Isabelle Redonnet‐Vernhet

744 total citations
26 papers, 398 citations indexed

About

Isabelle Redonnet‐Vernhet is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Isabelle Redonnet‐Vernhet has authored 26 papers receiving a total of 398 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 10 papers in Rheumatology. Recurrent topics in Isabelle Redonnet‐Vernhet's work include Metabolism and Genetic Disorders (10 papers), Folate and B Vitamins Research (7 papers) and Lysosomal Storage Disorders Research (5 papers). Isabelle Redonnet‐Vernhet is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Folate and B Vitamins Research (7 papers) and Lysosomal Storage Disorders Research (5 papers). Isabelle Redonnet‐Vernhet collaborates with scholars based in France, Canada and Belgium. Isabelle Redonnet‐Vernhet's co-authors include Thierry Levade, Robert Salvayre, Ralf‐Peter Jansen, Ron A. Wevers, Hans Kristian Ploos van Amstel, Pascal Barat, Nicole Barthe, Didier Lacombe, Cécile Ged and Samir Mesli and has published in prestigious journals such as Blood, Neurology and Journal of Investigative Dermatology.

In The Last Decade

Isabelle Redonnet‐Vernhet

23 papers receiving 391 citations

Peers

Countries citing papers authored by Isabelle Redonnet‐Vernhet

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Redonnet‐Vernhet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Isabelle Redonnet‐Vernhet. 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 Isabelle Redonnet‐Vernhet. The network helps show where Isabelle Redonnet‐Vernhet may publish in the future.

Co-authorship network of co-authors of Isabelle Redonnet‐Vernhet

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Redonnet‐Vernhet. A scholar is included among the top collaborators of Isabelle Redonnet‐Vernhet 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 Isabelle Redonnet‐Vernhet. Isabelle Redonnet‐Vernhet is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Preventing hyperhomocysteinemia using vitamin B6 supplementation in Givosiran-treated acute intermittent porphyria: Highlights from a case report and brief literature review 2024 ·Molecular Genetics and Metabolism Reports ·Isabelle Redonnet‐Vernhet, P. Mercié, (unknown), Jean‐Marc Blouin, Didier Brönnimann, Samir Mesli, (unknown), Emmanuel Ribeiro, Noémie Gensous, P. Duffau, Laurent Gouya, Emmanuel Richard	0
2	Biomarkers for the diagnosis and monitoring of nitrous oxide intoxication: objectives and methodology of the SFBC Working Group 2023 ·Annales de biologie clinique ·Damien Denimal, Stéphanie Badiou, (unknown), Mickaël Bonnan, Agnès Boullier, Anthony Chauvin, Annabelle Dupont, (unknown), Thierry Dupré, Nicolas Fabresse, (unknown), Apolline Imbard, (unknown), (unknown), (unknown), François Parant, Isabelle Redonnet‐Vernhet, Nathalie Trillot, Guillaume Grzych	0
3	Amino acids and vitamins status during continuous renal replacement therapy: An ancillary prospective observational study of a randomised control trial 2021 ·Anaesthesia Critical Care & Pain Medicine ·Antoine Schneider, Walter Picard, Patrick M. Honoré, Antoine Dewitte, Samir Mesli, Isabelle Redonnet‐Vernhet, Catherine Fleureau, Alexandre Ouattara, Mette M. Berger, Olivier Joannès-Boyau	5
4	Energy Metabolism Rewiring Precedes UVB-Induced Primary Skin Tumor Formation 2018 ·Cell Reports ·Mohsen Hosseini, L. Dousset, Walid Mahfouf, Martin Serrano-Sanchez, Isabelle Redonnet‐Vernhet, Samir Mesli, (unknown), Émilie Obre, Marc Bonneu, Stéphane Claverol, Marija Vlaski‐Lafarge, Zoran Ivanović, Walid Rachidi, Thierry Douki, Alain Taı̈eb, Anne‐Karine Bouzier‐Sore, Rodrigue Rossignol, Hamid Rezvani	48
5	Hyperhomocysteinemia and High Doses of Nilotinib Favour Cardio-Vascular Events in Chronic Phase Chronic Myelogenous Leukemia (CML) Patients 2014 ·Blood ·Gaëlle Fossard, Emilie Blond, Stéphane Giraudier, Stéphane Morisset, (unknown), Martine Escoffre‐Barbe, Hélène Labussière‐Wallet, Maël Heiblig, (unknown), Jocelyne Drai, Mohamad Sobh, Mauricette Michallet, Isabelle Redonnet‐Vernhet, Jean‐Christophe Lega, Gabriel Étienne, Franck E. Nicolini	1
6	Atteinte hépatique gravidique : mode de révélation d’une anomalie de la bêta-oxydation des acides gras chez l’enfant 2012 ·Archives de Pédiatrie ·Delphine Lamireau, (unknown), Isabelle Redonnet‐Vernhet, (unknown), Dominique Carles, Olivier Brissaud	10
7	Sight-Threatening Phenylketonuric Encephalopathy in a Young Adult, Reversed by Diet 2012 ·JIMD Reports ·Sébastien Rubin, (unknown), Marie‐Bénédicte Rougier, Marie‐Noëlle Delyfer, Jean‐François Korobelnik, Isabelle Redonnet‐Vernhet, Cécile Marchal, Cyril Goizet, Samir Mesli, (unknown), H. Gin, Vincent Rigalleau	12
8	Hypoketotic Hypoglycemia with Myolysis and Hypoparathyroidism: An Unusual Association in Medium Chain Acyl-CoA Desydrogenase Deficiency (MCADD) 2009 ·Journal of Pediatric Endocrinology and Metabolism ·Julien Baruteau, Thierry Levade, Isabelle Redonnet‐Vernhet, Samir Mesli, (unknown), (unknown)	9
9	Coagulopathies frequency in aseptic osteonecrosis patients 2009 ·Joint Bone Spine ·Nadia Mehsen, Thomas Barnetche, Isabelle Redonnet‐Vernhet, V. Guérin, (unknown), (unknown), Thierry Schaeverbeke	16
10	Tumoral calcinosis due to GALNT3 C.516-2A >T mutation in a black African family. 2008 ·PubMed ·(unknown), (unknown), (unknown), (unknown), (unknown), Isabelle Coupry, Isabelle Redonnet‐Vernhet, Sébastien Lepreux, (unknown), (unknown), Didier Lacombe, (unknown)	14
11	Detection of an Intragenic Deletion Expands the Spectrum of CTSC Mutations in Papillon–Lefèvre Syndrome 2007 ·Journal of Investigative Dermatology ·Thomas Jouary, Cyril Goizet, Isabelle Coupry, Isabelle Redonnet‐Vernhet, Thierry Levade, Ingrid Burgelin, Annick Toutain, Éric Delaporte, Claire Douillard, Didier Lacombe, Alain Taı̈eb, Benoı̂t Arveiler	7
12	Maladie de Fabry: propositions d'ungroupe d'experts français concernant le diagnostic, le traitement et le suivi des patients 2007 ·La Presse Médicale ·Olivier Lidove, Soumeya Bekri, Cyril Goizet, (unknown), S. Aractingi, Bertrand Knebelmann, Gabriel Choukroun, Michel Tsimaratos, Isabelle Redonnet‐Vernhet, Didier Lacombe, R. Jaussaud	10
13	Highly Efficient Lentiviral Gene Transfer in CD34 ⁺ and CD34 ⁺ /38 ⁻ /lin ⁻ Cells from Mobilized Peripheral Blood after Cytokine Prestimulation 2003 ·Stem Cells ·(unknown), Emmanuel Richard, Isabelle Redonnet‐Vernhet, Isabelle Lamrissi‐Garcia, Magalie Lalanne, Cécile Ged, François Moreau‐Gaudry, Hubert de Verneuil	20
14	Lentivirus-mediated gene transfer of uroporphyrinogen III synthase fully corrects the porphyric phenotype in human cells 2003 ·Journal of Molecular Medicine ·(unknown), Élodie Richard, Isabelle Lamrissi‐Garcia, Magalie Lalanne, Cécile Ged, Isabelle Redonnet‐Vernhet, François Moreau‐Gaudry, Hubert de Verneuil	15
15	The impact of the control of serum phenylalanine levels on osteopenia in patients with phenylketonuria 2002 ·European Journal of Pediatrics ·Pascal Barat, Nicole Barthe, Isabelle Redonnet‐Vernhet, (unknown)	38
16	Osteoporosis in late‐diagnosed adult homocystinuric patients 2000 ·Journal of Inherited Metabolic Disease ·(unknown), Isabelle Redonnet‐Vernhet, Didier Lacombe, H. Gin	19
17	A novel lysosomal acid lipase gene mutation in a patient with cholesteryl ester storage disease. 1998 ·PubMed ·Isabelle Redonnet‐Vernhet, (unknown), Robert Salvayre, Thierry Levade	11
18	Cholesteryl Ester Storage Disease: Relationship between Molecular Defects andin SituActivity of Lysosomal Acid Lipase 1997 ·Biochemical and Molecular Medicine ·Isabelle Redonnet‐Vernhet, (unknown), (unknown), Robert Salvayre, Thierry Levade	20
19	Significance of two point mutations present in each HEXB allele of patients with adult GM2 gangliosidosis (Sandhoff disease) Homozygosity for the Ile207 → Val substitution is not associated with a clinical or biochemical phenotype 1996 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Isabelle Redonnet‐Vernhet, Don J. Mahuran, Robert Salvayre, Frédéric Dubas, Thierry Levade	20
20	Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene. 1996 ·Journal of Medical Genetics ·Isabelle Redonnet‐Vernhet, Hans Kristian Ploos van Amstel, Ralf‐Peter Jansen, Ron A. Wevers, Robert Salvayre, Thierry Levade	78

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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