Sergey Stolyar

2.3k total citations
28 papers, 1.6k citations indexed

About

Sergey Stolyar is a scholar working on Molecular Biology, Ecology and Pollution. According to data from OpenAlex, Sergey Stolyar has authored 28 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 7 papers in Ecology and 4 papers in Pollution. Recurrent topics in Sergey Stolyar's work include Microbial Metabolic Engineering and Bioproduction (8 papers), Microbial Community Ecology and Physiology (7 papers) and Microbial metabolism and enzyme function (5 papers). Sergey Stolyar is often cited by papers focused on Microbial Metabolic Engineering and Bioproduction (8 papers), Microbial Community Ecology and Physiology (7 papers) and Microbial metabolism and enzyme function (5 papers). Sergey Stolyar collaborates with scholars based in United States, Canada and Russia. Sergey Stolyar's co-authors include David A. Stahl, Eugene Kolker, John A. Leigh, Nicolás Pinel, Kristina L. Hillesland, Thomas J. Lie, Andrew Keller, Alexey I. Nesvizhskii, David R. Goodlett and Samuel Purvine and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Bioinformatics.

In The Last Decade

Sergey Stolyar

28 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergey Stolyar United States 17 1.1k 403 238 192 180 28 1.6k
Biswarup Mukhopadhyay United States 26 1.1k 1.0× 282 0.7× 148 0.6× 131 0.7× 92 0.5× 65 1.6k
Jagroop Pandhal United Kingdom 26 900 0.8× 326 0.8× 228 1.0× 204 1.1× 168 0.9× 67 1.8k
Margaret Wexler United Kingdom 25 838 0.8× 654 1.6× 151 0.6× 324 1.7× 84 0.5× 33 2.0k
Hans C. Bernstein United States 22 1.0k 0.9× 521 1.3× 253 1.1× 150 0.8× 33 0.2× 56 1.7k
Jung-Hyun Lee South Korea 29 1.9k 1.7× 773 1.9× 312 1.3× 181 0.9× 31 0.2× 113 2.7k
Thomas Hübschmann Germany 26 1.1k 1.0× 428 1.1× 160 0.7× 145 0.8× 23 0.1× 40 1.8k
Muriel C. F. van Teeseling Germany 17 723 0.7× 437 1.1× 76 0.3× 154 0.8× 37 0.2× 24 1.2k
Yanfen Xue China 34 1.8k 1.6× 639 1.6× 914 3.8× 88 0.5× 43 0.2× 121 2.7k
Tatyana N. Chernikova Germany 24 1.0k 0.9× 745 1.8× 307 1.3× 59 0.3× 64 0.4× 41 2.1k
Yuri Grechkin United States 5 1.3k 1.2× 807 2.0× 146 0.6× 156 0.8× 16 0.1× 5 1.9k

Countries citing papers authored by Sergey Stolyar

Since Specialization
Citations

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

Fields of papers citing papers by Sergey Stolyar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergey Stolyar

This figure shows the co-authorship network connecting the top 25 collaborators of Sergey Stolyar. A scholar is included among the top collaborators of Sergey Stolyar 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 Sergey Stolyar. Sergey Stolyar 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.
2.
He, Lian, et al.. (2025). Growth Analysis of Methylotuvimicrobium buryatense 5GB1C and Its Utilization for Treating Low Methane Concentrations in a Packed-Bed Column Reactor. SHILAP Revista de lepidopterología. 4(4). 22–22. 1 indexed citations
3.
Leducq, Jean‐Baptiste, Geneviève Bourret, N. Cecilia Martínez-Gómez, et al.. (2022). Comprehensive Phylogenomics of Methylobacterium Reveals Four Evolutionary Distinct Groups and Underappreciated Phyllosphere Diversity. Genome Biology and Evolution. 14(8). 17 indexed citations
4.
Lee, Jessica A., Sergey Stolyar, & Christopher J. Marx. (2022). Aerobic Methoxydotrophy: Growth on Methoxylated Aromatic Compounds by Methylobacteriaceae. Frontiers in Microbiology. 13. 849573–849573. 9 indexed citations
5.
Dalia, Ankur B., Chelsea Hayes, Sergey Stolyar, Christopher J. Marx, & James B. McKinlay. (2017). Multiplex Genome Editing by Natural Transformation (MuGENT) for Synthetic Biology in Vibrio natriegens. ACS Synthetic Biology. 6(9). 1650–1655. 108 indexed citations
6.
Turkarslan, Serdar, Arjun V. Raman, Anne Thompson, et al.. (2017). Mechanism for microbial population collapse in a fluctuating resource environment. Molecular Systems Biology. 13(3). 919–919. 17 indexed citations
7.
Thompson, Anne, Matthew J. Crow, Serdar Turkarslan, et al.. (2015). A method to analyze, sort, and retain viability of obligate anaerobic microorganisms from complex microbial communities. Journal of Microbiological Methods. 117. 74–77. 12 indexed citations
8.
Stolyar, Sergey, et al.. (2014). Culturing Anaerobes to Use as a Model System for Studying the Evolution of Syntrophic Mutualism. Methods in molecular biology. 1151. 103–115. 2 indexed citations
9.
Stolyar, Sergey, Zhenfeng Liu, Vera Thiel, et al.. (2014). Genome Sequence of the Thermophilic Cyanobacterium Thermosynechococcus sp. Strain NK55a. Genome Announcements. 2(1). 15 indexed citations
10.
Melnicki, Matthew R., Grigoriy E. Pinchuk, Eric A. Hill, et al.. (2013). Feedback-controlled LED photobioreactor for photophysiological studies of cyanobacteria. Bioresource Technology. 134. 127–133. 32 indexed citations
11.
Rodionova, Irina A., Xiaoqing Li, Vera Thiel, et al.. (2013). Comparative genomics and functional analysis of rhamnose catabolic pathways and regulons in bacteria. Frontiers in Microbiology. 4. 407–407. 51 indexed citations
12.
Lindemann, Stephen R., James Moran, Alice Dohnálková, et al.. (2012). Microbial Diversity and Biogeochemical Function of the Phototrophic Microbial Mats of Epsomitic Hot Lake, WA. Microscopy and Microanalysis. 18(S2). 10–11. 2 indexed citations
13.
Walker, C. B., Zhili He, Zamin K. Yang, et al.. (2009). The Electron Transfer System of Syntrophically Grown Desulfovibrio vulgaris. Journal of Bacteriology. 191(18). 5793–5801. 115 indexed citations
14.
Walker, C. B., Sergey Stolyar, Dylan Chivian, et al.. (2009). Contribution of mobile genetic elements to Desulfovibrio vulgaris genome plasticity. Environmental Microbiology. 11(9). 2244–2252. 16 indexed citations
15.
Martens‐Habbena, Willm, Tiansong Wang, Murray Hackett, et al.. (2009). Methylophilaceae link methanol oxidation to denitrification in freshwater lake sediment as suggested by stable isotope probing and pure culture analysis. Environmental Microbiology Reports. 1(5). 385–392. 130 indexed citations
16.
Stolyar, Sergey, Qiang He, Marcin P. Joachimiak, et al.. (2007). Response of Desulfovibrio vulgaris to Alkaline Stress. Journal of Bacteriology. 189(24). 8944–8952. 49 indexed citations
17.
Kalyuzhnaya, Marina, Sergey Stolyar, Ann J. Auman, et al.. (2005). Methylosarcina lacus sp. nov., a methanotroph from Lake Washington, Seattle, USA, and emended description of the genus Methylosarcina. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 55(6). 2345–2350. 37 indexed citations
18.
Tjaden, Brian, David R. Haynor, Sergey Stolyar, Carsten Rosenow, & Eugene Kolker. (2002). Identifying operons and untranslated regions of transcripts using Escherichia coli RNA expression analysis. Bioinformatics. 18(suppl_1). S337–S344. 35 indexed citations
19.
Tjaden, Brian, et al.. (2002). Transcriptome analysis of Escherichia coli using high-density oligonucleotide probe arrays. Nucleic Acids Research. 30(17). 3732–3738. 142 indexed citations
20.
Pirog, Tatiana, et al.. (2000). Isolation and characterization ofAcinetobacter sp. mutants defective in exopolysaccharide biosynthesis. Microbiology. 69(5). 565–570. 3 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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