Stéphan Soullier

528 total citations
14 papers, 428 citations indexed

About

Stéphan Soullier is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Stéphan Soullier has authored 14 papers receiving a total of 428 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Surgery. Recurrent topics in Stéphan Soullier's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genomics and Chromatin Dynamics (4 papers) and Animal Genetics and Reproduction (2 papers). Stéphan Soullier is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genomics and Chromatin Dynamics (4 papers) and Animal Genetics and Reproduction (2 papers). Stéphan Soullier collaborates with scholars based in France, United Kingdom and Austria. Stéphan Soullier's co-authors include Françis Poulat, Philippe Berta, Philippe Jay, Marion Desclozeaux, Pascal de Santa Barbara, Brigitte Boizet, Brigitte Moniot, Nathalie Bonneaud, Jean‐Marc Vanacker and Vincent Laudet and has published in prestigious journals such as Journal of Biological Chemistry, Bioinformatics and FEBS Letters.

In The Last Decade

Stéphan Soullier

14 papers receiving 419 citations

Peers

Stéphan Soullier
Bela Patel United States
George J. Kargul United States
Anita K. Iyer United States
Koshi Kunimoto United States
Mark Hills Canada
Michael A. Charles United States
Stéphan Soullier
Citations per year, relative to Stéphan Soullier Stéphan Soullier (= 1×) peers Rieko Ajima

Countries citing papers authored by Stéphan Soullier

Since Specialization
Citations

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

Fields of papers citing papers by Stéphan Soullier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphan Soullier

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphan Soullier. A scholar is included among the top collaborators of Stéphan Soullier 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 Stéphan Soullier. Stéphan Soullier 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.
Gayrard, Nathalie, Ilan Szwarc, D.L. Andress, et al.. (2010). The use of SDS-PAGE scanning of spent dialysate to assess uraemic toxin removal by dialysis. Nephrology Dialysis Transplantation. 26(7). 2281–2289. 14 indexed citations
2.
Gayrard, Nathalie, et al.. (2009). Use of spent dialysate analysis to estimate blood levels of uraemic solutes without blood sampling: urea. Nephrology Dialysis Transplantation. 25(3). 873–879. 4 indexed citations
3.
Szwarc, Ilan, Stéphan Soullier, Nathalie Gayrard, et al.. (2007). Ischemic Postconditioning Prevents Ischemic Acute Renal Failure. Transplantation Proceedings. 39(8). 2554–2556. 33 indexed citations
4.
Soullier, Stéphan, et al.. (2005). Mécanismes moléculaires impliqués dans l'ischémie–reperfusion rénale. Néphrologie & Thérapeutique. 1(5). 315–321. 6 indexed citations
5.
Soullier, Stéphan, et al.. (2005). Foxn1 is required for tissue assembly and desmosomal cadherin expression in the hair shaft. Developmental Dynamics. 232(4). 1062–1068. 28 indexed citations
6.
Lawrence, Neil D., Marta Milo, Mahesan Niranjan, Penny Rashbass, & Stéphan Soullier. (2004). Reducing the variability in cDNA microarray image processing by Bayesian inference. Bioinformatics. 20(4). 518–526. 28 indexed citations
7.
Lawrence, Neil D., Marta Milo, Mahesan Niranjan, Penny Rashbass, & Stéphan Soullier. (2004). Bayesian processing of microarray images. 71–80. 5 indexed citations
8.
Soullier, Stéphan, Philippe Jay, Françis Poulat, et al.. (1999). Diversification Pattern of the HMG and SOX Family Members During Evolution. Journal of Molecular Evolution. 48(5). 517–527. 89 indexed citations
9.
Desclozeaux, Marion, Françis Poulat, Pascal de Santa Barbara, et al.. (1998). Characterization of two Sp1 binding sites of the human sex determining SRY promoter. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1397(3). 247–252. 25 indexed citations
10.
Crémazy, Frédéric, Stéphan Soullier, Philippe Berta, & Philippe Jay. (1998). Further complexity of the human SOX gene family revealed by the combined use of highly degenerate primers and nested PCR. FEBS Letters. 438(3). 311–314. 20 indexed citations
11.
Poulat, Françis, Pascal de Santa Barbara, Marion Desclozeaux, et al.. (1997). The Human Testis Determining Factor SRY Binds a Nuclear Factor Containing PDZ Protein Interaction Domains. Journal of Biological Chemistry. 272(11). 7167–7172. 135 indexed citations
12.
Gozé, Catherine, Stéphan Soullier, Françis Poulat, et al.. (1996). Le sexe et les SOX. médecine/sciences. 12(10). 1097–1097. 1 indexed citations
13.
Poulat, Françis, et al.. (1994). Description and functional implications of a novel mutation in the sex-determining gene SRY. Human Mutation. 3(3). 200–204. 37 indexed citations
14.
Soullier, Stéphan, Françis Poulat, Brigitte Boizet‐Bonhoure, et al.. (1994). The human testis determining factor SRY: A new member of the HMG box protein family. Biochimie. 76(10-11). 1075–1081. 3 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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