F. X. Coudé

1.1k total citations
33 papers, 709 citations indexed

About

F. X. Coudé is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, F. X. Coudé has authored 33 papers receiving a total of 709 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Clinical Biochemistry, 15 papers in Molecular Biology and 13 papers in Physiology. Recurrent topics in F. X. Coudé's work include Metabolism and Genetic Disorders (24 papers), Diet and metabolism studies (13 papers) and Biochemical and Molecular Research (7 papers). F. X. Coudé is often cited by papers focused on Metabolism and Genetic Disorders (24 papers), Diet and metabolism studies (13 papers) and Biochemical and Molecular Research (7 papers). F. X. Coudé collaborates with scholars based in France, Canada and United States. F. X. Coudé's co-authors include Lawrence Sweetman, William L. Nyhan, G Grimber, C. Charpentier, H. Ogier, L Cathelineau, Daniel Rabier, Jean‐Marie Saudubray, P Parvy and Stanislas Lyonnet and has published in prestigious journals such as Journal of Clinical Investigation, PEDIATRICS and Biochemical Journal.

In The Last Decade

F. X. Coudé

33 papers receiving 674 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F. X. Coudé France 16 484 292 183 177 97 33 709
Mohamed A. Nada United States 11 409 0.8× 424 1.5× 151 0.8× 60 0.3× 47 0.5× 30 636
F. A. M. Baumeister Germany 11 225 0.5× 203 0.7× 82 0.4× 106 0.6× 76 0.8× 27 528
Pascale Delonlay France 11 255 0.5× 304 1.0× 100 0.5× 62 0.4× 73 0.8× 13 530
J. M. Saudubray France 12 518 1.1× 392 1.3× 95 0.5× 140 0.8× 57 0.6× 26 660
F. J. van Spronsen Netherlands 13 410 0.8× 215 0.7× 224 1.2× 80 0.5× 91 0.9× 27 504
H Gröbe Germany 11 143 0.3× 237 0.8× 119 0.7× 69 0.4× 33 0.3× 30 680
Kathryn Moseley United States 17 672 1.4× 416 1.4× 410 2.2× 137 0.8× 103 1.1× 26 833
François Feillet France 15 251 0.5× 248 0.8× 212 1.2× 98 0.6× 31 0.3× 45 685
Elaina Jurecki United States 15 755 1.6× 426 1.5× 547 3.0× 133 0.8× 52 0.5× 31 899
H. R. Scholte Netherlands 13 293 0.6× 370 1.3× 66 0.4× 35 0.2× 64 0.7× 17 495

Countries citing papers authored by F. X. Coudé

Since Specialization
Citations

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

Fields of papers citing papers by F. X. Coudé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. X. Coudé. 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 F. X. Coudé. The network helps show where F. X. Coudé may publish in the future.

Co-authorship network of co-authors of F. X. Coudé

This figure shows the co-authorship network connecting the top 25 collaborators of F. X. Coudé. A scholar is included among the top collaborators of F. X. Coudé 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 F. X. Coudé. F. X. Coudé 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.
Coudé, F. X., Cyril Mignot, Stanislas Lyonnet, & Arnold Munnich. (2006). Academic Impairment is the Most Frequent Complication of Neurofibromatosis Type-1 (NF1) in Children. Behavior Genetics. 36(5). 660–664. 34 indexed citations
2.
Coudé, F. X., Cyril Mignot, Stanislas Lyonnet, & Arnold Münnich. (2006). Discontinuity in the fall of left-handedness in a French population: A May '68 effect?. Laterality Asymmetries of Body Brain and Cognition. 11(1). 33–35. 10 indexed citations
3.
Saudubray, Jean‐Marie, H. Ogier, C. Charpentier, et al.. (1984). Hudson Memorial Lecture Neonatal Management of Organic Acidurias. Clinical Update. PubMed. 7 Suppl 1. 2–9. 22 indexed citations
4.
Coudé, F. X., et al.. (1983). Inhibition of ureagenesis by valproate in rat hepatocytes. Role of N-acetylglutamate and acetyl-CoA. Biochemical Journal. 216(1). 233–236. 48 indexed citations
5.
Münnich, Arnold, J. M. Saudubray, C. Charpentier, et al.. (1983). Multiple molybdoenzyme deficiencies due to an inborn error of molybdenum cofactor metabolism: Two additional cases in a new family. Journal of Inherited Metabolic Disease. 6(S2). 95–96. 12 indexed citations
6.
Coudé, F. X., G Grimber, P Parvy, & Daniel Rabier. (1983). Role of N-acetylglutamate and acetyl-CoA in the inhibition of ureagenesis by isovaleric acid in isolated rat hepatocytes. Biochimica et Biophysica Acta (BBA) - General Subjects. 761(1). 13–16. 8 indexed citations
7.
Coudé, F. X., et al.. (1983). Characterization of enzymatic deficiencies of branched chain amino-acid catabolism in human fibroblasts by genetic complementation. Biochemical and Biophysical Research Communications. 114(1). 175–182. 3 indexed citations
8.
Coudé, F. X., et al.. (1983). Action of the antiepileptic drug, valproic acid, on fatty acid oxidation in isolated rat hepatocytes. Biochemical and Biophysical Research Communications. 115(2). 730–736. 54 indexed citations
9.
Coudé, F. X., et al.. (1982). Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemia.. PubMed. 69(1). 115–7. 20 indexed citations
10.
Münnich, Arnold, Jean‐Marie Saudubray, Jennifer Taylor, et al.. (1982). CONGENITAL LACTIC ACIDOSIS, α‐KETOGLUTARIC ACIDURIA AND VARIANT FORM OF MAPLE SYRUP URINE DISEASE DUE TO A SINGLE ENZYME DEFECT: DIHYDROLIPOYL DEHYDROGENASE DEFICIENCY. Acta Paediatrica. 71(1). 167–171. 38 indexed citations
11.
Saudubray, J. M., F. X. Coudé, H. Ogier, et al.. (1982). Hyperammonemia Secondary to Hereditary Organic Acidurias : A Study of 29 Cases. Advances in experimental medicine and biology. 153. 135–140. 3 indexed citations
12.
Coudé, F. X., et al.. (1982). Correlation Between Blood Ammonia Concentration and Organic Acid Accumulation in lsovaleric and Propionic Acidemia. PEDIATRICS. 69(1). 115–117. 19 indexed citations
13.
Charpentier, C., et al.. (1982). Amino acid profile in pyruvate carboxylase deficiency: Comparison with some other metabolic disorders. Journal of Inherited Metabolic Disease. 5(S1). 11–12. 10 indexed citations
14.
Coudé, F. X., H. Ogier, Arnold Münnich, et al.. (1982). Short Communication. Pediatric Research. 16(Supplement). 85–85. 1 indexed citations
15.
Saudubray, Jean Marie, C. Marsac, J.M. Limal, et al.. (1981). Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: Relationship to age. The Journal of Pediatrics. 98(6). 904–908. 44 indexed citations
16.
Coudé, F. X., H. Ogier, C. Charpentier, et al.. (1981). Neonatal glutaric aciduria type II: An X-linked recessive inherited disorder. Human Genetics. 59(3). 263–5. 25 indexed citations
17.
Coudé, F. X., et al.. (1981). N-Acetylglutamate synthetase in human liver: Regulation of activity by L-Arginine and N-Acetylglutamate. Biochemical and Biophysical Research Communications. 102(3). 1016–1020. 7 indexed citations
18.
Münnich, Arnold, Jean Marie Saudubray, H. Ogier, et al.. (1981). [Multiple biotin-dependent carboxylase deficiencies (author's transl)].. PubMed. 38(2). 83–90. 5 indexed citations
19.
Coudé, F. X., Lawrence Sweetman, & William L. Nyhan. (1979). Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia.. Journal of Clinical Investigation. 64(6). 1544–1551. 175 indexed citations
20.
Saudubray, J. M., O Amédée-Manesme, H. Ogier, et al.. (1979). [Emergency treatment of inborn amino errors of amino acid metabolism detected in the neonatal period].. PubMed. 36(10). 969–80. 2 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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