Inga R. Grin

683 total citations
34 papers, 540 citations indexed

About

Inga R. Grin is a scholar working on Molecular Biology, Plant Science and Infectious Diseases. According to data from OpenAlex, Inga R. Grin has authored 34 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 7 papers in Plant Science and 3 papers in Infectious Diseases. Recurrent topics in Inga R. Grin's work include DNA Repair Mechanisms (22 papers), Epigenetics and DNA Methylation (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). Inga R. Grin is often cited by papers focused on DNA Repair Mechanisms (22 papers), Epigenetics and DNA Methylation (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). Inga R. Grin collaborates with scholars based in Russia, France and United States. Inga R. Grin's co-authors include Dmitry O. Zharkov, Alexander A. Ishchenko, Murat Saparbaev, Georgy A. Nevinsky, S. Moréra, Armelle Vigouroux, Grigory L. Dianov, Sophie Couvé, Véronique Henriot and Anton V. Endutkin and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Inga R. Grin

33 papers receiving 533 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Inga R. Grin Russia 15 422 65 51 39 38 34 540
Andrew Harrison United Kingdom 12 268 0.6× 63 1.0× 34 0.7× 25 0.6× 20 0.5× 23 416
Esta Tamanaha United States 7 388 0.9× 20 0.3× 46 0.9× 54 1.4× 29 0.8× 8 498
Sanghamitra Mitra United States 7 303 0.7× 30 0.5× 155 3.0× 40 1.0× 26 0.7× 8 419
Victoria Korboukh United States 13 604 1.4× 34 0.5× 78 1.5× 57 1.5× 56 1.5× 17 812
Jacqueline Vitali United States 9 175 0.4× 86 1.3× 28 0.5× 27 0.7× 64 1.7× 25 321
Jennifer L. Fox United States 12 475 1.1× 25 0.4× 23 0.5× 11 0.3× 24 0.6× 16 580
Vincent T. Bicocca United States 8 160 0.4× 59 0.9× 60 1.2× 12 0.3× 9 0.2× 20 349
Rong Guo China 14 443 1.0× 59 0.9× 35 0.7× 83 2.1× 24 0.6× 32 578
Che-Fu Kuo United States 5 560 1.3× 57 0.9× 49 1.0× 90 2.3× 67 1.8× 6 645
Fiona C. Smith United Kingdom 8 290 0.7× 50 0.8× 39 0.8× 6 0.2× 60 1.6× 11 499

Countries citing papers authored by Inga R. Grin

Since Specialization
Citations

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

Fields of papers citing papers by Inga R. Grin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Inga R. Grin. 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 Inga R. Grin. The network helps show where Inga R. Grin may publish in the future.

Co-authorship network of co-authors of Inga R. Grin

This figure shows the co-authorship network connecting the top 25 collaborators of Inga R. Grin. A scholar is included among the top collaborators of Inga R. Grin 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 Inga R. Grin. Inga R. Grin 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
2.
Sun, Yutong, et al.. (2024). The dual role of methylglyoxal in plant stress response and regulation of DJ‐1 protein. Physiologia Plantarum. 176(6). e14608–e14608. 2 indexed citations
3.
Grin, Inga R., Anton V. Endutkin, Chunquan Ma, et al.. (2023). Base Excision DNA Repair in Plants: Arabidopsis and Beyond. International Journal of Molecular Sciences. 24(19). 14746–14746. 6 indexed citations
4.
Grin, Inga R., et al.. (2022). Characterization of demethylating DNA glycosylase ROS1 from Nicotiana tabacum L.. Vavilov Journal of Genetics and Breeding. 26(4). 341–348. 2 indexed citations
5.
Prorok, Paulina, Inga R. Grin, Bakhyt Matkarimov, et al.. (2021). Evolutionary Origins of DNA Repair Pathways: Role of Oxygen Catastrophe in the Emergence of DNA Glycosylases. Cells. 10(7). 1591–1591. 11 indexed citations
6.
Endutkin, Anton V., et al.. (2020). Displacement of Slow-Turnover DNA Glycosylases by Molecular Traffic on DNA. Genes. 11(8). 866–866. 8 indexed citations
7.
Grin, Inga R., et al.. (2019). Relative Efficiency of Recognition of 5-Methylcytosine and 5-Hydroxymethylcytosine by Methyl-Dependent DNA Endonuclease GlaI. Russian Journal of Bioorganic Chemistry. 45(6). 625–629. 3 indexed citations
8.
Grin, Inga R., et al.. (2019). Conformational Dynamics of Damage Processing by Human DNA Glycosylase NEIL1. Journal of Molecular Biology. 431(6). 1098–1112. 16 indexed citations
9.
Попов, А. В., Inga R. Grin, Bakhyt Matkarimov, et al.. (2019). Reading Targeted DNA Damage in the Active Demethylation Pathway: Role of Accessory Domains of Eukaryotic AP Endonucleases and Thymine-DNA Glycosylases. Journal of Molecular Biology. 432(6). 1747–1768. 13 indexed citations
10.
Mikhailov, Artem A., Evgeni M. Glebov, Vjacheslav P. Grivin, et al.. (2019). Photoinduced inhibition of DNA repair enzymes and the possible mechanism of photochemical transformations of the ruthenium nitrosyl complex [RuNO(β-Pic)2(NO2)2OH]. Metallomics. 11(12). 1999–2009. 21 indexed citations
11.
Shernyukov, Аndrey V., Alexey S. Kiryutin, Alexander A. Lomzov, et al.. (2018). Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation. Nucleic Acids Research. 46(20). 10827–10839. 27 indexed citations
12.
Redrejo‐Rodríguez, Modesto, Armelle Vigouroux, Inga R. Grin, et al.. (2016). Structural comparison of AP endonucleases from the exonuclease III family reveals new amino acid residues in human AP endonuclease 1 that are involved in incision of damaged DNA. Biochimie. 128-129. 20–33. 31 indexed citations
13.
Prorok, Paulina, Inga R. Grin, Dmitry O. Zharkov, et al.. (2014). Cloning and Characterization of a Wheat Homologue of Apurinic/Apyrimidinic Endonuclease Ape1L. PLoS ONE. 9(3). e92963–e92963. 16 indexed citations
14.
Grin, Inga R., et al.. (2013). Excision of 8‐oxoguanine from methylated CpG dinucleotides by human 8‐oxoguanine DNA glycosylase. FEBS Letters. 587(18). 3129–3134. 22 indexed citations
15.
Grin, Inga R., et al.. (2012). Human and bacterial DNA polymerases discriminate against 8-oxo-2'-deoxyadenosine- 5'-triphosphate. SHILAP Revista de lepidopterología. 28(4). 306–309. 3 indexed citations
16.
Grin, Inga R. & Dmitry O. Zharkov. (2011). Eukaryotic endonuclease VIII-Like proteins: New components of the base excision DNA repair system. Biochemistry (Moscow). 76(1). 80–93. 37 indexed citations
17.
Grin, Inga R., Robert Rieger, & Dmitry O. Zharkov. (2010). Inactivation of NEIL2 DNA glycosylase by pyridoxal phosphate reveals a loop important for substrate binding. Biochemical and Biophysical Research Communications. 394(1). 100–105. 11 indexed citations
18.
Grin, Inga R., Grigory L. Dianov, & Dmitry O. Zharkov. (2010). The role of mammalian NEIL1 protein in the repair of 8‐oxo‐7,8‐dihydroadenine in DNA. FEBS Letters. 584(8). 1553–1557. 32 indexed citations
19.
Grin, Inga R., et al.. (2009). Heavy metal ions affect the activity of DNA glycosylases of the Fpg family. Biochemistry (Moscow). 74(11). 1253–1259. 45 indexed citations
20.
Grin, Inga R., С. Н. Ходырева, Georgy A. Nevinsky, & Dmitry O. Zharkov. (2006). Deoxyribophosphate lyase activity of mammalian endonuclease VIII‐like proteins. FEBS Letters. 580(20). 4916–4922. 21 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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