Bertrand Friguet

15.1k total citations · 2 hit papers
171 papers, 12.2k citations indexed

About

Bertrand Friguet is a scholar working on Molecular Biology, Cell Biology and Clinical Biochemistry. According to data from OpenAlex, Bertrand Friguet has authored 171 papers receiving a total of 12.2k indexed citations (citations by other indexed papers that have themselves been cited), including 135 papers in Molecular Biology, 54 papers in Cell Biology and 49 papers in Clinical Biochemistry. Recurrent topics in Bertrand Friguet's work include Advanced Glycation End Products research (47 papers), Endoplasmic Reticulum Stress and Disease (43 papers) and Ubiquitin and proteasome pathways (40 papers). Bertrand Friguet is often cited by papers focused on Advanced Glycation End Products research (47 papers), Endoplasmic Reticulum Stress and Disease (43 papers) and Ubiquitin and proteasome pathways (40 papers). Bertrand Friguet collaborates with scholars based in France, United States and Germany. Bertrand Friguet's co-authors include Isabelle Petropoulos, Luke I. Szweda, Lisa Djavadi‐Ohaniance, Michel Goldberg, Anne‐Laure Bulteau, Alain Chaffotte, Earl R. Stadtman, Mariangela Conconi, Martín A. Baraibar and Géraldine Carrard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

Bertrand Friguet

168 papers receiving 11.9k citations

Hit Papers

Measurements of the true affinity constant in solution of... 1985 2026 1998 2012 1985 2015 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bertrand Friguet France 61 8.2k 2.6k 2.2k 1.7k 1.3k 171 12.2k
Carlotta Giorgi Italy 68 11.4k 1.4× 2.8k 1.1× 1.9k 0.8× 2.7k 1.6× 860 0.7× 180 16.9k
Orian S. Shirihai United States 63 11.2k 1.4× 1.5k 0.6× 3.9k 1.7× 4.4k 2.6× 1.9k 1.4× 163 16.8k
Ella Bossy‐Wetzel United States 47 11.9k 1.5× 1.8k 0.7× 1.9k 0.9× 1.8k 1.1× 901 0.7× 69 16.1k
Jean‐Claude Martinou Switzerland 79 22.0k 2.7× 2.3k 0.9× 2.2k 1.0× 3.1k 1.9× 1.9k 1.4× 194 27.9k
David C. Chan United States 68 23.9k 2.9× 2.4k 0.9× 4.6k 2.1× 5.3k 3.2× 5.4k 4.1× 128 30.7k
Jin Yao China 39 10.8k 1.3× 2.2k 0.8× 1.7k 0.8× 7.6k 4.5× 461 0.3× 90 18.5k
Biao Yan China 28 10.6k 1.3× 2.1k 0.8× 1.7k 0.8× 7.5k 4.5× 429 0.3× 97 17.9k
Guo-Fan Cao China 11 7.9k 1.0× 2.1k 0.8× 1.6k 0.7× 7.5k 4.5× 410 0.3× 17 14.4k
György Hajnóczky United States 69 14.2k 1.7× 3.3k 1.3× 2.6k 1.2× 2.1k 1.3× 1.7k 1.3× 163 18.0k
Junji Yodoi Japan 69 11.9k 1.5× 1.5k 0.6× 2.1k 0.9× 1000 0.6× 538 0.4× 271 19.2k

Countries citing papers authored by Bertrand Friguet

Since Specialization
Citations

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

Fields of papers citing papers by Bertrand Friguet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bertrand Friguet

This figure shows the co-authorship network connecting the top 25 collaborators of Bertrand Friguet. A scholar is included among the top collaborators of Bertrand Friguet 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 Bertrand Friguet. Bertrand Friguet 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.
Nemazanyy, Ivan, Susanne Brodesser, Gregory J. Dore, et al.. (2024). A homoeostatic switch causing glycerol-3-phosphate and phosphoethanolamine accumulation triggers senescence by rewiring lipid metabolism. Nature Metabolism. 6(2). 323–342. 34 indexed citations
2.
Couchie, Dominique, Nathalie Mougenot, Olaf Bergmann, et al.. (2023). Thioredoxin‐1 and its mimetic peptide improve systolic cardiac function and remodeling after myocardial infarction. The FASEB Journal. 38(1). 7 indexed citations
3.
Salnot, Virginie, et al.. (2021). Glyoxal Induces Senescence in Human Keratinocytes through Oxidative Stress and Activation of the Protein Kinase B/FOXO3a/p27KIP1 Pathway. Journal of Investigative Dermatology. 142(8). 2068–2078.e7. 13 indexed citations
4.
L’honoré, Aurore, Pierre‐Henri Commère, Elisa Négroni, et al.. (2018). The role of Pitx2 and Pitx3 in muscle stem cells gives new insights into P38α MAP kinase and redox regulation of muscle regeneration. eLife. 7. 59 indexed citations
5.
Rodier, Geneviève, Olivier Kirsh, Martín A. Baraibar, et al.. (2015). The Transcription Factor E4F1 Coordinates CHK1-Dependent Checkpoint and Mitochondrial Functions. Cell Reports. 11(2). 220–233. 33 indexed citations
6.
Yamada, Elizabeth Sumi, Gesine Respondek, Anderson de Andrade, et al.. (2014). Annonacin, a natural lipophilic mitochondrial complex I inhibitor, increases phosphorylation of tau in the brain of FTDP-17 transgenic mice. Experimental Neurology. 253. 113–125. 37 indexed citations
7.
Bayot, Aurélien, Monique Gareil, Laurent Chavatte, et al.. (2013). Effect of Lon protease knockdown on mitochondrial function in HeLa cells. Biochimie. 100. 38–47. 20 indexed citations
8.
Erjavec, Nika, Aurélien Bayot, Monique Gareil, et al.. (2012). Deletion of the mitochondrial Pim1/Lon protease in yeast results in accelerated aging and impairment of the proteasome. Free Radical Biology and Medicine. 56. 9–16. 55 indexed citations
9.
Baraibar, Martín A. & Bertrand Friguet. (2012). Changes of the Proteasomal System During the Aging Process. Progress in molecular biology and translational science. 109. 249–275. 52 indexed citations
10.
Sebban, C., Charles Cohen‐Salmon, Jacques Callebert, et al.. (2012). Aging of the dopaminergic system and motor behavior in mice intoxicated with the parkinsonian toxin 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine. Journal of Neurochemistry. 122(5). 1032–1046. 10 indexed citations
11.
Bakala, Hilaire, et al.. (2012). Catalase, a target of glycation damage in rat liver mitochondria with aging. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(10). 1527–1534. 52 indexed citations
12.
Friguet, Bertrand, Pierrette Gaudreau, & Karine Bédard. (2010). 30. Biologie du vieillissement. 2(3). 543–543. 1 indexed citations
13.
Pérez, Viviana, Rochelle Buffenstein, V. Pragathi Masamsetti, et al.. (2009). Protein stability and resistance to oxidative stress are determinants of longevity in the longest-living rodent, the naked mole-rat. Proceedings of the National Academy of Sciences. 106(9). 3059–3064. 331 indexed citations
14.
Karademir, Betül, Nicolle Breusing, A. Hoehn, et al.. (2009). The proteasome is an integral part of the signaling cascade leading to solar UVA-induced gene expression. Journal of Investigative Dermatology. 129. 1 indexed citations
15.
Bayot, Aurélien, Nicolas Basse, Irene Lee, et al.. (2007). Towards the control of intracellular protein turnover: Mitochondrial Lon protease inhibitors versus proteasome inhibitors. Biochimie. 90(2). 260–269. 47 indexed citations
16.
Cabreiro, Filipe, Martine Perichon, Marco Malavolta, et al.. (2007). Zinc supplementation in the elderly subjects: Effect on oxidized protein degradation and repair systems in peripheral blood lymphocytes. Experimental Gerontology. 43(5). 483–487. 20 indexed citations
17.
Adam, Emmanuelle, Vincent Quivy, Françoise Bex, et al.. (2003). Potentiation of Tumor Necrosis Factor-Induced NF-κB Activation by Deacetylase Inhibitors Is Associated with a Delayed Cytoplasmic Reappearance of IκBα. Molecular and Cellular Biology. 23(17). 6200–6209. 81 indexed citations
18.
Verbeke, Philippe, Martine Perichon, Bertrand Friguet, & Hilaire Bakala. (2000). Inhibition of nitric oxide synthase activity by early and advanced glycation end products in cultured rabbit proximal tubular epithelial cells. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1502(3). 481–494. 51 indexed citations
20.
Friguet, Bertrand, Lisa Djavadi‐Ohaniance, & Michel Goldberg. (1986). Conformational changes induced by domain assembly within the β2 subunit of Escherichia coli tryptophan synthase analysed with monoclonal antibodies. European Journal of Biochemistry. 160(3). 593–597. 30 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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