Gerardo Jiménez

2.8k total citations
44 papers, 2.2k citations indexed

About

Gerardo Jiménez is a scholar working on Molecular Biology, Plant Science and Cell Biology. According to data from OpenAlex, Gerardo Jiménez has authored 44 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 9 papers in Plant Science and 8 papers in Cell Biology. Recurrent topics in Gerardo Jiménez's work include Developmental Biology and Gene Regulation (22 papers), Genomics and Chromatin Dynamics (18 papers) and RNA Research and Splicing (10 papers). Gerardo Jiménez is often cited by papers focused on Developmental Biology and Gene Regulation (22 papers), Genomics and Chromatin Dynamics (18 papers) and RNA Research and Splicing (10 papers). Gerardo Jiménez collaborates with scholars based in Spain, United States and Israel. Gerardo Jiménez's co-authors include Ze’ev Paroush, David Ish‐Horowicz, Jordi Casanova, Stanislav Y. Shvartsman, Dirk Eberhard, Meinrad Busslinger, Barry Heavey, Antoine Guichet, Anne Ephrussi and Tariq Enver and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Genes & Development.

In The Last Decade

Gerardo Jiménez

41 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gerardo Jiménez Spain 26 1.8k 343 330 316 244 44 2.2k
Ze’ev Paroush Israel 25 2.4k 1.3× 303 0.9× 407 1.2× 410 1.3× 280 1.1× 38 2.8k
Dmitri Papatsenko United States 28 2.1k 1.1× 285 0.8× 343 1.0× 485 1.5× 330 1.4× 48 2.6k
Brian Gebelein United States 23 1.7k 1.0× 249 0.7× 481 1.5× 407 1.3× 113 0.5× 58 2.1k
Hamed Jafar‐Nejad United States 28 2.1k 1.2× 1.0k 3.0× 353 1.1× 533 1.7× 141 0.6× 52 2.9k
Elizabeth Noll United States 15 1.4k 0.8× 370 1.1× 216 0.7× 294 0.9× 137 0.6× 21 1.8k
Mario Chevrette Canada 23 1.9k 1.0× 440 1.3× 474 1.4× 115 0.4× 125 0.5× 42 2.5k
Bernard M. Mechler Germany 27 2.3k 1.3× 730 2.1× 365 1.1× 256 0.8× 260 1.1× 60 2.8k
Keith A. Wharton United States 20 1.5k 0.8× 270 0.8× 232 0.7× 259 0.8× 109 0.4× 36 2.1k
David A. Hartley United States 20 1.9k 1.0× 379 1.1× 401 1.2× 429 1.4× 259 1.1× 34 2.5k
Ralph A. Neumüller Austria 15 1.5k 0.8× 452 1.3× 197 0.6× 278 0.9× 196 0.8× 25 1.9k

Countries citing papers authored by Gerardo Jiménez

Since Specialization
Citations

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

Fields of papers citing papers by Gerardo Jiménez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gerardo Jiménez

This figure shows the co-authorship network connecting the top 25 collaborators of Gerardo Jiménez. A scholar is included among the top collaborators of Gerardo Jiménez 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 Gerardo Jiménez. Gerardo Jiménez 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.
Jiménez, Gerardo, et al.. (2025). Molecular basis of DNA recognition by the HMG-box-C1 module of capicua. Structure. 33(12). 2109–2121.e5.
2.
Bernués, Jordi, Mònica Torras‐Llort, Eulàlia Belloc, et al.. (2025). Maternal histone mRNAs are uniquely processed through polyadenylation in a Stem-Loop Binding Protein (SLBP) dependent manner. Nucleic Acids Research. 53(7).
3.
González‐Crespo, Sergio, et al.. (2022). Noncanonical function of Capicua as a growth termination signal inDrosophilaoogenesis. Proceedings of the National Academy of Sciences. 119(31). e2123467119–e2123467119. 1 indexed citations
4.
Simón-Carrasco, Lucía, Gerardo Jiménez, Mariano Barbacid, & Matthias Drosten. (2018). The Capicua tumor suppressor: a gatekeeper of Ras signaling in development and cancer. Cell Cycle. 17(6). 702–711. 35 indexed citations
5.
Papagianni, Αikaterini, Wanqing Shao, Shuonan He, et al.. (2018). Capicua controls Toll/IL-1 signaling targets independently of RTK regulation. Proceedings of the National Academy of Sciences. 115(8). 1807–1812. 26 indexed citations
6.
Simón-Carrasco, Lucía, Osvaldo Graña‐Castro, Harrys K.C. Jacob, et al.. (2017). Inactivation of Capicua in adult mice causes T-cell lymphoblastic lymphoma. Genes & Development. 31(14). 1456–1468. 38 indexed citations
7.
Simón-Carrasco, Lucía, Leiore Ajuria, Núria Samper, et al.. (2017). A new mode of DNA binding distinguishes Capicua from other HMG-box factors and explains its mutation patterns in cancer. PLoS Genetics. 13(3). e1006622–e1006622. 45 indexed citations
8.
Ajuria, Leiore, Núria Samper, Claudia Nieva, et al.. (2015). Origins of Context-Dependent Gene Repression by Capicua. PLoS Genetics. 11(1). e1004902–e1004902. 17 indexed citations
9.
Jin, Yinhua, Nati Ha, Jinyi Xiang, et al.. (2015). EGFR/Ras Signaling Controls Drosophila Intestinal Stem Cell Proliferation via Capicua-Regulated Genes. PLoS Genetics. 11(12). e1005634–e1005634. 103 indexed citations
10.
Azofeifa, Jorge, Meinhard Hahn, Edward Ruiz-Narváez, et al.. (2014). The STR polymorphism (AAAAT)n within the intron 1 of the tumor protein 53 (TP53) locus in 17 populations of different ethnic groups of Africa, America, Asia and Europe. Revista de Biología Tropical. 1(2). 645–645. 5 indexed citations
11.
Helman, Aharon, Bomyi Lim, María José Andreu, et al.. (2012). RTK signaling modulates the Dorsal gradient. Development. 139(16). 3032–3039. 20 indexed citations
12.
Andreu, María José, Leiore Ajuria, Núria Samper, et al.. (2012). Mirror represses pipe expression in follicle cells to initiate dorsoventral axis formation in Drosophila. Development. 139(6). 1110–1114. 24 indexed citations
13.
Helman, Aharon, Einat Cinnamon, Zvi Hayouka, et al.. (2011). Phosphorylation of Groucho Mediates RTK Feedback Inhibition and Prolonged Pathway Target Gene Expression. Current Biology. 21(13). 1102–1110. 22 indexed citations
14.
Kim, Yoosik, María José Andreu, Bomyi Lim, et al.. (2011). Gene Regulation by MAPK Substrate Competition. Developmental Cell. 20(6). 880–887. 52 indexed citations
15.
Cinnamon, Einat, Aharon Helman, Rachel Ben‐Haroush Schyr, et al.. (2008). Multiple RTK pathways downregulate Groucho-mediated repression in Drosophila embryogenesis. Development. 135(5). 829–837. 43 indexed citations
16.
Jiménez, Gerardo, et al.. (2007). Study of the genetic polymorphism of the αS1-casein in goats of Pernambuco State, Brazil.. Acta Scientiarum Animal Sciences. 29(3). 255–259.
17.
Cinnamon, Einat, Devorah Gur‐Wahnon, Aharon Helman, et al.. (2004). Capicua integrates input from two maternal systems in Drosophila terminal patterning. The EMBO Journal. 23(23). 4571–4582. 24 indexed citations
18.
Jiménez, Gerardo, Acaimo González‐Reyes, & Jordi Casanova. (2002). Cell surface proteins Nasrat and Polehole stabilize the Torso-like extracellular determinant in Drosophila oogenesis. Genes & Development. 16(8). 913–918. 40 indexed citations
19.
Goldstein, Robert E., et al.. (1999). Huckebein repressor activity in Drosophila terminal patterning is mediated by Groucho. Development. 126(17). 3747–3755. 49 indexed citations
20.
Rehm, Heidi L., Gustavo A. Gutiérrez‐Espeleta, Gerardo Jiménez, et al.. (1997). Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiency. Human Mutation. 9(5). 402–408. 25 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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