Alexander Y. Konev

723 total citations
20 papers, 583 citations indexed

About

Alexander Y. Konev is a scholar working on Molecular Biology, Plant Science and Physiology. According to data from OpenAlex, Alexander Y. Konev has authored 20 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Plant Science and 5 papers in Physiology. Recurrent topics in Alexander Y. Konev's work include Chromosomal and Genetic Variations (11 papers), Genomics and Chromatin Dynamics (10 papers) and Telomeres, Telomerase, and Senescence (5 papers). Alexander Y. Konev is often cited by papers focused on Chromosomal and Genetic Variations (11 papers), Genomics and Chromatin Dynamics (10 papers) and Telomeres, Telomerase, and Senescence (5 papers). Alexander Y. Konev collaborates with scholars based in United States, Russia and Austria. Alexander Y. Konev's co-authors include Alexander Emelyanov, Dmitry V. Fyodorov, James M. Mason, Harald Biessmann, James T. Kadonaga, Sung Yeon Park, Chin Yan Lim, Valerie Podhraski, Vincenzo Pirrotta and Alexandra Lusser and has published in prestigious journals such as Science, Journal of Biological Chemistry and Genes & Development.

In The Last Decade

Alexander Y. Konev

19 papers receiving 580 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexander Y. Konev United States 12 546 267 82 72 24 20 583
Paul Szauter United States 8 413 0.8× 175 0.7× 41 0.5× 107 1.5× 20 0.8× 12 468
Heiko Schober Switzerland 7 848 1.6× 136 0.5× 84 1.0× 60 0.8× 33 1.4× 7 895
L. S. Melnikova Russia 13 568 1.0× 350 1.3× 98 1.2× 68 0.9× 31 1.3× 49 613
Lutz R. Gehlen Switzerland 10 781 1.4× 142 0.5× 56 0.7× 71 1.0× 32 1.3× 11 818
Daniel Peric‐Hupkes Netherlands 8 599 1.1× 99 0.4× 31 0.4× 44 0.6× 21 0.9× 9 635
Pierre-Marie Dehé France 14 746 1.4× 99 0.4× 73 0.9× 51 0.7× 42 1.8× 15 786
Bhargavi Rao United States 6 907 1.7× 154 0.6× 14 0.2× 69 1.0× 15 0.6× 6 956
Ja-Hwan Seol United States 9 498 0.9× 71 0.3× 50 0.6× 57 0.8× 69 2.9× 9 545
Véra Schramke France 7 609 1.1× 221 0.8× 124 1.5× 40 0.6× 39 1.6× 7 671
Julien Soudet Switzerland 9 685 1.3× 52 0.2× 119 1.5× 32 0.4× 48 2.0× 13 745

Countries citing papers authored by Alexander Y. Konev

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Y. Konev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander Y. Konev. 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 Alexander Y. Konev. The network helps show where Alexander Y. Konev may publish in the future.

Co-authorship network of co-authors of Alexander Y. Konev

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Y. Konev. A scholar is included among the top collaborators of Alexander Y. Konev 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 Alexander Y. Konev. Alexander Y. Konev 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.
Konev, Alexander Y., et al.. (2019). The role of aTp-dependent chromatin remodeling factors in chromatin assembly in vivo. Vavilov Journal of Genetics and Breeding. 23(2). 160–167.
2.
Ilatovskiy, Andrey V., Igor Nazarov, А. В. Швецов, et al.. (2016). Partially Assembled Nucleosome Structures at Atomic Detail. Biophysical Journal. 112(3). 460–472. 44 indexed citations
3.
Konev, Alexander Y., et al.. (2013). [Structural features of chromatin organization of 3C6/C7 interband in Drosophila melanogaster polytene chromosomes].. PubMed. 55(3). 198–203. 1 indexed citations
4.
Emelyanov, Alexander, et al.. (2012). Identification and characterization of ToRC, a novel ISWI-containing ATP-dependent chromatin assembly complex. Genes & Development. 26(6). 603–614. 20 indexed citations
5.
Emelyanov, Alexander, et al.. (2010). Protein Complex of Drosophila ATRX/XNP and HP1a Is Required for the Formation of Pericentric Beta-heterochromatin in Vivo. Journal of Biological Chemistry. 285(20). 15027–15037. 31 indexed citations
6.
Lu, Xingwu, Sandeep N. Wontakal, Alexander Emelyanov, et al.. (2009). Linker histone H1 is essential for Drosophila development, the establishment of pericentric heterochromatin, and a normal polytene chromosome structure. Genes & Development. 23(4). 452–465. 77 indexed citations
7.
Konev, Alexander Y., Sung Yeon Park, Valerie Podhraski, et al.. (2007). CHD1 Motor Protein Is Required for Deposition of Histone Variant H3.3 into Chromatin in Vivo. Science. 317(5841). 1087–1090. 194 indexed citations
8.
Frydrychová, Radmila Čapková, Harald Biessmann, Alexander Y. Konev, et al.. (2007). Transcriptional Activity of the Telomeric Retrotransposon HeT-A in Drosophila melanogaster Is Stimulated as a Consequence of Subterminal Deficiencies at Homologous and Nonhomologous Telomeres. Molecular and Cellular Biology. 27(13). 4991–5001. 10 indexed citations
9.
Mason, James M., J. Ransom, & Alexander Y. Konev. (2004). A Deficiency Screen for Dominant Suppressors of Telomeric Silencing in Drosophila. Genetics. 168(3). 1353–1370. 21 indexed citations
10.
Mason, James M., Alexander Y. Konev, & Harald Biessmann. (2003). Telomeric Position Effect in Drosophila Melanogaster Reflects a Telomere Length Control Mechanism. Genetica. 117(2-3). 319–325. 15 indexed citations
11.
Konev, Alexander Y., Christopher M. Yan, Daniel Estrada Acevedo, et al.. (2003). Genetics of P-Element Transposition Into Drosophila melanogaster Centric Heterochromatin. Genetics. 165(4). 2039–2053. 26 indexed citations
12.
Mason, James M., Alexander Y. Konev, M. D. Golubovsky, & Harald Biessmann. (2003). Cis- and trans-acting Influences on Telomeric Position Effect in Drosophila melanogaster Detected With a Subterminal Transgene. Genetics. 163(3). 917–930. 21 indexed citations
13.
Yan, Christopher M., et al.. (2002). Efficient Recovery of Centric Heterochromatin P-Element Insertions in Drosophila melanogaster. Genetics. 161(1). 217–229. 31 indexed citations
14.
Golubovsky, M. D., Alexander Y. Konev, Marika F. Walter, Harald Biessmann, & James M. Mason. (2001). Terminal Retrotransposons Activate a Subtelomeric white Transgene at the 2L Telomere in Drosophila. Genetics. 158(3). 1111–1123. 50 indexed citations
15.
Haoudi, Abdelali, et al.. (2000). Control of Telomere Elongation and Telomeric Silencing in Drosophila Melanogaster. Genetica. 109(1-2). 61–70. 21 indexed citations
16.
Konev, Alexander Y., et al.. (1994). [Cytogenetic analysis of the chromosome region containing the Drosophila radiosensitivity gene. II. The vitally important loci of the 44F-45C region of chromosome 2].. PubMed. 30(2). 201–11. 7 indexed citations
17.
Konev, Alexander Y., et al.. (1994). [Cytogenetic analysis of the chromosome region containing the Drosophila radiosensitivity gene. I. Cytogenetic mapping of the radiosensitivity gene].. PubMed. 30(2). 192–200. 3 indexed citations
18.
Konev, Alexander Y., et al.. (1992). [Molecular-genetic analysis of radiation-induced mutation of the white gene, inserted in the 45D region of the second Drosophila melanogaster chromosome].. PubMed. 322(1). 161–5. 1 indexed citations
19.
Konev, Alexander Y., et al.. (1991). [Cytogenetic analysis of chromosome segments containing radiosensitivity genes in Drosophila. Radiation mutagenesis in the 44-45 region of chromosome 2 of Drosophila melanogaster].. PubMed. 27(1). 77–87. 4 indexed citations
20.
Konev, Alexander Y., et al.. (1991). [Cytogenetic analysis of the chromosomal region containing the radiosensitivity genes of Drosophila. Influence of pericentromeric heterochromatin on mutagenesis in the 44-45 region of chromosome 2].. PubMed. 27(4). 667–75. 6 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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