Elisabeth Perdu

2.4k total citations
36 papers, 2.1k citations indexed

About

Elisabeth Perdu is a scholar working on Health, Toxicology and Mutagenesis, Cancer Research and Molecular Biology. According to data from OpenAlex, Elisabeth Perdu has authored 36 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Health, Toxicology and Mutagenesis, 9 papers in Cancer Research and 5 papers in Molecular Biology. Recurrent topics in Elisabeth Perdu's work include Effects and risks of endocrine disrupting chemicals (19 papers), Carcinogens and Genotoxicity Assessment (9 papers) and Toxic Organic Pollutants Impact (6 papers). Elisabeth Perdu is often cited by papers focused on Effects and risks of endocrine disrupting chemicals (19 papers), Carcinogens and Genotoxicity Assessment (9 papers) and Toxic Organic Pollutants Impact (6 papers). Elisabeth Perdu collaborates with scholars based in France, Morocco and Spain. Elisabeth Perdu's co-authors include Daniel Zalko, Jean‐Pierre Cravedi, Carine Jacques, Laurent Debrauwer, Laurence Dolo, Hélène Duplan, Patrick Balaguer, Sandrine Bruel, Marina Grimaldi and Anne Riu and has published in prestigious journals such as Environmental Science & Technology, PLoS ONE and Hepatology.

In The Last Decade

Elisabeth Perdu

36 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elisabeth Perdu France	25	1.4k	453	344	332	161	36	2.1k
Chad R. Blystone United States	18	1.3k 1.0×	293 0.6×	264 0.8×	293 0.9×	120 0.7×	32	1.9k
Elisabete Silva United Kingdom	19	1.2k 0.9×	498 1.1×	221 0.6×	250 0.8×	98 0.6×	34	1.9k
Lichun Xu China	23	964 0.7×	248 0.5×	302 0.9×	327 1.0×	541 3.4×	69	1.8k
Otto Meyer Denmark	22	955 0.7×	243 0.5×	432 1.3×	380 1.1×	380 2.4×	59	2.3k
Majorie B.M. van Duursen Netherlands	25	773 0.6×	215 0.5×	408 1.2×	269 0.8×	101 0.6×	83	1.9k
Belma Giray Türkiye	30	1.2k 0.9×	228 0.5×	376 1.1×	342 1.0×	587 3.6×	99	2.5k
Jochem Louisse Netherlands	28	773 0.6×	178 0.4×	794 2.3×	310 0.9×	248 1.5×	83	2.5k
Janet J. Diliberto United States	28	1.8k 1.3×	207 0.5×	226 0.7×	892 2.7×	97 0.6×	53	2.3k
Francesca Maranghi Italy	25	886 0.6×	191 0.4×	247 0.7×	266 0.8×	346 2.1×	69	1.8k
Susan C. Maness United States	14	1.3k 0.9×	222 0.5×	253 0.7×	356 1.1×	160 1.0×	16	1.8k

Countries citing papers authored by Elisabeth Perdu

Since Specialization

Citations

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

Fields of papers citing papers by Elisabeth Perdu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Perdu

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

All Works

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20 of 20 papers shown

Corbel, Tanguy, Elisabeth Perdu, Véronique Gayrard, et al.. (2015). Conjugation and Deconjugation Reactions within the Fetoplacental Compartment in a Sheep Model: A Key Factor Determining Bisphenol A Fetal Exposure. Drug Metabolism and Disposition. 43(4). 467–476. 46 indexed citations

Maamar, Millissia Ben, Laurianne Lesné, Christèle Lethimonier, et al.. (2015). An Investigation of the Endocrine-Disruptive Effects of Bisphenol A in Human and Rat Fetal Testes. PLoS ONE. 10(2). e0117226–e0117226. 55 indexed citations

Jacques, Carine, Elisabeth Perdu, Emilien L. Jamin, et al.. (2014). Effect of Skin Metabolism on Dermal Delivery of Testosterone: Qualitative Assessment using a New Short-Term Skin Model. Skin Pharmacology and Physiology. 27(4). 188–188. 20 indexed citations

Riu, Anne, Catherine W. McCollum, Caroline Pinto, et al.. (2014). Halogenated Bisphenol-A Analogs Act as Obesogens in Zebrafish Larvae (Danio rerio). Toxicological Sciences. 139(1). 48–58. 111 indexed citations

Lethimonier, Christèle, O Albert, Bruno Le Bizec, et al.. (2012). Human testis steroidogenesis is inhibited by phthalates. Human Reproduction. 27(5). 1451–1459. 157 indexed citations

Muczynski, Vincent, Jean‐Pierre Cravedi, Abdelali Lehraiki, et al.. (2012). Effect of mono-(2-ethylhexyl) phthalate on human and mouse fetal testis: In vitro and in vivo approaches. Toxicology and Applied Pharmacology. 261(1). 97–104. 47 indexed citations

Audebert, Marc, Laurence Dolo, Elisabeth Perdu, Jean‐Pierre Cravedi, & Daniel Zalko. (2011). Use of the γH2AX assay for assessing the genotoxicity of bisphenol A and bisphenol F in human cell lines. Archives of Toxicology. 85(11). 1463–1473. 139 indexed citations

Riu, Anne, Marina Grimaldi, Albane le Maire, et al.. (2011). Peroxisome Proliferator-Activated Receptor γ Is a Target for Halogenated Analogs of Bisphenol A. Environmental Health Perspectives. 119(9). 1227–1232. 257 indexed citations

Jacques, Carine, Emilien L. Jamin, Elisabeth Perdu, et al.. (2010). Characterisation of B(a)P metabolites formed in an ex vivo pig skin model using three complementary analytical methods. Analytical and Bioanalytical Chemistry. 396(5). 1691–1701. 14 indexed citations

10.

Jacques, Carine, et al.. (2010). Percutaneous absorption and metabolism of [14C]-ethoxycoumarin in a pig ear skin model. Toxicology in Vitro. 24(5). 1426–1434. 24 indexed citations

11.

Zalko, Daniel, Carine Jacques, Hélène Duplan, Sandrine Bruel, & Elisabeth Perdu. (2010). Viable skin efficiently absorbs and metabolizes bisphenol A. Chemosphere. 82(3). 424–430. 199 indexed citations

12.

Pelletier, Laura, Sandra Rebouissou, Alain Paris, et al.. (2009). Loss of Hepatocyte Nuclear Factor 1α Function in Human Hepatocellular Adenomas Leads to Aberrant Activation of Signaling Pathways Involved in Tumorigenesis. Hepatology. 51(2). 557–566. 61 indexed citations

13.

Cabaton, Nicolas J., Isabelle Séverin, Elisabeth Perdu, et al.. (2008). Genotoxic and endocrine activities of bis(hydroxyphenyl)methane (bisphenol F) and its derivatives in the HepG2 cell line. Toxicology. 255(1-2). 15–24. 136 indexed citations

14.

Cabaton, Nicolas J., Daniel Zalko, Estelle Rathahao, et al.. (2008). Biotransformation of bisphenol F by human and rat liver subcellular fractions. Toxicology in Vitro. 22(7). 1697–1704. 55 indexed citations

15.

Perdu, Elisabeth, Katarina Pettersson, Ingemar Pongratz, et al.. (2008). Biotransformation of genistein and bisphenol A in cell lines used for screening endocrine disruptors. Toxicology in Vitro. 22(6). 1595–1604. 29 indexed citations

16.

Balaguer, Patrick, Elisabeth Perdu, Marchela Pandelova, et al.. (2008). Characterisation of bioactive compounds in infant formulas using immobilised recombinant estrogen receptor-α affinity columns. Food and Chemical Toxicology. 46(10). 3268–3278. 24 indexed citations

17.

Zalko, Daniel, Caroline Prouillac, Anne Riu, et al.. (2006). Biotransformation of the flame retardant tetrabromo-bisphenol A by human and rat sub-cellular liver fractions. Chemosphere. 64(2). 318–327. 50 indexed citations

18.

Cravedi, Jean‐Pierre, Michel Laurentie, Elisabeth Perdu, et al.. (2006). Disposition of genistein in rainbow trout (Oncorhynchus mykiss) and siberian sturgeon (Acipenser baeri). General and Comparative Endocrinology. 150(2). 298–308. 24 indexed citations

19.

Sturm, Armin, J.P Cravedi, Elisabeth Perdu, Maryse Baradat, & Helmut Segner. (2001). Effects of prochloraz and nonylphenol diethoxylate on hepatic biotransformation enzymes in trout: a comparative in vitro/in vivo-assessment using cultured hepatocytes. Aquatic Toxicology. 53(3-4). 229–245. 57 indexed citations

20.

Pérez‐López, Marcos, Patricia Anglade, Laurent Debrauwer, et al.. (2000). Characterization of hepatic and extrahepatic glutathione S-transferases in rainbow trout (Oncorhynchus mykiss) and their induction by 3,3′,4,4′-tetrachlorobiphenyl. Fish Physiology and Biochemistry. 22(1). 21–32. 31 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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