Igor V. Karpichev

593 total citations
21 papers, 465 citations indexed

About

Igor V. Karpichev is a scholar working on Molecular Biology, Plant Science and Biochemistry. According to data from OpenAlex, Igor V. Karpichev has authored 21 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Plant Science and 4 papers in Biochemistry. Recurrent topics in Igor V. Karpichev's work include Peroxisome Proliferator-Activated Receptors (6 papers), Plant Stress Responses and Tolerance (5 papers) and Photosynthetic Processes and Mechanisms (5 papers). Igor V. Karpichev is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (6 papers), Plant Stress Responses and Tolerance (5 papers) and Photosynthetic Processes and Mechanisms (5 papers). Igor V. Karpichev collaborates with scholars based in Russia, United States and Italy. Igor V. Karpichev's co-authors include Gillian M. Small, Yi Luo, Ronald A. Kohanski, Andrew Dillin, Alexey Shuvalov, Ardythe A. McCracken, William E. Courchesne, Yu. V. Balnokin, Eric D. Werner and В. П. Холодова and has published in prestigious journals such as Journal of Biological Chemistry, Molecular and Cellular Biology and Genetics.

In The Last Decade

Igor V. Karpichev

20 papers receiving 450 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Igor V. Karpichev 397 81 62 49 39 21 465
С. С. Соколов 398 1.0× 44 0.5× 63 1.0× 18 0.4× 42 1.1× 52 499
Pavlo Kyryakov 523 1.3× 101 1.2× 82 1.3× 64 1.3× 65 1.7× 17 639
Alice Zuin 451 1.1× 67 0.8× 88 1.4× 13 0.3× 46 1.2× 13 518
Cierra N. Sing 243 0.6× 43 0.5× 56 0.9× 39 0.8× 34 0.9× 11 307
Edith Bogengruber 442 1.1× 84 1.0× 80 1.3× 13 0.3× 36 0.9× 14 522
Naïma Belgareh‐Touzé 398 1.0× 80 1.0× 209 3.4× 24 0.5× 77 2.0× 19 513
Junsen Tong 378 1.0× 57 0.7× 209 3.4× 50 1.0× 46 1.2× 13 500
Fernando Alvarez‐Vasquez 468 1.2× 62 0.8× 78 1.3× 69 1.4× 32 0.8× 14 546
Inge Holsbeeks 241 0.6× 118 1.5× 42 0.7× 24 0.5× 28 0.7× 5 350
Y. Tsukagoshi 345 0.9× 77 1.0× 162 2.6× 128 2.6× 34 0.9× 8 471

Countries citing papers authored by Igor V. Karpichev

Since Specialization
Citations

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

Fields of papers citing papers by Igor V. Karpichev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Igor V. Karpichev. 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 Igor V. Karpichev. The network helps show where Igor V. Karpichev may publish in the future.

Co-authorship network of co-authors of Igor V. Karpichev

This figure shows the co-authorship network connecting the top 25 collaborators of Igor V. Karpichev. A scholar is included among the top collaborators of Igor V. Karpichev 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 Igor V. Karpichev. Igor V. Karpichev 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
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Karpichev, Igor V., et al.. (2023). Involvement of the Membrane Nanodomain Protein, AtFlot1, in Vesicular Transport of Plasma Membrane H+-ATPase in Arabidopsis thaliana under Salt Stress. International Journal of Molecular Sciences. 24(2). 1251–1251. 2 indexed citations
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Hoang, Giang Thi, et al.. (2021). An increased proportion of transgenic plants in the progeny of rapeseed (<i>Brassica napus</i> L.) transformants. Vavilov Journal of Genetics and Breeding. 25(2). 147–156. 2 indexed citations
5.
Shuvalov, Alexey, et al.. (2021). Identification of Some Anion Transporter Genes in the Halophyte Suaeda altissima (L.) Pall. and Their Expression under Nitrate Deficiency and Salinity. Russian Journal of Plant Physiology. 68(5). 873–882. 6 indexed citations
6.
Karpichev, Igor V., et al.. (2020). Arabidopsis thaliana Mutant with T-DNA Insertion in the Flot1 (At5g25250) Gene Promotor Possesses Increased Resistance to NaCl. Russian Journal of Plant Physiology. 67(2). 275–284. 7 indexed citations
7.
Karpichev, Igor V., et al.. (2019). Expression of P-Type ATPases of Marine Green Microalga Dunaliella maritima under Hyperosmotic Salt Shock. Doklady Biochemistry and Biophysics. 488(1). 327–331. 2 indexed citations
8.
Shuvalov, Alexey, et al.. (2019). Molecular cloning and characterisation of SaCLCa1, a novel protein of the chloride channel (CLC) family from the halophyte Suaeda altissima (L.) Pall. Journal of Plant Physiology. 240. 152995–152995. 12 indexed citations
9.
Shuvalov, Alexey, et al.. (2018). Cloning and Functional Analysis of SaCLCc1, a Gene Belonging to the Chloride Channel Family (CLC), from the Halophyte Suaeda altissima (L.) Pall.. Doklady Biochemistry and Biophysics. 481(1). 186–189. 11 indexed citations
10.
Karpichev, Igor V., et al.. (2018). Сloning and Functional Analysis of SaCLCc1, a Gene Belonging to Chloride Channel Family (CLC) from the Halophyte Suaeda altissima (L.) Pall. Доклады Академии наук. 481(1). 104–107. 1 indexed citations
11.
Mattana, Monica, et al.. (2018). Expression of rice OsMyb4 transcription factor improves tolerance to copper or zinc in canola plants. Biologia Plantarum. 62(3). 511–520. 13 indexed citations
12.
Karpichev, Igor V., et al.. (2009). Oleate β-oxidation in yeast involves thioesterase but not Yor180c protein that is not a dienoyl-CoA isomerase. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1791(5). 371–378. 5 indexed citations
13.
Karpichev, Igor V., et al.. (2008). Binding Characteristics and Regulatory Mechanisms of the Transcription Factors Controlling Oleate-responsive Genes in Saccharomyces cerevisiae. Journal of Biological Chemistry. 283(16). 10264–10275. 24 indexed citations
14.
Karpichev, Igor V., et al.. (2002). Multiple Regulatory Roles of a Novel Saccharomyces cerevisiae Protein, Encoded by YOL002c, in Lipid and Phosphate Metabolism. Journal of Biological Chemistry. 277(22). 19609–19617. 62 indexed citations
15.
Karpichev, Igor V. & Gillian M. Small. (2000). Evidence for a novel pathway for the targeting of a Saccharomyces cerevisiae peroxisomal protein belonging to the isomerase/hydratase family. Journal of Cell Science. 113(3). 533–544. 20 indexed citations
16.
Karpichev, Igor V. & Gillian M. Small. (1998). Global Regulatory Functions of Oaf1p and Pip2p (Oaf2p), Transcription Factors That Regulate Genes Encoding Peroxisomal Proteins in Saccharomyces cerevisiae. Molecular and Cellular Biology. 18(11). 6560–6570. 119 indexed citations
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Small, Gillian M., Igor V. Karpichev, & Yi Luo. (1997). Regulation of Peroxisomal Fatty Acyl-CoA Oxidase in the Yeast. Advances in experimental medicine and biology. 422. 157–166. 3 indexed citations
19.
Small, Gillian M., et al.. (1996). Molecular Regulation of Peroxisomal Acyl‐CoA Oxidase in Yeasta. Annals of the New York Academy of Sciences. 804(1). 362–372. 1 indexed citations
20.
Luo, Yi, Igor V. Karpichev, Ronald A. Kohanski, & Gillian M. Small. (1996). Purification, Identification, and Properties of a Saccharomyces cerevisiae Oleate-activated Upstream Activating Sequence-binding Protein That Is Involved in the Activation of POX1. Journal of Biological Chemistry. 271(20). 12068–12075. 62 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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