Edith Chevret

1.9k total citations
44 papers, 1.4k citations indexed

About

Edith Chevret is a scholar working on Molecular Biology, Dermatology and Epidemiology. According to data from OpenAlex, Edith Chevret has authored 44 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 15 papers in Dermatology and 10 papers in Epidemiology. Recurrent topics in Edith Chevret's work include Cutaneous lymphoproliferative disorders research (15 papers), Chromosomal and Genetic Variations (9 papers) and Fungal Infections and Studies (9 papers). Edith Chevret is often cited by papers focused on Cutaneous lymphoproliferative disorders research (15 papers), Chromosomal and Genetic Variations (9 papers) and Fungal Infections and Studies (9 papers). Edith Chevret collaborates with scholars based in France, Lebanon and Portugal. Edith Chevret's co-authors include Sophie Rousseaux, J. Cozzi, R. Pelletier, B Sèle, Denise Sheer, Emanuela V. Volpi, Jean‐Philippe Merlio, Michèle Monteil, M. Beylot‐Barry and T. Alwyn Jones and has published in prestigious journals such as Blood, PLoS ONE and Oncogene.

In The Last Decade

Edith Chevret

42 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edith Chevret France 18 695 451 284 257 237 44 1.4k
Shiyu Zhang China 12 524 0.8× 872 1.9× 45 0.2× 395 1.5× 51 0.2× 51 1.4k
Jeffrey W. Pollard United States 10 888 1.3× 299 0.7× 115 0.4× 239 0.9× 5 0.0× 11 1.6k
Masahiro Muto Japan 18 1.4k 2.0× 405 0.9× 95 0.3× 51 0.2× 5 0.0× 54 1.9k
Kathy M. Ensrud United States 13 343 0.5× 176 0.4× 20 0.1× 291 1.1× 26 0.1× 17 1.2k
N.G.J. Jaspers Netherlands 18 1.4k 2.1× 199 0.4× 123 0.4× 19 0.1× 62 0.3× 26 1.6k
Tim Lammens Belgium 23 1.3k 1.8× 103 0.2× 710 2.5× 40 0.2× 6 0.0× 64 1.9k
Susi Scappaticci Italy 18 374 0.5× 262 0.6× 153 0.5× 14 0.1× 25 0.1× 47 784
Masashi Yukawa Japan 16 743 1.1× 141 0.3× 111 0.4× 70 0.3× 4 0.0× 20 1.1k
Massimo Zani Italy 17 731 1.1× 345 0.8× 39 0.1× 40 0.2× 51 0.2× 31 1.1k
Kikuë Tachibana Germany 15 1000 1.4× 113 0.3× 200 0.7× 22 0.1× 9 0.0× 23 1.2k

Countries citing papers authored by Edith Chevret

Since Specialization
Citations

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

Fields of papers citing papers by Edith Chevret

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edith Chevret

This figure shows the co-authorship network connecting the top 25 collaborators of Edith Chevret. A scholar is included among the top collaborators of Edith Chevret 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 Edith Chevret. Edith Chevret 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.
Prochazkova‐Carlotti, Martina, Rui Batısta, Ana Pestana, et al.. (2023). Spotlight on hTERT Complex Regulation in Cutaneous T-Cell Lymphomas. Genes. 14(2). 439–439. 3 indexed citations
2.
Khalil, Charbel, et al.. (2023). T-cell lymphocytes’ aging clock: telomeres, telomerase and aging. Biogerontology. 25(2). 279–288. 10 indexed citations
3.
Prochazkova‐Carlotti, Martina, Jacky Ferrer, Chantal Farra, et al.. (2022). Telomeric Repeat-Containing RNA (TERRA): A Review of the Literature and First Assessment in Cutaneous T-Cell Lymphomas. Genes. 13(3). 539–539. 15 indexed citations
4.
Imre, Gergely, Stefan Kippenberger, Markus Meißner, et al.. (2021). C6 Ceramide (d18:1/6:0) as a Novel Treatment of Cutaneous T Cell Lymphoma. Cancers. 13(2). 270–270. 9 indexed citations
5.
Péloponèse, Jean‐Marie, et al.. (2020). hMZF-2, the Elusive Transcription Factor. Frontiers in Genetics. 11. 581115–581115. 1 indexed citations
6.
Chouery, Éliane, Hampig Raphaël Kourié, M. Beylot‐Barry, et al.. (2020). Diagnosis and treatment of lymphomas in the era of epigenetics. Blood Reviews. 48. 100782–100782. 12 indexed citations
7.
Gros, Audrey, Elodie Laharanne, Martina Prochazkova‐Carlotti, et al.. (2017). TP53 alterations in primary and secondary Sézary syndrome: A diagnostic tool for the assessment of malignancy in patients with erythroderma. PLoS ONE. 12(3). e0173171–e0173171. 13 indexed citations
8.
Andrique, Laëtitia, Sandrine Poglio, Martina Prochazkova‐Carlotti, et al.. (2016). Intrahepatic Xenograft of Cutaneous T-Cell Lymphoma Cell Lines. American Journal Of Pathology. 186(7). 1775–1785. 12 indexed citations
9.
Toutain, Jérôme, Martina Prochazkova‐Carlotti, J. Horovitz, et al.. (2015). Evaluation of Quantitative Fluorescence in situ Hybridization for Relative Measurement of Telomere Length in Placental Mesenchymal Core Cells. Gynecologic and Obstetric Investigation. 81(1). 54–60. 3 indexed citations
10.
Toutain, Jérôme, Martina Prochazkova‐Carlotti, David Cappellen, et al.. (2013). Reduced Placental Telomere Length during Pregnancies Complicated by Intrauterine Growth Restriction. PLoS ONE. 8(1). e54013–e54013. 39 indexed citations
11.
Laharanne, Elodie, Naïma Oumouhou, Françoise Bonnet, et al.. (2010). Genome-Wide Analysis of Cutaneous T-Cell Lymphomas Identifies Three Clinically Relevant Classes. Journal of Investigative Dermatology. 130(6). 1707–1718. 80 indexed citations
12.
Marty, Marion, Elodie Laharanne, Edith Chevret, et al.. (2008). Primary Cutaneous T-Cell Lymphomas Do not Show Specific NAV3 Gene Deletion or Translocation. Journal of Investigative Dermatology. 128(10). 2458–2466. 10 indexed citations
13.
Chevret, Edith, et al.. (2005). Large cell transformation of mycosis fungoides: tetraploidization within skin tumor large cells. Cancer Genetics and Cytogenetics. 163(1). 1–6. 14 indexed citations
14.
Chevret, Edith, Emanuela V. Volpi, & Denise Sheer. (2000). Mini review: Form and function in the human interphase chromosome. Cytogenetic and Genome Research. 90(1-2). 13–21. 34 indexed citations
15.
Chevret, Edith, Sophie Rousseaux, Michèle Monteil, et al.. (1997). Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35 142 sperm nuclei from two 47,XYY males. Human Genetics. 99(3). 407–412. 50 indexed citations
16.
Chevret, Edith, Sophie Rousseaux, Michèle Monteil, et al.. (1996). Increased incidence of hyperhaploid 24,XY spermatozoa detected by three-colour FISH in a 46,XY/47,XXY male. Human Genetics. 97(2). 171–175. 68 indexed citations
17.
Rousseaux, Sophie, Edith Chevret, Michèle Monteil, et al.. (1995). Meiotic segregation in males heterozygote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization. Cytogenetic and Genome Research. 71(3). 240–246. 54 indexed citations
18.
Cozzi, J., Edith Chevret, Sophie Rousseaux, R. Pelletier, & B Sèle. (1995). Human sperm chromosome analysis after microinjection into hamster oocytes. Journal of Assisted Reproduction and Genetics. 12(6). 384–388. 3 indexed citations
19.
Chevret, Edith, et al.. (1994). Male meiotic segregation of gonosomes analysed by two colour FISH in human interphase spermatozoa. Human Genetics. 94(6). 701–4. 11 indexed citations
20.
Rousseaux, Sophie, B Sèle, J. Cozzi, & Edith Chevret. (1993). Immediate rearrangements of human sperm chromosomes following in-vivo irradiation. Human Reproduction. 8(6). 903–907. 17 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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