Isabelle Pellerin

1.8k total citations
38 papers, 1.4k citations indexed

About

Isabelle Pellerin is a scholar working on Molecular Biology, Genetics and Obstetrics and Gynecology. According to data from OpenAlex, Isabelle Pellerin has authored 38 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Obstetrics and Gynecology. Recurrent topics in Isabelle Pellerin's work include Ion Transport and Channel Regulation (10 papers), Ion channel regulation and function (6 papers) and Developmental Biology and Gene Regulation (6 papers). Isabelle Pellerin is often cited by papers focused on Ion Transport and Channel Regulation (10 papers), Ion channel regulation and function (6 papers) and Developmental Biology and Gene Regulation (6 papers). Isabelle Pellerin collaborates with scholars based in France, Canada and United States. Isabelle Pellerin's co-authors include Daniel Guerrier, Stéphane Deschamps, Valérie Dupé, Audrey Laurent, Jean‐François Hubert, Daniel Thomas, Laurent Pasquier, Tanguy Watrin, Christian Delamarche and Christian Demers and has published in prestigious journals such as Journal of Biological Chemistry, Molecular and Cellular Biology and Endocrinology.

In The Last Decade

Isabelle Pellerin

38 papers receiving 1.4k citations

Peers

Isabelle Pellerin

GENET

PHEOH

PPCH

Yuko Matsubara Japan

Tatsuo Yamamoto Japan

Shintaro Yagi Japan

R. S. Gilmour United Kingdom

Shoshana Savion Israel

Monia Cecati Italy

Mariusz Zimmer Poland

S W Tsao Hong Kong

Thomas Vrekoussis Greece

Guillaume Pidoux France

Yuko Matsubara Japan

Isabelle Pellerin

636 ×0.8

403 ×1.4

489 ×2.0

GENET

71 ×0.4

PHEOH

252 ×1.6

PPCH

Citations per year, relative to Isabelle Pellerin Isabelle Pellerin (= 1×) peers Yuko Matsubara

Countries citing papers authored by Isabelle Pellerin

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Pellerin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Pellerin

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Pellerin. A scholar is included among the top collaborators of Isabelle Pellerin 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 Pellerin. Isabelle Pellerin 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

Morcel, Karine, Tanguy Watrin, Laurent Pasquier, et al.. (2011). Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci. Orphanet Journal of Rare Diseases. 6(1). 9–9. 42 indexed citations

Piquet‐Pellorce, Claire, et al.. (2011). ZFPIP/Zfp462 is involved in P19 cell pluripotency and in their neuronal fate. Experimental Cell Research. 317(13). 1922–1934. 15 indexed citations

Laurent, Audrey, et al.. (2010). Involvement of ZFPIP/Zfp462 in chromatin integrity and survival of P19 pluripotent cells. Experimental Cell Research. 316(7). 1190–1201. 12 indexed citations

Laurent, Audrey, Stéphane Deschamps, Agnès Burel, et al.. (2009). Interaction of ZFPIP with PBX1 is crucial for proper expression of neural genetic markers during Xenopus development. Development Growth & Differentiation. 51(8). 699–706. 5 indexed citations

Watrin, Tanguy, et al.. (2009). The developing female genital tract: from genetics to epigenetics. The International Journal of Developmental Biology. 53(2-3). 411–424. 92 indexed citations

Guerrier, Daniel, et al.. (2008). Le syndrome de Mayer-Rokitansky-Küster-Hauser (MRKH) : clinique et génétique. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 37(6). 539–546. 57 indexed citations

Laurent, Audrey, Francis Omilli, Stéphane Deschamps, et al.. (2008). ZFPIP/Zfp462 is maternally required for proper early Xenopus laevis development. Developmental Biology. 327(1). 169–176. 16 indexed citations

Laurent, Audrey, Stéphane Deschamps, Daniel Guerrier, et al.. (2007). Identification of a new type of PBX1 partner that contains zinc finger motifs and inhibits the binding of HOXA9-PBX1 to DNA. Mechanisms of Development. 124(5). 364–376. 18 indexed citations

Laurent, Audrey, et al.. (2007). PBX proteins: much more than Hox cofactors. The International Journal of Developmental Biology. 52(1). 9–20. 79 indexed citations

10.

Bendavid, Claude, Laurent Pasquier, Tanguy Watrin, et al.. (2006). Phenotypic variability of a 4q34 → qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother. European Journal of Medical Genetics. 50(1). 66–72. 27 indexed citations

11.

Burel, Agnès, et al.. (2006). Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina). Journal of Negative Results in BioMedicine. 5(1). 4–4. 61 indexed citations

12.

Guerrier, Daniel, et al.. (2006). The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina) – phenotypic manifestations and genetic approaches. Journal of Negative Results in BioMedicine. 5(1). 1–1. 123 indexed citations

13.

Duchesne, Laurence, Stéphane Deschamps, Isabelle Pellerin, et al.. (2001). Oligomerization of water and solute channels of the major intrinsic protein (MIP) family. Kidney International. 60(2). 422–426. 13 indexed citations

14.

Leblond, Agnès, Carl Guévin, Christian Demers, et al.. (2001). Downregulation of Hepatic Cytochrome P450 in Chronic Renal Failure. Journal of the American Society of Nephrology. 12(2). 326–332. 176 indexed citations

15.

Lagrée, Valérie, Alexandrine Froger, Stéphane Deschamps, et al.. (1999). Switch from an Aquaporin to a Glycerol Channel by Two Amino Acids Substitution. Journal of Biological Chemistry. 274(11). 6817–6819. 84 indexed citations

16.

Lagrée, Valérie, Isabelle Pellerin, Jean‐François Hubert, et al.. (1998). A Yeast Recombinant Aquaporin Mutant That Is Not Expressed or Mistargeted in Xenopus Oocyte Can Be Functionally Analyzed in Reconstituted Proteoliposomes. Journal of Biological Chemistry. 273(20). 12422–12426. 20 indexed citations

17.

Claveau, David, Isabelle Pellerin, M Leclerc, & M G Brunette. (1998). Characterization of the Na + /H + Exchanger in the Luminal Membrane of the Distal Nephron. The Journal of Membrane Biology. 165(3). 265–274. 6 indexed citations

18.

Cahérec, Françoise Le, Stéphane Deschamps, Christian Delamarche, et al.. (1996). Molecular Cloning and Characterization of an Insect Aquaporin. European Journal of Biochemistry. 241(3). 707–715. 78 indexed citations

19.

Vuillermoz, Cécile, et al.. (1992). Transfected endometrial cultured cells: A system to study gene regulation by estrogens. Molecular and Cellular Endocrinology. 87(1-3). R11–R17. 4 indexed citations

20.

Jouvenot, Michèle, et al.. (1990). Regulation of c-fos expression in primary culture of guinea pig glandular epithelial cells stimulated by growth factors and estradiol. annales de biologie animale biochimie biophysique. 30(3). 455–458. 4 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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