Zuzana Tóthová

12.8k total citations · 5 hit papers
47 papers, 8.4k citations indexed

About

Zuzana Tóthová is a scholar working on Molecular Biology, Hematology and Oncology. According to data from OpenAlex, Zuzana Tóthová has authored 47 papers receiving a total of 8.4k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 15 papers in Hematology and 9 papers in Oncology. Recurrent topics in Zuzana Tóthová's work include Acute Myeloid Leukemia Research (10 papers), FOXO transcription factor regulation (9 papers) and Genomics and Chromatin Dynamics (6 papers). Zuzana Tóthová is often cited by papers focused on Acute Myeloid Leukemia Research (10 papers), FOXO transcription factor regulation (9 papers) and Genomics and Chromatin Dynamics (6 papers). Zuzana Tóthová collaborates with scholars based in United States, Slovakia and United Kingdom. Zuzana Tóthová's co-authors include David E. Root, Ian C. P. Smith, Meagan E. Sullender, Mudra Hegde, John G. Doench, Katherine Donovan, Herbert W. Virgin, Jennifer Listgarten, Emma W Vaimberg and Robert C. Orchard and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Zuzana Tóthová

46 papers receiving 8.3k citations

Hit Papers

Optimized sgRNA design to maximize activity a... 2007 2026 2013 2019 2016 2007 2014 2007 2007 500 1000 1.5k 2.0k 2.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zuzana Tóthová United States 23 6.5k 1.1k 929 850 709 47 8.4k
Lihua Julie Zhu United States 54 6.8k 1.0× 383 0.4× 790 0.9× 656 0.8× 454 0.6× 165 9.3k
José M.P. Freije Spain 47 6.1k 0.9× 541 0.5× 1.6k 1.8× 475 0.6× 443 0.6× 98 9.2k
Noboru Motoyama Japan 36 5.1k 0.8× 497 0.5× 1.8k 1.9× 1.8k 2.2× 346 0.5× 63 7.6k
Robert Latek United States 17 5.4k 0.8× 496 0.5× 936 1.0× 1.2k 1.4× 124 0.2× 31 7.6k
William Biggs United States 27 6.0k 0.9× 224 0.2× 601 0.6× 712 0.8× 705 1.0× 33 8.1k
Bruce M. Paterson United States 33 5.9k 0.9× 916 0.8× 2.4k 2.6× 820 1.0× 185 0.3× 56 8.7k
Ivan Topisirović Canada 52 7.7k 1.2× 300 0.3× 960 1.0× 1.0k 1.2× 141 0.2× 111 9.6k
Homayoun Vaziri Canada 19 4.0k 0.6× 364 0.3× 1.2k 1.3× 933 1.1× 1.1k 1.6× 25 8.4k
Diane C. Fingar United States 33 6.2k 1.0× 195 0.2× 932 1.0× 981 1.2× 170 0.2× 49 8.7k
Christian Beauséjour Canada 25 5.1k 0.8× 140 0.1× 998 1.1× 1.1k 1.2× 572 0.8× 57 7.5k

Countries citing papers authored by Zuzana Tóthová

Since Specialization
Citations

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

Fields of papers citing papers by Zuzana Tóthová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zuzana Tóthová

This figure shows the co-authorship network connecting the top 25 collaborators of Zuzana Tóthová. A scholar is included among the top collaborators of Zuzana Tóthová 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 Zuzana Tóthová. Zuzana Tóthová 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.
Wong, Waihay J., Rebecca L. Zon, Caleb Ho, et al.. (2025). Somatic mutations in STAG2 are associated with separated megakaryocyte nuclear lobes in myelodysplastic syndromes. Blood Advances. 9(20). 5283–5288.
2.
Tóthová, Zuzana, et al.. (2025). Cohesin mutations and chromatin changes in cancer. International Journal of Cancer. 158(2). 368–381. 1 indexed citations
3.
Anczuków, Olga, Frédéric H.‐T. Allain, Brittany Angarola, et al.. (2024). Steering research on mRNA splicing in cancer towards clinical translation. Nature reviews. Cancer. 24(12). 887–905. 8 indexed citations
4.
Wheeler, Emily C., Benjamín Martín, Melanie Donahue, et al.. (2024). Splicing modulators impair DNA damage response and induce killing of cohesin-mutant MDS and AML. Science Translational Medicine. 16(728). eade2774–eade2774. 17 indexed citations
5.
Tóthová, Zuzana, Mangesh Bhide, Andrej Kováč, et al.. (2023). Differentially Expressed Genes Induced by Erythropoietin Receptor Overexpression in Rat Mammary Adenocarcinoma RAMA 37-28 Cells. International Journal of Molecular Sciences. 24(10). 8482–8482. 1 indexed citations
6.
Bondeson, Daniel P., Thomas C. Atack, Nolan Bick, et al.. (2022). Systematic profiling of conditional degron tag technologies for target validation studies. Nature Communications. 13(1). 5495–5495. 19 indexed citations
7.
Jann, Johann-Christoph & Zuzana Tóthová. (2021). Cohesin mutations in myeloid malignancies. Blood. 138(8). 649–661. 26 indexed citations
8.
Ji, Hye Young, Kai Yan, Qian Zhu, et al.. (2021). Inner nuclear protein Matrin-3 coordinates cell differentiation by stabilizing chromatin architecture. Nature Communications. 12(1). 6241–6241. 26 indexed citations
9.
Tóthová, Zuzana, et al.. (2021). STAT5 as a Key Protein of Erythropoietin Signalization. International Journal of Molecular Sciences. 22(13). 7109–7109. 35 indexed citations
10.
Tóthová, Zuzana, et al.. (2021). The Role of PI3K/AKT and MAPK Signaling Pathways in Erythropoietin Signalization. International Journal of Molecular Sciences. 22(14). 7682–7682. 62 indexed citations
11.
Lesch, Bluma J., Zuzana Tóthová, Elizabeth A. Morgan, et al.. (2019). Intergenerational epigenetic inheritance of cancer susceptibility in mammals. eLife. 8. 40 indexed citations
12.
Tóthová, Zuzana & Benjamin L. Ebert. (2017). Doubling Down on Mutant RAS Can MEK or Break Leukemia. Cell. 168(5). 749–750. 2 indexed citations
13.
Elf, Shannon, Nouran S. Abdelfattah, Edwin Chen, et al.. (2016). Mutant Calreticulin Requires Both Its Mutant C-terminus and the Thrombopoietin Receptor for Oncogenic Transformation. Cancer Discovery. 6(4). 368–381. 189 indexed citations
14.
Puram, Rishi V., Monika S. Kowalczyk, Carl G. de Boer, et al.. (2016). Core Circadian Clock Genes Regulate Leukemia Stem Cells in AML. Cell. 165(2). 303–316. 195 indexed citations
15.
Doench, John G., Nicolò Fusi, Meagan E. Sullender, et al.. (2016). Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9. Nature Biotechnology. 34(2). 184–191. 2646 indexed citations breakdown →
16.
Doench, John G., Ella Hartenian, Daniel B. Graham, et al.. (2014). Rational design of highly active sgRNAs for CRISPR-Cas9–mediated gene inactivation. Nature Biotechnology. 32(12). 1262–1267. 1157 indexed citations breakdown →
17.
Sykes, Stephen M., Lars Bullinger, Rukh Yusuf, et al.. (2011). Akt/foxo signaling pathway enforces the differentiation blockade in myeloid leukemias. Experimental Hematology. 39(8). 1 indexed citations
18.
Sykes, Stephen M., Steven Lane, Lars Bullinger, et al.. (2011). AKT/FOXO Signaling Enforces Reversible Differentiation Blockade in Myeloid Leukemias. Cell. 146(5). 697–708. 217 indexed citations
19.
Cornejo, Melanie, Stephen M. Sykes, Cristina Lo Celso, et al.. (2009). A Regulatory Network Between Notch and AKT Signaling Pathways Differentially Controls Megakaryocyte Development From Hematopoietic Stem or Committed Progenitor Cells.. Blood. 114(22). 384–384. 1 indexed citations
20.
Paik, Ji-Hye, Ramya Kollipara, Gerald Chu, et al.. (2007). FoxOs Are Lineage-Restricted Redundant Tumor Suppressors and Regulate Endothelial Cell Homeostasis. Cell. 128(2). 309–323. 859 indexed citations breakdown →

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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