Ildar Gainetdinov

2.8k total citations · 1 hit paper
26 papers, 1.8k citations indexed

About

Ildar Gainetdinov is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Ildar Gainetdinov has authored 26 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 17 papers in Plant Science and 5 papers in Genetics. Recurrent topics in Ildar Gainetdinov's work include Chromosomal and Genetic Variations (17 papers), CRISPR and Genetic Engineering (12 papers) and Advanced biosensing and bioanalysis techniques (7 papers). Ildar Gainetdinov is often cited by papers focused on Chromosomal and Genetic Variations (17 papers), CRISPR and Genetic Engineering (12 papers) and Advanced biosensing and bioanalysis techniques (7 papers). Ildar Gainetdinov collaborates with scholars based in United States, Russia and Belarus. Ildar Gainetdinov's co-authors include Phillip D. Zamore, Deniz M. Özata, Ansgar Zoch, Dónal O’Carroll, Cansu Colpan, Katharine Cecchini, Amena Arif, Zhiping Weng, Erik J. Sontheimer and Alireza Edraki and has published in prestigious journals such as Nature, Cell and Nature Genetics.

In The Last Decade

Ildar Gainetdinov

24 papers receiving 1.8k citations

Hit Papers

PIWI-interacting RNAs: sm... 2018 2026 2020 2023 2018 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ildar Gainetdinov United States 17 1.6k 842 296 259 74 26 1.8k
Constance Ciaudo Switzerland 22 1.6k 1.0× 577 0.7× 539 1.8× 380 1.5× 44 0.6× 41 2.1k
Kai Xu China 19 1.5k 1.0× 241 0.3× 321 1.1× 222 0.9× 54 0.7× 54 1.8k
Mikel Zaratiegui United States 20 1.6k 1.0× 618 0.7× 191 0.6× 303 1.2× 38 0.5× 31 2.0k
Fedor V. Karginov United States 17 1.8k 1.1× 120 0.1× 827 2.8× 160 0.6× 38 0.5× 28 2.0k
Jonathan Strecker United States 14 1.4k 0.9× 211 0.3× 27 0.1× 292 1.1× 77 1.0× 18 1.6k
Kazumichi M. Nishida Japan 14 2.3k 1.4× 1.9k 2.2× 257 0.9× 243 0.9× 75 1.0× 20 2.5k
Sergei Ryazansky Russia 16 982 0.6× 549 0.7× 97 0.3× 149 0.6× 19 0.3× 33 1.1k
Christian B. Matranga United States 10 1.7k 1.1× 495 0.6× 666 2.3× 104 0.4× 74 1.0× 14 2.0k
Elitza Deltcheva United Kingdom 7 1.9k 1.2× 180 0.2× 43 0.1× 423 1.6× 219 3.0× 10 2.0k

Countries citing papers authored by Ildar Gainetdinov

Since Specialization
Citations

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

Fields of papers citing papers by Ildar Gainetdinov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ildar Gainetdinov

This figure shows the co-authorship network connecting the top 25 collaborators of Ildar Gainetdinov. A scholar is included among the top collaborators of Ildar Gainetdinov 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 Ildar Gainetdinov. Ildar Gainetdinov 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.
Sieriebriennikov, Bogdan, Jennifer Wu, Ildar Gainetdinov, et al.. (2025). Transcriptional interferences ensure one olfactory receptor per ant neuron. Nature. 648(8093). 418–426.
3.
Lee, Seung Kyu, Weiping Shen, William Wen, et al.. (2025). Topoisomerase 3b facilitates piRNA biogenesis to promote transposon silencing and germ cell development. Cell Reports. 44(4). 115495–115495. 1 indexed citations
4.
Venkei, Zsolt, Ildar Gainetdinov, Margaret R. Starostik, et al.. (2023). A maternally programmed intergenerational mechanism enables male offspring to make piRNAs from Y-linked precursor RNAs in Drosophila. Nature Cell Biology. 25(10). 1495–1505. 6 indexed citations
5.
Gainetdinov, Ildar, Joel Vega‐Badillo, Katharine Cecchini, et al.. (2023). Relaxed targeting rules help PIWI proteins silence transposons. Nature. 619(7969). 394–402. 42 indexed citations
6.
Arif, Amena, Shannon M. Bailey, Natsuko Izumi, et al.. (2022). GTSF1 accelerates target RNA cleavage by PIWI-clade Argonaute proteins. Nature. 608(7923). 618–625. 39 indexed citations
7.
Cecchini, Katharine, Tianxiong Yu, Haiwei Mou, et al.. (2022). The transcription factor TCFL5 responds to A-MYB to elaborate the male meiotic program in mice. Reproduction. 165(2). 183–196. 16 indexed citations
8.
Gainetdinov, Ildar, Cansu Colpan, Katharine Cecchini, et al.. (2021). Terminal modification, sequence, length, and PIWI-protein identity determine piRNA stability. Molecular Cell. 81(23). 4826–4842.e8. 41 indexed citations
9.
Wu, Pei-Hsuan, Yu Fu, Katharine Cecchini, et al.. (2020). The evolutionarily conserved piRNA-producing locus pi6 is required for male mouse fertility. Nature Genetics. 52(7). 728–739. 93 indexed citations
10.
Jolly, Samson M., Ildar Gainetdinov, Karina Jouravleva, et al.. (2020). Thermus thermophilus Argonaute Functions in the Completion of DNA Replication. Cell. 182(6). 1545–1559.e18. 81 indexed citations
11.
Özata, Deniz M., Tianxiong Yu, Haiwei Mou, et al.. (2019). Evolutionarily conserved pachytene piRNA loci are highly divergent among modern humans. Nature Ecology & Evolution. 4(1). 156–168. 68 indexed citations
12.
Gainetdinov, Ildar, et al.. (2018). Assessment of piRNA biogenesis and function in testicular germ cell tumors and their precursor germ cell neoplasia in situ. BMC Cancer. 18(1). 20–20. 21 indexed citations
13.
Özata, Deniz M., Ildar Gainetdinov, Ansgar Zoch, Dónal O’Carroll, & Phillip D. Zamore. (2018). PIWI-interacting RNAs: small RNAs with big functions. Nature Reviews Genetics. 20(2). 89–108. 778 indexed citations breakdown →
14.
Lee, Jooyoung, Aamir Mir, Alireza Edraki, et al.. (2018). Potent Cas9 Inhibition in Bacterial and Human Cells by AcrIIC4 and AcrIIC5 Anti-CRISPR Proteins. mBio. 9(6). 79 indexed citations
15.
Gainetdinov, Ildar, Cansu Colpan, Amena Arif, Katharine Cecchini, & Phillip D. Zamore. (2018). A Single Mechanism of Biogenesis, Initiated and Directed by PIWI Proteins, Explains piRNA Production in Most Animals. Molecular Cell. 71(5). 775–790.e5. 149 indexed citations
16.
Gainetdinov, Ildar, et al.. (2017). Two modes of targeting transposable elements by piRNA pathway in human testis. RNA. 23(11). 1614–1625. 34 indexed citations
17.
Zinovyeva, M. V., et al.. (2016). Intragenic Locus in Human PIWIL2 Gene Shares Promoter and Enhancer Functions. PLoS ONE. 11(6). e0156454–e0156454. 3 indexed citations
18.
Gainetdinov, Ildar, Elena Y. Rykova, Anastasia A. Ponomaryova, et al.. (2016). Hypomethylation of human-specific family of LINE-1 retrotransposons in circulating DNA of lung cancer patients. Lung Cancer. 99. 127–130. 21 indexed citations
20.
Azhikina, Tatyana, et al.. (2003). Non-methylated Genomic Sites Coincidence Cloning (NGSCC): an approach to large scale analysis of hypomethylated CpG patterns at predetermined genomic loci. Molecular Genetics and Genomics. 271(1). 22–32. 15 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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