Claude Adenis

562 total citations
12 papers, 244 citations indexed

About

Claude Adenis is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Claude Adenis has authored 12 papers receiving a total of 244 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Claude Adenis's work include BRCA gene mutations in cancer (8 papers), Genetic factors in colorectal cancer (3 papers) and Ovarian cancer diagnosis and treatment (3 papers). Claude Adenis is often cited by papers focused on BRCA gene mutations in cancer (8 papers), Genetic factors in colorectal cancer (3 papers) and Ovarian cancer diagnosis and treatment (3 papers). Claude Adenis collaborates with scholars based in France and Italy. Claude Adenis's co-authors include Philippe Vennin, Fabrice Narducci, Sylvie Galiègue‐Zouitina, Marie‐Paule Hildebrand, Jean‐Pierre Kerckaert, Isabelle Farré, F Bauters, Claude Preudhomme, Agnès Daudignon and Christophe Roumier and has published in prestigious journals such as Oncogene, European Journal of Cancer and Gynecologic Oncology.

In The Last Decade

Claude Adenis

12 papers receiving 240 citations

Peers

Claude Adenis
Samantha Cohen United States
Ryan Noss United States
Diana Johnson United Kingdom
Talia Boshari United Kingdom
Ching Hang Wong United States
Judith Carser United Kingdom
Andrea Jewell United States
Sara Alavi Germany
Samantha Cohen United States
Claude Adenis
Citations per year, relative to Claude Adenis Claude Adenis (= 1×) peers Samantha Cohen

Countries citing papers authored by Claude Adenis

Since Specialization
Citations

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

Fields of papers citing papers by Claude Adenis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claude Adenis

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

All Works

12 of 12 papers shown
1.
Leblanc, Éric, Philippe Vennin, Fabrice Narducci, et al.. (2014). Chirurgie annexielle prophylactique des femmes à risque héréditaire : vers de nouvelles pistes ?. ONCOLOGIE. 16(9-10). 438–444. 1 indexed citations
2.
Christophe, Véronique, et al.. (2013). Comparison of the Screening Practices of Unaffected Noncarriers under 40 and between 40 and 49 in BRCA1/2 Families. Journal of Genetic Counseling. 22(4). 469–481. 3 indexed citations
3.
Taïeb, S., N. Rocourt, Fabrice Narducci, et al.. (2011). Inefficacité du dépistage des cancers tubo-ovariens dans les situations de risque héréditaire de cancer de l’ovaire ; l’expérience du Centre Oscar-Lambret. Bulletin du Cancer. 98(2). 113–119. 3 indexed citations
4.
Leblanc, Éric, Fabrice Narducci, Isabelle Farré, et al.. (2011). Radical fimbriectomy: A reasonable temporary risk-reducing surgery for selected women with a germ line mutation of BRCA 1 or 2 genes? Rationale and preliminary development. Gynecologic Oncology. 121(3). 472–476. 53 indexed citations
5.
Christophe, Véronique, et al.. (2009). Social sharing of genetic information in the family. Journal of Health Psychology. 14(7). 855–860. 6 indexed citations
6.
Fournier, Marion, Claude Adenis, H. Fontaine, Bruno Carnaille, & Jenny Goudemand. (2008). Evaluation and use of the white blood cell differential provided by the Coulter® STKS in a children's hospital. Clinical & Laboratory Haematology. 16(1). 33–42. 1 indexed citations
7.
Christophe, Véronique, Tanguy Leroy, Claude Adenis, M. Reich, & Philippe Vennin. (2008). [Information spreading about hereditary carriage of a BRCA1/2 mutation and ovarian cancer and rate of consultation of the concerned relatives].. PubMed. 95(4). 395–402. 2 indexed citations
8.
Mancini, Julien, Catherine Noguès, Claude Adenis, et al.. (2006). Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing. European Journal of Cancer. 42(7). 871–881. 39 indexed citations
9.
Mancini, Julien, Catherine Noguès, Claude Adenis, et al.. (2006). Patients’ characteristics and rate of Internet use to obtain cancer information. Journal of Public Health. 28(3). 235–237. 32 indexed citations
10.
Nicolas, C., Claude Adenis, Patrick Dhellemmes, et al.. (2003). Large-cell medulloblastoma with arrestin-like protein expression.. PubMed. 22(1). 1–9. 3 indexed citations
11.
Preudhomme, Claude, Christophe Roumier, Marie‐Paule Hildebrand, et al.. (2000). Nonrandom 4p13 rearrangements of the RhoH/TTF gene, encoding a GTP-binding protein, in non-Hodgkin's lymphoma and multiple myeloma. Oncogene. 19(16). 2023–2032. 96 indexed citations
12.
Peyrat, J.P., Philippe Vennin, Louis Hornez, et al.. (1998). Germline BRCA1 mutations in patients from 84 families with breast and/or ovarian cancers in northern France. European Journal of Cancer Prevention. 7. S7–S12. 5 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026