Igor Iatsenko

1.3k total citations
21 papers, 795 citations indexed

About

Igor Iatsenko is a scholar working on Insect Science, Immunology and Molecular Biology. According to data from OpenAlex, Igor Iatsenko has authored 21 papers receiving a total of 795 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Insect Science, 12 papers in Immunology and 6 papers in Molecular Biology. Recurrent topics in Igor Iatsenko's work include Invertebrate Immune Response Mechanisms (12 papers), Insect symbiosis and bacterial influences (10 papers) and Genetics, Aging, and Longevity in Model Organisms (5 papers). Igor Iatsenko is often cited by papers focused on Invertebrate Immune Response Mechanisms (12 papers), Insect symbiosis and bacterial influences (10 papers) and Genetics, Aging, and Longevity in Model Organisms (5 papers). Igor Iatsenko collaborates with scholars based in Germany, Switzerland and Japan. Igor Iatsenko's co-authors include Bruno Lemaître, Jean‐Philippe Boquete, Ralf J. Sommer, Shu Kondo, Mark A. Hanson, Alice Marra, Robbie Rae, Dominique Mengin‐Lecreulx, Jan P. Dudzic and Jasquelin Peña and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Immunity.

In The Last Decade

Igor Iatsenko

21 papers receiving 792 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Igor Iatsenko Germany 15 429 336 260 111 107 21 795
Jean‐Philippe Boquete Switzerland 10 386 0.9× 484 1.4× 260 1.0× 79 0.7× 43 0.4× 11 844
Samuel Liégeois France 12 473 1.1× 480 1.4× 464 1.8× 149 1.3× 51 0.5× 18 1.1k
Dani Osman Lebanon 15 456 1.1× 578 1.7× 325 1.3× 79 0.7× 54 0.5× 26 994
Takayuki Kuraishi Japan 17 555 1.3× 782 2.3× 374 1.4× 68 0.6× 59 0.6× 31 1.3k
W. Robert Shaw United States 15 453 1.1× 148 0.4× 218 0.8× 68 0.6× 95 0.9× 24 981
Olivier Binggeli Switzerland 7 507 1.2× 457 1.4× 176 0.7× 18 0.2× 91 0.9× 8 746
Eileen Knorr Germany 14 461 1.1× 220 0.7× 435 1.7× 18 0.2× 169 1.6× 20 761
Hyuck‐Jin Nam South Korea 12 584 1.4× 743 2.2× 287 1.1× 38 0.3× 46 0.4× 16 1.0k
Young Seok Hong United States 14 220 0.5× 140 0.4× 393 1.5× 23 0.2× 205 1.9× 28 735
Jonathan Revah United States 7 296 0.7× 353 1.1× 144 0.6× 38 0.3× 23 0.2× 7 542

Countries citing papers authored by Igor Iatsenko

Since Specialization
Citations

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

Fields of papers citing papers by Igor Iatsenko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Igor Iatsenko

This figure shows the co-authorship network connecting the top 25 collaborators of Igor Iatsenko. A scholar is included among the top collaborators of Igor Iatsenko 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 Igor Iatsenko. Igor Iatsenko 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.
Hurwitz, Robert, et al.. (2025). Infection-induced elevation of gut glycosaminoglycans fosters microbiota expansion in Drosophila melanogaster. Cell Reports. 44(12). 116598–116598. 1 indexed citations
2.
Iatsenko, Igor, et al.. (2025). Colonization island directs L. plantarum to its niche. Cell Host & Microbe. 33(2). 168–170. 2 indexed citations
3.
Arifah, Adini Qisthi, Georgia Angelidou, Volker Brinkmann, et al.. (2024). MprF-mediated immune evasion is necessary for Lactiplantibacillus plantarum resilience in the Drosophila gut during inflammation. PLoS Pathogens. 20(8). e1012462–e1012462. 5 indexed citations
4.
5.
Hurwitz, Robert, et al.. (2023). Resistance to host antimicrobial peptides mediates resilience of gut commensals during infection and aging in Drosophila. Proceedings of the National Academy of Sciences. 120(36). e2305649120–e2305649120. 21 indexed citations
6.
7.
Iatsenko, Igor, et al.. (2022). The Role of Microbiota in Drosophila melanogaster Aging. SHILAP Revista de lepidopterología. 3. 909509–909509. 26 indexed citations
8.
Hanson, Mark A., Lianne B. Cohen, Alice Marra, et al.. (2021). The Drosophila Baramicin polypeptide gene protects against fungal infection. PLoS Pathogens. 17(8). e1009846–e1009846. 40 indexed citations
9.
Iatsenko, Igor, et al.. (2021). The roles of metals in insect–microbe interactions and immunity. Current Opinion in Insect Science. 49. 71–77. 35 indexed citations
10.
Iatsenko, Igor, Alice Marra, Jean‐Philippe Boquete, Jasquelin Peña, & Bruno Lemaître. (2020). Iron sequestration by transferrin 1 mediates nutritional immunity in Drosophila melanogaster. Proceedings of the National Academy of Sciences. 117(13). 7317–7325. 90 indexed citations
11.
Dudzic, Jan P., Mark A. Hanson, Igor Iatsenko, Shu Kondo, & Bruno Lemaître. (2019). More Than Black or White: Melanization and Toll Share Regulatory Serine Proteases in Drosophila. Cell Reports. 27(4). 1050–1061.e3. 95 indexed citations
12.
Iatsenko, Igor, Jean‐Philippe Boquete, & Bruno Lemaître. (2018). Microbiota-Derived Lactate Activates Production of Reactive Oxygen Species by the Intestinal NADPH Oxidase Nox and Shortens Drosophila Lifespan. Immunity. 49(5). 929–942.e5. 165 indexed citations
13.
Iatsenko, Igor, Shu Kondo, Dominique Mengin‐Lecreulx, & Bruno Lemaître. (2016). PGRP-SD, an Extracellular Pattern-Recognition Receptor, Enhances Peptidoglycan-Mediated Activation of the Drosophila Imd Pathway. Immunity. 45(5). 1013–1023. 82 indexed citations
14.
Iatsenko, Igor, Joshua J. Yim, Frank C. Schroeder, & Ralf J. Sommer. (2014). B. subtilis GS67 Protects C. elegans from Gram-Positive Pathogens via Fengycin-Mediated Microbial Antagonism. Current Biology. 24(22). 2720–2727. 32 indexed citations
15.
Iatsenko, Igor, Iuliia Boichenko, & Ralf J. Sommer. (2014). Bacillus thuringiensis DB27 Produces Two Novel Protoxins, Cry21Fa1 and Cry21Ha1, Which Act Synergistically against Nematodes. Applied and Environmental Microbiology. 80(10). 3266–3275. 36 indexed citations
16.
Iatsenko, Igor, Craig Corton, Derek Pickard, Gordon Dougan, & Ralf J. Sommer. (2014). Draft Genome Sequence of Highly Nematicidal Bacillus thuringiensis DB27. Genome Announcements. 2(1). 10 indexed citations
17.
18.
Iatsenko, Igor, Amit Sinha, Christian Rödelsperger, & Ralf J. Sommer. (2013). New Role for DCR-1/Dicer in Caenorhabditis elegans Innate Immunity against the Highly Virulent Bacterium Bacillus thuringiensis DB27. Infection and Immunity. 81(10). 3942–3957. 22 indexed citations
19.
Sinha, Amit, Robbie Rae, Igor Iatsenko, & Ralf J. Sommer. (2012). System Wide Analysis of the Evolution of Innate Immunity in the Nematode Model Species Caenorhabditis elegans and Pristionchus pacificus. PLoS ONE. 7(9). e44255–e44255. 43 indexed citations
20.
Rae, Robbie, et al.. (2010). A subset of naturally isolated Bacillus strains show extreme virulence to the free‐living nematodes Caenorhabditis elegans and Pristionchus pacificus. Environmental Microbiology. 12(11). 3007–3021. 44 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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