Dmitry Temiakov

3.6k total citations
42 papers, 2.4k citations indexed

About

Dmitry Temiakov is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Dmitry Temiakov has authored 42 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Clinical Biochemistry. Recurrent topics in Dmitry Temiakov's work include RNA and protein synthesis mechanisms (25 papers), Mitochondrial Function and Pathology (16 papers) and RNA modifications and cancer (11 papers). Dmitry Temiakov is often cited by papers focused on RNA and protein synthesis mechanisms (25 papers), Mitochondrial Function and Pathology (16 papers) and RNA modifications and cancer (11 papers). Dmitry Temiakov collaborates with scholars based in United States, Germany and Japan. Dmitry Temiakov's co-authors include Michael Anikin, Yaroslav I. Morozov, Patrick Cramer, William T. McAllister, Dmitry G. Vassylyev, Karen Agaronyan, Shigeyuki Yokoyama, Hauke S. Hillen, T.H. Tahirov and Azadeh Sarfallah and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Dmitry Temiakov

39 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dmitry Temiakov United States 25 2.2k 374 349 234 110 42 2.4k
Laurie S. Kaguni United States 36 3.3k 1.5× 479 1.3× 913 2.6× 193 0.8× 132 1.2× 97 3.8k
Linda Spremulli United States 39 4.4k 2.0× 361 1.0× 449 1.3× 150 0.6× 153 1.4× 147 4.7k
Basil J. Greber United States 26 2.3k 1.1× 221 0.6× 72 0.2× 166 0.7× 111 1.0× 37 2.6k
Kai Hell Germany 32 3.6k 1.6× 263 0.7× 643 1.8× 51 0.2× 56 0.5× 41 3.9k
Thomas W. O’Brien United States 25 1.7k 0.8× 141 0.4× 365 1.0× 66 0.3× 80 0.7× 43 2.0k
Abdussalam Azem Israel 32 2.3k 1.1× 150 0.4× 178 0.5× 77 0.3× 35 0.3× 85 2.7k
Eva Kutějová Slovakia 24 1.4k 0.6× 325 0.9× 104 0.3× 67 0.3× 63 0.6× 57 1.6k
Kaye N. Truscott Australia 31 3.8k 1.7× 235 0.6× 745 2.1× 53 0.2× 66 0.6× 50 4.1k
Marie Sissler France 24 2.4k 1.1× 212 0.6× 321 0.9× 52 0.2× 71 0.6× 40 2.5k
Dusanka Milenkovic Germany 31 4.1k 1.8× 218 0.6× 1.1k 3.1× 45 0.2× 169 1.5× 40 4.4k

Countries citing papers authored by Dmitry Temiakov

Since Specialization
Citations

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

Fields of papers citing papers by Dmitry Temiakov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dmitry Temiakov

This figure shows the co-authorship network connecting the top 25 collaborators of Dmitry Temiakov. A scholar is included among the top collaborators of Dmitry Temiakov 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 Dmitry Temiakov. Dmitry Temiakov 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.
Zhao, Caifeng, et al.. (2025). Maackia amurensis seed lectin structure and sequence comparison with other M. amurensis lectins. Journal of Biological Chemistry. 301(5). 108466–108466.
2.
Temiakov, Dmitry, et al.. (2025). Structural basis for promoter recognition and transcription factor binding and release in human mitochondria. Molecular Cell. 85(16). 3123–3136.e7.
3.
Temiakov, Dmitry, et al.. (2024). Structural basis for substrate binding and selection by human mitochondrial RNA polymerase. Nature Communications. 15(1). 7134–7134. 3 indexed citations
4.
Sarfallah, Azadeh, et al.. (2023). Structural basis for DNA proofreading. Nature Communications. 14(1). 8501–8501. 12 indexed citations
5.
Sarfallah, Azadeh & Dmitry Temiakov. (2020). In Vitro Reconstitution of Human Mitochondrial Transcription. Methods in molecular biology. 2192. 35–41. 4 indexed citations
6.
Jones, Julia, Katharina Hofmann, Andrew T. Cowan, et al.. (2019). Yeast mitochondrial protein Pet111p binds directly to two distinct targets in COX2 mRNA, suggesting a mechanism of translational activation. Journal of Biological Chemistry. 294(18). 7528–7536. 14 indexed citations
7.
King, Graeme A., Ashutosh Pandey, Sundararajan Venkatesh, et al.. (2018). Acetylation and phosphorylation of human TFAM regulate TFAM–DNA interactions via contrasting mechanisms. Nucleic Acids Research. 46(7). 3633–3642. 68 indexed citations
8.
Hillen, Hauke S., Yaroslav I. Morozov, Azadeh Sarfallah, Dmitry Temiakov, & Patrick Cramer. (2017). Structural Basis of Mitochondrial Transcription Initiation. Cell. 171(5). 1072–1081.e10. 128 indexed citations
9.
Hillen, Hauke S., Karen Agaronyan, Yaroslav I. Morozov, et al.. (2017). Mechanism of Transcription Anti-termination in Human Mitochondria. Cell. 171(5). 1082–1093.e13. 67 indexed citations
10.
Morozov, Yaroslav I., Karen Agaronyan, Alan C. M. Cheung, et al.. (2014). A novel intermediate in transcription initiation by human mitochondrial RNA polymerase. Nucleic Acids Research. 42(6). 3884–3893. 55 indexed citations
11.
Cheung, Alan C. M., et al.. (2013). Structure of human mitochondrial RNA polymerase elongation complex. Nature Structural & Molecular Biology. 20(11). 1298–1303. 63 indexed citations
12.
Lü, Bin, Jae Lee, Xiaobo Nie, et al.. (2012). Phosphorylation of Human TFAM in Mitochondria Impairs DNA Binding and Promotes Degradation by the AAA+ Lon Protease. Molecular Cell. 49(1). 121–132. 253 indexed citations
13.
Morozov, Yaroslav I., et al.. (2011). Structure of human mitochondrial RNA polymerase. Nature. 478(7368). 269–273. 144 indexed citations
14.
Shi, Yonghong, M. V. Savkina, Michael Anikin, et al.. (2010). Human Mitochondrial Transcription Revisited. Journal of Biological Chemistry. 285(24). 18129–18133. 159 indexed citations
15.
Savkina, M. V., Dmitry Temiakov, William T. McAllister, & Michael Anikin. (2009). Multiple Functions of Yeast Mitochondrial Transcription Factor Mtf1p during Initiation. Journal of Biological Chemistry. 285(6). 3957–3964. 25 indexed citations
16.
Kashkina, Ekaterina, Michael Anikin, T.H. Tahirov, et al.. (2006). Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations. Nucleic Acids Research. 34(14). 4036–4045. 30 indexed citations
17.
Kashkina, Ekaterina, Michael Anikin, Florian Brueckner, et al.. (2006). Template Misalignment in Multisubunit RNA Polymerases and Transcription Fidelity. Molecular Cell. 24(2). 257–266. 34 indexed citations
18.
Temiakov, Dmitry, Nikolay Zenkin, Marina N. Vassylyeva, et al.. (2005). Structural Basis of Transcription Inhibition by Antibiotic Streptolydigin. Molecular Cell. 19(5). 655–666. 126 indexed citations
19.
Tahirov, T.H., Dmitry Temiakov, Michael Anikin, et al.. (2002). Structure of a T7 RNA polymerase elongation complex at 2.9 Å resolution. Nature. 420(6911). 43–50. 208 indexed citations
20.
Tonevitsky, Alexander, et al.. (1997). Preliminary crystallographic characterization of ricin agglutinin. Proteins Structure Function and Bioinformatics. 28(4). 586–589. 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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