Philippe Couvert

2.5k total citations
32 papers, 1.3k citations indexed

About

Philippe Couvert is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Philippe Couvert has authored 32 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 11 papers in Surgery. Recurrent topics in Philippe Couvert's work include Epigenetics and DNA Methylation (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Drug Transport and Resistance Mechanisms (6 papers). Philippe Couvert is often cited by papers focused on Epigenetics and DNA Methylation (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Drug Transport and Resistance Mechanisms (6 papers). Philippe Couvert collaborates with scholars based in France, Lebanon and Germany. Philippe Couvert's co-authors include Alain Carrié, Philippe Giral, Jamel Chelly, T. Bienvenu, Chérif Beldjord, Wilfried Le Goff, Maryse Guérin, M. John Chapman, Éric Bruckert and Thierry Huby and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Immunology and Gastroenterology.

In The Last Decade

Philippe Couvert

31 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippe Couvert France 18 649 476 344 206 152 32 1.3k
Andrew P. Boright Canada 13 404 0.6× 223 0.5× 194 0.6× 68 0.3× 106 0.7× 18 1.2k
Sampathkumar Rangasamy United States 20 611 0.9× 286 0.6× 210 0.6× 33 0.2× 173 1.1× 44 1.9k
Richard Pang China 19 324 0.5× 108 0.2× 217 0.6× 35 0.2× 82 0.5× 45 1.1k
Mirko Pinotti Italy 30 1.1k 1.7× 272 0.6× 161 0.5× 23 0.1× 113 0.7× 122 3.1k
Kimihiko Oishi United States 15 463 0.7× 99 0.2× 224 0.7× 31 0.2× 108 0.7× 34 1.1k
Martine Géhin Switzerland 13 452 0.7× 447 0.9× 92 0.3× 21 0.1× 146 1.0× 28 1.1k
Masanori Kurimoto Japan 23 379 0.6× 89 0.2× 368 1.1× 26 0.1× 315 2.1× 135 1.9k
Yoshikazu Saito Japan 15 355 0.5× 90 0.2× 194 0.6× 42 0.2× 125 0.8× 41 1.0k
Joana Visa Spain 14 466 0.7× 307 0.6× 197 0.6× 26 0.1× 27 0.2× 16 936
Lu Yu China 15 297 0.5× 44 0.1× 433 1.3× 177 0.9× 61 0.4× 45 965

Countries citing papers authored by Philippe Couvert

Since Specialization
Citations

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

Fields of papers citing papers by Philippe Couvert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Couvert

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe Couvert. A scholar is included among the top collaborators of Philippe Couvert 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 Philippe Couvert. Philippe Couvert 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.
Guillas, Isabelle, Marie Lhomme, Cédric Pionneau, et al.. (2023). Identification of the specific molecular and functional signatures of pre-beta-HDL: relevance to cardiovascular disease. Basic Research in Cardiology. 118(1). 33–33. 9 indexed citations
2.
Couvert, Philippe, et al.. (2022). Rotor Syndrome Presenting as Dubin-Johnson Syndrome. Case Reports in Gastroenterology. 16(2). 452–455.
3.
Small, Lewin, Lars R. Ingerslev, Rhianna C. Laker, et al.. (2021). Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity. PLoS Genetics. 17(1). e1009325–e1009325. 11 indexed citations
4.
Khoury, Petra El, Philippe Couvert, Sandy Elbitar, et al.. (2018). Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1. Journal of clinical lipidology. 12(6). 1374–1382. 10 indexed citations
5.
Vekić, Jelena, Aleksandra Zeljković, Alain Carrié, et al.. (2017). The usefulness of advanced lipid and oxidative stress testing for diagnosis and management of low HDL-cholesterol phenotype: A case report. Clinical Biochemistry. 50(18). 1323–1325. 5 indexed citations
6.
Villard, Elise F., Éric Bruckert, Karine Clément, et al.. (2013). Endogenous CETP activity as a predictor of cardiovascular risk: Determination of the optimal range. Atherosclerosis. 227(1). 165–171. 12 indexed citations
7.
Abifadel, Marianne, Maryse Guérin, Suzanne Benjannet, et al.. (2012). Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia. Atherosclerosis. 223(2). 394–400. 87 indexed citations
8.
Couvert, Philippe, Alain Carrié, Sophie Tézenas du Montcel, et al.. (2012). Insulin-like growth factor 2 gene methylation in peripheral blood mononuclear cells of patients with hepatitis C related cirrhosis or hepatocellular carcinoma. Clinics and Research in Hepatology and Gastroenterology. 36(4). 345–351. 13 indexed citations
9.
Giral, Philippe, Vlad Ratziu, Philippe Couvert, et al.. (2009). Plasma bilirubin and gamma-glutamyltransferase activity are inversely related in dyslipidemic patients with metabolic syndrome: Relevance to oxidative stress. Atherosclerosis. 210(2). 607–613. 49 indexed citations
10.
Prieur, Xavier, Thierry Huby, Joan Rodríguez, Philippe Couvert, & John Chapman. (2008). Apolipoprotein AV: gene expression,physiological role in lipid metabolism and clinical relevance. 3(4). 371–384. 4 indexed citations
11.
Théaudin, Marie, Philippe Couvert, Emmanuel Fournier, et al.. (2008). Lewis-Sumner Syndrome and Tangier Disease. Archives of Neurology. 65(7). 968–70. 9 indexed citations
12.
Nahon, Pierre, Angéla Sutton, Pierre Rufat, et al.. (2007). Liver Iron, HFE Gene Mutations, and Hepatocellular Carcinoma Occurrence in Patients With Cirrhosis. Gastroenterology. 134(1). 102–110. 100 indexed citations
13.
Poirier, Karine, Céline Chalas, Frédérique Tissier, et al.. (2003). Loss of parental‐specific methylation at the IGF2 locus in human hepatocellular carcinoma. The Journal of Pathology. 201(3). 473–479. 27 indexed citations
14.
Gomot, Marie, Chantal Gendrot, Alain Verloès, et al.. (2003). MECP2 gene mutations in non‐syndromic X‐linked mental retardation: Phenotype–genotype correlation. American Journal of Medical Genetics Part A. 123A(2). 129–139. 30 indexed citations
15.
Kerjean, Antoine, Philippe Couvert, Thomas Heams, et al.. (2003). In vitro follicular growth affects oocyte imprinting establishment in mice. European Journal of Human Genetics. 11(7). 493–496. 69 indexed citations
16.
Benchoua, Alexandra, et al.. (2002). Active Caspase-8 Translocates into the Nucleus of Apoptotic Cells to Inactivate Poly(ADP-ribose) Polymerase-2. Journal of Biological Chemistry. 277(37). 34217–34222. 69 indexed citations
17.
Couvert, Philippe. (2001). MECP2 is highly mutated in X-linked mental retardation. Human Molecular Genetics. 10(9). 941–946. 214 indexed citations
18.
Bienvenu, Thierry, Isabelle Souville, Karine Poirier, et al.. (2001). Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy. Human Mutation. 18(3). 251–252. 8 indexed citations
19.
Girard, M, Philippe Couvert, Alain Carrié, et al.. (2001). Parental origin of de novo MECP2 mutations in Rett syndrome. European Journal of Human Genetics. 9(3). 231–236. 92 indexed citations
20.

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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