Alain Fairand

641 total citations
21 papers, 536 citations indexed

About

Alain Fairand is a scholar working on Clinical Biochemistry, Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Alain Fairand has authored 21 papers receiving a total of 536 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Clinical Biochemistry, 7 papers in Biochemistry and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Alain Fairand's work include Metabolism and Genetic Disorders (13 papers), Amino Acid Enzymes and Metabolism (6 papers) and Neonatal Health and Biochemistry (6 papers). Alain Fairand is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Amino Acid Enzymes and Metabolism (6 papers) and Neonatal Health and Biochemistry (6 papers). Alain Fairand collaborates with scholars based in France. Alain Fairand's co-authors include Annie Husson, Alain Lavoinne, Carole Brasse‐Lagnel, Sylvie Renouf, R Vaillant, Muriel Quillard, Catherine Buquet, Christine Bôle‐Feysot, Jean Demarquoy and D.A.S. Loeber and has published in prestigious journals such as Journal of Biological Chemistry, Biochemical Journal and FEBS Letters.

In The Last Decade

Alain Fairand

21 papers receiving 519 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Alain Fairand France 11 220 144 113 109 107 21 536
Sylvie Renouf France 13 200 0.9× 152 1.1× 80 0.7× 78 0.7× 72 0.7× 19 644
Juan J. Aragón Spain 18 525 2.4× 175 1.2× 153 1.4× 38 0.3× 54 0.5× 40 841
Marian J. Jackson United States 11 167 0.8× 41 0.3× 124 1.1× 27 0.2× 110 1.0× 15 456
Amy Ciccarella United States 3 286 1.3× 158 1.1× 99 0.9× 82 0.8× 67 0.6× 3 499
B Lederer Belgium 8 569 2.6× 215 1.5× 125 1.1× 10 0.1× 82 0.8× 14 903
Bookyung Ko United States 8 503 2.3× 347 2.4× 105 0.9× 18 0.2× 56 0.5× 9 738
V. S. Shapot United Kingdom 11 263 1.2× 108 0.8× 103 0.9× 14 0.1× 29 0.3× 43 420
W. J. Salsgiver United States 12 301 1.4× 89 0.6× 100 0.9× 12 0.1× 52 0.5× 18 612
Yuko Kikuchi Japan 11 373 1.7× 52 0.4× 32 0.3× 20 0.2× 18 0.2× 25 575
Thomas A. Tedesco United States 20 407 1.9× 41 0.3× 169 1.5× 16 0.1× 166 1.6× 47 1.0k

Countries citing papers authored by Alain Fairand

Since Specialization
Citations

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

Fields of papers citing papers by Alain Fairand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alain Fairand

This figure shows the co-authorship network connecting the top 25 collaborators of Alain Fairand. A scholar is included among the top collaborators of Alain Fairand 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 Alain Fairand. Alain Fairand 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.
Brasse‐Lagnel, Carole, Alain Lavoinne, D.A.S. Loeber, et al.. (2007). Glutamine and interleukin‐1β interact at the level of Sp1 and nuclear factor‐κB to regulate argininosuccinate synthetase gene expression. FEBS Journal. 274(20). 5250–5262. 32 indexed citations
2.
Brasse‐Lagnel, Carole, et al.. (2005). IL-1β stimulates argininosuccinate synthetase gene expression through NF-κB in Caco-2 cells. Biochimie. 87(5). 403–409. 18 indexed citations
3.
Brasse‐Lagnel, Carole, et al.. (2005). Biphasic effect of IL-1β on the activity of argininosuccinate synthetase in Caco-2 cells. Involvement of nitric oxide production. Biochimie. 88(6). 607–612. 4 indexed citations
4.
Brasse‐Lagnel, Carole, Alain Fairand, Alain Lavoinne, & Annie Husson. (2003). Glutamine Stimulates Argininosuccinate Synthetase Gene Expression through Cytosolic O-Glycosylation of Sp1 in Caco-2 Cells. Journal of Biological Chemistry. 278(52). 52504–52510. 61 indexed citations
5.
Husson, Annie, Carole Brasse‐Lagnel, Alain Fairand, Sylvie Renouf, & Alain Lavoinne. (2003). Argininosuccinate synthetase from the urea cycle to the citrulline–NO cycle. European Journal of Biochemistry. 270(9). 1887–1899. 252 indexed citations
6.
Fairand, Alain, et al.. (1999). Expression of the Genes of Arginine-Synthesizing Enzymes in the Rat Kidney during Development. Neonatology. 76(4). 253–260. 11 indexed citations
7.
Renouf, Sylvie, Alain Fairand, & Annie Husson. (1998). Developmental Control of Argininosuccinate Lyase Gene by Methylation. Neonatology. 73(3). 190–197. 3 indexed citations
9.
Renouf, Sylvie, et al.. (1997). Regulation of Argininosuccinate Synthetase mRNA Level in Rat Foetal Hepatocytes. European Journal of Biochemistry. 249(3). 669–674. 14 indexed citations
10.
Lavoinne, Alain, et al.. (1996). Glutamine Inhibits the Lowering Effect of Glucose on the Level of Phosphoenol pyruvate Carboxykinase mRNA in Isolated Rat Hepatocytes. European Journal of Biochemistry. 242(3). 537–543. 18 indexed citations
11.
Husson, Annie, et al.. (1996). Hypoosmolarity and glutamine increased the β‐actin gene transcription in isolated rat hepatocytes. FEBS Letters. 394(3). 353–355. 23 indexed citations
12.
Demarquoy, Jean, et al.. (1995). Regulation of argininosuccinate synthetase level by corticosteroid and pancreatic hormones during perinatal period. Molecular and Cellular Biochemistry. 143(1). 47–51. 8 indexed citations
13.
Renouf, Sylvie, Alain Fairand, & Annie Husson. (1995). Glucocorticoid-Dependent Induction of the mRNA Coding for Argininosuccinate Lyase in Cultured Fetal Rat Hepatocytes. Neonatology. 68(3). 221–228. 2 indexed citations
14.
Renouf, Sylvie, et al.. (1993). Changes in levels of argininosuccinate lyase mRNA during induction by glucagon and cyclic AMP in cultured foetal-rat hepatocytes. Biochemical Journal. 291(2). 609–613. 16 indexed citations
15.
Renouf, Sylvie, et al.. (1992). Changes in Argininosuccinate Lyase Gene Expression in the Rat Liver during Development. Neonatology. 61(6). 381–390. 6 indexed citations
16.
Demarquoy, Jean, et al.. (1991). Development and hormonal control of thioredoxin and the thioredoxin-reductase system in the rat liver during the perinatal period. Cellular and Molecular Life Sciences. 47(5). 497–500. 9 indexed citations
17.
Husson, Annie, et al.. (1990). Expression of argininosuccinate lyase mRNA in foetal hepatocytes. European Journal of Biochemistry. 192(3). 677–681. 22 indexed citations
19.
Husson, Annie, et al.. (1982). Regulation of Ureagenesis in Neonatal Rat Liver: Influence of Cycloheximide in vivo and in vitro. Neonatology. 42(1-2). 39–45. 2 indexed citations
20.
Husson, Annie, Alain Fairand, & R Vaillant. (1981). Control of Urea Synthesis in Fetal Rat Liver Slices. Neonatology. 40(5-6). 224–231. 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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