Joëlle Aupetit

1.0k total citations
23 papers, 812 citations indexed

About

Joëlle Aupetit is a scholar working on Rheumatology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Joëlle Aupetit has authored 23 papers receiving a total of 812 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Rheumatology, 11 papers in Clinical Biochemistry and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Joëlle Aupetit's work include Folate and B Vitamins Research (14 papers), Metabolism and Genetic Disorders (10 papers) and Neonatal Health and Biochemistry (6 papers). Joëlle Aupetit is often cited by papers focused on Folate and B Vitamins Research (14 papers), Metabolism and Genetic Disorders (10 papers) and Neonatal Health and Biochemistry (6 papers). Joëlle Aupetit collaborates with scholars based in France, United States and Canada. Joëlle Aupetit's co-authors include P. Kamoun, B. Chadefaux, Philippe Chauveau, M. Coudé, P Jungers, T Hannedouche, Bernadette Chadefaux-Vekemans, A. Chabli, Jean‐Paul Bonnefont and Daniel Rabier and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neurochemistry.

In The Last Decade

Joëlle Aupetit

23 papers receiving 791 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joëlle Aupetit France 14 392 205 179 162 157 23 812
B. Chadefaux France 18 579 1.5× 204 1.0× 321 1.8× 214 1.3× 69 0.4× 32 1.1k
Brigitte Kohl Germany 10 562 1.4× 111 0.5× 241 1.3× 136 0.8× 56 0.4× 11 921
Jovan Evrovski Canada 14 305 0.8× 67 0.3× 183 1.0× 131 0.8× 60 0.4× 24 762
William Owen United States 12 57 0.1× 73 0.4× 84 0.5× 107 0.7× 23 0.1× 23 699
Maddalena L. Zighetti Italy 18 309 0.8× 44 0.2× 243 1.4× 173 1.1× 26 0.2× 27 1.3k
P. Clifton‐Bligh Australia 21 111 0.3× 49 0.2× 332 1.9× 201 1.2× 30 0.2× 54 1.1k
Mitsumine Fukui Japan 18 40 0.1× 157 0.8× 119 0.7× 246 1.5× 38 0.2× 46 1.0k
Yoshio Konishi Japan 21 89 0.2× 28 0.1× 104 0.6× 151 0.9× 27 0.2× 57 1.1k
Isabella Catalano Italy 10 114 0.3× 48 0.2× 296 1.7× 64 0.4× 79 0.5× 22 964
Rosanna Capasso Italy 13 121 0.3× 45 0.2× 53 0.3× 122 0.8× 137 0.9× 23 544

Countries citing papers authored by Joëlle Aupetit

Since Specialization
Citations

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

Fields of papers citing papers by Joëlle Aupetit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joëlle Aupetit

This figure shows the co-authorship network connecting the top 25 collaborators of Joëlle Aupetit. A scholar is included among the top collaborators of Joëlle Aupetit 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 Joëlle Aupetit. Joëlle Aupetit 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.
Anne, Christine, Sylvie Kieffer‐Jaquinod, S O’Regan, et al.. (2012). Heptahelical protein PQLC2 is a lysosomal cationic amino acid exporter underlying the action of cysteamine in cystinosis therapy. Proceedings of the National Academy of Sciences. 109(50). E3434–43. 135 indexed citations
2.
Monnot, Sophie, Bernadette Chadefaux-Vekemans, Joëlle Aupetit, et al.. (2009). Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiency. Human Mutation. 30(5). 734–740. 25 indexed citations
3.
Ottolenghi, Chris, Nasséra Abermil, Alain Lescoat, et al.. (2009). Gestational age‐related reference values for amniotic fluid organic acids. Prenatal Diagnosis. 30(1). 43–48. 9 indexed citations
4.
Chabli, A., et al.. (2007). Measurement of cystine in granulocytes using liquid chromatography-tandem mass spectrometry. Clinical Biochemistry. 40(9-10). 692–698. 33 indexed citations
5.
Chadefaux-Vekemans, Bernadette, Daniel Rabier, Alain Lescoat, et al.. (2006). Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experience. Prenatal Diagnosis. 26(9). 814–818. 5 indexed citations
6.
Santiard-Baron, Dominique, Joëlle Aupetit, & Nathalie Janel. (2005). Plasma homocysteine levels are not increased in murine models of Alzheimer's disease. Neuroscience Research. 53(4). 447–449. 13 indexed citations
7.
Robert, Karine, Dominique Santiard-Baron, Jean-François Chassé, et al.. (2004). The neuronal SAPK/JNK pathway is altered in a murine model of hyperhomocysteinemia. Journal of Neurochemistry. 89(1). 33–43. 20 indexed citations
8.
Robert, Karine, Dominique Santiard-Baron, Catherine Vayssettes, et al.. (2003). Altered Gene Expression in Liver from a Murine Model of Hyperhomocysteinemia. Journal of Biological Chemistry. 278(34). 31504–31511. 50 indexed citations
9.
Bonnefont, Jean‐Paul, et al.. (2003). Prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency in chorionic villi: a novel approach. Prenatal Diagnosis. 23(11). 884–887. 6 indexed citations
10.
Chadefaux-Vekemans, Bernadette, Daniel Rabier, A. Chabli, et al.. (2002). Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluid. Prenatal Diagnosis. 22(6). 456–458. 12 indexed citations
11.
Thuillier, Laure, Caroline Sevin, France Demaugre, et al.. (2000). Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patient. Neuromuscular Disorders. 10(3). 200–205. 25 indexed citations
12.
Jungers, Paul, Dominique Joly, Ziad A. Massy, et al.. (1999). Sustained reduction of hyperhomocysteinaemia with folic acid supplementation in predialysis patients. Nephrology Dialysis Transplantation. 14(12). 2903–2906. 53 indexed citations
13.
Thuillier, Laure, Bernadette Chadefaux-Vekemans, Jean‐Paul Bonnefont, et al.. (1998). Does the polymorphism 677C‐T of the 5,10‐methylenetetrahydrofolate reductase gene contribute to homocysteine‐related vascular disease?. Journal of Inherited Metabolic Disease. 21(8). 812–822. 15 indexed citations
14.
Coudé, M., Joëlle Aupetit, M. T. Zabot, P. Kamoun, & Bernadette Chadefaux-Vekemans. (1998). Four novel mutations at the cystathionine β‐synthase locus causing homocystinuria. Journal of Inherited Metabolic Disease. 21(8). 823–828. 6 indexed citations
15.
Aral, Bernard, Marie Coudé, Jacqueline London, et al.. (1997). Two novel mutations (K384E and L539S) in the C-terminal moiety of the cystathionine β-synthase protein in two French pyridoxine-responsive homocystinuria patients. Human Mutation. 9(1). 81–82. 11 indexed citations
16.
Rabier, Daniel, Bernadette Chadefaux-Vekemans, J.-F. Oury, et al.. (1996). GESTATIONAL AGE-RELATED REFERENCE VALUES FOR AMNIOTIC FLUID AMINO ACIDS: A USEFUL TOOL FOR PRENATAL DIAGNOSIS OF AMINOACIDOPATHIES. Prenatal Diagnosis. 16(7). 623–628. 13 indexed citations
17.
Chauveau, Philippe, B. Chadefaux, M. Coudé, et al.. (1993). Hyperhomocysteinemia, a risk factor for atherosclerosis in chronic uremic patients.. PubMed. 41. S72–7. 187 indexed citations
18.
Bonnefont, Jean‐Paul, Dominique Chrétien, Pierre Rustin, et al.. (1992). Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis. The Journal of Pediatrics. 121(2). 255–258. 56 indexed citations
19.
Chadefaux, B., M. Coudé, M. Hamet, et al.. (1990). [Radioisotopic assay of total L-homocysteine in plasma and urine: application to serial determinations].. PubMed. 48(1). 33–6. 1 indexed citations
20.
Chadefaux, B., M. Coudé, M. Hamet, Joëlle Aupetit, & P. Kamoun. (1989). Rapid determination of total homocysteine in plasma.. Clinical Chemistry. 35(9). 2002–2002. 23 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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