Anita Göndör

3.0k total citations · 2 hit papers
27 papers, 2.1k citations indexed

About

Anita Göndör is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anita Göndör has authored 27 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anita Göndör's work include Genomics and Chromatin Dynamics (16 papers), Epigenetics and DNA Methylation (10 papers) and Genetic Syndromes and Imprinting (7 papers). Anita Göndör is often cited by papers focused on Genomics and Chromatin Dynamics (16 papers), Epigenetics and DNA Methylation (10 papers) and Genetic Syndromes and Imprinting (7 papers). Anita Göndör collaborates with scholars based in Sweden, Japan and China. Anita Göndör's co-authors include Rolf Ohlsson, Andrew P. Feinberg, Michael A. Koldobskiy, Vijay Tiwari, Chandrasekhar Kanduri, Mikael Sjölinder, Zhihu Zhao, Kuljeet Singh Sandhu, Vinod Pant and Umashankar Singh and has published in prestigious journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Anita Göndör

26 papers receiving 2.1k citations

Hit Papers

Circular chromosome conformation capture (4C) uncovers ex... 2006 2026 2012 2019 2006 2016 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anita Göndör Sweden 15 1.9k 421 338 308 162 27 2.1k
Marco Barchi Italy 22 1.8k 1.0× 348 0.8× 348 1.0× 303 1.0× 308 1.9× 41 2.3k
Robin Andersson Denmark 30 2.4k 1.3× 470 1.1× 473 1.4× 311 1.0× 116 0.7× 59 2.9k
Ryuichiro Nakato Japan 27 2.2k 1.2× 291 0.7× 207 0.6× 283 0.9× 209 1.3× 67 2.5k
Henriette O’Geen United States 28 2.4k 1.3× 527 1.3× 202 0.6× 275 0.9× 118 0.7× 43 2.7k
Jolyon Terragni United States 15 2.0k 1.1× 279 0.7× 427 1.3× 428 1.4× 446 2.8× 17 2.4k
Kashyap Dave Finland 11 1.7k 0.9× 302 0.7× 166 0.5× 212 0.7× 82 0.5× 12 2.0k
Roland Green United States 18 1.9k 1.0× 372 0.9× 252 0.7× 296 1.0× 288 1.8× 21 2.3k
Hauke Cornils Switzerland 13 1.3k 0.7× 228 0.5× 343 1.0× 222 0.7× 287 1.8× 15 1.8k
Reini F. Luco France 15 1.9k 1.0× 329 0.8× 425 1.3× 166 0.5× 79 0.5× 22 2.3k
Achim Breiling Germany 19 2.1k 1.1× 350 0.8× 422 1.2× 181 0.6× 125 0.8× 27 2.5k

Countries citing papers authored by Anita Göndör

Since Specialization
Citations

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

Fields of papers citing papers by Anita Göndör

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anita Göndör

This figure shows the co-authorship network connecting the top 25 collaborators of Anita Göndör. A scholar is included among the top collaborators of Anita Göndör 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 Anita Göndör. Anita Göndör 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.
Fonseca, Pedro, Weiyingqi Cui, Le Tong, et al.. (2024). A phenotypic screening approach to target p60AmotL2-expressing invasive cancer cells. Journal of Experimental & Clinical Cancer Research. 43(1). 107–107.
2.
Chachoua, Ilyas, Hao Dai, Jia Pei Lim, et al.. (2022). Canonical WNT signaling-dependent gating of MYC requires a noncanonical CTCF function at a distal binding site. Nature Communications. 13(1). 204–204. 15 indexed citations
3.
Scholz, Barbara A., Noriyuki Sumida, Ilyas Chachoua, et al.. (2020). Author Correction: WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating. Nature Genetics. 52(11). 1265–1265. 4 indexed citations
4.
Scholz, Barbara A., Noriyuki Sumida, Ilyas Chachoua, et al.. (2019). WNT signaling and AHCTF1 promote oncogenic MYC expression through super-enhancer-mediated gene gating. Nature Genetics. 51(12). 1723–1731. 65 indexed citations
5.
Yin, Chang Shik, Temesgen Fufa, Gayathri Chandrasekar, et al.. (2017). Phenotypic Screen Identifies a Small Molecule Modulating ERK2 and Promoting Stem Cell Proliferation. Frontiers in Pharmacology. 8. 726–726. 3 indexed citations
6.
Feinberg, Andrew P., Michael A. Koldobskiy, & Anita Göndör. (2016). Epigenetic modulators, modifiers and mediators in cancer aetiology and progression. Nature Reviews Genetics. 17(5). 284–299. 610 indexed citations breakdown →
7.
Zhao, Honglei, Emmanouil G. Sifakis, Noriyuki Sumida, et al.. (2015). PARP1- and CTCF-Mediated Interactions between Active and Repressed Chromatin at the Lamina Promote Oscillating Transcription. Molecular Cell. 59(6). 984–997. 105 indexed citations
8.
Chen, Xingqi, et al.. (2014). The visualization of large organized chromatin domains enriched in the H3K9me2 mark within a single chromosome in a single cell. Epigenetics. 9(11). 1439–1445. 14 indexed citations
9.
Göndör, Anita. (2013). Dynamic chromatin loops bridge health and disease in the nuclear landscape. Seminars in Cancer Biology. 23(2). 90–98. 7 indexed citations
10.
Guibert, Sylvain, Zhihu Zhao, Mikael Sjölinder, et al.. (2012). CTCF-binding sites within theH19ICR differentially regulate local chromatin structures and cis-acting functions. Epigenetics. 7(4). 361–369. 14 indexed citations
11.
Holmgren, Claes, Anita Göndör, Mattias Vesterlund, et al.. (2012). Cell type and context-specific function of PLAG1 for IGF2 P3 promoter activity. International Journal of Oncology. 41(6). 1959–1966. 22 indexed citations
12.
Göndör, Anita, et al.. (2010). Window into the Complexities of Chromosome Interactomes. Cold Spring Harbor Symposia on Quantitative Biology. 75(0). 493–500. 4 indexed citations
14.
Göndör, Anita & Rolf Ohlsson. (2009). Replication timing and epigenetic reprogramming of gene expression: a two-way relationship?. Nature Reviews Genetics. 10(4). 269–276. 51 indexed citations
15.
Göndör, Anita & Rolf Ohlsson. (2009). Chromosome crosstalk in three dimensions. Nature. 461(7261). 212–217. 117 indexed citations
16.
Sandhu, Kuljeet Singh, Mikael Sjölinder, Zhihu Zhao, et al.. (2009). Nonallelic transvection of multiple imprinted loci is organized by the H19 imprinting control region during germline development. Genes & Development. 23(22). 2598–2603. 68 indexed citations
17.
Göndör, Anita, et al.. (2008). High-resolution circular chromosome conformation capture assay. Nature Protocols. 3(2). 303–313. 72 indexed citations
18.
Ohlsson, Rolf & Anita Göndör. (2007). The 4C technique: the ‘Rosetta stone’ for genome biology in 3D?. Current Opinion in Cell Biology. 19(3). 321–325. 22 indexed citations
19.
Zhao, Zhihu, Gholamreza Tavoosidana, Mikael Sjölinder, et al.. (2006). Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions. Nature Genetics. 38(11). 1341–1347. 717 indexed citations breakdown →
20.
Thakur, Noopur, Vijay Tiwari, Hélène Thomassin, et al.. (2004). An Antisense RNA Regulates the Bidirectional Silencing Property of the Kcnq1 Imprinting Control Region. Molecular and Cellular Biology. 24(18). 7855–7862. 116 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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