Igor I. Kireev

2.5k total citations
97 papers, 1.7k citations indexed

About

Igor I. Kireev is a scholar working on Molecular Biology, Cell Biology and Biomaterials. According to data from OpenAlex, Igor I. Kireev has authored 97 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 20 papers in Cell Biology and 11 papers in Biomaterials. Recurrent topics in Igor I. Kireev's work include Genomics and Chromatin Dynamics (19 papers), DNA Repair Mechanisms (14 papers) and RNA Research and Splicing (12 papers). Igor I. Kireev is often cited by papers focused on Genomics and Chromatin Dynamics (19 papers), DNA Repair Mechanisms (14 papers) and RNA Research and Splicing (12 papers). Igor I. Kireev collaborates with scholars based in Russia, Tajikistan and United States. Igor I. Kireev's co-authors include Andrew S. Belmont, Margot Lakonishok, Olga Strelkova, Tatsuya Hirano, Rustem Uzbekov, Yan Hu, Irina B. Alieva, Sergey V. Razin, Paul Sinclair and B. F. Vanyushin and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and The Journal of Cell Biology.

In The Last Decade

Igor I. Kireev

90 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Igor I. Kireev Russia 20 1.1k 238 194 181 131 97 1.7k
Xiong Liu China 27 801 0.7× 151 0.6× 223 1.1× 201 1.1× 102 0.8× 90 1.7k
Kaustuv Basu Canada 19 848 0.8× 108 0.5× 303 1.6× 114 0.6× 73 0.6× 34 1.4k
Rosa M. Lozano Spain 23 971 0.9× 122 0.5× 407 2.1× 188 1.0× 155 1.2× 64 1.6k
Yun Gao China 27 1.2k 1.1× 142 0.6× 103 0.5× 372 2.1× 332 2.5× 62 2.2k
Andreas Maurer Germany 26 1.3k 1.2× 249 1.0× 207 1.1× 233 1.3× 93 0.7× 100 2.7k
Fernando Domı́nguez Spain 31 1.3k 1.2× 469 2.0× 174 0.9× 179 1.0× 186 1.4× 85 2.5k
Sheng Wang China 23 836 0.8× 102 0.4× 67 0.3× 235 1.3× 179 1.4× 90 1.6k
Shintaro Maeda Japan 20 1.2k 1.2× 110 0.5× 283 1.5× 81 0.4× 91 0.7× 47 2.0k

Countries citing papers authored by Igor I. Kireev

Since Specialization
Citations

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

Fields of papers citing papers by Igor I. Kireev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Igor I. Kireev

This figure shows the co-authorship network connecting the top 25 collaborators of Igor I. Kireev. A scholar is included among the top collaborators of Igor I. Kireev 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 I. Kireev. Igor I. Kireev 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.
Chikina, Aleksandra, Igor I. Kireev, Alexander А. Minin, et al.. (2024). Plasma Membrane Blebbing Is Controlled by Subcellular Distribution of Vimentin Intermediate Filaments. Cells. 13(1). 105–105. 4 indexed citations
2.
Dubinin, Mikhail V., et al.. (2024). Mitochondrial Transplantation Therapy Ameliorates Muscular Dystrophy in mdx Mouse Model. Biomolecules. 14(3). 316–316. 15 indexed citations
3.
4.
Kireev, Igor I., et al.. (2023). Expression, Intracellular Localization, and Maturation of Cysteine Cathepsins in Renal Embryonic and Cancer Cell Lines. Biochemistry (Moscow). 88(7). 1034–1044. 9 indexed citations
5.
Papusha, L. I., et al.. (2023). Supratentorial tumor resembling anaplastic ependymoma in an adolescent. Brain Pathology. 33(2). e13137–e13137. 1 indexed citations
6.
7.
Dubinin, Mikhail V., Vlada S. Starinets, Natalia V. Belosludtseva, et al.. (2023). Effect of the large-conductance calcium-dependent k<sup>+</sup> channel activator NS1619 on the function of mitochondria in the heart of dystrophin-deficient mice. 88(2). 228–242. 1 indexed citations
8.
Dubinin, Mikhail V., Vlada S. Starinets, Natalia V. Belosludtseva, et al.. (2023). Effect of Large-Conductance Calcium-Dependent K+ Channel Activator NS1619 on Function of Mitochondria in the Heart of Dystrophin-Deficient Mice. Biochemistry (Moscow). 88(2). 189–201. 2 indexed citations
9.
Dubinin, Mikhail V., Natalia V. Belosludtseva, I. B. Mikheeva, et al.. (2023). Uridine Administration Promotes Normalization of Heart Mitochondrial Function in Dystrophin-Deficient Mice and Decreases Tissue Fibrosis. Bulletin of Experimental Biology and Medicine. 176(1). 54–59. 3 indexed citations
10.
Ulianov, Sergey V., Artem K. Velichko, Mikhail Magnitov, et al.. (2021). Suppression of liquid–liquid phase separation by 1,6-hexanediol partially compromises the 3D genome organization in living cells. Nucleic Acids Research. 49(18). 10524–10541. 82 indexed citations
11.
Velichko, Artem K., Nadezhda V. Petrova, Artem V. Luzhin, et al.. (2021). Treacle and TOPBP1 control replication stress response in the nucleolus. The Journal of Cell Biology. 220(8). 12 indexed citations
12.
Alexandrov, Alexander I., Vitaly V. Kushnirov, Roman N. Chuprov‐Netochin, et al.. (2019). Analysis of novel hyperosmotic shock response suggests “beads in liquid” cytosol structure. Biology Open. 8(7). 16 indexed citations
13.
Kosenko, Еlena, et al.. (2017). Rapid Elimination of Blood Alcohol Using Erythrocytes: Mathematical Modeling and In Vitro Study. BioMed Research International. 2017. 1–14. 10 indexed citations
14.
Kireev, Igor I.. (2016). An orthogonal power method of solving the partial eigenproblem for a symmetric nonnegative definite matrix. Vyčislitelʹnye metody i programmirovanie. 44–54. 1 indexed citations
15.
Fetisova, E. K., et al.. (2015). Mitochondria-targeted antioxidant SkQR1 selectively protects MDR-negative cells from ionizing radiation. Cell and Tissue Biology. 9(2). 87–95. 4 indexed citations
16.
Strelkova, Olga, et al.. (2015). Overcoming steric hindrances during replication of peripheral heterochromatin. Cell and Tissue Biology. 9(2). 110–118. 4 indexed citations
17.
Skachkov, Ilya, et al.. (2009). Serum-induced inhibition of the phagocytic activity of cultured macrophages IC-21. Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology. 3(4). 417–424. 8 indexed citations
18.
Kireev, Igor I., et al.. (2008). In vivo immunogold labeling confirms large-scale chromatin folding motifs. Nature Methods. 5(4). 311–313. 34 indexed citations
19.
Kireev, Igor I., et al.. (2007). High-pressure treatment of polytene chromosomes improves structural resolution. Nature Methods. 4(6). 483–485. 12 indexed citations
20.
Sheval, Eugene V., Igor I. Kireev, & V. Yu. Polyakov. (2004). Stabilization of macromolecular chromatin complexes in mitotic chromosomes by light irradiation in the presence of ethidium bromide. Cell Biology International. 28(12). 835–843. 5 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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