads to lipotoxicity and cardiomyopathy. Journal of Clinical Investigation. 124(11). 4795–4806. 33 indexed citations
6.
Bayeva, Marina, Konrad Teodor Sawicki, Javed Butler, Mihai Gheorghiade, & Hossein Ardehali. (2014). Molecular and Cellular Basis of Viable Dysfunctional Myocardium. Circulation Heart Failure. 7(4). 680–691. 38 indexed citations
7.
Bayeva, Marina, Konrad Teodor Sawicki, & Hossein Ardehali. (2013). Taking Diabetes to Heart—Deregulation of Myocardial Lipid Metabolism in Diabetic Cardiomyopathy. Journal of the American Heart Association. 2(6). e000433–e000433. 125 indexed citations
8.
Bayeva, Marina, Arineh Khechaduri, Rongxue Wu, et al.. (2013). ATP-Binding Cassette B10 Regulates Early Steps of Heme Synthesis. Circulation Research. 113(3). 279–287. 52 indexed citations
9.
Khechaduri, Arineh, Marina Bayeva, Hsiang‐Chun Chang, & Hossein Ardehali. (2013). Heme Levels Are Increased in Human Failing Hearts. Journal of the American College of Cardiology. 61(18). 1884–1893. 58 indexed citations
10.
Bayeva, Marina, Hsiang‐Chun Chang, Rongxue Wu, & Hossein Ardehali. (2013). When less is more: novel mechanisms of iron conservation. Trends in Endocrinology and Metabolism. 24(11). 569–577. 29 indexed citations
11.
Bayeva, Marina, Arineh Khechaduri, Sergi Puig, et al.. (2012). mTOR Regulates Cellular Iron Homeostasis through Tristetraprolin. Cell Metabolism. 16(5). 645–657. 158 indexed citations
12.
Bayeva, Marina, Mihai Gheorghiade, & Hossein Ardehali. (2012). Mitochondria as a Therapeutic Target in Heart Failure. Journal of the American College of Cardiology. 61(6). 599–610. 272 indexed citations
13.
Ichikawa, Yoshihiko, Marina Bayeva, Mohsen Ghanefar, et al.. (2012). Disruption of ATP-binding cassette B8 in mice leads to cardiomyopathy through a decrease in mitochondrial iron export. Proceedings of the National Academy of Sciences. 109(11). 4152–4157. 126 indexed citations
14.
Ichikawa, Yoshihiko, Marina Bayeva, Mohsen Ghanefar, et al.. (2011). Abstract 16027: Mitochondrial ATP-Binding Cassette Protein-1 (mABC1) Protects Against Doxorubicin-Mediated Cardiotoxicity. Circulation. 124(3). 1 indexed citations
15.
Bayeva, Marina, Yoshihiko Ichikawa, Mohsen Ghanefar, et al.. (2011). Abstract 16497: Characterization of ATP Binding Cassette Protein B8 (ABCB8) as a Mitochondrial Iron and Glutathione Exporter. Circulation. 124. 1 indexed citations
16.
Bayeva, Marina & Hossein Ardehali. (2010). Mitochondrial Dysfunction and Oxidative Damage to Sarcomeric Proteins. Current Hypertension Reports. 12(6). 426–432. 46 indexed citations
17.
Damer, Cynthia Kay, Marina Bayeva, Eric S. Eberhardt, et al.. (2007). Copine A Is Required for Cytokinesis, Contractile Vacuole Function, and Development inDictyostelium. Eukaryotic Cell. 6(3). 430–442. 33 indexed citations
18.

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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