Aurora Ruiz‐Herrera

4.3k total citations
78 papers, 2.1k citations indexed

About

Aurora Ruiz‐Herrera is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, Aurora Ruiz‐Herrera has authored 78 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Plant Science, 52 papers in Molecular Biology and 50 papers in Genetics. Recurrent topics in Aurora Ruiz‐Herrera's work include Chromosomal and Genetic Variations (58 papers), Genomics and Chromatin Dynamics (18 papers) and Genomics and Phylogenetic Studies (17 papers). Aurora Ruiz‐Herrera is often cited by papers focused on Chromosomal and Genetic Variations (58 papers), Genomics and Chromatin Dynamics (18 papers) and Genomics and Phylogenetic Studies (17 papers). Aurora Ruiz‐Herrera collaborates with scholars based in Spain, Australia and South Africa. Aurora Ruiz‐Herrera's co-authors include Terence J. Robinson, M. Garcı́a, Elena Giulotto, Marta Farré, F. García, M. Ponsà, Solomon G. Nergadze, Marco Santagostino, Laia Capilla and José Castresana and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Aurora Ruiz‐Herrera

71 papers receiving 2.1k citations

Peers

Aurora Ruiz‐Herrera
Aurora Ruiz‐Herrera
Citations per year, relative to Aurora Ruiz‐Herrera Aurora Ruiz‐Herrera (= 1×) peers M. Garcı́a

Countries citing papers authored by Aurora Ruiz‐Herrera

Since Specialization
Citations

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

Fields of papers citing papers by Aurora Ruiz‐Herrera

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aurora Ruiz‐Herrera. 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 Aurora Ruiz‐Herrera. The network helps show where Aurora Ruiz‐Herrera may publish in the future.

Co-authorship network of co-authors of Aurora Ruiz‐Herrera

This figure shows the co-authorship network connecting the top 25 collaborators of Aurora Ruiz‐Herrera. A scholar is included among the top collaborators of Aurora Ruiz‐Herrera 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 Aurora Ruiz‐Herrera. Aurora Ruiz‐Herrera 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.
Ayroles, Julien F., Mayra Furlan-Magaril, Luisa F. Pallares, et al.. (2025). The Genomic Kaleidoscope: On the Hidden Dimensions of Within-Species Genomic Diversity. Genome Biology and Evolution. 17(11).
2.
Patel, Hardip R., Hyungtaek Jung, Jillian M. Hammond, et al.. (2025). A near telomere-to-telomere phased genome assembly and annotation for the Australian central bearded dragon Pogona vitticeps. GigaScience. 14.
3.
Jeffries, Daniel L., Chiara Benvenuto, Astrid Böhne, et al.. (2025). The Tree of Sex consortium: a global initiative for studying the evolution of reproduction in eukaryotes. Journal of Evolutionary Biology. 38(7). 861–886.
4.
Álvarez-González, Lucía, Zhiqiang Wu, Eugenia E. Montiel, et al.. (2024). De novo genome assemblies of two cryptodiran turtles with ZZ/ZW and XX/XY sex chromosomes provide insights into patterns of genome reshuffling and uncover novel 3D genome folding in amniotes. Genome Research. 34(10). 1553–1569. 2 indexed citations
5.
Patel, Hardip R., Shafagh A. Waters, Alexandra Livernois, et al.. (2024). Incomplete transcriptional dosage compensation of chicken and platypus sex chromosomes is balanced by post-transcriptional compensation. Proceedings of the National Academy of Sciences. 121(32). e2322360121–e2322360121. 5 indexed citations
6.
Grady, Patrick G. S., Donna M. Bond, Timothy A. Hore, et al.. (2024). Imprinted X chromosome inactivation in marsupials: The paternal X arrives at the egg with a silent DNA methylation profile. Proceedings of the National Academy of Sciences. 121(36). e2412185121–e2412185121. 1 indexed citations
7.
Álvarez-González, Lucía & Aurora Ruiz‐Herrera. (2024). Evolution of 3D Chromatin Folding. Annual Review of Animal Biosciences. 13(1). 49–71. 6 indexed citations
8.
Solé, M, Roberto de la Fuente, Marilyn B. Renfree, et al.. (2023). Divergent patterns of meiotic double strand breaks and synapsis initiation dynamics suggest an evolutionary shift in the meiosis program between American and Australian marsupials. Frontiers in Cell and Developmental Biology. 11. 1147610–1147610. 4 indexed citations
9.
Vara, Covadonga, Soledad Berríos, Raúl Fernández‐Donoso, et al.. (2022). Strategies for meiotic sex chromosome dynamics and telomeric elongation in Marsupials. PLoS Genetics. 18(2). e1010040–e1010040. 15 indexed citations
10.
Waters, Paul D., Hardip R. Patel, Aurora Ruiz‐Herrera, et al.. (2021). Microchromosomes are building blocks of bird, reptile, and mammal chromosomes. Proceedings of the National Academy of Sciences. 118(45). 93 indexed citations
11.
Vara, Covadonga, Andreu Paytuví-Gallart, Yasmina Cuartero, et al.. (2021). The impact of chromosomal fusions on 3D genome folding and recombination in the germ line. Nature Communications. 12(1). 48 indexed citations
12.
Waters, Paul D. & Aurora Ruiz‐Herrera. (2020). Meiotic Executioner Genes Protect the Y from Extinction. Trends in Genetics. 36(10). 728–738. 23 indexed citations
13.
Deakin, Janine E., Sally Potter, Rachel J. O’Neill, et al.. (2019). Chromosomics: Bridging the Gap between Genomes and Chromosomes. Genes. 10(8). 627–627. 76 indexed citations
14.
Vara, Covadonga, Andreu Paytuví-Gallart, Yasmina Cuartero, et al.. (2019). Three-Dimensional Genomic Structure and Cohesin Occupancy Correlate with Transcriptional Activity during Spermatogenesis. Cell Reports. 28(2). 352–367.e9. 108 indexed citations
15.
Vozdová, Miluše, Aurora Ruiz‐Herrera, Halina Černohorská, et al.. (2016). Meiotic behaviour of evolutionary sex-autosome translocations in Bovidae. Chromosome Research. 24(3). 325–338. 21 indexed citations
16.
Capilla, Laia, Rosa Ana Sánchez‐Guillén, Marta Farré, et al.. (2016). Mammalian comparative genomics reveals genetic and epigenetic features associated with genome reshuffling in Rodentia. Genome Biology and Evolution. 8(12). evw276–evw276. 21 indexed citations
17.
Reig‐Viader, Rita, Miguel A. Brieño‐Enríquez, Núria Torán, et al.. (2012). Telomeric repeat-containing RNA and telomerase in human fetal oocytes. Human Reproduction. 28(2). 414–422. 30 indexed citations
18.
Raimondi, Elena, Francesca M. Piras, Solomon G. Nergadze, et al.. (2011). Polymorphic organization of constitutive heterochromatin in Equus asinus (2n = 62) chromosome 1. Hereditas. 148(3). 110–113. 8 indexed citations
19.
Robinson, Terence J. & Aurora Ruiz‐Herrera. (2008). Defining the ancestral eutherian karyotype: A cladistic interpretation of chromosome painting and genome sequence assembly data. Chromosome Research. 16(8). 1133–1141. 25 indexed citations
20.
Ruiz‐Herrera, Aurora, M. Ponsà, F. García, J. Egozcue, & M. Garcı́a. (2002). Fragile Sites in Human and Macaca Fascicularis Chromosomes are Breakpoints in Chromosome Evolution. Chromosome Research. 10(1). 33–44. 42 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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