Violeta Morı́n

972 total citations
36 papers, 624 citations indexed

About

Violeta Morı́n is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Violeta Morı́n has authored 36 papers receiving a total of 624 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Physiology. Recurrent topics in Violeta Morı́n's work include Genomics and Chromatin Dynamics (13 papers), Epigenetics and DNA Methylation (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Violeta Morı́n is often cited by papers focused on Genomics and Chromatin Dynamics (13 papers), Epigenetics and DNA Methylation (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Violeta Morı́n collaborates with scholars based in Chile, France and United Kingdom. Violeta Morı́n's co-authors include Marcia Puchi, Marı́a Imschenetzky, Ariane Abrieu, Julien Espeut, Susana Prieto, Franz Hozer, Jean-François Costemale-Lacoste, Martı́n Montecino, Amaury Gaussen and Didier Fesquet and has published in prestigious journals such as Nature Communications, Molecular Cell and PLoS ONE.

In The Last Decade

Violeta Morı́n

35 papers receiving 617 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Violeta Morı́n Chile 14 462 148 89 80 46 36 624
Nannan Chang China 11 918 2.0× 154 1.0× 124 1.4× 212 2.6× 25 0.5× 15 1.1k
Brigitte L. Arduini United States 11 405 0.9× 140 0.9× 85 1.0× 72 0.9× 33 0.7× 15 650
Norma Towers United Kingdom 17 769 1.7× 68 0.5× 31 0.3× 162 2.0× 34 0.7× 22 867
Igor Kondrychyn Singapore 15 483 1.0× 258 1.7× 51 0.6× 124 1.6× 20 0.4× 23 779
Amanda Hall United Kingdom 5 333 0.7× 205 1.4× 43 0.5× 88 1.1× 15 0.3× 5 507
Yoshikazu Haramoto Japan 14 412 0.9× 56 0.4× 27 0.3× 111 1.4× 25 0.5× 41 584
Panna Tandon United States 14 435 0.9× 76 0.5× 49 0.6× 96 1.2× 53 1.2× 20 699
Laixin Xia China 18 1.0k 2.2× 87 0.6× 312 3.5× 211 2.6× 46 1.0× 34 1.3k
Cynthia D. Cooper United States 13 551 1.2× 180 1.2× 43 0.5× 80 1.0× 16 0.3× 21 721

Countries citing papers authored by Violeta Morı́n

Since Specialization
Citations

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

Fields of papers citing papers by Violeta Morı́n

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Violeta Morı́n

This figure shows the co-authorship network connecting the top 25 collaborators of Violeta Morı́n. A scholar is included among the top collaborators of Violeta Morı́n 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 Violeta Morı́n. Violeta Morı́n 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.
Alarcón, Carolina, et al.. (2024). Biodegradation of Polystyrene by Galleria mellonella: Identification of Potential Enzymes Involved in the Degradative Pathway. International Journal of Molecular Sciences. 25(3). 1576–1576. 6 indexed citations
2.
Torres-Méndez, Antonio, Sophie Bonnal, Isabel Almudí, et al.. (2022). Parallel evolution of a splicing program controlling neuronal excitability in flies and mammals. Science Advances. 8(4). eabk0445–eabk0445. 25 indexed citations
3.
Morı́n, Violeta, et al.. (2022). Blocking the Farnesyl Pocket of PDEδ Reduces Rheb-Dependent mTORC1 Activation and Survival of Tsc2-Null Cells. Frontiers in Pharmacology. 13. 912688–912688. 2 indexed citations
4.
Bawankar, Praveen, Tina Lenče, Chiara Paolantoni, et al.. (2021). Hakai is required for stabilization of core components of the m6A mRNA methylation machinery. Nature Communications. 12(1). 3778–3778. 113 indexed citations
5.
6.
Troncoso, Rodrigo, et al.. (2016). Rapamycin requires AMPK activity and p27 expression for promoting autophagy-dependent Tsc2 -null cell survival. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1863(6). 1200–1207. 16 indexed citations
7.
Trombly, Daniel J., et al.. (2016). Transcriptional Auto-Regulation of RUNX1 P1 Promoter. PLoS ONE. 11(2). e0149119–e0149119. 24 indexed citations
8.
9.
Puchi, Marcia, Rodrigo Aguilar, Estefanie Dufey, et al.. (2010). A new nuclear protease with cathepsin L properties is present in HeLa and Caco‐2 cells. Journal of Cellular Biochemistry. 111(5). 1099–1106. 9 indexed citations
10.
Espeut, Julien, Amaury Gaussen, Peter Bieling, et al.. (2008). Phosphorylation Relieves Autoinhibition of the Kinetochore Motor Cenp-E. Molecular Cell. 29(5). 637–643. 86 indexed citations
11.
Morı́n, Violeta, et al.. (2007). Nuclear cysteine‐protease involved in male chromatin remodeling after fertilization is ubiquitously distributed during sea urchin development. Journal of Cellular Biochemistry. 101(1). 1–8. 4 indexed citations
12.
Morı́n, Violeta, et al.. (2007). Sperm nucleosomes disassembly is a requirement for histones proteolysis during male pronucleus formation. Journal of Cellular Biochemistry. 103(2). 447–455. 7 indexed citations
13.
Morı́n, Violeta, et al.. (2005). During male pronuclei formation chromatin remodeling is uncoupled from nucleus decondensation. Journal of Cellular Biochemistry. 96(2). 235–241. 6 indexed citations
14.
Even, Yasmine, et al.. (2005). Inhibition of cysteine protease activity disturbs DNA replication and prevents mitosis in the early mitotic cell cycles of sea urchin embryos. Journal of Cellular Physiology. 204(2). 693–703. 19 indexed citations
15.
Concha, Carolina, Violeta Morı́n, Paula Bustos, et al.. (2004). Cysteine‐protease involved in male chromatin remodeling after fertilization co‐localizes with α‐tubulin at mitosis. Journal of Cellular Physiology. 202(2). 602–607. 9 indexed citations
16.
Imschenetzky, Marı́a, Marcia Puchi, Violeta Morı́n, Ricardo Medina, & Martı́n Montecino. (2003). Chromatin remodeling during sea urchin early development: molecular determinants for pronuclei formation and transcriptional activation. Gene. 322. 33–46. 14 indexed citations
17.
Oliver-Ferrándiz, María, Paula Bustos, Violeta Morı́n, et al.. (2002). Conservative segregation of maternally inherited CS histone variants in larval stages of sea urchin development. Journal of Cellular Biochemistry. 88(4). 643–649. 4 indexed citations
18.
Morı́n, Violeta, et al.. (2001). Variability of sperm specific histones in sea urchins. Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 128(3). 451–457. 3 indexed citations
19.
Imschenetzky, Marı́a, María Oliver-Ferrándiz, Soraya Gutiérrez, et al.. (1996). Hybrid nucleoprotein particles containing a subset of male and female histone variants form during male pronucleus formation in sea urchins. Journal of Cellular Biochemistry. 63(4). 385–394. 8 indexed citations
20.
Imschenetzky, Marı́a, Violeta Morı́n, Nelson Carvajal, Martı́n Montecino, & Marcia Puchi. (1996). Decreased heterogeneity of CS histone variants after hydrolysis of the ADP-ribose moiety. Journal of Cellular Biochemistry. 61(1). 109–117. 5 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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