Idan Cohen

1.5k total citations
34 papers, 1.0k citations indexed

About

Idan Cohen is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Idan Cohen has authored 34 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 7 papers in Cell Biology and 6 papers in Oncology. Recurrent topics in Idan Cohen's work include Epigenetics and DNA Methylation (9 papers), Genomics and Chromatin Dynamics (6 papers) and Polyomavirus and related diseases (5 papers). Idan Cohen is often cited by papers focused on Epigenetics and DNA Methylation (9 papers), Genomics and Chromatin Dynamics (6 papers) and Polyomavirus and related diseases (5 papers). Idan Cohen collaborates with scholars based in Israel, United States and Japan. Idan Cohen's co-authors include Elena Ezhkova, Ohad S. Birk, Barak Markus, Sara Sivan, Daniella Landau, Víctor Julián Valdés, Deyou Zheng, Dejian Zhao, Hagit Flusser and Rotem Kadir and has published in prestigious journals such as Nature Communications, Genes & Development and PLoS ONE.

In The Last Decade

Idan Cohen

34 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Idan Cohen Israel 18 669 189 173 135 77 34 1.0k
A.F. Markham United Kingdom 16 566 0.8× 194 1.0× 147 0.8× 122 0.9× 80 1.0× 35 1.0k
Nuno Miguel Luis France 13 442 0.7× 124 0.7× 108 0.6× 57 0.4× 46 0.6× 18 712
Adi D. Dubash United States 17 759 1.1× 466 2.5× 65 0.4× 134 1.0× 76 1.0× 22 1.2k
Olga Ermakova Italy 16 440 0.7× 90 0.5× 84 0.5× 66 0.5× 65 0.8× 29 725
Marc Thiry Belgium 17 707 1.1× 98 0.5× 169 1.0× 212 1.6× 173 2.2× 32 1.2k
Ian R. Kill United Kingdom 22 1.7k 2.5× 249 1.3× 195 1.1× 139 1.0× 91 1.2× 36 2.0k
Sandra Pankow United States 14 432 0.6× 199 1.1× 68 0.4× 65 0.5× 47 0.6× 20 784
Toru Hiratsuka Japan 12 527 0.8× 308 1.6× 36 0.2× 140 1.0× 42 0.5× 21 990
Chitra Kannabiran India 21 847 1.3× 80 0.4× 341 2.0× 173 1.3× 84 1.1× 71 1.5k
Jennifer N. Cech United States 10 892 1.3× 182 1.0× 201 1.2× 109 0.8× 115 1.5× 13 1.2k

Countries citing papers authored by Idan Cohen

Since Specialization
Citations

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

Fields of papers citing papers by Idan Cohen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Idan Cohen

This figure shows the co-authorship network connecting the top 25 collaborators of Idan Cohen. A scholar is included among the top collaborators of Idan Cohen 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 Idan Cohen. Idan Cohen 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.
Sklarz, Menachem Y., Ehud Ohana, Idan Cohen, et al.. (2025). Pharmacological activation of SIRT6 suppresses progression of head and neck and esophageal squamous cell carcinoma by modulation of cellular metabolism and protein translation. Cell Death and Disease. 16(1). 727–727. 1 indexed citations
2.
Cohen, Idan, H W Levi, Yuval Yogev, et al.. (2024). Heterozygous THBS2 pathogenic variant causes Ehlers–Danlos syndrome with prominent vascular features in humans and mice. European Journal of Human Genetics. 32(5). 550–557. 7 indexed citations
3.
Pu, Hong, José Silva, Idan Cohen, et al.. (2021). UV-induced reduction in Polycomb repression promotes epidermal pigmentation. Developmental Cell. 56(18). 2547–2561.e8. 15 indexed citations
4.
Cohen, Idan, Hequn Liu, Víctor Julián Valdés, et al.. (2021). Polycomb complexes redundantly maintain epidermal stem cell identity during development. Genes & Development. 35(5-6). 354–366. 26 indexed citations
5.
Miroshnikova, Yekaterina A., Idan Cohen, Elena Ezhkova, & Sara A. Wickström. (2019). Epigenetic gene regulation, chromatin structure, and force-induced chromatin remodelling in epidermal development and homeostasis. Current Opinion in Genetics & Development. 55. 46–51. 32 indexed citations
6.
Cohen, Idan, Dejian Zhao, Venu Pothula, et al.. (2019). Polycomb Repressive Complex 1 Controls Maintenance of Fungiform Papillae by Repressing Sonic Hedgehog Expression. Cell Reports. 28(1). 257–266.e5. 10 indexed citations
7.
Nguyen, Minh, Víctor Julián Valdés, Idan Cohen, et al.. (2019). Dissection of Merkel cell formation in hairy and glabrous skin reveals a common requirement for FGFR2‐mediated signalling. Experimental Dermatology. 28(4). 374–382. 16 indexed citations
8.
Cohen, Idan, Dejian Zhao, Víctor Julián Valdés, et al.. (2018). PRC1 Fine-tunes Gene Repression and Activation to Safeguard Skin Development and Stem Cell Specification. Cell stem cell. 22(5). 726–739.e7. 92 indexed citations
9.
Cohen, Idan, Dejian Zhao, Deyou Zheng, & Elena Ezhkova. (2018). 1358 PRC1 fine-tunes gene repression and activation to safeguard skin epithelium development and stem cell specification. Journal of Investigative Dermatology. 138(5). S231–S231. 1 indexed citations
10.
Nguyen, Minh, Idan Cohen, Zijian Xu, et al.. (2018). FGF signalling controls the specification of hair placode-derived SOX9 positive progenitors to Merkel cells. Nature Communications. 9(1). 2333–2333. 35 indexed citations
11.
Cohen, Idan, Dejian Zhao, Gopinathan K. Menon, et al.. (2018). PRC1 preserves epidermal tissue integrity independently of PRC2. Genes & Development. 33(1-2). 55–60. 33 indexed citations
12.
Cohen, Idan, Orna Staretz‐Chacham, Ohad Wormser, et al.. (2017). A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansion. American Journal of Medical Genetics Part A. 176(2). 330–336. 13 indexed citations
13.
Perdigoto, Carolina N., Víctor Julián Valdés, Idan Cohen, et al.. (2016). Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development. PLoS Genetics. 12(7). e1006151–e1006151. 51 indexed citations
14.
Perez, Yonatan, Libe Gradstein, Hagit Flusser, et al.. (2013). Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation. European Journal of Human Genetics. 22(5). 703–706. 38 indexed citations
15.
Cohen, Idan, Eldad Silberstein, Yonatan Perez, et al.. (2013). Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase. European Journal of Human Genetics. 22(3). 374–378. 45 indexed citations
16.
Cohen, Idan, et al.. (2012). ZNF750 Is Expressed in Differentiated Keratinocytes and Regulates Epidermal Late Differentiation Genes. PLoS ONE. 7(8). e42628–e42628. 38 indexed citations
17.
Cohen, Idan, Daniella Landau, Baruch Yerushalmi, et al.. (2012). Meconium Ileus Caused by Mutations in GUCY2C, Encoding the CFTR-Activating Guanylate Cyclase 2C. The American Journal of Human Genetics. 90(5). 893–899. 73 indexed citations
18.
Markus, Barak, Ginat Narkis, Daniella Landau, et al.. (2012). Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1. Human Mutation. 33(10). 1435–1438. 45 indexed citations
19.
Birnbaum, Ramon Y., Genki Hayashi, Idan Cohen, et al.. (2011). Association analysis identifies ZNF750 regulatory variants in psoriasis. BMC Medical Genetics. 12(1). 167–167. 16 indexed citations
20.
Markus, Barak, Iris Noyman, Hagit Flusser, et al.. (2010). Pelizaeus-Merzbacher-like Disease Caused by AIMP1/p43 Homozygous Mutation. The American Journal of Human Genetics. 87(6). 820–828. 62 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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