Olga Protchenko

2.5k total citations · 1 hit paper
29 papers, 1.9k citations indexed

About

Olga Protchenko is a scholar working on Molecular Biology, Cell Biology and Nutrition and Dietetics. According to data from OpenAlex, Olga Protchenko has authored 29 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Cell Biology and 10 papers in Nutrition and Dietetics. Recurrent topics in Olga Protchenko's work include Trace Elements in Health (10 papers), Iron Metabolism and Disorders (9 papers) and Fungal and yeast genetics research (9 papers). Olga Protchenko is often cited by papers focused on Trace Elements in Health (10 papers), Iron Metabolism and Disorders (9 papers) and Fungal and yeast genetics research (9 papers). Olga Protchenko collaborates with scholars based in United States, Ukraine and Poland. Olga Protchenko's co-authors include Caroline C. Philpott, Minoo Shakoury‐Elizeh, Shyamalagauri Jadhav, Sarju J. Patel, James E. Cox, Yulia Y. Tyurina, Vladimir A. Tyurin, Valerian E. Kagan, Hülya Bayır and Xiaojing Yuan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Olga Protchenko

27 papers receiving 1.9k citations

Hit Papers

Iron catalysis of lipid peroxidation in ferroptosis: Regu... 2018 2026 2020 2023 2018 50 100 150 200 250

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Olga Protchenko United States 21 1.2k 402 313 285 281 29 1.9k
Morgane Le Bras France 23 1.7k 1.5× 87 0.2× 68 0.2× 261 0.9× 263 0.9× 43 2.3k
Roger T. Snowden United Kingdom 26 1.7k 1.5× 69 0.2× 161 0.5× 240 0.8× 122 0.4× 50 2.7k
Toshifumi Akizawa Japan 21 666 0.6× 129 0.3× 84 0.3× 244 0.9× 81 0.3× 80 1.6k
Katalin Sipos Hungary 20 760 0.7× 60 0.1× 237 0.8× 84 0.3× 154 0.5× 55 1.5k
Ruth Freudinger Germany 31 1.1k 1.0× 202 0.5× 109 0.3× 265 0.9× 29 0.1× 48 2.2k
Carlo Alberto Palmerini Italy 23 759 0.7× 119 0.3× 208 0.7× 153 0.5× 27 0.1× 101 2.0k
Hiroshi Kaneko Japan 20 1.1k 0.9× 81 0.2× 81 0.3× 75 0.3× 89 0.3× 71 1.8k
Federica Gibellini United States 18 1.1k 0.9× 80 0.2× 49 0.2× 234 0.8× 139 0.5× 27 2.1k
Khurshid Iqbal Andrabi India 22 1.5k 1.3× 104 0.3× 46 0.1× 170 0.6× 70 0.2× 71 2.2k
Lisa C. Crowley Australia 15 909 0.8× 88 0.2× 46 0.1× 217 0.8× 72 0.3× 19 1.8k

Countries citing papers authored by Olga Protchenko

Since Specialization
Citations

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

Fields of papers citing papers by Olga Protchenko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olga Protchenko

This figure shows the co-authorship network connecting the top 25 collaborators of Olga Protchenko. A scholar is included among the top collaborators of Olga Protchenko 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 Olga Protchenko. Olga Protchenko 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.
Protchenko, Olga, Shyamalagauri Jadhav, Deliang Zhang, et al.. (2023). Vitamin E Induces Liver Iron Depletion and Alters Iron Regulation in Mice. Journal of Nutrition. 153(7). 1866–1876. 6 indexed citations
2.
Philpott, Caroline C., et al.. (2023). Iron-tracking strategies: Chaperones capture iron in the cytosolic labile iron pool. Frontiers in Molecular Biosciences. 10. 1127690–1127690. 23 indexed citations
3.
Jadhav, Shyamalagauri, Olga Protchenko, Feng‐Min Li, et al.. (2021). Mitochondrial dysfunction in mouse livers depleted of iron chaperone PCBP1. Free Radical Biology and Medicine. 175. 18–27. 31 indexed citations
4.
Queralt-Martín, María, Lucie Bergdoll, Oscar Teijido, et al.. (2020). A lower affinity to cytosolic proteins reveals VDAC3 isoform-specific role in mitochondrial biology. The Journal of General Physiology. 152(2). 46 indexed citations
5.
Philpott, Caroline C., Sarju J. Patel, & Olga Protchenko. (2020). Management versus miscues in the cytosolic labile iron pool: The varied functions of iron chaperones. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1867(11). 118830–118830. 66 indexed citations
6.
Stoyanovsky, Detcho A., Yulia Y. Tyurina, Indira H. Shrivastava, et al.. (2018). Iron catalysis of lipid peroxidation in ferroptosis: Regulated enzymatic or random free radical reaction?. Free Radical Biology and Medicine. 133. 153–161. 278 indexed citations breakdown →
7.
Gurnev, Philip A., Tatiana K. Rostovtseva, David P. Hoogerheide, et al.. (2015). Alpha-Synuclein Blocks VDAC Suggesting Mechanism of Mitochondrial Regulation and Toxicity in Parkinson Disease. Biophysical Journal. 108(2). 607a–607a.
8.
Rostovtseva, Tatiana K., Philip A. Gurnev, Olga Protchenko, et al.. (2015). α-Synuclein Shows High Affinity Interaction with Voltage-dependent Anion Channel, Suggesting Mechanisms of Mitochondrial Regulation and Toxicity in Parkinson Disease. Journal of Biological Chemistry. 290(30). 18467–18477. 152 indexed citations
9.
Huynh, Chau, Xiaojing Yuan, Danilo C. Miguel, et al.. (2012). Heme Uptake by Leishmania amazonensis Is Mediated by the Transmembrane Protein LHR1. PLoS Pathogens. 8(7). e1002795–e1002795. 92 indexed citations
10.
11.
Yuan, Xiaojing, Olga Protchenko, Caroline C. Philpott, & Iqbal Hamza. (2011). Topologically Conserved Residues Direct Heme Transport in HRG-1-related Proteins. Journal of Biological Chemistry. 287(7). 4914–4924. 56 indexed citations
12.
Shakoury‐Elizeh, Minoo, Olga Protchenko, Alvin Berger, et al.. (2010). Metabolic Response to Iron Deficiency in Saccharomyces cerevisiae. Journal of Biological Chemistry. 285(19). 14823–14833. 150 indexed citations
13.
Boretsky, Yuriy R., Daria V. Fedorovych, Lyubov Fayura, et al.. (2009). Deficiency in frataxin homologue YFH1 in the yeast Pichia guilliermondii leads to missregulation of iron acquisition and riboflavin biosynthesis and affects sulfate assimilation. BioMetals. 22(6). 1051–1061. 10 indexed citations
14.
Boretsky, Yuriy R., et al.. (2007). Development of a transformation system for gene knock-out in the flavinogenic yeast Pichia guilliermondii. Journal of Microbiological Methods. 70(1). 13–19. 23 indexed citations
15.
16.
Philpott, Caroline C. & Olga Protchenko. (2007). Response to Iron Deprivation in Saccharomyces cerevisiae. Eukaryotic Cell. 7(1). 20–27. 202 indexed citations
17.
Protchenko, Olga, et al.. (2006). A Screen for Genes of Heme Uptake Identifies the FLC Family Required for Import of FAD into the Endoplasmic Reticulum. Journal of Biological Chemistry. 281(30). 21445–21457. 59 indexed citations
18.
Protchenko, Olga & Caroline C. Philpott. (2003). Regulation of Intracellular Heme Levels by HMX1, a Homologue of Heme Oxygenase, in Saccharomyces cerevisiae. Journal of Biological Chemistry. 278(38). 36582–36587. 77 indexed citations
19.
Protchenko, Olga, et al.. (2001). Three Cell Wall Mannoproteins Facilitate the Uptake of Iron in Saccharomyces cerevisiae. Journal of Biological Chemistry. 276(52). 49244–49250. 131 indexed citations
20.
Protchenko, Olga, et al.. (1999). Iron uptake by the yeast Pichia guilliermondii. Flavinogenesis and reductive iron assimilation are co-regulated processes. BioMetals. 12(4). 295–300. 26 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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