Frédéric Bienvenu

1.1k total citations
10 papers, 861 citations indexed

About

Frédéric Bienvenu is a scholar working on Molecular Biology, Oncology and Pathology and Forensic Medicine. According to data from OpenAlex, Frédéric Bienvenu has authored 10 papers receiving a total of 861 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Oncology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Frédéric Bienvenu's work include Cancer-related Molecular Pathways (4 papers), RNA Research and Splicing (2 papers) and Advanced biosensing and bioanalysis techniques (2 papers). Frédéric Bienvenu is often cited by papers focused on Cancer-related Molecular Pathways (4 papers), RNA Research and Splicing (2 papers) and Advanced biosensing and bioanalysis techniques (2 papers). Frédéric Bienvenu collaborates with scholars based in France, United Kingdom and United States. Frédéric Bienvenu's co-authors include Olivier Coqueret, Hugues Gascan, Piotr Siciński, Sylvie Avril, Sandrine Giraud, Joshua E. Elias, Siwanon Jirawatnotai, Steven P. Gygi, Agnieszka Zagożdżon and David M. Heery and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Blood.

In The Last Decade

Frédéric Bienvenu

9 papers receiving 855 citations

Peers

Frédéric Bienvenu

MB

ONCOL

CB

CR

PFM

Jean‐Bernard Lazaro United States

Ivan Nicola Colaluca Italy

Katherine Dunn Canada

Raouf Fetni Canada

Nicole Falette France

Jia-Ling Teo United States

Thomas R. Geiger United States

Nathalie Cahuzac France

Yow-Ling Shiue Taiwan

Cédric Barrière France

Jean‐Bernard Lazaro United States

Frédéric Bienvenu

701 ×1.3

MB

385 ×0.8

ONCOL

125 ×0.9

CB

95 ×0.7

CR

39 ×0.4

PFM

Citations per year, relative to Frédéric Bienvenu Frédéric Bienvenu (= 1×) peers Jean‐Bernard Lazaro

Countries citing papers authored by Frédéric Bienvenu

Since Specialization

Citations

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

Fields of papers citing papers by Frédéric Bienvenu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frédéric Bienvenu

This figure shows the co-authorship network connecting the top 25 collaborators of Frédéric Bienvenu. A scholar is included among the top collaborators of Frédéric Bienvenu 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 Frédéric Bienvenu. Frédéric Bienvenu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Dumas, Jonathan, et al.. (2023). Dynamic sizing of required balancing capacities: the operational approach in France. 1 indexed citations

2.

Champagne, Julien, Laëtitia K. Linares, Emeric Dubois, et al.. (2019). TAG-RNAi overcomes off-target effects in cancer models. Oncogene. 39(4). 935–945. 5 indexed citations

3.

Champagne, Julien, et al.. (2015). Hyper sensitive protein detection by Tandem-HTRF reveals Cyclin D1 dynamics in adult mouse. Scientific Reports. 5(1). 15739–15739. 1 indexed citations

4.

Jirawatnotai, Siwanon, Yiduo Hu, Wojciech Michowski, et al.. (2011). A function for cyclin D1 in DNA repair uncovered by protein interactome analyses in human cancers. Nature. 474(7350). 230–234. 255 indexed citations

5.

Odajima, Junko, Zachary P. Wills, Miho Terunuma, et al.. (2011). Cyclin E Constrains Cdk5 Activity to Regulate Synaptic Plasticity and Memory Formation. Developmental Cell. 21(4). 655–668. 99 indexed citations

6.

Bienvenu, Frédéric, Siwanon Jirawatnotai, Joshua E. Elias, et al.. (2010). Transcriptional role of cyclin D1 in development revealed by a genetic–proteomic screen. Nature. 463(7279). 374–378. 220 indexed citations

7.

Bienvenu, Frédéric, Benjamin Barré, Sandrine Giraud, Sylvie Avril, & Olivier Coqueret. (2005). Transcriptional Regulation by a DNA-associated Form of Cyclin D1. Molecular Biology of the Cell. 16(4). 1850–1858. 39 indexed citations

8.

Barré, Benjamin, et al.. (2003). Kaposi sarcoma–associated viral cyclin K overrides cell growth inhibition mediated by oncostatin M through STAT3 inhibition. Blood. 101(10). 4070–4077. 18 indexed citations

9.

Giraud, Sandrine, Frédéric Bienvenu, Sylvie Avril, et al.. (2002). Functional Interaction of STAT3 Transcription Factor with the Coactivator NcoA/SRC1a. Journal of Biological Chemistry. 277(10). 8004–8011. 121 indexed citations

10.

Bienvenu, Frédéric, Hugues Gascan, & Olivier Coqueret. (2001). Cyclin D1 Represses STAT3 Activation through a Cdk4-independent Mechanism. Journal of Biological Chemistry. 276(20). 16840–16847. 102 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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