Christine Conesa

1.2k total citations
28 papers, 1.0k citations indexed

About

Christine Conesa is a scholar working on Molecular Biology, Plant Science and Epidemiology. According to data from OpenAlex, Christine Conesa has authored 28 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 2 papers in Plant Science and 1 paper in Epidemiology. Recurrent topics in Christine Conesa's work include Fungal and yeast genetics research (21 papers), Genomics and Chromatin Dynamics (20 papers) and RNA Research and Splicing (15 papers). Christine Conesa is often cited by papers focused on Fungal and yeast genetics research (21 papers), Genomics and Chromatin Dynamics (20 papers) and RNA Research and Splicing (15 papers). Christine Conesa collaborates with scholars based in France, Spain and United States. Christine Conesa's co-authors include André Sentenac, Olivier Lefebvre, Joël Acker, Christophe Carles, R. N. Swanson, Giorgio Dieci, Janine Huet, Rosalía Arrebola, Salam Shaaban and Michel Riva and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Christine Conesa

28 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christine Conesa France 19 968 75 65 27 23 28 1.0k
Anne Cosset France 20 891 0.9× 147 2.0× 40 0.6× 42 1.6× 17 0.7× 24 992
Saskia Gressel Germany 6 773 0.8× 49 0.7× 67 1.0× 22 0.8× 21 0.9× 7 801
Sundaresan Tharun United States 12 972 1.0× 89 1.2× 46 0.7× 26 1.0× 11 0.5× 15 1.0k
Stephanie Schroeder United States 13 1.0k 1.1× 48 0.6× 54 0.8× 11 0.4× 19 0.8× 18 1.1k
Purusharth I Rajyaguru India 12 633 0.7× 37 0.5× 103 1.6× 27 1.0× 9 0.4× 25 698
Christopher Marshallsay Switzerland 12 781 0.8× 193 2.6× 62 1.0× 17 0.6× 17 0.7× 16 840
Nono Takeuchi Japan 17 763 0.8× 39 0.5× 94 1.4× 40 1.5× 33 1.4× 24 840
Patricia Compagnone-Post United States 6 620 0.6× 46 0.6× 46 0.7× 14 0.5× 35 1.5× 7 678
Christiane Rammelt Germany 10 628 0.6× 38 0.5× 50 0.8× 15 0.6× 23 1.0× 13 680
Vladimir Podolny United States 7 1.1k 1.1× 169 2.3× 64 1.0× 19 0.7× 28 1.2× 7 1.1k

Countries citing papers authored by Christine Conesa

Since Specialization
Citations

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

Fields of papers citing papers by Christine Conesa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Conesa

This figure shows the co-authorship network connecting the top 25 collaborators of Christine Conesa. A scholar is included among the top collaborators of Christine Conesa 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 Christine Conesa. Christine Conesa 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.
Garrido-Godino, Ana I., et al.. (2024). Maf1 phosphorylation is regulated through the action of prefoldin-like Bud27 on PP4 phosphatase in Saccharomyces cerevisiae. Nucleic Acids Research. 52(12). 7081–7095. 1 indexed citations
2.
Huecas, Sonia, Christine Conesa, Joël Acker, et al.. (2023). Structural basis of Ty1 integrase tethering to RNA polymerase III for targeted retrotransposon integration. Nature Communications. 14(1). 1729–1729. 5 indexed citations
3.
Conesa, Christine, et al.. (2021). Ty1 integrase is composed of an active N-terminal domain and a large disordered C-terminal module dispensable for its activity in vitro. Journal of Biological Chemistry. 297(4). 101093–101093. 2 indexed citations
4.
Conesa, Christine, et al.. (2020). A small targeting domain in Ty1 integrase is sufficient to direct retrotransposon integration upstream of tRNA genes. The EMBO Journal. 39(17). e104337–e104337. 14 indexed citations
5.
Acker, Joël, et al.. (2014). Sub1 and Maf1, Two Effectors of RNA Polymerase III, Are Involved in the Yeast Quiescence Cycle. PLoS ONE. 9(12). e114587–e114587. 11 indexed citations
6.
7.
Graczyk, Damian, et al.. (2013). Maf1, repressor of tRNA transcription, is involved in the control of gluconeogenetic genes in Saccharomyces cerevisiae. Gene. 526(1). 16–22. 13 indexed citations
8.
Acker, Joël, Christine Conesa, & Olivier Lefebvre. (2012). Yeast RNA polymerase III transcription factors and effectors. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1829(3-4). 283–295. 43 indexed citations
9.
Conesa, Christine & Joël Acker. (2010). Sub1/PC4 a chromatin associated protein with multiple functions in transcription. RNA Biology. 7(3). 287–290. 52 indexed citations
10.
Conesa, Christine, Roberta Ruotolo, Pascal Soularue, et al.. (2005). Modulation of Yeast Genome Expression in Response to Defective RNA Polymerase III-Dependent Transcription. Molecular and Cellular Biology. 25(19). 8631–8642. 28 indexed citations
11.
Siaut, Magali, Cécile Zaros, Magali Court, et al.. (2002). An Rpb4/Rpb7-Like Complex in Yeast RNA Polymerase III Contains the Orthologue of Mammalian CGRP-RCP. Molecular and Cellular Biology. 23(1). 195–205. 41 indexed citations
12.
Peyroche, Gérald, Magali Siaut, Olivier Lefebvre, et al.. (2000). A Novel Subunit of Yeast RNA Polymerase III Interacts with the TFIIB-Related Domain of TFIIIB70. Molecular and Cellular Biology. 20(2). 488–495. 67 indexed citations
13.
Deprez, Eric, Rosalía Arrebola, Christine Conesa, & André Sentenac. (1999). A Subunit of Yeast TFIIIC Participates in the Recruitment of TATA-Binding Protein. Molecular and Cellular Biology. 19(12). 8042–8051. 32 indexed citations
14.
Arrebola, Rosalía, Marie‐Claude Marsolier, Olivier Lefebvre, et al.. (1998). τ91, an Essential Subunit of Yeast Transcription Factor IIIC, Cooperates with τ138 in DNA Binding. Molecular and Cellular Biology. 18(1). 1–9. 53 indexed citations
15.
Arrebola, Rosalía, Bénédicte Buffin‐Meyer, Olivier Lefebvre, et al.. (1998). A Chimeric Subunit of Yeast Transcription Factor IIIC Forms a Subcomplex with τ95. Molecular and Cellular Biology. 18(6). 3191–3200. 30 indexed citations
16.
Huet, Janine, Giorgio Dieci, Gérald Peyroche, et al.. (1996). [22] RNA polymerase III and class III transcription factors from Saccharomyces cerevisiae. Methods in enzymology on CD-ROM/Methods in enzymology. 273. 249–267. 45 indexed citations
17.
Conesa, Christine, et al.. (1995). Complex Interactions between Yeast TFIIIB and TFIIIC. Journal of Biological Chemistry. 270(25). 15353–15358. 72 indexed citations
18.
Huet, Janine, et al.. (1994). Interactions between yeast TFIIIB components. Nucleic Acids Research. 22(16). 3433–3439. 49 indexed citations
19.
Huet, Janine, et al.. (1994). Interactions between yeast TFIIIB components. Nucleic Acids Research. 22(12). 2282–2288. 11 indexed citations
20.
Lygerou, Zoi, Christine Conesa, Pascale Lesage, et al.. (1994). The yeast BDF1 gene encodes a transcription factor involved in the expression of a broad class of genes including snRNAs. Nucleic Acids Research. 22(24). 5332–5340. 66 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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