Agnès Chompret

7.3k total citations
49 papers, 1.7k citations indexed

About

Agnès Chompret is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Agnès Chompret has authored 49 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 19 papers in Oncology and 14 papers in Genetics. Recurrent topics in Agnès Chompret's work include BRCA gene mutations in cancer (11 papers), Cutaneous Melanoma Detection and Management (8 papers) and Cancer-related Molecular Pathways (7 papers). Agnès Chompret is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Cutaneous Melanoma Detection and Management (8 papers) and Cancer-related Molecular Pathways (7 papers). Agnès Chompret collaborates with scholars based in France, United Kingdom and United States. Agnès Chompret's co-authors include Brigitte Bressac–de Paillerets, Gilbert Lenoir, Caroline Kannengiesser, Marie‐Françoise Avril, Michel Barrois, Florence Démenais, Laurence Brugières, Thomas Tursz, Philippe Terrier and Catherine Bonaïti‐Pellié and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and JNCI Journal of the National Cancer Institute.

In The Last Decade

Agnès Chompret

47 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Agnès Chompret France 20 550 541 414 322 309 49 1.7k
Eva van den Berg Netherlands 28 711 1.3× 648 1.2× 754 1.8× 178 0.6× 143 0.5× 88 2.6k
Jonathan Keith Killian United States 23 725 1.3× 382 0.7× 478 1.2× 114 0.4× 169 0.5× 62 1.6k
Kerrington D. Smith United States 23 681 1.2× 979 1.8× 619 1.5× 37 0.1× 320 1.0× 50 2.2k
Ronald L. Richardson United States 27 588 1.1× 1.1k 2.0× 949 2.3× 55 0.2× 143 0.5× 79 2.3k
Michael C. Luce United States 18 653 1.2× 949 1.8× 223 0.5× 34 0.1× 230 0.7× 27 2.3k
Arto Leminen Finland 28 415 0.8× 538 1.0× 256 0.6× 27 0.1× 71 0.2× 60 1.9k
Najat Mourra France 23 293 0.5× 609 1.1× 251 0.6× 72 0.2× 43 0.1× 79 1.5k
Tsunehisa Kaku Japan 30 512 0.9× 454 0.8× 311 0.8× 31 0.1× 67 0.2× 107 2.5k
Ian M. Frayling United Kingdom 31 998 1.8× 1.4k 2.7× 414 1.0× 75 0.2× 394 1.3× 72 3.3k
Albiruni Ryan Abdul Razak Canada 18 410 0.7× 661 1.2× 375 0.9× 47 0.1× 44 0.1× 100 1.3k

Countries citing papers authored by Agnès Chompret

Since Specialization
Citations

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

Fields of papers citing papers by Agnès Chompret

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Agnès Chompret

This figure shows the co-authorship network connecting the top 25 collaborators of Agnès Chompret. A scholar is included among the top collaborators of Agnès Chompret 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 Agnès Chompret. Agnès Chompret 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.
Ghiringhelli, François, Lionel Apétoh, Antoine Tesnière, et al.. (2007). The TLR4 polymorphism predicts the response of breast cancer patients to anthracyclins. Journal of Clinical Oncology. 25(18_suppl). 10612–10612. 3 indexed citations
2.
Pontual, Loïc de, Delphine Trochet, Franck Bourdeaut, et al.. (2007). Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma. European Journal of Cancer. 43(16). 2366–2372. 19 indexed citations
3.
Chompret, Agnès, Catherine Noguès, & Dominique Stoppa‐Lyonnet. (2007). Consultation d'oncogénétique pour le cancer du sein. La Presse Médicale. 36(2). 357–363. 1 indexed citations
4.
Pasini, Barbara, Sarah R. McWhinney, Thalia Bei, et al.. (2007). Clinical and molecular genetics of patients with the Carney–Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. European Journal of Human Genetics. 16(1). 79–88. 327 indexed citations
5.
Monnerat, Christian, Agnès Chompret, Caroline Kannengiesser, et al.. (2007). BRCA1, BRCA2, TP53, and CDKN2A germline mutations in patients with breast cancer and cutaneous melanoma. Familial Cancer. 6(4). 453–461. 30 indexed citations
6.
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
7.
Satgé, Daniel, Louis H. Honoré, A J Sasco, et al.. (2006). An ovarian dysgerminoma in Down syndrome. Hypothesis about the association. International Journal of Gynecological Cancer. 16(S1). 375–379. 8 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.
Sasco, A J, et al.. (2006). An ovarian dysgerminoma in Down syndrome. Hypothesis about the association. International Journal of Gynecological Cancer. 16. 375–379. 2 indexed citations
10.
Laud, Karine, Cătălin Marian, Marie‐Françoise Avril, et al.. (2005). Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma. Journal of Medical Genetics. 43(1). 39–47. 41 indexed citations
11.
Satgé, Daniel, Annie J. Sasco, Agnès Chompret, et al.. (2003). A 22-year French Experience with Solid Tumors in Children with Down Syndrome. Pediatric Hematology and Oncology. 20(7). 517–529. 16 indexed citations
12.
Chompret, Agnès. (2003). [Clinical and molecular diagnosis of inherited breast-ovarian cancer].. PubMed. 32(2). 101–19. 4 indexed citations
13.
Deley, Marie‐Cécile Le, Thierry Leblanc, Akthar Shamsaldin, et al.. (2003). Risk of Secondary Leukemia After a Solid Tumor in Childhood According to the Dose of Epipodophyllotoxins and Anthracyclines: A Case-Control Study by the Société Française d’Oncologie Pédiatrique. Journal of Clinical Oncology. 21(6). 1074–1081. 153 indexed citations
14.
Chompret, Agnès, Anne S. Abel, Florent de Vathaire, et al.. (2003). Genetic epidemiology of neuroblastoma: A study of 426 cases at the Institut Gustave‐Roussy in France. Pediatric Blood & Cancer. 42(1). 99–105. 27 indexed citations
15.
Paillerets, Brigitte Bressac–de, Marie‐Françoise Avril, Agnès Chompret, & Florence Démenais. (2002). Genetic and environmental factors in cutaneous malignant melanoma. Biochimie. 84(1). 67–74. 38 indexed citations
16.
Chompret, Agnès. (2002). The Li–Fraumeni syndrome. Biochimie. 84(1). 75–82. 61 indexed citations
17.
Avril, M.-F., Agnès Chompret, Marie‐José Terrier‐Lacombe, et al.. (2001). Association between germ cell tumours, large numbers of naevi, atypical naevi and melanoma. Melanoma Research. 11(2). 117–122. 5 indexed citations
18.
Briollais, Laurent, Agnès Chompret, M Guilloud-Bataille, et al.. (2000). Patterns of familial aggregation of three melanoma risk factors: great number of naevi, light phototype and high degree of sun exposure. International Journal of Epidemiology. 29(3). 408–415. 2 indexed citations
19.
Moutou, Céline, Christine Le Bihan-Benjamin, Agnès Chompret, et al.. (1996). Genetic transmission of susceptibility to cancer in families of children with soft tissue sarcomas. Cancer. 78(7). 1483–1491. 17 indexed citations
20.
Moutou, Céline, Joëlle Hochez, Agnès Chompret, et al.. (1994). The French Wilms' tumour study: no clear evidence for cancer prone families.. Journal of Medical Genetics. 31(6). 429–434. 8 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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