Sergei Gaidamakov

1.5k total citations
17 papers, 1.2k citations indexed

About

Sergei Gaidamakov is a scholar working on Molecular Biology, Ecology and Infectious Diseases. According to data from OpenAlex, Sergei Gaidamakov has authored 17 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 3 papers in Ecology and 2 papers in Infectious Diseases. Recurrent topics in Sergei Gaidamakov's work include RNA and protein synthesis mechanisms (10 papers), RNA Research and Splicing (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). Sergei Gaidamakov is often cited by papers focused on RNA and protein synthesis mechanisms (10 papers), RNA Research and Splicing (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). Sergei Gaidamakov collaborates with scholars based in United States, Russia and Canada. Sergei Gaidamakov's co-authors include Robert J. Crouch, Marcin Nowotny, Wei Yang, Susana M. Cerritelli, Rodolfo Ghirlando, Richard J Maraia, Guennadi Kozlov, Joowon Lee, Kalle Gehring and Sandy Mattijssen and has published in prestigious journals such as Cell, Nucleic Acids Research and The EMBO Journal.

In The Last Decade

Sergei Gaidamakov

17 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergei Gaidamakov United States 13 1.0k 186 138 132 118 17 1.2k
Peter Frank United States 18 1.2k 1.2× 134 0.7× 153 1.1× 81 0.6× 74 0.6× 36 1.4k
Marta del Álamo Spain 11 506 0.5× 111 0.6× 85 0.6× 164 1.2× 140 1.2× 15 684
U. Sen India 16 591 0.6× 87 0.5× 239 1.7× 133 1.0× 97 0.8× 45 830
Gilles Mirambeau France 18 1.1k 1.0× 268 1.4× 188 1.4× 421 3.2× 194 1.6× 29 1.4k
Zhufang Li United States 16 454 0.4× 255 1.4× 126 0.9× 204 1.5× 40 0.3× 23 824
Ravi Vinayak United States 17 840 0.8× 86 0.5× 78 0.6× 67 0.5× 79 0.7× 35 937
Elisabetta Viani Puglisi United States 15 624 0.6× 115 0.6× 84 0.6× 118 0.9× 45 0.4× 27 723
Michelle West Frey United States 8 506 0.5× 112 0.6× 153 1.1× 130 1.0× 95 0.8× 9 664
Alexander Litovchick Israel 14 625 0.6× 71 0.4× 60 0.4× 139 1.1× 93 0.8× 17 738
Akash Bhattacharya United States 13 521 0.5× 216 1.2× 53 0.4× 337 2.6× 48 0.4× 35 809

Countries citing papers authored by Sergei Gaidamakov

Since Specialization
Citations

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

Fields of papers citing papers by Sergei Gaidamakov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergei Gaidamakov

This figure shows the co-authorship network connecting the top 25 collaborators of Sergei Gaidamakov. A scholar is included among the top collaborators of Sergei Gaidamakov 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 Sergei Gaidamakov. Sergei Gaidamakov is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Kozlov, Guennadi, Sandy Mattijssen, Tara Sprules, et al.. (2022). Structural basis of 3′-end poly(A) RNA recognition by LARP1. Nucleic Acids Research. 50(16). 9534–9547. 19 indexed citations
2.
Mattijssen, Sandy, Guennadi Kozlov, Sergei Gaidamakov, et al.. (2020). The isolated La-module of LARP1 mediates 3’ poly(A) protection and mRNA stabilization, dependent on its intrinsic PAM2 binding to PABPC1. RNA Biology. 18(2). 275–289. 26 indexed citations
3.
Tian, Yi, Zhouhao Zeng, Xiang Li, et al.. (2020). Transcriptome-wide stability analysis uncovers LARP4-mediated NFκB1 mRNA stabilization during T cell activation. Nucleic Acids Research. 48(15). 8724–8739. 10 indexed citations
4.
Blewett, Nathan H., James Iben, Sergei Gaidamakov, & Richard J Maraia. (2017). La Deletion from Mouse Brain Alters Pre-tRNA Metabolism and Accumulation of Pre-5.8S rRNA, with Neuron Death and Reactive Astrocytosis. Molecular and Cellular Biology. 37(10). 8 indexed citations
5.
Mattijssen, Sandy, Gopalakrishnan Aneeshkumar Arimbasseri, James Iben, et al.. (2017). LARP4 mRNA codon-tRNA match contributes to LARP4 activity for ribosomal protein mRNA poly(A) tail length protection. eLife. 6. 40 indexed citations
6.
Gaidamakov, Sergei, Olga A. Maximova, Hyongi Chon, et al.. (2013). Targeted Deletion of the Gene Encoding the La Autoantigen (Sjögren's Syndrome Antigen B) in B Cells or the Frontal Brain Causes Extensive Tissue Loss. Molecular and Cellular Biology. 34(1). 123–131. 21 indexed citations
7.
Yang, Ruiqing, Sergei Gaidamakov, Jingwei Xie, et al.. (2010). La-Related Protein 4 Binds Poly(A), Interacts with the Poly(A)-Binding Protein MLLE Domain via a Variant PAM2w Motif, and Can Promote mRNA Stability. Molecular and Cellular Biology. 31(3). 542–556. 81 indexed citations
8.
Nowotny, Marcin, Susana M. Cerritelli, Rodolfo Ghirlando, et al.. (2008). Specific recognition of RNA/DNA hybrid and enhancement of human RNase H1 activity by HBD. The EMBO Journal. 27(7). 1172–1181. 82 indexed citations
9.
Nowotny, Marcin, et al.. (2007). Structure of Human RNase H1 Complexed with an RNA/DNA Hybrid: Insight into HIV Reverse Transcription. Molecular Cell. 28(3). 513–513. 12 indexed citations
10.
Nowotny, Marcin, Sergei Gaidamakov, Rodolfo Ghirlando, et al.. (2007). Structure of Human RNase H1 Complexed with an RNA/DNA Hybrid: Insight into HIV Reverse Transcription. Molecular Cell. 28(2). 264–276. 265 indexed citations
11.
Nowotny, Marcin, Sergei Gaidamakov, Robert J. Crouch, & Wei Yang. (2005). Crystal Structures of RNase H Bound to an RNA/DNA Hybrid: Substrate Specificity and Metal-Dependent Catalysis. Cell. 121(7). 1005–1016. 498 indexed citations
12.
Gaidamakov, Sergei. (2005). Eukaryotic RNases H1 act processively by interactions through the duplex RNA-binding domain. Nucleic Acids Research. 33(7). 2166–2175. 45 indexed citations
13.
Chan, King C., Scott R. Budihas, Stuart F.J. Le Grice, et al.. (2004). A capillary electrophoretic assay for ribonuclease H activity. Analytical Biochemistry. 331(2). 296–302. 24 indexed citations
14.
Gaidamakov, Sergei, et al.. (1999). [Sensitized photomodification of DNA with binary systems of oligonucleotide conjugates. IV. Photoinduced electron transfer].. PubMed. 25(1). 31–9. 1 indexed citations
15.
Gaidamakov, Sergei, et al.. (1997). Sensitized Photomodification of Single-Stranded DNA by a Binary System of Oligonucleotide Conjugates. Antisense and Nucleic Acid Drug Development. 7(4). 309–317. 17 indexed citations
16.
Vlassov, Valentin V., et al.. (1988). Sequence-specific chemical modification of double-stranded DNA with alkylating oligodeoxyribonucleotide derivatives. Gene. 72(1-2). 313–322. 31 indexed citations
17.
Vlassov, Valentin V., Sergei Gaidamakov, Vladimir V. Gorn, & S. A. Grachev. (1985). Sequence‐specific chemical modification of a 365‐nucleotide‐long DNA fragment with an alkylating oligonucleotide derivative. FEBS Letters. 182(2). 415–418. 7 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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