J. Labat‐Robert
- Immunology and Allergy top 1%
- Cell Adhesion Molecules Research 53
- Aging top 2%
- Genetics, Aging, and Longevity in Model Organisms 8
- Dermatology top 2%
- Cancer Research top 5%
- Protease and Inhibitor Mechanisms 31
- Cell Biology top 5%
- Proteoglycans and glycosaminoglycans research 7
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- Connective tissue disorders research 10
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- Advanced Glycation End Products research 9
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- Glycosylation and Glycoproteins Research 7
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- Peptidase Inhibition and Analysis 7
J. Labat‐Robert
104 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 125
- Immunology and Allergy 475
- Aging 92
- Dermatology 233
- Cancer Research 368
- Cell Biology 342
Countries citing papers authored by J. Labat‐Robert
This map shows the geographic impact of J. Labat‐Robert'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 J. Labat‐Robert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Labat‐Robert more than expected).
Fields of papers citing papers by J. Labat‐Robert
This network shows the impact of papers produced by J. Labat‐Robert. 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 J. Labat‐Robert. The network helps show where J. Labat‐Robert may publish in the future.
Co-authorship network
The 25 scholars most cited alongside J. Labat‐Robert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 15 | |
| 2 | 2014 | 12 | |
| 3 | 2014 | 6 | |
| 4 | 2013 | 18 | |
| 5 | 2012 | 11 | |
| 6 | 2009 | 18 | |
| 7 | 2009 | 6 | |
| 8 | 2005 | 3 | |
| 9 | 2000 | 19 | |
| 10 | 2000 | 77 | |
| 11 | 1998 | 47 | |
| 12 | 1996 | 6 | |
| 13 | 1992 | 32 | |
| 14 | Modifications of the biosynthesis of type-I and type-III collagens and fibronectin during diabetes and atherosclerosis. | 1991 | 8 |
| 15 | 1991 | 56 | |
| 16 | 1990 | 74 | |
| 17 | 1990 | 15 | |
| 18 | 1989 | 16 | |
| 19 | 1983 | 15 | |
| 20 | Glycoprotéines du mucus gastrique: structure, fonctions et pathologie. | 1979 | 1 |
About J. Labat‐Robert
J. Labat‐Robert is a scholar working on Immunology and Allergy, Aging and Cancer Research, having authored 107 papers that have together received 1.8k indexed citations. Recurring topics across this work include Cell Adhesion Molecules Research (53 papers), Protease and Inhibitor Mechanisms (31 papers), Connective tissue disorders research (10 papers), Advanced Glycation End Products research (9 papers), Genetics, Aging, and Longevity in Model Organisms (8 papers), Glycosylation and Glycoproteins Research (7 papers), Peptidase Inhibition and Analysis (7 papers) and Proteoglycans and glycosaminoglycans research (7 papers). The work is most often cited by research in Immunology and Allergy (475 citations), Aging (92 citations) and Dermatology (233 citations). J. Labat‐Robert has collaborated with scholars based in France, Hungary and Canada. Frequent co-authors include L. Robert, Patrick Kern, A.M. Robert, Ladislas Robert, M Bihari-Varga, Gaston Godeau, M Szendröi, Yasmina Benazzoug, Daniel Hantaı̈ and Philippe Birembaut. Their work appears in journals such as Biochemical Pharmacology, Archives of Gerontology and Geriatrics, Annals of the New York Academy of Sciences, Experimental Gerontology and Biogerontology.
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.