Catherine Caillaud
Impact in
- Physiology top 0.5%
- Lysosomal Storage Disorders Research
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Papers in
- Physiology 83
- Lysosomal Storage Disorders Research 81
- Rheumatology 29
- Glycogen Storage Diseases and Myoclonus 24
- Co-authors
- Livia Poënaru (17 shared papers)Axel Kahn (4 shared papers)Roseline Froissart (12 shared papers)Michel Perricaudet (4 shared papers)Emmanuelle Vigne (4 shared papers)Saïd Akli (4 shared papers)Marc Peschanski (3 shared papers)Leslie D. Stratford-Perricaudet (3 shared papers)
- Journals
- Molecular Genetics and Metabolism (5 papers)Human Molecular Genetics (4 papers)Journal of Inherited Metabolic Disease (3 papers)Human Mutation (3 papers)Neurology (3 papers)
- Partner nations
- FranceUnited StatesTunisia
In The Last Decade
Catherine Caillaud
108 papers receiving 3.6k citations
Catherine Caillaud's Hit Papers
Peers
Comparison fields: 5 of 89
- Physiology 2.1k
- Clinical Biochemistry 320
- Rheumatology 590
- Cell Biology 691
- Physiology 152
Countries citing papers authored by Catherine Caillaud
This map shows the geographic impact of Catherine Caillaud'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 Catherine Caillaud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catherine Caillaud more than expected).
Fields of papers citing papers by Catherine Caillaud
This network shows the impact of papers produced by Catherine Caillaud. 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 Catherine Caillaud. The network helps show where Catherine Caillaud may publish in the future.
Co-authors
The 25 scholars most cited alongside Catherine Caillaud, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 108 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A Review of Gaucher Disease Pathophysiology, Clinical Presentation and Treatments Hit paper breakdown → | 2017 | 524 |
| 2 | 1993 | 432 | |
| 3 | 2000 | 157 | |
| 4 | 2010 | 130 | |
| 5 | 2013 | 91 | |
| 6 | 2005 | 85 | |
| 7 | 1989 | 81 | |
| 8 | 2005 | 80 | |
| 9 | 2004 | 80 | |
| 10 | Gene delivery into the central nervous system by nasal instillation in rats. | 1995 | 72 |
| 11 | 2008 | 70 | |
| 12 | 2010 | 68 | |
| 13 | 2008 | 67 | |
| 14 | Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency. | 1989 | 64 |
| 15 | 1993 | 60 | |
| 16 | 2018 | 60 | |
| 17 | 1999 | 55 | |
| 18 | 2009 | 53 | |
| 19 | 2000 | 53 | |
| 20 | 2017 | 48 |
About Catherine Caillaud
Catherine Caillaud is a scholar working on Physiology, Rheumatology, Epidemiology, Molecular Biology and Organic Chemistry, having authored 108 papers that have together received 3.7k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (81 papers), Glycogen Storage Diseases and Myoclonus (24 papers), Carbohydrate Chemistry and Synthesis (22 papers), Trypanosoma species research and implications (21 papers), Cellular transport and secretion (19 papers), Metabolism and Genetic Disorders (11 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Virus-based gene therapy research (6 papers). The work is most often cited by research in Physiology (2.1k citations), Clinical Biochemistry (320 citations), Rheumatology (590 citations), Cell Biology (691 citations) and Physiology (152 citations). Catherine Caillaud has collaborated with scholars based in France, United States and Tunisia. Frequent co-authors include Livia Poënaru, Axel Kahn, Roseline Froissart, Michel Perricaudet, Emmanuelle Vigne, Saïd Akli, Marc Peschanski, Leslie D. Stratford-Perricaudet, Thierry Levade and Thierry Billette de Villemeur. Their work appears in journals such as Molecular Genetics and Metabolism, Human Molecular Genetics, Journal of Inherited Metabolic Disease, Human Mutation and Neurology.
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.