B. Chadefaux

1.5k total citations
32 papers, 1.1k citations indexed

About

B. Chadefaux is a scholar working on Clinical Biochemistry, Rheumatology and Molecular Biology. According to data from OpenAlex, B. Chadefaux has authored 32 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Clinical Biochemistry, 16 papers in Rheumatology and 13 papers in Molecular Biology. Recurrent topics in B. Chadefaux's work include Metabolism and Genetic Disorders (16 papers), Folate and B Vitamins Research (16 papers) and Mitochondrial Function and Pathology (5 papers). B. Chadefaux is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Folate and B Vitamins Research (16 papers) and Mitochondrial Function and Pathology (5 papers). B. Chadefaux collaborates with scholars based in France, United Kingdom and Qatar. B. Chadefaux's co-authors include P. Kamoun, M. Coudé, Philippe Chauveau, Joëlle Aupetit, P Jungers, T Hannedouche, Annick Ankri, T. Bienvenu, Delphine Allard and Gilles Montalescot and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and Clinical Chemistry.

In The Last Decade

B. Chadefaux

32 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. Chadefaux France 18 579 321 214 204 196 32 1.1k
Brigitte Kohl Germany 10 562 1.0× 241 0.8× 136 0.6× 111 0.5× 82 0.4× 11 921
McCully Ks United States 7 1.3k 2.2× 528 1.6× 183 0.9× 222 1.1× 174 0.9× 10 1.6k
Joëlle Aupetit France 14 392 0.7× 179 0.6× 162 0.8× 205 1.0× 109 0.6× 23 812
Arzu Ergen Türkiye 20 198 0.3× 213 0.7× 463 2.2× 91 0.4× 75 0.4× 109 1.1k
Israel Roisenberg Brazil 19 136 0.2× 73 0.2× 236 1.1× 159 0.8× 138 0.7× 47 953
Jovan Evrovski Canada 14 305 0.5× 183 0.6× 131 0.6× 67 0.3× 78 0.4× 24 762
Markéta Pavlı́ková Czechia 19 332 0.6× 300 0.9× 195 0.9× 62 0.3× 31 0.2× 64 977
D. G. Franken Netherlands 9 826 1.4× 430 1.3× 62 0.3× 111 0.5× 212 1.1× 9 978
Maddalena L. Zighetti Italy 18 309 0.5× 243 0.8× 173 0.8× 44 0.2× 567 2.9× 27 1.3k
R. M. McCredie Australia 14 175 0.3× 417 1.3× 145 0.7× 32 0.2× 116 0.6× 41 1.3k

Countries citing papers authored by B. Chadefaux

Since Specialization
Citations

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

Fields of papers citing papers by B. Chadefaux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Chadefaux

This figure shows the co-authorship network connecting the top 25 collaborators of B. Chadefaux. A scholar is included among the top collaborators of B. Chadefaux 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 B. Chadefaux. B. Chadefaux 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.
Heslegrave, Amanda, Ritika R. Kapoor, Simon Eaton, et al.. (2012). Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase. Orphanet Journal of Rare Diseases. 7(1). 25–25. 33 indexed citations
2.
Kapoor, Ritika R., Sarah E. Flanagan, Anupam Chakrapani, et al.. (2009). Hyperinsulinism–hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype–phenotype correlations. European Journal of Endocrinology. 161(5). 731–735. 76 indexed citations
3.
Nübel, Tobias, Yalin Emre, Daniel Rabier, et al.. (2007). Modified glutamine catabolism in macrophages of Ucp2 knock-out mice. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1777(1). 48–54. 33 indexed citations
4.
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
5.
Chadefaux, B., et al.. (1994). Homocysteine: relationship to serum cobalamin, serum folate, erythrocyte folate, and lobation of neutrophils.. PubMed. 17(6). 540–50. 12 indexed citations
6.
Marquet, J, B. Chadefaux, Jean‐Paul Bonnefont, Jean‐Marie Saudubray, & J Zittoun. (1994). Methylenetetrahydrofolate reductase deficiency: Prenatal diagnosis and family studies. Prenatal Diagnosis. 14(1). 29–33. 11 indexed citations
7.
Vilarinho, Laura, et al.. (1994). Citrullinaemia and isolated sulphite oxidase deficiency in two siblings. Journal of Inherited Metabolic Disease. 17(5). 638–639. 5 indexed citations
8.
Bienvenu, T., Annick Ankri, B. Chadefaux, Gilles Montalescot, & P. Kamoun. (1993). Elevated total plasma homocysteine, a risk factor for thrombosis. Relation to coagulation and fibrinolytic parameters. Thrombosis Research. 70(2). 123–129. 83 indexed citations
9.
Bienvenu, T., B. Chadefaux, Annick Ankri, et al.. (1991). Antithrombin III Activity Is Not Related to Plasma Homocysteine Concentrations. Pathophysiology of Haemostasis and Thrombosis. 21(2). 65–67. 5 indexed citations
10.
Visy, Jean-Marc, B. Chadefaux, Catherine Fressinaud, et al.. (1991). Homocystinuria due to 5,10‐methylenetetra‐hydrofolate reductase deficiency revealed by stroke in adult siblings. Neurology. 41(8). 1313–1313. 51 indexed citations
11.
Kamoun, P. & B. Chadefaux. (1991). Eleventh week amniocentesis for prenatal diagnosis of some metabolic diseases. Prenatal Diagnosis. 11(9). 691–696. 12 indexed citations
12.
Coudé, M., B. Chadefaux, Daniel Rabier, & P. Kamoun. (1990). Early amniocentesis and amniotic fluid organic acid levels in the prenatal diagnosis of organic acidemias. Clinica Chimica Acta. 187(3). 329–332. 14 indexed citations
13.
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
14.
Chadefaux, B., et al.. (1990). Concentrations of total homocysteine in plasma in chronic renal failure. Clinical Chemistry. 36(12). 2137–2138. 62 indexed citations
15.
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
16.
Chadefaux, B., Daniel Rabier, & P Kamoun. (1988). [Prenatal diagnosis of enzymopathies of the urea cycle].. PubMed. 46(7). 471–6. 2 indexed citations
17.
Chadefaux, B., Daniel Rabier, F. Rocchiccioli, et al.. (1988). Prenatal diagnosis of propionic acidemia in chorionic villi by direct assay of propionyl CoA carboxylase. Prenatal Diagnosis. 8(2). 161–164. 9 indexed citations
18.
Gilgenkrantz, S, Fryns Jp, P. Droullé, et al.. (1987). [Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21].. PubMed. 35(1). 51–61. 3 indexed citations
19.
Sinet, P.-M., B. Chadefaux, Annie Nicole, et al.. (1987). Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome). Human Genetics. 76(3). 225–229. 25 indexed citations
20.
Chadefaux, B., et al.. (1984). Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221. Human Genetics. 66(2-3). 190–192. 29 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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