Э. М. Баричева

628 total citations
45 papers, 453 citations indexed

About

Э. М. Баричева is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Э. М. Баричева has authored 45 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 16 papers in Genetics and 13 papers in Plant Science. Recurrent topics in Э. М. Баричева's work include Developmental Biology and Gene Regulation (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers) and Chromosomal and Genetic Variations (9 papers). Э. М. Баричева is often cited by papers focused on Developmental Biology and Gene Regulation (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers) and Chromosomal and Genetic Variations (9 papers). Э. М. Баричева collaborates with scholars based in Russia, United States and Iran. Э. М. Баричева's co-authors include E. S. Belyaeva, И. Ф. Жимулев, V. F. Semeshin, Anna A. Ogienko, Evgeniya S. Omelina, Igor V. Sharakhov, Т. И. Меркулова, Maria V. Sharakhova, Dmitry Oshchepkov and Anastasia N. Naumenko and has published in prestigious journals such as FEBS Letters, International Journal of Molecular Sciences and Molecular Ecology.

In The Last Decade

Э. М. Баричева

45 papers receiving 449 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Э. М. Баричева Russia 14 343 155 103 55 43 45 453
Inna Biryukova Sweden 14 366 1.1× 106 0.7× 62 0.6× 45 0.8× 55 1.3× 23 498
Susan E. Lott United States 10 394 1.1× 107 0.7× 149 1.4× 20 0.4× 17 0.4× 15 491
Josefa Steinhauer United States 13 268 0.8× 55 0.4× 148 1.4× 33 0.6× 34 0.8× 17 480
Diane Bortolamiol-Bécet United States 11 486 1.4× 164 1.1× 46 0.4× 23 0.4× 63 1.5× 15 636
Olga Grushko United States 11 183 0.5× 71 0.5× 94 0.9× 152 2.8× 33 0.8× 12 381
Nina Bausek United Kingdom 10 175 0.5× 41 0.3× 132 1.3× 92 1.7× 63 1.5× 13 409
Jeremy E. Sandler United States 7 384 1.1× 82 0.5× 59 0.6× 80 1.5× 51 1.2× 9 468
Ok-Kyung Lee United States 7 368 1.1× 87 0.6× 146 1.4× 28 0.5× 28 0.7× 16 460
Pauline Cottee Australia 12 368 1.1× 88 0.6× 35 0.3× 28 0.5× 28 0.7× 15 636
C. Sim United States 8 196 0.6× 126 0.8× 71 0.7× 56 1.0× 46 1.1× 10 355

Countries citing papers authored by Э. М. Баричева

Since Specialization
Citations

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

Fields of papers citing papers by Э. М. Баричева

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Э. М. Баричева. 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 Э. М. Баричева. The network helps show where Э. М. Баричева may publish in the future.

Co-authorship network of co-authors of Э. М. Баричева

This figure shows the co-authorship network connecting the top 25 collaborators of Э. М. Баричева. A scholar is included among the top collaborators of Э. М. Баричева 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 Э. М. Баричева. Э. М. Баричева 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.
Yurchenko, Andrey A., Anastasia N. Naumenko, Gleb N. Artemov, et al.. (2023). Phylogenomics revealed migration routes and adaptive radiation timing of Holarctic malaria mosquito species of the Maculipennis Group. BMC Biology. 21(1). 63–63. 2 indexed citations
3.
Баричева, Э. М., et al.. (2023). The misregulation of mitochondria-associated genes caused by GAGA-factor lack promotes autophagic germ cell death in Drosophila testes. Genetica. 151(6). 349–355. 1 indexed citations
4.
Баричева, Э. М., et al.. (2021). Lack of GAGA protein in Trl mutants causes massive cell death in Drosophila spermatogenesis and oogenesis. Vavilov Journal of Genetics and Breeding. 25(3). 292–300. 1 indexed citations
5.
Ogienko, Anna A., et al.. (2020). GAGA Regulates Border Cell Migration in Drosophila. International Journal of Molecular Sciences. 21(20). 7468–7468. 3 indexed citations
6.
Naumenko, Anastasia N., Andrey A. Yurchenko, Э. М. Баричева, et al.. (2020). Chromosome and Genome Divergence between the Cryptic Eurasian Malaria Vector-Species Anopheles messeae and Anopheles daciae. Genes. 11(2). 165–165. 17 indexed citations
7.
Баричева, Э. М., et al.. (2020). Loss of Drosophila E3 Ubiquitin Ligase Hyd Promotes Extra Mitosis in Germline Cysts and Massive Cell Death During Oogenesis. Frontiers in Cell and Developmental Biology. 8. 600868–600868. 1 indexed citations
8.
Ogienko, Anna A., et al.. (2018). New slbo-Gal4 driver lines for the analysis of border cell migration during Drosophila oogenesis. Chromosoma. 127(4). 475–487. 6 indexed citations
9.
Меркулова, Т. И., et al.. (2016). The reasons of Trithorax-like expression disturbance in Trl 3609 allele of Drosophila melanogaster. Doklady Biochemistry and Biophysics. 471(1). 443–446. 3 indexed citations
10.
Omelina, Evgeniya S., et al.. (2013). Identification of functionally significant elements in the second intron of the Drosophila melanogaster Trithorax-like gene. Gene. 520(2). 178–184. 6 indexed citations
11.
Kamali, Maryam, et al.. (2011). An Integrated Chromosome Map of Microsatellite Markers and Inversion Breakpoints for an Asian Malaria Mosquito, Anopheles stephensi. Journal of Heredity. 102(6). 719–726. 13 indexed citations
12.
Omelina, Evgeniya S., N. V. Pavlova, Anna A. Ogienko, & Э. М. Баричева. (2011). The GAGA protein is essential for dorsal appendage formation during Drosophila melanogaster oogenesis. Doklady Biochemistry and Biophysics. 436(1). 32–34. 4 indexed citations
13.
Omelina, Evgeniya S., Э. М. Баричева, Dmitry Oshchepkov, & Т. И. Меркулова. (2011). Analysis and recognition of the GAGA transcription factor binding sites in Drosophila genes. Computational Biology and Chemistry. 35(6). 363–370. 29 indexed citations
14.
Voronin, Denis, et al.. (2009). [Influence of Drosophila melanogaster genotype on biological effects of endocymbiont Wolbachia (stamm wMelPop)].. PubMed. 51(4). 335–45. 2 indexed citations
15.
Савватеева-Попова, Е. В., Н. Г. Камышев, А. В. Попов, et al.. (2002). Complex Study of Drosophila Mutants in the agnostic Locus: A Model for Coupling Chromosomal Architecture and Cognitive Functions. Journal of Evolutionary Biochemistry and Physiology. 38(6). 706–733. 4 indexed citations
16.
Баричева, Э. М., et al.. (1993). A molecular and cytogenetic analysis of λ 20p7 fragment DNA from the proximal β-heterochromatin of Drosophila melanogaster. Gene. 134(2). 175–181. 4 indexed citations
17.
Belyaeva, E. S., et al.. (1991). Cytogenetic and molecular aspects of position effect variegation in Drosophila melanogaster. Chromosoma. 101(1). 55–61. 46 indexed citations
18.
Жимулев, И. Ф., et al.. (1988). Cytogenetic and molecular aspects of position effect variegation in Drosophila melanogaster. Chromosoma. 96(3). 255–261. 25 indexed citations
19.
Semeshin, V. F., Э. М. Баричева, E. S. Belyaeva, & И. Ф. Жимулев. (1985). Electron microscopical analysis of Drosophila polytene chromosomes. Chromosoma. 91(3-4). 210–233. 45 indexed citations
20.
Баричева, Э. М., et al.. (1979). Drosophila virilis puffs induced by temperature and other environmental factors. Genetika. 15(8). 1399–1414. 12 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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