Régine Perrichot

1.0k total citations
14 papers, 508 citations indexed

About

Régine Perrichot is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Régine Perrichot has authored 14 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Nephrology. Recurrent topics in Régine Perrichot's work include Renal and related cancers (5 papers), Genetic and Kidney Cyst Diseases (5 papers) and Genetic Syndromes and Imprinting (2 papers). Régine Perrichot is often cited by papers focused on Renal and related cancers (5 papers), Genetic and Kidney Cyst Diseases (5 papers) and Genetic Syndromes and Imprinting (2 papers). Régine Perrichot collaborates with scholars based in France, Switzerland and Belgium. Régine Perrichot's co-authors include Claude Férec, B. Whebe, Jian‐Min Chen, Marie-Pascale Morin, Yannick Le Meur, Philippe Saliou, Christophe Charasse, Marie-Paule Guillodo, Maryvonne Hourmant and Anne Grall-Jézéquel and has published in prestigious journals such as Biochemical Journal, Journal of the American Society of Nephrology and Nephrology Dialysis Transplantation.

In The Last Decade

Régine Perrichot

12 papers receiving 501 citations

Peers

Régine Perrichot
Sumaya Alkanderi United Kingdom
Ryan J. Russo United States
Raoul Zeltner United States
Rachel M. Sinders United States
Sarah R. Senum United States
Régine Perrichot
Citations per year, relative to Régine Perrichot Régine Perrichot (= 1×) peers Masatomo Kusaka

Countries citing papers authored by Régine Perrichot

Since Specialization
Citations

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

Fields of papers citing papers by Régine Perrichot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Régine Perrichot

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

All Works

14 of 14 papers shown
1.
Mauhin, Wladimir, Javier I. Ottaviani, Olivier Lidove, et al.. (2024). Lysosphingolipid Quantitation in Plasma and Dried‐Blood Spots Using Targeted High‐Resolution Mass Spectrometry. Journal of Clinical Laboratory Analysis. 39(1). e25131–e25131.
3.
Audrézet, Marie‐Pierre, Jean‐Michel Halimi, Cécile Vigneau, et al.. (2019). SaO006PREVALENCE OF DETECTED INTRACRANIAL ANEURYSMS IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE (ADPKD) IN 2796 PATIENTS FROM THE GENKYST COHORT. Nephrology Dialysis Transplantation. 34(Supplement_1). 1 indexed citations
4.
Gall, Émilie Cornec-Le, Marie‐Pierre Audrézet, Jian‐Min Chen, et al.. (2013). Type of PKD1 Mutation Influences Renal Outcome in ADPKD. Journal of the American Society of Nephrology. 24(6). 1006–1013. 365 indexed citations
5.
Clèdes, J, et al.. (2006). Insuffisance rénale chronique du sujet âgé et traitement par dialyse et transplantation. 1(1). 1–12. 1 indexed citations
6.
Clèdes, J, et al.. (2006). Évolution des reins au cours du vieillissement. 1(1). 1–13. 1 indexed citations
7.
Perrichot, Régine, Bernard Mercier, L de Parscau, et al.. (2001). Inheritance of a Stable Mutation in a Family with Early-Onset Disease. ˜The œNephron journals/Nephron journals. 87(4). 340–345. 7 indexed citations
8.
Perrichot, Régine, Bernard Mercier, Aurore Carré, J Clèdes, & Claude Férec. (2000). Identification of 3 novel mutations (Y4236X, Q3820X, 11745+2 ins3) in autosomal dominant polycystic kidney disease 1 gene (PKD1). Human Mutation. 15(6). 582–582. 9 indexed citations
9.
Perrichot, Régine, Bernard Mercier, I. Quéré, et al.. (2000). Novel mutations in the duplicated region of PKD1 gene. European Journal of Human Genetics. 8(5). 353–359. 21 indexed citations
10.
Clèdes, J, Régine Perrichot, & Catherine Hanrotel‐Saliou. (2000). [Symptomatic treatment of nephrotic syndrome].. PubMed. 29(8). 430–8. 1 indexed citations
11.
Perrichot, Régine, Bernard Mercier, Pierre Simon, et al.. (1999). DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patients. Human Genetics. 105(3). 231–239. 28 indexed citations
12.
Giral, Magali, Régine Perrichot, Dominique Latinne, et al.. (1997). Idiopathic and secondary membranous nephropathy and polymorphism at TAP1 and HLA‐DMA loci. Tissue Antigens. 50(2). 164–169. 9 indexed citations
13.
Dueymes, Maryvonne, Régine Perrichot, Christelle Basset, et al.. (1996). Aberrant glycosylation of IgA from patients with IgA nephropathy. Glycoconjugate Journal. 13(4). 505–511. 29 indexed citations
14.
Perrichot, Régine, Adolfo Garcı́a-Ocaña, Sylviane Couette, et al.. (1995). Locally formed dopamine modulates renal Na-Pi co-transport through DA1 and DA2 receptors. Biochemical Journal. 312(2). 433–437. 35 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026