Stéphanie Cherqui

3.7k total citations
56 papers, 2.3k citations indexed

About

Stéphanie Cherqui is a scholar working on Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Biochemistry. According to data from OpenAlex, Stéphanie Cherqui has authored 56 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Pathology and Forensic Medicine, 35 papers in Pediatrics, Perinatology and Child Health and 25 papers in Biochemistry. Recurrent topics in Stéphanie Cherqui's work include Biomedical Research and Pathophysiology (41 papers), Neonatal Health and Biochemistry (35 papers) and Amino Acid Enzymes and Metabolism (25 papers). Stéphanie Cherqui is often cited by papers focused on Biomedical Research and Pathophysiology (41 papers), Neonatal Health and Biochemistry (35 papers) and Amino Acid Enzymes and Metabolism (25 papers). Stéphanie Cherqui collaborates with scholars based in United States, France and Belgium. Stéphanie Cherqui's co-authors include Corinne Antignac, Céline J. Rocca, Pierre J. Courtoy, M. Broyer, G Jean, Marlene Attard, William van’t Hoff, Lionel Forestier, Daniel R. Salomon and Vasiliki Kalatzis and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Stéphanie Cherqui

52 papers receiving 2.3k citations

Peers

Stéphanie Cherqui
Terttu Suormala Switzerland
Thierry Vilboux United States
Diana Escalante‐Alcalde Mexico
Kanya Suphapeetiporn Thailand
Jacinthe Sirois Canada
Guanqing Wu United States
Murat Bastepe United States
Eleonora Lamantea Italy
Gayle B. Collin United States
Meral Özgüç Türkiye
Terttu Suormala Switzerland
Stéphanie Cherqui
Citations per year, relative to Stéphanie Cherqui Stéphanie Cherqui (= 1×) peers Terttu Suormala

Countries citing papers authored by Stéphanie Cherqui

Since Specialization
Citations

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

Fields of papers citing papers by Stéphanie Cherqui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphanie Cherqui

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

All Works

20 of 20 papers shown
1.
2.
Johnson, Jennifer L., Aparna Shukla, Danni Chen, et al.. (2024). Reconstitution of Rab11-FIP4 Expression Rescues Cellular Homeostasis in Cystinosis. Molecular and Cellular Biology. 44(12). 577–589. 1 indexed citations
3.
Cherqui, Stéphanie, et al.. (2024). Targeted gene therapy for rare genetic kidney diseases. Kidney International. 106(6). 1051–1061. 1 indexed citations
4.
Mishra, Priyanka, Jay Sharma, Jacqueline Nguyen, et al.. (2023). Rescue of Alzheimer’s disease phenotype in a mouse model by transplantation of wild-type hematopoietic stem and progenitor cells. Cell Reports. 42(8). 112956–112956. 32 indexed citations
5.
Rocca, Céline J., et al.. (2020). CRISPR-Cas9 Gene Editing of Hematopoietic Stem Cells from Patients with Friedreich’s Ataxia. Molecular Therapy — Methods & Clinical Development. 17. 1026–1036. 23 indexed citations
6.
Névo, Nathalie, Céline J. Rocca, Marie-Claire Gübler, et al.. (2018). New interaction between galectin-3 and cystinosin reveals a role of inflammation in kidney pathogenesis in cystinosis. Molecular Genetics and Metabolism. 123(2). S88–S88. 1 indexed citations
7.
Rocca, Céline J., Spencer Goodman, Jennifer N. Dulin, et al.. (2017). Transplantation of wild-type mouse hematopoietic stem and progenitor cells ameliorates deficits in a mouse model of Friedreich’s ataxia. Science Translational Medicine. 9(413). 50 indexed citations
8.
Cherqui, Stéphanie & Pierre J. Courtoy. (2016). The renal Fanconi syndrome in cystinosis: pathogenic insights and therapeutic perspectives. Nature Reviews Nephrology. 13(2). 115–131. 112 indexed citations
9.
Rocca, Céline J., Sarah N. Ur, F. Harrison, & Stéphanie Cherqui. (2014). rAAV9 combined with renal vein injection is optimal for kidney-targeted gene delivery: conclusion of a comparative study. Gene Therapy. 21(6). 618–628. 64 indexed citations
10.
Chevronnay, Héloïse P. Gaide, Patrick Van Deŕ Smissen, Francisca N’Kuli, et al.. (2014). Time Course of Pathogenic and Adaptation Mechanisms in Cystinotic Mouse Kidneys. Journal of the American Society of Nephrology. 25(6). 1256–1269. 62 indexed citations
11.
Johnson, Jennifer L., Gennaro Napolitano, Jlenia Monfregola, et al.. (2013). Upregulation of the Rab27a-Dependent Trafficking and Secretory Mechanisms Improves Lysosomal Transport, Alleviates Endoplasmic Reticulum Stress, and Reduces Lysosome Overload in Cystinosis. Molecular and Cellular Biology. 33(15). 2950–2962. 43 indexed citations
12.
Cherqui, Stéphanie, et al.. (2011). Kidney repair and stem cells: a complex and controversial process. Pediatric Nephrology. 26(9). 1427–1434. 31 indexed citations
13.
Cherqui, Stéphanie, et al.. (2007). Lentiviral Gene Delivery of vMIP-II to Transplanted Endothelial Cells and Endothelial Progenitors Is Proangiogenic In Vivo. Molecular Therapy. 15(7). 1264–1272. 23 indexed citations
14.
Kurian, Sunil M., et al.. (2005). Pseudotyping of Porcine Endogenous Retrovirus by Xenotropic Murine Leukemia Virus in a Pig Islet Xenotransplantation Model. American Journal of Transplantation. 5(8). 1837–1847. 28 indexed citations
15.
Chol, Marie, Nathalie Névo, Stéphanie Cherqui, Corinne Antignac, & Pierre Rustin. (2004). Glutathione precursors replenish decreased glutathione pool in cystinotic cell lines. Biochemical and Biophysical Research Communications. 324(1). 231–235. 39 indexed citations
16.
Kalatzis, Vasiliki, Stéphanie Cherqui, G Jean, et al.. (2001). Characterization of a Putative Founder Mutation that Accounts for the High Incidence of Cystinosis in Brittany. Journal of the American Society of Nephrology. 12(10). 2170–2174. 23 indexed citations
17.
Cherqui, Stéphanie, Vasiliki Kalatzis, Germain Trugnan, & Corinne Antignac. (2001). The Targeting of Cystinosin to the Lysosomal Membrane Requires a Tyrosine-based Signal and a Novel Sorting Motif. Journal of Biological Chemistry. 276(16). 13314–13321. 109 indexed citations
18.
Cherqui, Stéphanie, Vasiliki Kalatzis, Lionel Forestier, Isabelle Poras, & Corinne Antignac. (2000). Identification and Characterisation of the Murine Homologue of the Gene Responsible for Cystinosis, Ctns. BMC Genomics. 1(1). 2–2. 12 indexed citations
19.
Jean, G, Marlene Attard, Stéphanie Cherqui, et al.. (1999). Molecular Characterization of CTNS Deletions in Nephropathic Cystinosis: Development of a PCR-Based Detection Assay. The American Journal of Human Genetics. 65(2). 353–359. 73 indexed citations
20.
Town, Margaret, G Jean, Stéphanie Cherqui, et al.. (1998). A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. Nature Genetics. 18(4). 319–324. 447 indexed citations

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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