Régis Roche

2.1k total citations · 1 hit paper
33 papers, 1.8k citations indexed

About

Régis Roche is a scholar working on Surgery, Epidemiology and Genetics. According to data from OpenAlex, Régis Roche has authored 33 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Surgery, 10 papers in Epidemiology and 8 papers in Genetics. Recurrent topics in Régis Roche's work include Adipokines, Inflammation, and Metabolic Diseases (9 papers), Mesenchymal stem cell research (8 papers) and Pancreatic function and diabetes (7 papers). Régis Roche is often cited by papers focused on Adipokines, Inflammation, and Metabolic Diseases (9 papers), Mesenchymal stem cell research (8 papers) and Pancreatic function and diabetes (7 papers). Régis Roche collaborates with scholars based in France, Réunion and Italy. Régis Roche's co-authors include Franck Festy, Laurence Hoareau, Marie‐Paule Gonthier, Maya Césari, Vincenzo Di Marzo, Isabel Matias, Stefania Petrosino, Palmiero Monteleone, Luciano De Petrocellis and Uberto Pagotto and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Biochemical Journal and Annals of Oncology.

In The Last Decade

Régis Roche

32 papers receiving 1.7k citations

Hit Papers

Regulation, Function, and Dysregulation of Endocannabinoi... 2006 2026 2012 2019 2006 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Régis Roche France 20 805 521 495 448 278 33 1.8k
Laurence Hoareau France 17 805 1.0× 507 1.0× 436 0.9× 470 1.0× 265 1.0× 26 1.6k
Franck Festy France 15 708 0.9× 455 0.9× 448 0.9× 381 0.9× 243 0.9× 25 1.5k
Malcolm Begg United Kingdom 20 451 0.6× 215 0.4× 325 0.7× 102 0.2× 132 0.5× 43 1.6k
Maya Césari France 15 269 0.3× 278 0.5× 143 0.3× 154 0.3× 238 0.9× 25 924
Katriina Vuolteenaho Finland 32 445 0.6× 711 1.4× 259 0.5× 81 0.2× 680 2.4× 73 2.8k
Fraser D. Russell Australia 25 361 0.4× 470 0.9× 463 0.9× 200 0.4× 61 0.2× 73 1.8k
David A. Essig United States 21 222 0.3× 595 1.1× 288 0.6× 109 0.2× 208 0.7× 79 1.9k
Sylvie Manin France 14 468 0.6× 138 0.3× 165 0.3× 187 0.4× 224 0.8× 16 1.1k
Romana Tomaszewska Poland 26 252 0.3× 332 0.6× 958 1.9× 281 0.6× 379 1.4× 112 2.1k
Kenji Uno Japan 24 131 0.2× 673 1.3× 738 1.5× 457 1.0× 646 2.3× 72 2.4k

Countries citing papers authored by Régis Roche

Since Specialization
Citations

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

Fields of papers citing papers by Régis Roche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Régis Roche

This figure shows the co-authorship network connecting the top 25 collaborators of Régis Roche. A scholar is included among the top collaborators of Régis Roche 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 Régis Roche. Régis Roche 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.
Grimaud, Fanny, Jérôme Guicheux, Sophie Portron, et al.. (2019). Comparing “intra operative” tissue engineering strategies for the repair of craniofacial bone defects. Journal of Stomatology Oral and Maxillofacial Surgery. 120(5). 432–442. 5 indexed citations
2.
Gunasekaran, Manoj Kumar, Cynthia Planesse, Alexis Guérin-Dubourg, et al.. (2016). TLR4-dependant pro-inflammatory effects of HMGB1 on human adipocyte. Adipocyte. 5(4). 384–388. 21 indexed citations
3.
Guicheux, Jérôme, et al.. (2015). Autologous Fat Grafting in the Breast: Critical Points and Technique Improvements. Aesthetic Plastic Surgery. 39(4). 547–561. 40 indexed citations
4.
Festy, Franck, et al.. (2015). Effect of Washes and Centrifugation on the Efficacy of Lipofilling With or Without Local Anesthetic. Plastic & Reconstructive Surgery Global Open. 3(8). e496–e496. 20 indexed citations
5.
Atlan, Michaël, et al.. (2013). De la biología al injerto de tejido adiposo: cómo mejorar el lipoinjerto. Cirugía Plástica Ibero-Latinoamericana. 39. 33–38.
6.
Hoareau, Laurence, et al.. (2013). Effect of centrifugation and washing on adipose graft viability: A new method to improve graft efficiency. Journal of Plastic Reconstructive & Aesthetic Surgery. 66(5). 712–719. 59 indexed citations
7.
Gunasekaran, Manoj Kumar, Wildriss Viranaïcken, Franck Festy, et al.. (2013). Inflammation triggers high mobility group box 1 (HMGB1) secretion in adipose tissue, a potential link to obesity. Cytokine. 64(1). 103–111. 55 indexed citations
8.
Atlan, Michaël, Karima Bencharif, Manoj Kumar Gunasekaran, et al.. (2012). New Insights into Lidocaine and Adrenaline Effects on Human Adipose Stem Cells. Aesthetic Plastic Surgery. 37(1). 144–152. 51 indexed citations
9.
Gunasekaran, Manoj Kumar, Karima Bencharif, Franck Festy, et al.. (2012). Fatty acids do not pay the toll: effect of SFA and PUFA on human adipose tissue and mature adipocytes inflammation. Lipids in Health and Disease. 11(1). 175–175. 68 indexed citations
10.
Bencharif, Karima, Amritendu Bhattacharya, Frank Tallet, et al.. (2011). Effect of the Cannabinoid Receptor-1 antagonist SR141716A on human adipocyte inflammatory profile and differentiation. Journal of Inflammation. 8(1). 33–33. 25 indexed citations
11.
Bencharif, Karima, Laurence Hoareau, Evelyne Tarnus, et al.. (2010). Effect of apoA-I on cholesterol release and apoE secretion in human mature adipocytes. Lipids in Health and Disease. 9(1). 75–75. 14 indexed citations
12.
Roche, Régis, Franck Festy, & Xavier Fritel. (2009). Stem cells for stress urinary incontinence: the adipose promise. Journal of Cellular and Molecular Medicine. 14(1-2). 135–142. 28 indexed citations
13.
Gonthier, Marie‐Paule, Laurence Hoareau, Franck Festy, et al.. (2007). Identification of Endocannabinoids and Related Compounds in Human Fat Cells. Obesity. 15(4). 837–845. 74 indexed citations
14.
Matias, Isabel, Stefania Petrosino, Ludovico Docimo, et al.. (2007). Role and regulation of acylethanolamides in energy balance: focus on adipocytes and β‐cells. British Journal of Pharmacology. 152(5). 676–690. 92 indexed citations
15.
Roche, Régis, et al.. (2007). Adult stem cells for cardiovascular diseases: the adipose tissue potential. Expert Opinion on Biological Therapy. 7(6). 791–798. 6 indexed citations
16.
Roche, Régis, Laurence Hoareau, Marie‐Paule Gonthier, et al.. (2006). Presence of functional TLR2 and TLR4 on human adipocytes. Histochemistry and Cell Biology. 127(2). 131–137. 88 indexed citations
17.
Roche, Régis, Laurence Hoareau, Marie‐Paule Gonthier, et al.. (2006). Presence of the cannabinoid receptors, CB1 and CB2, in human omental and subcutaneous adipocytes. Histochemistry and Cell Biology. 126(2). 177–187. 144 indexed citations
18.
Roche, Régis, Isabelle Poizot‐Martin, Emmanuel Compe, et al.. (2002). Effects of antiretroviral drug combinations on the differentiation of adipocytes. AIDS. 16(1). 13–20. 60 indexed citations
20.
Bossavy, Jean-Pierre, et al.. (1990). Nosocomial Infection Surveillance in a Vascular Surgery Unit. Annals of Vascular Surgery. 4(6). 553–557. 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.

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