Irina Stancheva

3.5k total citations
28 papers, 2.0k citations indexed

About

Irina Stancheva is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Irina Stancheva has authored 28 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 12 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Irina Stancheva's work include Epigenetics and DNA Methylation (24 papers), Cancer-related gene regulation (11 papers) and Genomics and Chromatin Dynamics (8 papers). Irina Stancheva is often cited by papers focused on Epigenetics and DNA Methylation (24 papers), Cancer-related gene regulation (11 papers) and Genomics and Chromatin Dynamics (8 papers). Irina Stancheva collaborates with scholars based in United Kingdom, France and Switzerland. Irina Stancheva's co-authors include Thomas Clouaire, Kevin Myant, Richard R. Meehan, Adrian Bird, Shireen A. Sarraf, Robert J. Klose, Lars Schmiedeberg, Matthew J. Lyst, Suzanne M. McDermott and Slimane Ait‐Si‐Ali and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Genes & Development.

In The Last Decade

Irina Stancheva

28 papers receiving 1.9k citations

Peers

Irina Stancheva
Daniel J. Turner United Kingdom
Serge Saxonov United States
Jacqueline E. Mermoud United Kingdom
Peri Tate United Kingdom
Paul A. Ginno United States
Tomas Fitzgerald United Kingdom
Florian Lienert United States
Daniel J. Turner United Kingdom
Irina Stancheva
Citations per year, relative to Irina Stancheva Irina Stancheva (= 1×) peers Daniel J. Turner

Countries citing papers authored by Irina Stancheva

Since Specialization
Citations

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

Fields of papers citing papers by Irina Stancheva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irina Stancheva

This figure shows the co-authorship network connecting the top 25 collaborators of Irina Stancheva. A scholar is included among the top collaborators of Irina Stancheva 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 Irina Stancheva. Irina Stancheva 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.
Zhang, Tuo, Jayne Culley, Flávia de Lima Alves, et al.. (2016). G9a/GLP Complex Maintains Imprinted DNA Methylation in Embryonic Stem Cells. Cell Reports. 15(1). 77–85. 84 indexed citations
2.
Culley, Jayne, et al.. (2016). The SNF2 family ATPase LSH promotes cell-autonomousde novoDNA methylation in somatic cells. Nucleic Acids Research. 44(16). 7592–7604. 23 indexed citations
3.
Stancheva, Irina & Eric C. Schirmer. (2014). Nuclear Envelope: Connecting Structural Genome Organization to Regulation of Gene Expression. Advances in experimental medicine and biology. 773. 209–244. 25 indexed citations
4.
Gendrel, Anne-Valérie, Anwyn Apedaile, Heather Coker, et al.. (2012). Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome. Developmental Cell. 23(2). 265–279. 148 indexed citations
5.
Burrage, Joe, et al.. (2012). SNF2 family ATPase LSH promotes phosphorylation of H2AX and efficient repair of DNA double-strand breaks in mammalian cells. Journal of Cell Science. 125(Pt 22). 5524–34. 48 indexed citations
6.
Stancheva, Irina. (2011). Revisiting Heterochromatin in Embryonic Stem Cells. PLoS Genetics. 7(6). e1002093–e1002093. 7 indexed citations
7.
Newbery, Helen J., Irina Stancheva, Lyle B. Zimmerman, & Catherine M. Abbott. (2011). Evolutionary importance of translation elongation factor eEF1A variant switching: eEF1A1 down-regulation in muscle is conserved in Xenopus but is controlled at a post-transcriptional level. Biochemical and Biophysical Research Communications. 411(1). 19–24. 9 indexed citations
8.
Defossez, Pierre‐Antoine & Irina Stancheva. (2011). Biological Functions of Methyl-CpG-Binding Proteins. Progress in molecular biology and translational science. 101. 377–398. 65 indexed citations
9.
Athanasiadou, Rodoniki, Dina De Sousa, Kevin Myant, et al.. (2010). Targeting of De Novo DNA Methylation Throughout the Oct-4 Gene Regulatory Region in Differentiating Embryonic Stem Cells. PLoS ONE. 5(4). e9937–e9937. 54 indexed citations
10.
Myant, Kevin, Arvind Y. M. Sundaram, Chao Li, et al.. (2010). LSH and G9a/GLP complex are required for developmentally programmed DNA methylation. Genome Research. 21(1). 83–94. 95 indexed citations
11.
Clouaire, Thomas, Jose I. de las Heras, Cara Merusi, & Irina Stancheva. (2010). Recruitment of MBD1 to target genes requires sequence-specific interaction of the MBD domain with methylated DNA. Nucleic Acids Research. 38(14). 4620–4634. 72 indexed citations
12.
Clouaire, Thomas & Irina Stancheva. (2008). Methyl-CpG binding proteins: specialized transcriptional repressors or structural components of chromatin?. Cellular and Molecular Life Sciences. 65(10). 1509–1522. 166 indexed citations
13.
Klose, Robert J., Shireen A. Sarraf, Lars Schmiedeberg, et al.. (2005). DNA Binding Selectivity of MeCP2 Due to a Requirement for A/T Sequences Adjacent to Methyl-CpG. Molecular Cell. 19(5). 667–678. 262 indexed citations
14.
Stancheva, Irina. (2005). Caught in conspiracy: cooperation between DNA methylation and histone H3K9 methylation in the establishment and maintenance of heterochromatin. Biochemistry and Cell Biology. 83(3). 385–395. 50 indexed citations
15.
Stancheva, Irina, Osman El‐Maarri, Joern Walter, Alain Niveleau, & Richard R. Meehan. (2002). DNA Methylation at Promoter Regions Regulates the Timing of Gene Activation in Xenopus laevis Embryos. Developmental Biology. 243(1). 155–165. 88 indexed citations
16.
Stancheva, Irina. (2001). Loss of the maintenance methyltransferase, xDnmt1, induces apoptosis in Xenopus embryos. The EMBO Journal. 20(8). 1963–1973. 68 indexed citations
17.
Meehan, Richard R. & Irina Stancheva. (2001). DNA methylation and control of gene expression in vertebrate development. Essays in Biochemistry. 37. 59–70. 33 indexed citations
18.
Meehan, Richard R., Sari Pennings, & Irina Stancheva. (2001). Lashings of DNA methylation, forkfuls of chromatin remodeling. Genes & Development. 15(24). 3231–3236. 30 indexed citations
19.
Stancheva, Irina, Theodor Koller, & José M. Sogo. (1999). Asymmetry of Dam remethylation on the leading and lagging arms of plasmid replicative intermediates. The EMBO Journal. 18(22). 6542–6551. 29 indexed citations
20.
Stancheva, Irina, Roberto G. Lucchini, T. Köller, & José M. Sogo. (1997). Chromatin structure and methylation of rat rRNA genes studied by formaldehyde fixation and psoralen cross-linking. Nucleic Acids Research. 25(9). 1727–1735. 46 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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