C. Beaumont

3.0k total citations
48 papers, 2.4k citations indexed

About

C. Beaumont is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, C. Beaumont has authored 48 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Hematology, 22 papers in Molecular Biology and 18 papers in Genetics. Recurrent topics in C. Beaumont's work include Iron Metabolism and Disorders (28 papers), Hemoglobinopathies and Related Disorders (18 papers) and Trace Elements in Health (13 papers). C. Beaumont is often cited by papers focused on Iron Metabolism and Disorders (28 papers), Hemoglobinopathies and Related Disorders (18 papers) and Trace Elements in Health (13 papers). C. Beaumont collaborates with scholars based in France, Italy and United Kingdom. C. Beaumont's co-authors include Des R. Richardson, Prem Ponka, F Trivin, J Emerit, Bernard Grandchamp, Y Nordmann, Achille Iolascon, Luigia De Falco, Jean‐Charles Deybach and F Renaudie and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

C. Beaumont

48 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Beaumont France 26 1.2k 900 731 727 313 48 2.4k
Alex D. Sheftel Canada 24 801 0.7× 1.3k 1.5× 786 1.1× 451 0.6× 155 0.5× 36 2.6k
Sylvia S. Bottomley United States 26 430 0.4× 1.1k 1.3× 285 0.4× 359 0.5× 509 1.6× 53 1.9k
Zoubida Karim France 31 578 0.5× 1.3k 1.5× 451 0.6× 368 0.5× 219 0.7× 70 2.3k
De‐Liang Zhang United States 22 1.1k 1.0× 581 0.6× 667 0.9× 720 1.0× 92 0.3× 39 2.1k
Giorgio Biasiotto Italy 28 903 0.8× 752 0.8× 714 1.0× 454 0.6× 173 0.6× 75 2.4k
Caroline Chauvet France 14 2.1k 1.8× 399 0.4× 1.1k 1.5× 1.6k 2.2× 113 0.4× 19 2.9k
Debbie Trinder Australia 29 1.4k 1.2× 356 0.4× 833 1.1× 721 1.0× 113 0.4× 66 2.5k
Maura Poli Italy 32 1.4k 1.2× 1.3k 1.4× 825 1.1× 700 1.0× 120 0.4× 77 3.2k
Sandro Altamura Germany 28 1.1k 0.9× 1.0k 1.2× 555 0.8× 708 1.0× 88 0.3× 70 2.7k
Ivana De Domenico United States 27 2.8k 2.4× 885 1.0× 1.9k 2.5× 1.9k 2.6× 154 0.5× 39 4.1k

Countries citing papers authored by C. Beaumont

Since Specialization
Citations

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

Fields of papers citing papers by C. Beaumont

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Beaumont

This figure shows the co-authorship network connecting the top 25 collaborators of C. Beaumont. A scholar is included among the top collaborators of C. Beaumont 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 C. Beaumont. C. Beaumont 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.
Beaumont, C. & Zoubida Karim. (2012). Actualité du métabolisme du fer. La Revue de Médecine Interne. 34(1). 17–25. 13 indexed citations
2.
Arlet, Jean‐Benoît, et al.. (2012). Supplémentation en fer : indications, limites et modalités. La Revue de Médecine Interne. 34(1). 26–31. 5 indexed citations
3.
Montalembert, Mariane de, et al.. (2012). Exploration d’une anémie microcytaire chez l’enfant. Archives de Pédiatrie. 19(3). 295–304. 5 indexed citations
4.
Brasse‐Lagnel, Carole, Maura Poli, C. Lesueur, et al.. (2010). Immunoassay for human serum hemojuvelin. Haematologica. 95(12). 2031–2037. 25 indexed citations
5.
Kannengiesser, Caroline, Gilles Hetet, Annick Mosser, et al.. (2009). A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload. Haematologica. 94(3). 335–339. 61 indexed citations
6.
Iolascon, Achille, Luigia De Falco, & C. Beaumont. (2009). Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis. Haematologica. 94(3). 395–408. 96 indexed citations
7.
Beaumont, C.. (2009). Actualités du métabolisme du fer. La Revue de Médecine Interne. 30. S307–S310. 3 indexed citations
8.
Lasocki, Sigismond, et al.. (2008). La prescription martiale en réanimation aujourd’hui : une enquête de pratique. Annales Françaises d Anesthésie et de Réanimation. 27(11). 909–914. 3 indexed citations
9.
Delaby, Constance, Jean‐Charles Deybach, & C. Beaumont. (2007). L'hepcidine et le métabolisme du fer. La Revue de Médecine Interne. 28(7). 510–512. 9 indexed citations
10.
11.
Cynober, Thérèse, Gordon W. Stewart, Bernard Grandchamp, et al.. (2006). Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis. Clinical & Laboratory Haematology. 28(4). 270–274. 25 indexed citations
12.
Beaumont, C. & François Canonne‐Hergaux. (2005). Erythrophagocytose et recyclage du fer héminique dans les conditions normales et pathologiques ; régulation par l'hepcidine. Transfusion Clinique et Biologique. 12(2). 123–130. 37 indexed citations
13.
Beaumont, C.. (2000). [Intracellular iron metabolism].. PubMed. 184(2). 313–23; discussion 323. 3 indexed citations
14.
Milon, Béatrice & C. Beaumont. (1998). Génétique moléculaire du syndrome héréditaire cataracte-hyperferritinémie. Annales de biologie clinique. 56. 36–40. 1 indexed citations
15.
Bonneau, Dominique, et al.. (1996). Bilateral cataract and high serum ferritin: a new dominant genetic disorder?. American Journal of Ophthalmology. 121(2). 232–232. 5 indexed citations
16.
Gouya, Laurent, Jean‐Charles Deybach, J. Lamoril, et al.. (1996). Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase allele.. PubMed. 58(2). 292–9. 81 indexed citations
17.
Raja, K.B., Bénédicte Gérard, Andrew T. McKie, et al.. (1995). Duodenal expression of NF‐E2 in mouse models of altered iron metabolism. British Journal of Haematology. 91(2). 483–489. 5 indexed citations
18.
Bonneau, Dominique, et al.. (1995). Bilateral cataract and high serum ferritin: a new dominant genetic disorder?. Journal of Medical Genetics. 32(10). 778–779. 65 indexed citations
19.
Mattéi, Marie‐Geneviève, et al.. (1991). Mouse ferritin H sequences map to chromosomes 3, 6, and 19. Genomics. 9(1). 204–206. 9 indexed citations
20.
Grandchamp, Bernard, C. Picat, Felix de Rooij, et al.. (1989). A point mutation G—A in exon 12 of the porphoblllnogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria. Nucleic Acids Research. 17(16). 6637–6649. 106 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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