Claude Bendavid

3.4k total citations
81 papers, 1.7k citations indexed

About

Claude Bendavid is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Claude Bendavid has authored 81 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 20 papers in Genetics and 11 papers in Surgery. Recurrent topics in Claude Bendavid's work include Hedgehog Signaling Pathway Studies (15 papers), Genomic variations and chromosomal abnormalities (12 papers) and Breast Cancer Treatment Studies (5 papers). Claude Bendavid is often cited by papers focused on Hedgehog Signaling Pathway Studies (15 papers), Genomic variations and chromosomal abnormalities (12 papers) and Breast Cancer Treatment Studies (5 papers). Claude Bendavid collaborates with scholars based in France, United States and United Kingdom. Claude Bendavid's co-authors include Christèle Dubourg, Laurent Pasquier, Sylvie Odent, Véronique David, Cathérine Henry, Sylvie Odent, Véronique David, Isabelle Gicquel, Philippe Loget and Lucie Rochard and has published in prestigious journals such as Journal of Clinical Oncology, Hepatology and The FASEB Journal.

In The Last Decade

Claude Bendavid

75 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
Claude Bendavid France 23 994 727 384 149 145 81 1.7k
Andrew Dauber United States 31 1.3k 1.3× 1.3k 1.8× 354 0.9× 241 1.6× 117 0.8× 109 2.8k
U. Heinrich Germany 26 1.2k 1.2× 1.2k 1.6× 461 1.2× 231 1.6× 196 1.4× 70 2.8k
Véronique David France 19 523 0.5× 406 0.6× 173 0.5× 127 0.9× 68 0.5× 40 1.6k
Leonard Pinsky Canada 28 1.4k 1.4× 852 1.2× 105 0.3× 169 1.1× 116 0.8× 77 2.4k
Özgür Çoğulu Türkiye 19 515 0.5× 320 0.4× 153 0.4× 129 0.9× 86 0.6× 133 1.2k
Narsingh D. Agnish United States 9 934 0.9× 468 0.6× 283 0.7× 170 1.1× 29 0.2× 13 1.7k
Anthony Lipson Australia 20 422 0.4× 303 0.4× 508 1.3× 427 2.9× 42 0.3× 49 1.4k
Florence Fellmann Switzerland 18 417 0.4× 691 1.0× 188 0.5× 66 0.4× 98 0.7× 54 1.4k
Guiomar Pérez de Nanclares Spain 29 1.2k 1.2× 1.5k 2.0× 316 0.8× 507 3.4× 32 0.2× 115 2.2k
Ping Hu China 22 730 0.7× 501 0.7× 563 1.5× 137 0.9× 97 0.7× 110 1.6k

Countries citing papers authored by Claude Bendavid

Since Specialization
Citations

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

Fields of papers citing papers by Claude Bendavid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claude Bendavid

This figure shows the co-authorship network connecting the top 25 collaborators of Claude Bendavid. A scholar is included among the top collaborators of Claude Bendavid 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 Bendavid. Claude Bendavid 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.
Rauch, Claudine, Tifenn Le Charpentier, Luis Cano, et al.. (2025). PPARγ, a key modulator of metabolic reprogramming, stemness and chemoresistance associated with retrodifferentiation in human hepatocellular carcinomas. Cell Death and Disease. 16(1). 831–831.
2.
Bertrand, Michel, et al.. (2024). Biochemical exploration of cholestasis: interpretation, traps and interferences. Clinical Biochemistry. 135. 110852–110852.
3.
Lefèvre, Claude, B. Vigier, Josselin Garnier, et al.. (2024). A simple algorithm based on complete blood count and haemolysis index to enable potassium determination in haemolysed samples. Clinica Chimica Acta. 558. 119614–119614. 1 indexed citations
4.
Bendavid, Claude, et al.. (2024). Monitoring Variability of Laboratory Results in a Clinical Data Warehouse Using Automatic Dashboard. Studies in health technology and informatics. 316. 1577–1581. 1 indexed citations
5.
Luque-Paz, David, et al.. (2023). Validation of a short turnaround time automated method for the 24/7 determination of plasma d-lactate on Roche Cobas c502. Practical Laboratory Medicine. 36. e00317–e00317.
6.
Labarthe, François, Caroline Moreau, Jean‐Baptiste Arnoux, et al.. (2023). Newborn Screening of Primary Carnitine Deficiency: An Overview of Worldwide Practices and Pitfalls to Define an Algorithm before Expansion of Newborn Screening in France. International Journal of Neonatal Screening. 9(1). 6–6. 9 indexed citations
7.
Luque-Paz, David, Céline René, Nicolas Collet, et al.. (2023). Early detection of plasma d-lactate: Toward a new highly-specific biomarker of bacteraemia?. Heliyon. 9(6). e16466–e16466. 6 indexed citations
8.
Denolle, Thierry, J.F. Heautot, T. Frouget, et al.. (2021). Adrenalectomy for pheochromocytoma: Complications and predictive factors of intraoperative hemodynamic instability. European Urology. 79. S951–S951. 3 indexed citations
9.
10.
Ropert, Martine, et al.. (2019). Metals: common clinical applications in inductively coupled plasma mass spectrometry. Annales de biologie clinique. 77(5). 495–504. 6 indexed citations
11.
Bendavid, Claude, Mathilde Doyard, Patricia Leroyer, et al.. (2018). Iron excess upregulates SPNS2 mRNA levels but reduces sphingosine-1-phosphate export in human osteoblastic MG-63 cells. Osteoporosis International. 29(8). 1905–1915. 8 indexed citations
12.
Findeisen, Peter, Martin Fiedler, Alexander Leichtle, et al.. (2018). Doubling immunochemistry laboratory testing efficiency with the cobas e 801 module while maintaining consistency in analytical performance. Clinical Biochemistry. 58. 86–93. 4 indexed citations
13.
Ropert, Martine, Marie de Tayrac, Edouard Bardou‐Jacquet, et al.. (2015). Mouse genetic background impacts both on iron and non-iron metals parameters and on their relationships. BioMetals. 28(4). 733–743. 16 indexed citations
14.
Poli, Caroline, Delphine Rossille, Pascale Jeannin, et al.. (2015). Comparison of two enzymatic immunoassays, high resolution mass spectrometry method and radioimmunoassay for the quantification of human plasma histamine. Journal of Pharmaceutical and Biomedical Analysis. 118. 307–314. 19 indexed citations
15.
Dubourg, Christèle, Frédérique Bonnet‐Brilhault, Annick Toutain, et al.. (2014). Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions. Molecular Syndromology. 5(2). 57–64. 20 indexed citations
16.
Morcel, Karine, Tanguy Watrin, Laurent Pasquier, et al.. (2011). Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci. Orphanet Journal of Rare Diseases. 6(1). 9–9. 42 indexed citations
17.
Boudreau, Eilis, Kyle Johnson, Angela R. Jackman, et al.. (2009). Review of disrupted sleep patterns in Smith–Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion. American Journal of Medical Genetics Part A. 149A(7). 1382–1391. 36 indexed citations
18.
Bendavid, Claude, Lucie Rochard, Jonathan Séguin, et al.. (2009). Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci. Human Mutation. 30(8). 1175–1182. 35 indexed citations
19.
20.
Bendavid, Claude, Robert Kleta, Robert T. Long, et al.. (2004). FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosis. Human Genetics. 115(6). 510–514. 21 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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