Robert Rousson

3.1k citations

61 papers · 2.4k indexed · h-index 30

Impact in

Physiology top 5%
- Lysosomal Storage Disorders Research
Cardiology and Cardiovascular Medicine top 5%
- Cardiomyopathy and Myosin Studies
- Cardiac electrophysiology and arrhythmias

Papers in ⓘ

Cardiology and Cardiovascular Medicine 22
- Cardiomyopathy and Myosin Studies 10
- Cardiac electrophysiology and arrhythmias 9
Physiology 19
- Lysosomal Storage Disorders Research 16
- Erythrocyte Function and Pathophysiology 6

Co-authors: Claire Rodriguez‐Lafrasse (27 shared papers)Pierre Louisot (19 shared papers)Gilles Millat (18 shared papers)Peter G. Pentchev (4 shared papers)Marie T. Vanier (9 shared papers)Valérie Chanavat (9 shared papers)Gersende Alphonse (8 shared papers)Marie‐Thérèse Aloy (6 shared papers)
Journals: Clinica Chimica Acta (5 papers)European Journal of Medical Genetics (4 papers)Biochemical Journal (4 papers)Clinical Genetics (3 papers)Clinical Biochemistry (2 papers)
Partner nations: France United States Canada

In The Last Decade

Robert Rousson

60 papers receiving 2.4k citations

Peers

Countries citing papers authored by Robert Rousson

Since Specialization

Citations

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

Fields of papers citing papers by Robert Rousson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Robert Rousson, 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 Robert Rousson Line = papers co-authored together Robert Rousson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 61 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Type C Niemann-Pick disease: spectrum of phenotypic variation in disruption of intracellular LDL-derived cholesterol processing Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Marie T. Vanier, Claire Rodriguez‐Lafrasse, Robert Rousson, Noureddine Gazzah, Marie‐Christine Juge, Peter G. Pentchev, André Revol, Pierre Louisot	1991	186
2	A Major Determinant for Binding and Aminoacylation of tRNAAla in Cytoplasmic Alanyl-tRNA Synthetase Is Mutated in Dominant Axonal Charcot-Marie-Tooth Disease The American Journal of Human Genetics ·Philippe Latour, Christel Thauvin‐Robinet, Chantal Baudelet-Méry, P Soichot, Véronica Cusin, Laurence Faivre, Marie-Claire Locatelli, Martine Mayençon, Annie Sarcey, Emmanuel Broussolle, William Camu, Albert David, Robert Rousson	2010	171
3	Niemann‐Pick disease group C: clinical variability and diagnosis based on defective cholesterol esterification: A collaborative study on 70 patients Clinical Genetics ·Marie T. Vanier, David A. Wenger, Marcella Comly, Robert Rousson, Roscoe O. Brady, Peter G. Pentchev	1988	146
4	Usefulness of procalcitonin for diagnosis of infection in cardiac surgical patients Critical Care Medicine ·A. Aouifi, Vincent Piriou, Olivier Bastien, Pascale Blanc, H. Bouvier, Rhys Evans, M. Célard, François Vandenesch, Robert Rousson, Jean-Jacques Lehot	2000	121
5	Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy European Journal of Medical Genetics ·Gilles Millat, Patrice Bouvagnet, Philippe Chevalier, Claire Dauphin, Pierre‐Simon Jouk, Antoine Da Costa, Fabienne Prieur, J. Bresson, Laurence Bonhomme‐Faivre, Jean‐Christophe Eicher, Nicolas Chassaing, Hervé Crehalet, Raphaël Porcher, Claire Rodriguez‐Lafrasse, Robert Rousson	2010	115
6	Effect of cardiopulmonary bypass on serum procalcitonin and C-reactive protein concentrations British Journal of Anaesthesia ·A. Aouifi, Vincent Piriou, Pascale Blanc, H. Bouvier, Olivier Bastien, Pascal Chiari, Robert Rousson, Rhys Evans, Jean-Jacques Lehot	1999	89
7	Type C Niemann-Pick Disease: Biochemical Aspects and Phenotypic Heterogeneity Developmental Neuroscience ·Marie T. Vanier, Claire Rodriguez‐Lafrasse, Robert Rousson, Sylvie Duthel, K. Harzer, P. G. Pentchev, André Revol, Pierre Louisot	1991	82
8	Abnormal cholesterol metabolism in imipramine-treated fibroblast cultures. Similarities with Niemann-Pick type C disease Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism ·Claire Rodriguez-Lafrasse, Robert Rousson, Jean Jacques Bonnet, P. G. Pentchev, Pierre Louisot, Marie T. Vanier	1990	79
9	Protective Role of Hsp27 Protein Against Gamma Radiation–Induced Apoptosis and Radiosensitization Effects of Hsp27 Gene Silencing in Different Human Tumor Cells International Journal of Radiation OncologyBiologyPhysics ·Marie‐Thérèse Aloy, Élie Hadchity, Clara Bionda, Chantal Diaz‐Latoud, L. Claude, Robert Rousson, André‐Patrick Arrigo, Claire Rodriguez‐Lafrasse	2008	76
10	Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy European Journal of Medical Genetics ·Gilles Millat, Patrice Bouvagnet, Philippe Chevalier, Laurent Sebbag, Arnaud Dulac, Claire Dauphin, Pierre‐Simon Jouk, Marie‐Ange Delrue, Jean‐Benoît Thambo, Philippe Le Métayer, Marie‐France Seronde, Laurence Bonhomme‐Faivre, Jean‐Christophe Eicher, Robert Rousson	2011	75
11	Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome Clinical Genetics ·Gilles Millat, Philippe Chevalier, Lioara Restier‐Miron, Antoine Da Costa, Patrice Bouvagnet, B. Kugener, Laurence Fayol, Carmen González Armengod, B Oddou, Valérie Chanavat, E Froidefond, R Perraudin, Robert Rousson, Claire Rodriguez‐Lafrasse	2006	73
12	Free sphingoid bases in tissues from patients with type C Niemann-Pick disease and other lysosomal storage disorders Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Claire Rodriguez‐Lafrasse, Robert Rousson, Peter G. Pentchev, Pierre Louisot, Marie T. Vanier	1994	70
13	Contribution of Long-QT Syndrome Genetic Variants in Sudden Infant Death Syndrome Pediatric Cardiology ·Gilles Millat, B. Kugener, Philippe Chevalier, Mohamed Chahine, Hai Huang, Daniel Malicier, Claire Rodriguez‐Lafrasse, Robert Rousson	2009	54
14	Overcoming resistance to γ-rays in squamous carcinoma cells by poly-drug elevation of ceramide levels Oncogene ·Gersende Alphonse, Clara Bionda, Marie‐Thérèse Aloy, Dominique Ardail, Robert Rousson, Claire Rodriguez‐Lafrasse	2004	54
15	Deletion of arginine (608) in acid sphingomyelinase is the prevalent mutation among Niemann-Pick disease type B patients from northern Africa Human Genetics ·Marie T. Vanier, Klaus Ferlinz, Robert Rousson, Sylvie Duthel, Pierre Louisot, Konrad Sandhoff, Kunihiko Suzuki	1993	49
16	Increasing endogenous ceramide using inhibitors of sphingolipid metabolism maximizes ionizing radiation‐induced mitochondrial injury and apoptotic cell killing International Journal of Cancer ·Claire Rodriguez‐Lafrasse, Gersende Alphonse, Marie‐Thérèse Aloy, Dominique Ardail, Jean‐Pierre Gérard, Pierre Louisot, Robert Rousson	2002	49
17	Niemann‐Pick disease type C: An update Journal of Inherited Metabolic Disease ·M. T. Vanier, Peter G. Pentchev, Claire Rodriguez‐Lafrasse, Robert Rousson	1991	48
18	Transient Alteration of Cellular Redox Buffering before Irradiation Triggers Apoptosis in Head and Neck Carcinoma Stem and Non-Stem Cells PLoS ONE ·Anthony Boivin, Maïté Hanot, Céline Malésys, Mira Maalouf, Robert Rousson, Claire Rodriguez‐Lafrasse, Dominique Ardail	2011	46
19	Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at risk. PubMed ·M. T. Vanier, Claire Rodriguez‐Lafrasse, Robert Rousson, G. Mandon, J Boué, Agnès Choiset, M F Peyrat, C Dumontel, Marie‐Christine Juge, P. G. Pentchev	1992	45
20	Biochemical studies in Niemann‐Pick disease. III: In vitro and in vivo assays of sphingomyelin degradation in cultured skin fibroblasts and amniotic fluid cells for the diagnosis of the various forms of the disease Clinical Genetics ·Marie T. Vanier, Robert Rousson, Isabelle Garcia, Geneviève Bailloud, Marie‐Christine Juge, A Revol, Pierre Louisot	1985	45

About Robert Rousson

Robert Rousson is a scholar working on Cardiology and Cardiovascular Medicine, Physiology, Molecular Biology, Developmental Neuroscience and Physiology, having authored 61 papers that have together received 2.4k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (16 papers), Sphingolipid Metabolism and Signaling (11 papers), Cardiomyopathy and Myosin Studies (10 papers), Cardiac electrophysiology and arrhythmias (9 papers), Erythrocyte Function and Pathophysiology (6 papers), Lipid Membrane Structure and Behavior (6 papers), Ion channel regulation and function (6 papers) and Carbohydrate Chemistry and Synthesis (5 papers). The work is most often cited by research in Physiology (754 citations), Physiology (121 citations), Cardiology and Cardiovascular Medicine (584 citations), Molecular Biology (1.2k citations) and Critical Care and Intensive Care Medicine (81 citations). Robert Rousson has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Claire Rodriguez‐Lafrasse, Pierre Louisot, Gilles Millat, Peter G. Pentchev, Marie T. Vanier, Valérie Chanavat, Gersende Alphonse, Marie‐Thérèse Aloy, Marie T. Vanier and Dominique Ardail. Their work appears in journals such as Clinica Chimica Acta, European Journal of Medical Genetics, Biochemical Journal, Clinical Genetics and Clinical Biochemistry.

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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