Ruslan Strogantsev

1.1k total citations
10 papers, 420 citations indexed

About

Ruslan Strogantsev is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ruslan Strogantsev has authored 10 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ruslan Strogantsev's work include Epigenetics and DNA Methylation (7 papers), Genetic Syndromes and Imprinting (5 papers) and Prenatal Screening and Diagnostics (4 papers). Ruslan Strogantsev is often cited by papers focused on Epigenetics and DNA Methylation (7 papers), Genetic Syndromes and Imprinting (5 papers) and Prenatal Screening and Diagnostics (4 papers). Ruslan Strogantsev collaborates with scholars based in United Kingdom, United States and Australia. Ruslan Strogantsev's co-authors include Anne C. Ferguson‐Smith, Hui Shi, Adam G. West, Gary Felsenfeld, Miklós Gaszner, Humaira Gowher, Alan Hair, Jacqueline Dickson, Felix Krueger and Bowen Sun and has published in prestigious journals such as Nature Communications, Blood and The Journal of Immunology.

In The Last Decade

Ruslan Strogantsev

10 papers receiving 420 citations

Peers

Ruslan Strogantsev
Rachel Byron United States
Maxine Tevendale United Kingdom
Joanna E. Huddleston United Kingdom
Anastasiya Kazachenka United Kingdom
J. Stamberg United States
Ruslan Strogantsev
Citations per year, relative to Ruslan Strogantsev Ruslan Strogantsev (= 1×) peers Stéphanie Maupetit‐Mehouas

Countries citing papers authored by Ruslan Strogantsev

Since Specialization
Citations

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

Fields of papers citing papers by Ruslan Strogantsev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruslan Strogantsev

This figure shows the co-authorship network connecting the top 25 collaborators of Ruslan Strogantsev. A scholar is included among the top collaborators of Ruslan Strogantsev 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 Ruslan Strogantsev. Ruslan Strogantsev is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Strogantsev, Ruslan, Hong Lin, Majid Mohammadhosseini, et al.. (2023). Clonal hematopoiesis related TET2 loss-of-function impedes IL1β-mediated epigenetic reprogramming in hematopoietic stem and progenitor cells. Nature Communications. 14(1). 8102–8102. 29 indexed citations
2.
Shi, Hui, Ruslan Strogantsev, Nozomi Takahashi, et al.. (2019). ZFP57 regulation of transposable elements and gene expression within and beyond imprinted domains. Epigenetics & Chromatin. 12(1). 49–49. 47 indexed citations
3.
Takahashi, Nozomi, Dionne Gray, Ruslan Strogantsev, et al.. (2015). ZFP57and the Targeted Maintenance of Postfertilization Genomic Imprints. Cold Spring Harbor Symposia on Quantitative Biology. 80. 177–187. 29 indexed citations
4.
Strogantsev, Ruslan, Felix Krueger, Kazuki Yamazawa, et al.. (2015). Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression. Genome Biology. 16(1). 112–112. 111 indexed citations
5.
Das, Radhika, Yew Kok Lee, Ruslan Strogantsev, et al.. (2013). DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation. BMC Genomics. 14(1). 685–685. 38 indexed citations
6.
Zhou, Yan, Sreenivasulu Kurukuti, Peter Saffrey, et al.. (2013). Chromatin looping defines expression of TAL1, its flanking genes, and regulation in T-ALL. Blood. 122(26). 4199–4209. 26 indexed citations
7.
Weyden, Louise van der, Alistair G. Rust, Rebecca E. McIntyre, et al.. (2012). Jdp2 downregulates Trp53 transcription to promote leukaemogenesis in the context of Trp53 heterozygosity. Oncogene. 32(3). 397–402. 19 indexed citations
8.
Strogantsev, Ruslan & Anne C. Ferguson‐Smith. (2012). Proteins involved in establishment and maintenance of imprinted methylation marks. Briefings in Functional Genomics. 11(3). 227–239. 32 indexed citations
9.
Baxter, Euan W., Fabio Mirabella, Sarion R. Bowers, et al.. (2012). The Inducible Tissue-Specific Expression of the Human IL-3/GM-CSF Locus Is Controlled by a Complex Array of Developmentally Regulated Enhancers. The Journal of Immunology. 189(9). 4459–4469. 8 indexed citations
10.
Dickson, Jacqueline, Humaira Gowher, Ruslan Strogantsev, et al.. (2010). VEZF1 Elements Mediate Protection from DNA Methylation. PLoS Genetics. 6(1). e1000804–e1000804. 81 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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