Isabelle Coupier

4.9k total citations
35 papers, 834 citations indexed

About

Isabelle Coupier is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Isabelle Coupier has authored 35 papers receiving a total of 834 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 13 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Isabelle Coupier's work include BRCA gene mutations in cancer (17 papers), Prenatal Screening and Diagnostics (6 papers) and Hedgehog Signaling Pathway Studies (5 papers). Isabelle Coupier is often cited by papers focused on BRCA gene mutations in cancer (17 papers), Prenatal Screening and Diagnostics (6 papers) and Hedgehog Signaling Pathway Studies (5 papers). Isabelle Coupier collaborates with scholars based in France, Burkina Faso and United Kingdom. Isabelle Coupier's co-authors include Dominique Stoppa‐Lyonnet, Pascal Pujol, Laurence Amar, Nelly Burnichon, Anne‐Paule Gimenez‐Roqueplo, Jérôme Bertherat, Philippe Herman, Jean‐Pierre Fricker, Frédéric Chabolle and Pierre‐François Plouin and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Isabelle Coupier

33 papers receiving 819 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabelle Coupier France 14 275 275 274 255 231 35 834
Fabiano Sandrini United States 17 508 1.8× 356 1.3× 125 0.5× 344 1.3× 262 1.1× 25 1.2k
Anita K. Ying United States 19 438 1.6× 160 0.6× 180 0.7× 206 0.8× 810 3.5× 35 1.2k
Jessica N. Everett United States 16 253 0.9× 397 1.4× 316 1.2× 149 0.6× 86 0.4× 30 985
A. Eisenhardt Germany 16 163 0.6× 103 0.4× 67 0.2× 257 1.0× 141 0.6× 48 729
Matthias W. Beckmann Germany 17 56 0.2× 224 0.8× 539 2.0× 415 1.6× 170 0.7× 51 1.2k
Valentina Elisabetta Bounous Italy 18 123 0.4× 176 0.6× 176 0.6× 55 0.2× 199 0.9× 43 858
Shanna Gustafson United States 12 122 0.4× 173 0.6× 290 1.1× 95 0.4× 46 0.2× 16 636
K.-D. Schulz Germany 15 75 0.3× 111 0.4× 170 0.6× 140 0.5× 137 0.6× 31 634
Alison H. Trainer Australia 22 157 0.6× 363 1.3× 791 2.9× 455 1.8× 116 0.5× 78 1.5k
Marit Holmqvist Sweden 15 74 0.3× 293 1.1× 277 1.0× 91 0.4× 133 0.6× 19 766

Countries citing papers authored by Isabelle Coupier

Since Specialization
Citations

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

Fields of papers citing papers by Isabelle Coupier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Coupier

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Coupier. A scholar is included among the top collaborators of Isabelle Coupier 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 Isabelle Coupier. Isabelle Coupier 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.
Montgolfier, Sandrine de, Anne‐Paule Gimenez‐Roqueplo, Cécile Flahault, et al.. (2024). Psychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients. European Journal of Human Genetics. 32(11). 1446–1455. 3 indexed citations
2.
Benusiglio, Patrick R., Chrystelle Colas, Erell Guillerm, et al.. (2018). Clinical implications of CTNNA1 germline mutations in asymptomatic carriers. Gastric Cancer. 22(4). 899–903. 26 indexed citations
3.
Girardet, Anne, Stéphanie Plaza, S. Hamamah, et al.. (2017). Thirteen years' experience of 893 PGD cycles for monogenic disorders in a publicly funded, nationally regulated regional hospital service. Reproductive BioMedicine Online. 36(2). 154–163. 9 indexed citations
4.
Pellegrini, Isabelle, et al.. (2014). Avoir un enfant et accéder au DPN/DPI pour des femmes porteuses d’une mutation BRCA ? Malades et indemnes appréhendent la question différemment. Bulletin du Cancer. 101(11). 1001–1008. 5 indexed citations
5.
Abadie, Caroline, Marion Gauthier‐Villars, Nicolas Sirvent, & Isabelle Coupier. (2012). Mise au pointOncogénétique en oncopédiatrieGenetic predisposition to childhood cancer. Archives de Pédiatrie. 19(8). 1 indexed citations
6.
Julian‐Reynier, Claire, Roxane Fabre, Isabelle Coupier, et al.. (2012). BRCA1/2 carriers: their childbearing plans and theoretical intentions about having preimplantation genetic diagnosis and prenatal diagnosis. Genetics in Medicine. 14(5). 527–534. 33 indexed citations
7.
Abadie, Caroline, Marion Gauthier‐Villars, Nicolas Sirvent, & Isabelle Coupier. (2012). Oncogénétique en oncopédiatrie. Archives de Pédiatrie. 19(8). 863–875. 2 indexed citations
8.
Lecarpentier, Julie, Catherine Noguès, Emmanuelle Mouret‐Fourme, et al.. (2011). Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO). Breast Cancer Research and Treatment. 130(3). 927–938. 30 indexed citations
9.
Raingeard, I., et al.. (2010). Le syndrome de Cowden ou syndrome des hamartomes multiples en endocrinologie clinique. Annales d Endocrinologie. 71(4). 264–273. 2 indexed citations
10.
Abadie, Caroline, et al.. (2010). Acute lymphocytic leukaemia in a child with Beckwith–Wiedemann syndrome harbouring a CDKN1C mutation. European Journal of Medical Genetics. 53(6). 400–403. 3 indexed citations
11.
Kluger, Nicolas, Sophie Giraud, Isabelle Coupier, et al.. (2009). Birt-Hogg-Dubé syndrome: clinical and genetic studies of 10 French families. British Journal of Dermatology. 162(3). 527–537. 78 indexed citations
12.
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
13.
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
14.
Noruzinia, Mehrdad, Isabelle Coupier, & Pascal Pujol. (2005). Is BRCA1/BRCA2‐related breast carcinogenesis estrogen dependent?. Cancer. 104(8). 1567–1574. 24 indexed citations
15.
Coupier, Isabelle & Pascal Pujol. (2005). Prédispositions héréditaires aux cancers gynécologiques. Gynécologie Obstétrique & Fertilité. 33(11). 851–856. 1 indexed citations
16.
Hughes, David J., Isabelle Coupier, Laure Barjhoux, et al.. (2004). Analysis of breast cancer risk modifying candidate genes in BRCA1 and BRCA2 mutation carriers. Cancer Research. 64. 301–301. 2 indexed citations
17.
Gauthier‐Villars, Marion, Gudrun Schleiermacher, Isabelle Coupier, & Dominique Stoppa‐Lyonnet. (2003). Prédispositions génétiques aux cancers de l‘enfant. Le point en 2003. MTP. Médecine thérapeutique pédiatrie. 6(3). 153–161. 1 indexed citations
18.
Coupier, Isabelle, Céline Baldeyron, Alexandra Rousseau, et al.. (2003). Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations. Oncogene. 23(4). 914–919. 27 indexed citations
19.
Gad, Sophie, Virginie Caux‐Moncoutier, Sabine Pagès-Berhouet, et al.. (2002). Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families. Oncogene. 21(44). 6841–6847. 115 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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