Catherine Caillaud

107 papers receiving 3.6k citations

Catherine Caillaud's Hit Papers

A Review of Gaucher Disease Pathophysiology, Clinical Presentation and Treatments 2017 · 510 citations
5100+3+6Years since publication100200300400500

Peers

Catherine Caillaud
Comparison fields: 5 of 93
  • Physiology 2.1k
  • Cell Biology 803
  • Clinical Biochemistry 333
  • Rheumatology 712
  • Physiology 163
Replace Anna‐Elina Lehesjoki with:
Anna‐Elina Lehesjoki Finland
Annick Raas‐Rothschild Israel
Brian Bigger United Kingdom
Jaana Tyynelä Finland
Mary E. LaMarca United States
Roberta Biancheri Italy
Livia Poënaru France
Donna M. Krasnewich United States
David Konecki United States
A. T. Hoogeveen Netherlands
Catherine Caillaud relative to Anna‐Elina Lehesjoki Finland Anna‐Elina Lehesjoki's profile →
Citations per field
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Anna‐Elina Lehesjoki · 1×
Citations per year

Countries citing papers authored by Catherine Caillaud

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Catherine Caillaud Line = papers co-authored together Catherine Caillaud links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 107 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 →
2017510
2 1993431
3 2000157
4 2010128
5 201389
6 200584
7 198981
8 200480
9 200578
10
Gene delivery into the central nervous system by nasal instillation in rats.
199572
11 200870
12 201068
13 200866
14
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.
198964
15 199360
16 201859
17 199955
18 200052
19 200949
20 201748

About Catherine Caillaud

Catherine Caillaud is a scholar working on Physiology, Rheumatology, Epidemiology, Molecular Biology and Cell Biology, having authored 107 papers that have together received 3.6k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (81 papers), Glycogen Storage Diseases and Myoclonus (29 papers), Carbohydrate Chemistry and Synthesis (24 papers), Cellular transport and secretion (24 papers), Trypanosoma species research and implications (23 papers), Metabolism and Genetic Disorders (13 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Virus-based gene therapy research (7 papers). The work is most often cited by research in Physiology (2.1k citations), Cell Biology (803 citations), Clinical Biochemistry (333 citations), Rheumatology (712 citations) and Physiology (163 citations). Catherine Caillaud has collaborated with scholars based in France, United States and Tunisia. Frequent co-authors include Livia Poënaru, Axel Kahn, Emmanuelle Vigne, Roseline Froissart, Michel Perricaudet, 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, Neurology, Journal of Inherited Metabolic Disease and Human Mutation.

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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