Attila Tóth

5.9k total citations · 2 hit papers
45 papers, 4.3k citations indexed

About

Attila Tóth is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Attila Tóth has authored 45 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 18 papers in Cell Biology and 8 papers in Plant Science. Recurrent topics in Attila Tóth's work include DNA Repair Mechanisms (29 papers), Microtubule and mitosis dynamics (18 papers) and Genomics and Chromatin Dynamics (14 papers). Attila Tóth is often cited by papers focused on DNA Repair Mechanisms (29 papers), Microtubule and mitosis dynamics (18 papers) and Genomics and Chromatin Dynamics (14 papers). Attila Tóth collaborates with scholars based in Germany, United States and United Kingdom. Attila Tóth's co-authors include Kim Nasmyth, Marta Gálová, Rafal Ciosk, Masaki Shirayama, Alexander Schleiffer, Frank Uhlmann, Katrin Daniel, Andrej Shevchenko, Anna Shevchenko and Tomoyuki Tanaka and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Attila Tóth

44 papers receiving 4.2k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Cohesin's Binding to Chromosomes Depends on a Separate Complex Consisting of Scc2 and Scc4 Proteins

2000 586 citations Rafal Ciosk, Masaki Shirayama et al. Molecular Cell profile →
Yeast Cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication

1999 505 citations Attila Tóth, Rafal Ciosk et al. Genes & Development profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Attila Tóth Germany	29	3.8k	1.4k	872	581	425	45	4.3k
Martin Anger Czechia	19	2.1k 0.6×	594 0.4×	605 0.7×	382 0.7×	667 1.6×	43	2.6k
Maria‐Elena Torres‐Padilla Germany	34	4.2k 1.1×	159 0.1×	815 0.9×	575 1.0×	555 1.3×	79	4.5k
Paul Kalitsis Australia	30	2.6k 0.7×	804 0.6×	1.7k 1.9×	854 1.5×	78 0.2×	59	3.3k
Corinne Grey France	20	2.0k 0.5×	157 0.1×	548 0.6×	747 1.3×	258 0.6×	30	2.4k
Rafal Ciosk Switzerland	25	3.8k 1.0×	1.5k 1.0×	858 1.0×	308 0.5×	194 0.5×	38	4.2k
Satoshi H. Namekawa United States	32	2.4k 0.6×	110 0.1×	597 0.7×	1.1k 1.9×	417 1.0×	89	3.0k
Rika Suzuki Japan	18	1.6k 0.4×	201 0.1×	141 0.2×	696 1.2×	300 0.7×	57	2.3k
Eva Brundell Sweden	14	1.2k 0.3×	298 0.2×	193 0.2×	351 0.6×	268 0.6×	15	1.5k
Paul E. Mains Canada	28	1.8k 0.5×	995 0.7×	284 0.3×	407 0.7×	367 0.9×	53	2.6k
Marek Bartkuhn Germany	28	2.5k 0.7×	115 0.1×	551 0.6×	515 0.9×	108 0.3×	65	3.0k

Countries citing papers authored by Attila Tóth

Since Specialization

Citations

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

Fields of papers citing papers by Attila Tóth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Attila Tóth

This figure shows the co-authorship network connecting the top 25 collaborators of Attila Tóth. A scholar is included among the top collaborators of Attila Tóth 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 Attila Tóth. Attila Tóth 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

Guerquin, Marie-Justine, Antoine D. Rolland, Sébastien Messiaen, et al.. (2025). Genome-wide transcriptional silencing and mRNA stabilization allow the coordinated expression of the meiotic program in mice. Nucleic Acids Research. 53(5). 1 indexed citations

Gómez, Rocío, et al.. (2023). Kinase PLK1 regulates the disassembly of the lateral elements and the assembly of the inner centromere during the diakinesis/metaphase I transition in male mouse meiosis. Frontiers in Cell and Developmental Biology. 10. 1069946–1069946.

Slotman, Johan A., Esther Sleddens–Linkels, Wiggert A. van Cappellen, et al.. (2022). Multi-color dSTORM microscopy in Hormad1-/- spermatocytes reveals alterations in meiotic recombination intermediates and synaptonemal complex structure. PLoS Genetics. 18(7). e1010046–e1010046. 4 indexed citations

Candi, Eleonora, Gerry Melino, Attila Tóth, & Volker Dötsch. (2021). Mechanisms of quality control differ in male and female germ cells. Cell Death and Differentiation. 28(7). 2300–2302. 4 indexed citations

Papanikos, Frantzeskos, Julie A. J. Clément, Corinne Grey, et al.. (2019). Mouse ANKRD31 Regulates Spatiotemporal Patterning of Meiotic Recombination Initiation and Ensures Recombination between X and Y Sex Chromosomes. Molecular Cell. 74(5). 1069–1085.e11. 65 indexed citations

Ye, Qiaozhen, Dong Hyun Kim, Ihsan Dereli, et al.. (2017). The AAA + ATP ase TRIP 13 remodels HORMA domains through N‐terminal engagement and unfolding. The EMBO Journal. 36(16). 2419–2434. 61 indexed citations

Gómez-H, Laura, Natalia Felipe‐Medina, Manuel Sánchez‐Martín, et al.. (2016). C14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertility. Nature Communications. 7(1). 13298–13298. 73 indexed citations

Papanikos, Frantzeskos, Katrin Daniel, Ji‐Feng Fei, et al.. (2016). The enigmatic meiotic dense body and its newly discovered component, SCML1, are dispensable for fertility and gametogenesis in mice. Chromosoma. 126(3). 399–415. 3 indexed citations

Cloutier, Jeffrey M., Shantha K. Mahadevaiah, Elias Elinati, Attila Tóth, & James M. A. Turner. (2015). Mammalian meiotic silencing exhibits sexually dimorphic features. Chromosoma. 125(2). 215–226. 25 indexed citations

10.

Muñoz‐Fuentes, Violeta, Gorka Alkorta‐Aranburu, Catharina Linde Forsberg, et al.. (2014). Strong Artificial Selection in Domestic Mammals Did Not Result in an Increased Recombination Rate. Molecular Biology and Evolution. 32(2). 510–523. 31 indexed citations

11.

Cloutier, Jeffrey M., Katrin Daniel, János Varga, et al.. (2012). Meiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanisms. Genes & Development. 26(9). 958–973. 121 indexed citations

12.

Daniel, Katrin, Julian Lange, Khaled Hached, et al.. (2011). Meiotic homologue alignment and its quality surveillance are controlled by mouse HORMAD1. Nature Cell Biology. 13(5). 599–610. 182 indexed citations

13.

Daniel, Katrin, Ignasi Roig, Ewelina Bolcun‐Filas, et al.. (2009). Mouse HORMAD1 and HORMAD2, Two Conserved Meiotic Chromosomal Proteins, Are Depleted from Synapsed Chromosome Axes with the Help of TRIP13 AAA-ATPase. PLoS Genetics. 5(10). e1000702–e1000702. 311 indexed citations

14.

Fukuda, Tomoyuki, et al.. (2009). A novel mammalian HORMA domain-containing protein, HORMAD1, preferentially associates with unsynapsed meiotic chromosomes. Experimental Cell Research. 316(2). 158–171. 106 indexed citations

15.

Buonomo, Sara B.C., Jörg Fuchs, Stephan Gruber, et al.. (2003). Division of the Nucleolus and Its Release of CDC14 during Anaphase of Meiosis I Depends on Separase, SPO12, and SLK19. Developmental Cell. 4(5). 727–739. 96 indexed citations

16.

Tóth, Attila, Marta Gálová, Alexander Schleiffer, et al.. (2001). A screen for genes required for meiosis and spore formation based on whole-genome expression. Current Biology. 11(13). 1001–1009. 224 indexed citations

17.

Ciosk, Rafal, Masaki Shirayama, Anna Shevchenko, et al.. (2000). Cohesin's Binding to Chromosomes Depends on a Separate Complex Consisting of Scc2 and Scc4 Proteins. Molecular Cell. 5(2). 243–254. 586 indexed citations breakdown →

18.

Tóth, Attila, et al.. (2000). Functional Genomics Identifies Monopolin. Cell. 103(7). 1155–1168. 244 indexed citations

19.

Shirayama, Masaki, Attila Tóth, Marta Gálová, & Kim Nasmyth. (1999). APCCdc20 promotes exit from mitosis by destroying the anaphase inhibitor Pds1 and cyclin Clb5. Nature. 402(6758). 203–207. 293 indexed citations

20.

Tóth, Attila. (1979). Reversible Toxic Effect of Salicylazosulf Apyridine on Semen Quality. Fertility and Sterility. 31(5). 538–540. 99 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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