Lucie Vérot

1.4k total citations
11 papers, 1.0k citations indexed

About

Lucie Vérot is a scholar working on Physiology, Organic Chemistry and Cell Biology. According to data from OpenAlex, Lucie Vérot has authored 11 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Physiology, 4 papers in Organic Chemistry and 4 papers in Cell Biology. Recurrent topics in Lucie Vérot's work include Lysosomal Storage Disorders Research (9 papers), Cellular transport and secretion (4 papers) and Carbohydrate Chemistry and Synthesis (4 papers). Lucie Vérot is often cited by papers focused on Lysosomal Storage Disorders Research (9 papers), Cellular transport and secretion (4 papers) and Carbohydrate Chemistry and Synthesis (4 papers). Lucie Vérot collaborates with scholars based in France, United States and Italy. Lucie Vérot's co-authors include Lisa Griffin, Wenhui Gong, Synthia H. Mellon, Marie T. Vanier, Nathalie Desmaris, Steven U. Walkley, Jennifer A. Wiseman, Sandy M. Price, Michael M. Shen and G S Tint and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Journal of Neuroscience.

In The Last Decade

Lucie Vérot

11 papers receiving 1.0k citations

Peers

Countries citing papers authored by Lucie Vérot

Since Specialization

Citations

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

Fields of papers citing papers by Lucie Vérot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucie Vérot

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Niemann–Pick C disease: functional characterization of three NPC2 mutations and clinical and molecular update on patients with NPC2 2007 ·Clinical Genetics ·Lucie Vérot, Karim Chikh, (unknown), (unknown), (unknown), Gilles Millat	46
2	Bone marrow transplantation for feline mucopolysaccharidosis I 2007 ·Molecular Genetics and Metabolism ·N. Matthew Ellinwood, Marie‐Anne Colle, Margaret A. Weil, Margret L. Casal, Charles H. Vite, (unknown), (unknown), Thomas O’Malley, Xingxuan He, (unknown), Lucie Vérot, John R. Melniczek, (unknown), Geoffrey K. Aguirre, Van W. Knox, Sydney M. Evans, Marie T. Vanier, Edward H. Schuchman, Steven U. Walkley, Mark E. Haskins	21
3	Partial cure of established disease in an animal model of metachromatic leukodystrophy after intracerebral adeno-associated virus-mediated gene transfer 2006 ·Gene Therapy ·Caroline Sevin, Lucie Vérot, Abdellatif Benraiss, Debby Van Dam, (unknown), Guy Nagels, Françoise Fouquet, Volkmar Gieselmann, M. T. Vanier, Peter Paul De Deyn, Patrick Aubourg, Nathalie Cartier	49
4	Gene therapy of the brain in the dog model of Hurler's syndrome 2006 ·Annals of Neurology ·Carine Ciron, Nathalie Desmaris, Marie-Anne Colle, Sylvie Raoul, Béatrice Joussemet, Lucie Vérot, Jérôme Ausseil, Roseline Froissart, Françoise Roux, Yan Chérel, (unknown), Y Lajat, Bertrand Schwartz, Marie‐Thérèse Vanier, Irène Maire, Marc Tardieu, Philippe Moullier, Jean‐Michel Heard	79
5	Forme respiratoire néonatale létale de la maladie de Niemann-Pick C2 et diagnostic anténatal par l'étude des mutations du gène HE1/NPC2 2005 ·Archives de Pédiatrie ·(unknown), Gilles Millat, (unknown), (unknown), (unknown), D. Dobbelaere, Lucie Vérot, (unknown), Claudine Le Vaillant, Frédèric Gottrand, E. Bogaert, (unknown), S Klosowski, (unknown), (unknown), Sylvie Manouvrier, M. T. Vanier	10
6	Intracerebral adeno-associated virus-mediated gene transfer in rapidly progressive forms of metachromatic leukodystrophy 2005 ·Human Molecular Genetics ·Caroline Sevin, Abdellatif Benraiss, Debby Van Dam, (unknown), Guy Nagels, Lucie Vérot, Ingrid Laurendeau, Michel Vidaud, Volkmar Gieselmann, Marie T. Vanier, Peter Paul De Deyn, Patrick Aubourg, Nathalie Cartier	72
7	Improved Behavior and Neuropathology in the Mouse Model of Sanfilippo Type IIIB Disease after Adeno-Associated Virus-Mediated Gene Transfer in the Striatum 2004 ·Journal of Neuroscience ·Arnaud Cressant, Nathalie Desmaris, Lucie Vérot, (unknown), Roseline Froissart, (unknown), Irène Maire, Jean Michel Heard	112
8	Niemann–Pick type C disease involves disrupted neurosteroidogenesis and responds to allopregnanolone 2004 ·Nature Medicine ·Lisa Griffin, Wenhui Gong, Lucie Vérot, Synthia H. Mellon	295
9	Prevention of neuropathology in the mouse model of hurler syndrome 2004 ·Annals of Neurology ·Nathalie Desmaris, Lucie Vérot, (unknown), Catherine Caillaud, Marie T. Vanier, Jean Michel Heard	80
10	Genetic evidence for nonredundant functional cooperativity between NPC1 and NPC2 in lipid transport 2004 ·Proceedings of the National Academy of Sciences ·David E. Sleat, Jennifer A. Wiseman, Mukarram El-Banna, Sandy M. Price, Lucie Vérot, Michael M. Shen, G S Tint, Marie T. Vanier, Steven U. Walkley, Peter Lobel	276
11	Localization of a non‐syndromic X‐linked mental retardation gene (MRX80) to Xq22‐q24 2003 ·American Journal of Medical Genetics Part A ·Lucie Vérot, Nicole Alloisio, Laurette Morlé, Muriel Bozon, Renaud Touraine, Henri Plauchu, Patrick Edery	5

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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