R Aquaron

1.4k total citations
64 papers, 929 citations indexed

About

R Aquaron is a scholar working on Molecular Biology, Clinical Biochemistry and Cell Biology. According to data from OpenAlex, R Aquaron has authored 64 papers receiving a total of 929 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 12 papers in Cell Biology. Recurrent topics in R Aquaron's work include Metabolism and Genetic Disorders (17 papers), melanin and skin pigmentation (12 papers) and Mitochondrial Function and Pathology (7 papers). R Aquaron is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), melanin and skin pigmentation (12 papers) and Mitochondrial Function and Pathology (7 papers). R Aquaron collaborates with scholars based in France, Spain and United States. R Aquaron's co-authors include Serge Lissitzky, J. Gergely, Marcel Rolland, Paul C. Leavis, Santiago Rodrı́guez de Córdoba, G Serratrice, Donna Durham‐Pierre, Hervé Puy, Y Nordmann and H Roux and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Analytical Biochemistry.

In The Last Decade

R Aquaron

59 papers receiving 854 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R Aquaron France	18	503	211	209	121	114	64	929
Robin Casey Canada	16	348 0.7×	181 0.9×	97 0.5×	90 0.7×	52 0.5×	27	817
George K. Summer United States	14	345 0.7×	284 1.3×	101 0.5×	48 0.4×	45 0.4×	41	800
A. K. Sen Canada	18	967 1.9×	188 0.9×	172 0.8×	53 0.4×	56 0.5×	38	1.3k
B. J. H. M. Poorthuis Netherlands	13	342 0.7×	94 0.4×	159 0.8×	84 0.7×	35 0.3×	30	915
W. Endres Germany	20	471 0.9×	381 1.8×	61 0.3×	44 0.4×	59 0.5×	73	1.0k
K. Keller Germany	22	772 1.5×	144 0.7×	85 0.4×	49 0.4×	86 0.8×	52	1.3k
V. Barash Israel	22	483 1.0×	229 1.1×	45 0.2×	49 0.4×	84 0.7×	49	1.1k
Franz‐X. Beck Germany	23	651 1.3×	55 0.3×	389 1.9×	68 0.6×	52 0.5×	39	1.1k
S.F. Contractor United Kingdom	17	227 0.5×	122 0.6×	42 0.2×	67 0.6×	47 0.4×	53	914
Chike Bellarmine Item Austria	17	348 0.7×	360 1.7×	301 1.4×	18 0.1×	46 0.4×	38	879

Countries citing papers authored by R Aquaron

Since Specialization

Citations

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

Fields of papers citing papers by R Aquaron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R Aquaron

This figure shows the co-authorship network connecting the top 25 collaborators of R Aquaron. A scholar is included among the top collaborators of R Aquaron 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 R Aquaron. R Aquaron is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Aquaron, R, Eulalie Lasseaux, Nathalie Bonello‐Palot, et al.. (2022). Co-occurrence of oculocutaneous albinism type 2 and mild sickle cell disease explained by HbS/βthal genotype in an individual from the Democratic Republic of Congo. European Journal of Medical Genetics. 65(10). 104594–104594. 1 indexed citations

Aquaron, R, et al.. (2016). Report from the 1st international workshop on oculocutaneous albinism in subsaharan Africa, Douala, Cameroon, July 24-25th 2015. Médecine et Santé Tropicales. 26(2). 118–121. 1 indexed citations

Delmont, Émilien, Sabrina Sacconi, J.-L. Bergé-Lefranc, et al.. (2008). Maladie de McArdle (glycogénose de type V) : étude clinique, biochimique et génétique d’une cohorte de cinq patients français. Revue Neurologique. 164(11). 912–916. 3 indexed citations

Aquaron, R, Jean‐Louis Bergé‐Lefranc, Jean‐François Pellissier, et al.. (2007). Molecular characterization of myophosphorylase deficiency (McArdle disease) in 34 patients from Southern France: Identification of 10 new mutations. Absence of genotype–phenotype correlation. Neuromuscular Disorders. 17(3). 235–241. 34 indexed citations

Córdoba, Santiago Rodrı́guez de, et al.. (2005). Ochronotic rheumatism in Algeria: clinical, radiological, biological and molecular studies—a case study of 14 patients in 11 families. Joint Bone Spine. 73(3). 284–292. 23 indexed citations

Aquaron, R. (2002). Type 2 oculocutaneous albinism (OCA2) in Cameroon : distribution of the 2.7-kb deletion allele of the P gene among various ethnic groups. Pigment Cell Research. 15(9). 63. 3 indexed citations

Puy, Hervé, et al.. (2000). Porphobilinogen deaminase gene in African and Afro-Caribbean ethnic groups: mutations causing acute intermittent porphyria and specific intragenic polymorphisms. Human Genetics. 107(2). 150–159. 14 indexed citations

Bernabé, Daniel Beltrán-Valero de, F. Javier Jiménez, R Aquaron, & Santiago Rodrı́guez de Córdoba. (1999). Analysis of Alkaptonuria (AKU) Mutations and Polymorphisms Reveals that the CCC Sequence Motif Is a Mutational Hot Spot in the Homogentisate 1,2 Dioxygenase Gene (HGO). The American Journal of Human Genetics. 64(5). 1316–1322. 22 indexed citations

Bernabé, Daniel Beltrán-Valero de, Begoña Granadino, Berardino Porfirio, et al.. (1998). Mutation and Polymorphism Analysis of the Human Homogentisate 1,2-Dioxygenase Gene in Alkaptonuria Patients. The American Journal of Human Genetics. 62(4). 776–784. 57 indexed citations

10.

Gouya, Laurent, X. Schneider‐Yin, Hervé Puy, et al.. (1998). Systematic Analysis of Molecular Defects in the Ferrochelatase Gene from Patients with Erythropoietic Protoporphyria. The American Journal of Human Genetics. 62(6). 1341–1352. 97 indexed citations

11.

Durham‐Pierre, Donna, et al.. (1997). Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene. Human Genetics. 100(5-6). 651–656. 27 indexed citations

12.

Puy, Hervé, et al.. (1997). Acute intermittent porphyria: rapid molecular diagnosis.. PubMed. 43(1). 37–45. 14 indexed citations

13.

Durham‐Pierre, Donna, John M. Gardner, Yoshimichi Nakatsu, et al.. (1994). African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism. Nature Genetics. 7(2). 176–179. 92 indexed citations

14.

Aquaron, R, et al.. (1993). Endemic goiter in Morocco (Skoura-Toundoute areas in the high atlas). Journal of Endocrinological Investigation. 16(1). 9–14. 18 indexed citations

15.

Aquaron, R. (1990). Oculocutaneous albinism in Cameroon a 15-year follow-up study. Ophthalmic Paediatrics and Genetics. 11(4). 255–263. 23 indexed citations

16.

Aquaron, R, et al.. (1978). Caroténoides et vitamine A sériques au Cameroun chez des sujets mélanodermes et albinos. International Journal for Vitamin and Nutrition Research. 48(2). 105–112. 1 indexed citations

17.

Aquaron, R, et al.. (1977). Biological study of endemic goitre in Bamoun (Cameroun).. 24(3). 183–190.

18.

Jaquet, P, et al.. (1972). Effets de l'administration de TRH synthetique chez le sujet normal.. Annales d Endocrinologie. 33(4). 3 indexed citations

19.

Roux, Hélène, et al.. (1972). [Serum basic amino acids in rheumatoid arthritis].. PubMed. 39(11). 677–80. 1 indexed citations

20.

Busson, F., et al.. (1962). Chemical study of millets and sorghums. Effect of variety and ecology on the amino acid composition of Pennisetum millet and sorghum.. 17. 752–764. 1 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.

Explore authors with similar magnitude of impact