Ilona Dunkel

2.1k total citations
26 papers, 1.2k citations indexed

About

Ilona Dunkel is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Ilona Dunkel has authored 26 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Ilona Dunkel's work include Genomics and Chromatin Dynamics (9 papers), CRISPR and Genetic Engineering (7 papers) and Pluripotent Stem Cells Research (4 papers). Ilona Dunkel is often cited by papers focused on Genomics and Chromatin Dynamics (9 papers), CRISPR and Genetic Engineering (7 papers) and Pluripotent Stem Cells Research (4 papers). Ilona Dunkel collaborates with scholars based in Germany, United Kingdom and United States. Ilona Dunkel's co-authors include Silke Sperling, Martin Lange, Jenny Schlesinger, Hans Lehrach, Jenny J. Fischer, Martje Tönjes, Marcel Grunert, Felix Berger, Siegrun Mebus and Christina Grimm and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Ilona Dunkel

25 papers receiving 1.2k citations

Peers

Ilona Dunkel

GENET

EPIDE

CMN

Hanneke Okkenhaug United Kingdom

Gil Bu Kang South Korea

Christine Powers United States

Felix Kraus United States

Hervé Barrière Canada

Arno Kalkuhl Germany

Silvia Vergarajauregui United States

John Anagli United States

Ruhee Dere United States

Serge Grégoire Canada

Hanneke Okkenhaug United Kingdom

Ilona Dunkel

698 ×0.7

64 ×0.3

GENET

268 ×1.5

EPIDE

103 ×0.9

CMN

99 ×1.0

Citations per year, relative to Ilona Dunkel Ilona Dunkel (= 1×) peers Hanneke Okkenhaug

Countries citing papers authored by Ilona Dunkel

Since Specialization

Citations

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

Fields of papers citing papers by Ilona Dunkel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilona Dunkel

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

All Works

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20 of 20 papers shown

Khoei, Heidar Heidari, Harunobu Kagawa, Saurabh J. Pradhan, et al.. (2024). mTOR activity paces human blastocyst stage developmental progression. Cell. 187(23). 6566–6583.e22. 18 indexed citations

Klinger, Bertram, et al.. (2023). Modeling unveils sex differences of signaling networks in mouse embryonic stem cells. Molecular Systems Biology. 19(11). e11510–e11510. 1 indexed citations

Wong, Chee-Wai, Ilona Dunkel, Philipp Voigt, et al.. (2023). Epigenetic dynamics during capacitation of naïve human pluripotent stem cells. Science Advances. 9(39). eadg1936–eadg1936. 9 indexed citations

Kumar, Abhishek Sampath, Ilona Dunkel, Guido Pacini, et al.. (2023). GATA transcription factors drive initial Xist upregulation after fertilization through direct activation of long-range enhancers. Nature Cell Biology. 25(11). 1704–1715. 10 indexed citations

Gjaltema, Rutger A. F., Michael I. Robson, Robert Schöpflin, et al.. (2021). Distal and proximal cis-regulatory elements sense X chromosome dosage and developmental state at the Xist locus. Molecular Cell. 82(1). 190–208.e17. 31 indexed citations

Dunkel, Ilona, et al.. (2021). Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach. Genome biology. 22(1). 110–110. 31 indexed citations

Pacini, Guido, et al.. (2021). Integrated analysis of Xist upregulation and X-chromosome inactivation with single-cell and single-allele resolution. Nature Communications. 12(1). 3638–3638. 29 indexed citations

Li, Na, et al.. (2020). EPIGENE: genome-wide transcription unit annotation using a multivariate probabilistic model of histone modifications. Epigenetics & Chromatin. 13(1). 20–20. 1 indexed citations

Grunert, Marcel, Sandra Appelt, Ilona Dunkel, Felix Berger, & Silke Sperling. (2019). Altered microRNA and target gene expression related to Tetralogy of Fallot. Scientific Reports. 9(1). 19063–19063. 19 indexed citations

10.

Okamoto, Ikuhiro, Ilona Dunkel, Mitinori Saitou, et al.. (2019). A symmetric toggle switch explains the onset of random X inactivation in different mammals. Nature Structural & Molecular Biology. 26(5). 350–360. 33 indexed citations

11.

Chung, Ho‐Ryun, Chao Xu, Andreas Mund, et al.. (2016). PHF13 is a molecular reader and transcriptional co-regulator of H3K4me2/3. eLife. 5. 24 indexed citations

12.

Kinkley, Sarah, Johannes Helmuth, Julia K. Polansky, et al.. (2016). reChIP-seq reveals widespread bivalency of H3K4me3 and H3K27me3 in CD4+ memory T cells. Nature Communications. 7(1). 12514–12514. 50 indexed citations

13.

Grunert, Marcel, Huanhuan Cui, Ilona Dunkel, et al.. (2016). Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases. Cardiovascular Research. 112(1). 464–477. 59 indexed citations

14.

Cui, Huanhuan, Jenny Schlesinger, Martje Tönjes, et al.. (2015). Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA. Nucleic Acids Research. 44(6). 2538–2553. 32 indexed citations

15.

Grunert, Marcel, C. Dorn, Markus Schueler, et al.. (2014). Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot. Human Molecular Genetics. 23(12). 3115–3128. 38 indexed citations

16.

Chung, Ho‐Ryun, Ilona Dunkel, Christian Linke, et al.. (2010). The Effect of Micrococcal Nuclease Digestion on Nucleosome Positioning Data. PLoS ONE. 5(12). e15754–e15754. 95 indexed citations

17.

Schlesinger, Jenny, Martje Tönjes, Markus Schueler, et al.. (2010). Evaluation of the LightCycler® 1536 Instrument for high-throughput quantitative real-time PCR. Methods. 50(4). S19–S22. 10 indexed citations

18.

Hammer, Stefanie, Martin Lange, Jenny J. Fischer, et al.. (2008). Characterization of TBX20 in human hearts and its regulation by TFAP2. Journal of Cellular Biochemistry. 104(3). 1022–1033. 49 indexed citations

19.

Sperling, Silke, Christina Grimm, Ilona Dunkel, et al.. (2005). Identification and functional analysis ofCITED2 mutations in patients with congenital heart defects. Human Mutation. 26(6). 575–582. 104 indexed citations

20.

Schalkwyk, Leonard C., Brian Cusack, Ilona Dunkel, et al.. (2001). Advanced Integrated Mouse YAC Map Including BAC Framework. Genome Research. 11(12). 2142–2150. 4 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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