Н. И. Речкунова

1.1k total citations
72 papers, 904 citations indexed

About

Н. И. Речкунова is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Н. И. Речкунова has authored 72 papers receiving a total of 904 indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 21 papers in Oncology and 17 papers in Cancer Research. Recurrent topics in Н. И. Речкунова's work include DNA Repair Mechanisms (56 papers), DNA and Nucleic Acid Chemistry (31 papers) and Carcinogens and Genotoxicity Assessment (17 papers). Н. И. Речкунова is often cited by papers focused on DNA Repair Mechanisms (56 papers), DNA and Nucleic Acid Chemistry (31 papers) and Carcinogens and Genotoxicity Assessment (17 papers). Н. И. Речкунова collaborates with scholars based in Russia, United States and France. Н. И. Речкунова's co-authors include Olga I. Lavrik, Н. А. Лебедева, Ekaterina A. Maltseva, N. Lebedeva, I. O. Petruseva, С. Н. Ходырева, Maria V. Sukhanova, Orlando D. Schärer, Sherif F. El‐Khamisy and Dmitry M. Kolpashchikov and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Н. И. Речкунова

68 papers receiving 893 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Н. И. Речкунова Russia 18 850 206 159 63 62 72 904
Varun Bodepudi United States 10 1.1k 1.3× 101 0.5× 274 1.7× 70 1.1× 122 2.0× 23 1.2k
H.H.K. Winterwerp Netherlands 17 1.1k 1.2× 118 0.6× 113 0.7× 89 1.4× 126 2.0× 21 1.2k
Soenita S. Goerdayal Netherlands 13 581 0.7× 131 0.6× 87 0.5× 100 1.6× 37 0.6× 15 797
Paul W. Doetsch United States 17 1.1k 1.3× 128 0.6× 179 1.1× 90 1.4× 163 2.6× 25 1.2k
Stephen A. Shinsky United States 15 833 1.0× 130 0.6× 50 0.3× 52 0.8× 50 0.8× 18 905
Jeffrey J. Pouliot United States 9 1.2k 1.4× 399 1.9× 101 0.6× 156 2.5× 26 0.4× 10 1.2k
Dennis Gómez France 25 2.2k 2.6× 210 1.0× 65 0.4× 79 1.3× 63 1.0× 38 2.4k
Alokes Majumdar United States 19 958 1.1× 60 0.3× 91 0.6× 59 0.9× 101 1.6× 29 1.0k
Gerald W. Hsu United States 7 535 0.6× 83 0.4× 108 0.7× 29 0.5× 53 0.9× 7 621

Countries citing papers authored by Н. И. Речкунова

Since Specialization
Citations

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

Fields of papers citing papers by Н. И. Речкунова

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Н. И. Речкунова. 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 Н. И. Речкунова. The network helps show where Н. И. Речкунова may publish in the future.

Co-authorship network of co-authors of Н. И. Речкунова

This figure shows the co-authorship network connecting the top 25 collaborators of Н. И. Речкунова. A scholar is included among the top collaborators of Н. И. Речкунова 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 Н. И. Речкунова. Н. И. Речкунова 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.
Maltseva, Ekaterina A., et al.. (2024). Does the XPA–FEN1 Interaction Concern to Nucleotide Excision Repair or Beyond?. Biomolecules. 14(7). 814–814.
2.
Maltseva, Ekaterina A., Н. И. Речкунова, & Olga I. Lavrik. (2023). NON-CATALYTIC DOMAINS OF DNA POLYMERASE λ: INFLUENCE ON ENZYME ACTIVITY AND ITS REGULATION. 512(1). 422–427.
3.
Maltseva, Ekaterina A., Н. И. Речкунова, & Olga I. Lavrik. (2023). Non-Catalytic Domains of DNA Polymerase λ: Influence on Enzyme Activity and Its Regulation. Doklady Biochemistry and Biophysics. 512(1). 245–250. 1 indexed citations
4.
Речкунова, Н. И., et al.. (2021). Интерактом систем репарации оснований и нуклеотидов. Молекулярная биология. 55(2). 181–193. 2 indexed citations
5.
Dyrkheeva, Nadezhda S., Rashid O. Anarbaev, Н. А. Лебедева, et al.. (2020). Human Tyrosyl-DNA Phosphodiesterase 1 Possesses Transphosphooligonucleotidation Activity With Primary Alcohols. Frontiers in Cell and Developmental Biology. 8. 604732–604732. 10 indexed citations
7.
8.
Речкунова, Н. И., et al.. (2016). Processing of the abasic sites clustered with the benzo[a]pyrene adducts by the base excision repair enzymes. DNA repair. 50. 43–53. 4 indexed citations
9.
Maltseva, Ekaterina A., Н. И. Речкунова, Maria V. Sukhanova, & Olga I. Lavrik. (2015). Poly(ADP-ribose) Polymerase 1 Modulates Interaction of the Nucleotide Excision Repair Factor XPC-RAD23B with DNA via Poly(ADP-ribosyl)ation. Journal of Biological Chemistry. 290(36). 21811–21820. 32 indexed citations
11.
Lebedeva, N., et al.. (2012). Interaction of nucleotide excision repair proteins with DNA containing bulky lesion and apurinic/apyrimidinic site. Biochemistry (Moscow). 77(5). 524–531. 3 indexed citations
12.
Maltseva, Ekaterina A., Н. И. Речкунова, I. O. Petruseva, et al.. (2006). Interaction of nucleotide excision repair factors RPA and XPA with DNA containing bulky photoreactive groups imitating damages. Biochemistry (Moscow). 71(3). 270–278. 12 indexed citations
13.
Belousova, E. A., Н. И. Речкунова, & Olga I. Lavrik. (2005). Thermostable DNA polymerases can perform translesion synthesis using 8-oxoguanine and tetrahydrofuran-containing DNA templates. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1764(1). 97–104. 16 indexed citations
14.
Лебедева, Н. А., Vladimir N. Silnikov, Tatyana V. Abramova, et al.. (2005). Analysis of Interactions of DNA polymerase β and reverse transcriptases of human immunodeficiency and mouse leukemia viruses with dNTP analogs containing a modified sugar residue. Biochemistry (Moscow). 70(1). 1–7. 2 indexed citations
15.
Lebedeva, N., Ekaterina A. Maltseva, E. A. Belousova, et al.. (2004). Interaction of Replication Protein A with Photoreactive DNA Structures. Biochemistry (Moscow). 69(2). 208–215. 3 indexed citations
16.
Ходырева, С. Н., et al.. (2003). A Comparative Study of the Modification Efficiency of DNA Polymerases and DNA Template by the DNA Primers with Various Photoreactive Groups at Their 3"-Termini. Russian Journal of Bioorganic Chemistry. 29(1). 66–72. 3 indexed citations
17.
Лебедева, Н. А., Dmitry M. Kolpashchikov, Н. И. Речкунова, С. Н. Ходырева, & Olga I. Lavrik. (2002). Highly Efficient Labeling of DNA Polymerases by a Binary System of Photoaffinity Reagents. Biochemistry (Moscow). 67(7). 807–814. 2 indexed citations
18.
Речкунова, Н. И., et al.. (2001). Affinity Labeling of Flap-endonuclease FEN-1 by Photoreactive DNAs. Biochemistry (Moscow). 66(7). 733–739. 3 indexed citations
19.
Речкунова, Н. И., et al.. (2001). Interaction of Human Replication Protein A with DNA Duplexes Containing Gaps of Varying Size. Molecular Biology. 35(5). 702–708. 8 indexed citations
20.
Buryanov, Yaroslav I., V. V. Zinoviev, Ф. В. Тузиков, et al.. (1988). Interaction of the EcoDam methyltransferase with synthetic oligodeoxyribonucleotides. Gene. 74(1). 67–69. 13 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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