Isabelle Creveaux

1.7k total citations
34 papers, 690 citations indexed

About

Isabelle Creveaux is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Surgery. According to data from OpenAlex, Isabelle Creveaux has authored 34 papers receiving a total of 690 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 7 papers in Surgery. Recurrent topics in Isabelle Creveaux's work include Axon Guidance and Neuronal Signaling (6 papers), RNA regulation and disease (5 papers) and Neurogenesis and neuroplasticity mechanisms (5 papers). Isabelle Creveaux is often cited by papers focused on Axon Guidance and Neuronal Signaling (6 papers), RNA regulation and disease (5 papers) and Neurogenesis and neuroplasticity mechanisms (5 papers). Isabelle Creveaux collaborates with scholars based in France, United States and Tunisia. Isabelle Creveaux's co-authors include B. Dastugue, Annie Meiniel, R Meiniel, Stéphane Gobron, Hubert Monnerie, Werner Lehmann, Mahchid Bamdad, A. Herbet, Banumathi Ramakrishna and Vincent Sapin and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Journal of Cell Science.

In The Last Decade

Isabelle Creveaux

34 papers receiving 664 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 Creveaux France 16 307 185 135 114 83 34 690
Yasuo Ouchi Japan 20 677 2.2× 111 0.6× 81 0.6× 176 1.5× 61 0.7× 34 1.0k
John Yeh United States 18 209 0.7× 192 1.0× 102 0.8× 52 0.5× 41 0.5× 37 780
Masato Nagahama Japan 17 258 0.8× 177 1.0× 55 0.4× 42 0.4× 34 0.4× 40 685
Caroline R. Sussman United States 19 514 1.7× 81 0.4× 86 0.6× 257 2.3× 49 0.6× 30 833
Andrew J. Latimer United States 16 464 1.5× 150 0.8× 269 2.0× 74 0.6× 296 3.6× 46 1.0k
Geraldine M. Grant United States 14 299 1.0× 151 0.8× 107 0.8× 38 0.3× 36 0.4× 22 870
Deon Wolpowitz United States 9 250 0.8× 223 1.2× 76 0.6× 48 0.4× 65 0.8× 17 826
Bartolomeo Augello Italy 18 439 1.4× 58 0.3× 101 0.7× 199 1.7× 53 0.6× 33 882
Elisabeth L. Hooghe‐Peters Belgium 20 304 1.0× 109 0.6× 33 0.2× 124 1.1× 29 0.3× 33 981

Countries citing papers authored by Isabelle Creveaux

Since Specialization
Citations

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

Fields of papers citing papers by Isabelle Creveaux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Creveaux

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Creveaux. A scholar is included among the top collaborators of Isabelle Creveaux 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 Creveaux. Isabelle Creveaux 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.
Lasseaux, Eulalie, et al.. (2023). A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a Moroccan family. Clinical and Experimental Dermatology. 48(12). 1414–1417. 1 indexed citations
2.
Ginzac, Angeline, Émilie Thivat, Caroline Pétorin, et al.. (2023). A phase-II study based on dose adjustment according to UGT1A1 polymorphism: is irinotecan underdosed in first-line FOLFIRI regimen for mCRC?. Cancer Chemotherapy and Pharmacology. 93(3). 225–236. 3 indexed citations
3.
Jabaudon, Matthieu, Isabelle Creveaux, Corinne Belville, et al.. (2019). Pathological Implications of Receptor for Advanced Glycation End-Product (AGER) Gene Polymorphism. Disease Markers. 2019. 1–17. 64 indexed citations
4.
Woillard, Jean‐Baptiste, et al.. (2017). Genetic Analysis of Mu and Kappa Opioid Receptor and COMT Enzyme in Cancer Pain Tunisian Patients Under Opioid Treatment. SHILAP Revista de lepidopterología. 7 indexed citations
5.
Pugazhendhi, Srinivasan, Srikanth Santhanam, Jayanthi Venkataraman, Isabelle Creveaux, & Banumathi Ramakrishna. (2012). NOD2 gene mutations associate weakly with ulcerative colitis but not with Crohn's disease in Indian patients with inflammatory bowel disease. Gene. 512(2). 309–313. 26 indexed citations
6.
Harbuz, Radu, James Lespinasse, Christine Francannet, et al.. (2010). Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome. Prenatal Diagnosis. 30(11). 1072–1078. 34 indexed citations
7.
André, Marc, O. Aumaître, Gilles Grateau, et al.. (2009). Longest Form of CCTG Microsatellite Repeat in the Promoter of the CD2BP1/PSTPIP1 Gene Is Associated with Aseptic Abscesses and with Crohn Disease in French Patients. Digestive Diseases and Sciences. 55(6). 1681–1688. 27 indexed citations
8.
9.
Chiambaretta, F., et al.. (2004). Récidive d’une dystrophie de Groenouw de type I après photokératectomie thérapeutique. Journal Français d Ophtalmologie. 27(5). 449–456. 7 indexed citations
10.
Chiambaretta, F., et al.. (2004). La photokératectomie thérapeutique dans le traitement de la dystrophie grillagée de type I. Journal Français d Ophtalmologie. 27(7). 747–753. 5 indexed citations
11.
Tachdjian, Gérard, Moncef Benkhalifa, Isabelle Creveaux, et al.. (2004). De novo interstitial direct duplication of Xq21.1q25 associated with skewed X‐inactivation pattern. American Journal of Medical Genetics Part A. 131A(3). 273–280. 20 indexed citations
12.
Vaurs‐Barrière, Catherine, Kondi Wong, Mones Abu‐Asab, et al.. (2003). Insertion of mutant proteolipid protein results in missorting of myelin proteins. Annals of Neurology. 54(6). 769–780. 19 indexed citations
13.
Solassol, Jérôme, Vincent Sapin, Didier Lémery, et al.. (2003). Detection of trisomy 21 by quantitative fluorescent–polymerase chain reaction in uncultured amniocytes. Prenatal Diagnosis. 23(4). 287–291. 6 indexed citations
14.
Gonçalves-Mendes, Nicolas, Dominique Simon‐Chazottes, Isabelle Creveaux, et al.. (2003). Mouse SCO-spondin, a gene of the thrombospondin type 1 repeat (TSR) superfamily expressed in the brain. Gene. 312. 263–270. 13 indexed citations
15.
Meiniel, Annie, et al.. (2003). The Thrombospondin Type 1 Repeat (TSR) and Neuronal Differentiation: Roles of SCO-Spondin Oligopeptides on Neuronal Cell Types and Cell Lines∗. International review of cytology. 1–39. 23 indexed citations
16.
Bouchard, Philippe, Viviane Ravet, R Meiniel, et al.. (1999). Use of a heterologous monoclonal antibody for cloning and detection of glial fibrillary acidic protein in the bovine ventricular ependyma. Cell and Tissue Research. 298(2). 207–216. 4 indexed citations
17.
Creveaux, Isabelle, Stéphane Gobron, R Meiniel, B. Dastugue, & Annie Meiniel. (1998). Complex expression pattern of the SCO-spondin gene in the bovine subcommissural organ: toward an explanation for Reissner's fiber complexity?. Molecular Brain Research. 55(1). 45–53. 23 indexed citations
18.
Popescu, C.P., H. Hayes, R Meiniel, Isabelle Creveaux, & Annie Meiniel. (1997). Short Communications: Localization of the SCO-spondin gene to cattle chromosome 4. Chromosome Research. 5(4). 276–277. 4 indexed citations
19.
Meiniel, Annie, R Meiniel, Isabelle Creveaux, et al.. (1996). The Subcommissural Organ and Reissner's Fiber Complex. Progress in Histochemistry and Cytochemistry. 30(2). III–66. 36 indexed citations
20.
Gobron, Stéphane, Hubert Monnerie, R Meiniel, et al.. (1996). SCO-spondin: a new member of the thrombospondin family secreted by the subcommissural organ is a candidate in the modulation of neuronal aggregation. Journal of Cell Science. 109(5). 1053–1061. 115 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

Breakdown of academic impact, for papers by Yasuo Ouchi Breakdown of academic impact, for papers by John Yeh Breakdown of academic impact, for papers by Masato Nagahama Breakdown of academic impact, for papers by Caroline R. Sussman Breakdown of academic impact, for papers by Andrew J. Latimer Breakdown of academic impact, for papers by Geraldine M. Grant Breakdown of academic impact, for papers by Deon Wolpowitz Breakdown of academic impact, for papers by Bartolomeo Augello Breakdown of academic impact, for papers by Elisabeth L. Hooghe‐Peters
Rankless by CCL
2026