Jean Rey

1.5k total citations
45 papers, 1.1k citations indexed

About

Jean Rey is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics. According to data from OpenAlex, Jean Rey has authored 45 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Clinical Biochemistry, 17 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Jean Rey's work include Metabolism and Genetic Disorders (22 papers), Folate and B Vitamins Research (7 papers) and Infant Nutrition and Health (6 papers). Jean Rey is often cited by papers focused on Metabolism and Genetic Disorders (22 papers), Folate and B Vitamins Research (7 papers) and Infant Nutrition and Health (6 papers). Jean Rey collaborates with scholars based in France, Spain and United Kingdom. Jean Rey's co-authors include Françoise Rey, Véronique Abadie, Peter Burgard, J Frézal, Arnold Münnich, Stanislas Lyonnet, F.A. Rey, Catherine Caillaud, M. Berthelon and Valentino Romano and has published in prestigious journals such as Nature, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Jean Rey

45 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean Rey France	20	692	585	252	237	172	45	1.1k
F. Güttler Denmark	21	917 1.3×	681 1.2×	302 1.2×	346 1.5×	92 0.5×	67	1.2k
J. B. C. de Klerk Netherlands	21	601 0.9×	569 1.0×	174 0.7×	364 1.5×	84 0.5×	42	1.0k
N. J. Brandt Denmark	24	773 1.1×	729 1.2×	139 0.6×	149 0.6×	147 0.9×	66	1.4k
Philip P. Dembure United States	16	606 0.9×	403 0.7×	184 0.7×	200 0.8×	91 0.5×	26	1.0k
Shigeaki Miyabayashi Japan	20	708 1.0×	1.0k 1.7×	110 0.4×	131 0.6×	102 0.6×	62	1.3k
M. van Rijn Netherlands	15	994 1.4×	547 0.9×	257 1.0×	628 2.6×	114 0.7×	28	1.3k
Joy Yaplito‐Lee Australia	17	575 0.8×	653 1.1×	163 0.6×	193 0.8×	144 0.8×	29	1.1k
B. William Uhlendorf United States	20	650 0.9×	714 1.2×	575 2.3×	431 1.8×	132 0.8×	26	1.6k
Cristina Amat Di San Filippo United States	13	594 0.9×	554 0.9×	115 0.5×	178 0.8×	65 0.4×	13	858
Cecilia Teng United States	23	458 0.7×	472 0.8×	187 0.7×	136 0.6×	83 0.5×	41	1.6k

Countries citing papers authored by Jean Rey

Since Specialization

Citations

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

Fields of papers citing papers by Jean Rey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jean Rey

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

All Works

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20 of 20 papers shown

Hernell, Olle, Peter Aggett, Mary Fewtrell, Berthold Koletzko, & Jean Rey. (2018). Chapter 7. The Contributions of the ESPGHAN Committees on Nutrition to Paediatric Nutrition. Journal of Pediatric Gastroenterology and Nutrition. 66(S1). S144–S153. 1 indexed citations

Motta, Fábio, Renata Canalle, Lívio César Cunha Nunes, et al.. (2014). Association of the rs7903146 and rs12255372 polymorphisms in the TCF7L2 gene with type 2 diabetes in a population from northeastern Brazil. Genetics and Molecular Research. 13(3). 7889–7898. 18 indexed citations

Motta, Fábio, Renata Canalle, João Farias Guerreiro, et al.. (2013). Prevalence of variants that confer risk for venous thromboembolism in an elderly population of northeastern Brazil. Genetics and Molecular Research. 12(3). 3698–3707. 4 indexed citations

Almeida, Luciana O., Giovanny R. Pinto, María José Santos, et al.. (2011). Analysis of the polymorphisms XRCC1Arg194Trp and XRCC1Arg399Gln in gliomas. Genetics and Molecular Research. 10(2). 1120–1129. 23 indexed citations

Rey, Jean, Peter Aggett, & Berthold Koletzko. (2004). Thirty Years of the ESPGAN/ESPGHAN Committee on Nutrition. Journal of Pediatric Gastroenterology and Nutrition. 39(5). 474–479. 2 indexed citations

García‐Ródenas, Clara L., et al.. (2003). Potential effects of supplementation with amino acids, choline or sialic acid on cognitive development in young infants. Acta Paediatrica. 92(s442). 42–46. 31 indexed citations

Rey, Jean. (2003). Breastfeeding and cognitive development. Acta Paediatrica. 92(s442). 11–18. 45 indexed citations

Sermet‐Gaudelus, Isabelle, Michèle Garabédian, M Déchaux, et al.. (2001). Hereditary Hypophosphatemic Rickets with Hypercalciuria: Report of a New Kindred. The Nephron journals/Nephron journals. 88(1). 83–86. 11 indexed citations

Alonso, M., M. Bellò, J Lomas, et al.. (2001). Absence of mutation of the p73 gene in astrocytic neoplasms. International Journal of Oncology. 19(3). 609–12. 18 indexed citations

10.

Rey, Jean. (1998). Expression of oestrogen receptor-alpha splicing variants and oestrogen receptor-beta in endometrium of infertile patients. Molecular Human Reproduction. 4(7). 641–647. 27 indexed citations

11.

Guldberg, Per, Françoise Rey, Johannes Zschocke, et al.. (1998). A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype. The American Journal of Human Genetics. 63(1). 71–79. 278 indexed citations

12.

Galactéros, Frederic, Josiane Bardakdjian‐Michau, Frédéric Galactéros, et al.. (1996). Détection néonatale de la drépanocytose en France métropolitaine. Archives de Pédiatrie. 3(10). 1026–1031. 11 indexed citations

13.

Rey, F.A., et al.. (1996). Long-term follow up of patients with classical phenylketonuria after diet relaxation at 5 years of age. European Journal of Pediatrics. 155(S1). S39–S44. 23 indexed citations

14.

Bénit, Paule, et al.. (1994). Novel frame shift deletions of the phenylalanine hydroxylase gene in phenylketonuria. Human Molecular Genetics. 3(4). 675–676. 4 indexed citations

15.

Bénit, Paule, et al.. (1994). Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuria. Human Mutation. 4(3). 229–231. 10 indexed citations

16.

Caillaud, Catherine, Françoise Rey, Philippe Labrune, et al.. (1991). Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus. Human Genetics. 86(4). 355–358. 25 indexed citations

17.

Abadie, Véronique, Stanislas Lyonnet, Nicole Maurin, et al.. (1989). CpG dinucleotides are mutation hot spots in phenylketonuria. Genomics. 5(4). 936–939. 81 indexed citations

18.

Lyonnet, Stanislas, Catherine Caillaud, F. Rey, et al.. (1989). Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.. PubMed. 44(4). 511–7. 64 indexed citations

19.

Saudubray, J. M., F.A. Rey, H. Ogier, et al.. (1987). Intellectual and school performances in early-treated classical PKU patients. European Journal of Pediatrics. 146(1). A20–A22. 31 indexed citations

20.

Rey, Jean & J Frézal. (1966). Pathogenesis of vitamin-resistant familial hypophosphataemic rickets.. 11. 771–776. 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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