G. Mérault

490 total citations
22 papers, 366 citations indexed

About

G. Mérault is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, G. Mérault has authored 22 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 8 papers in Hematology and 6 papers in Molecular Biology. Recurrent topics in G. Mérault's work include Hemoglobinopathies and Related Disorders (13 papers), Iron Metabolism and Disorders (8 papers) and Hemoglobin structure and function (5 papers). G. Mérault is often cited by papers focused on Hemoglobinopathies and Related Disorders (13 papers), Iron Metabolism and Disorders (8 papers) and Hemoglobin structure and function (5 papers). G. Mérault collaborates with scholars based in France, Guadeloupe and Jamaica. G. Mérault's co-authors include C Berchel, Frédéric Galactéros, Bernard Labouesse, Julie Labouesse, Pierre‐Vincent Graves, J. Rosa, Y. Blouquit, Claire Poyart, Marc Romana and C. Saint‐Martin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and FEBS Letters.

In The Last Decade

G. Mérault

22 papers receiving 344 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G. Mérault France 12 226 152 123 48 48 22 366
G Fioretti Italy 14 188 0.8× 133 0.9× 131 1.1× 73 1.5× 41 0.9× 28 402
C Altay United States 12 476 2.1× 375 2.5× 121 1.0× 113 2.4× 23 0.5× 29 561
G. V. Sciarratta Italy 11 292 1.3× 193 1.3× 108 0.9× 88 1.8× 40 0.8× 27 387
Piera Samperi Italy 12 243 1.1× 241 1.6× 25 0.2× 70 1.5× 9 0.2× 36 353
Konstantinos Varvagiannis Greece 5 309 1.4× 243 1.6× 75 0.6× 96 2.0× 14 0.3× 11 373
T. H. J. Huisman United States 8 349 1.5× 269 1.8× 32 0.3× 89 1.9× 19 0.4× 14 381
Jean Atwater United States 12 336 1.5× 249 1.6× 37 0.3× 88 1.8× 56 1.2× 20 393
John Brewin United Kingdom 11 176 0.8× 150 1.0× 61 0.5× 36 0.8× 14 0.3× 33 307
WA Schroeder United States 5 345 1.5× 283 1.9× 100 0.8× 124 2.6× 6 0.1× 8 419
JG Mears United States 8 393 1.7× 361 2.4× 64 0.5× 40 0.8× 18 0.4× 13 470

Countries citing papers authored by G. Mérault

Since Specialization
Citations

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

Fields of papers citing papers by G. Mérault

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Mérault

This figure shows the co-authorship network connecting the top 25 collaborators of G. Mérault. A scholar is included among the top collaborators of G. Mérault 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 G. Mérault. G. Mérault 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.
Mukisi-Mukaza, Martin, et al.. (2000). Prevalence, Clinical Features, and Risk Factors of Osteonecrosis of the Femoral Head Among Adults With Sickle Cell Disease. Orthopedics. 23(4). 357–363. 44 indexed citations
2.
Romana, Marc, et al.. (2000). Diverse Genetic Mechanisms Operate to Generate Atypical βsHaplotypes in the Population of Guadeloupe. Hemoglobin. 24(2). 77–87. 13 indexed citations
3.
Mérault, G., et al.. (1999). Morphological features of the human umbilical vein in normal, sickle cell trait, and sickle cell disease pregnancies. Human Pathology. 30(1). 13–20. 12 indexed citations
4.
El‐Baz, Ayman, et al.. (1998). Prevalence of fragile‐X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies. Journal of Intellectual Disability Research. 42(1). 81–89. 13 indexed citations
5.
Préhu, Claude, G. Mérault, Françoise Roudot‐Thoraval, et al.. (1998). Genetic and hematological studies in a group of 114 adult patients with SC sickle cell disease. American Journal of Hematology. 59(1). 15–21. 11 indexed citations
6.
Romana, Marc, et al.. (1998). Spectrum of β‐Thalassemia Mutations in Guadeloupe (French West Indies) and Interactions with Other Hemoglobinopathies. Annals of the New York Academy of Sciences. 850(1). 423–425. 1 indexed citations
7.
Romana, Marc, et al.. (1997). Sickle cell disorder, β-globin gene cluster haplotypes and α-thalassemia in neonates and adults from Guadeloupe. American Journal of Hematology. 55(1). 24–27. 23 indexed citations
8.
Romana, Marc, et al.. (1997). Hemoglobin Sickle-Lepore: An Unusual Case of Sickle Cell Disease. Acta Haematologica. 98(3). 170–171. 2 indexed citations
9.
Romana, Marc, et al.. (1997). Efficiency of prenatal counselling for sickle cell disease in Guadeloupe.. PubMed. 8(1). 25–32. 7 indexed citations
10.
Romana, Marc, et al.. (1996). Molecular characterization of β‐thalassemia mutations in Guadeloupe. American Journal of Hematology. 53(4). 228–233. 21 indexed citations
11.
Berchel, C, et al.. (1996). βsHaplotypes, α-Globin Gene Status, and Hematological Data of Sickle Cell Disease Patients in Guadeloupe (F.W.I.). Hemoglobin. 20(1). 63–74. 22 indexed citations
12.
Hardy‐Dessources, Marie‐Dominique, et al.. (1993). Characterization of phosphoinositide kinases in normal and sickle anaemia red cells. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1181(1). 90–96. 3 indexed citations
13.
Zohoun, I., et al.. (1992). [Health policies and sickle cell disease].. PubMed. 42(15). 1873–7. 2 indexed citations
14.
Mérault, G., et al.. (1990). Hemoglobin Nevers [αβ2 130(H8)TYR↣R]; A New Silent Variant Found in France. Hemoglobin. 14(1). 103–107. 4 indexed citations
15.
Mérault, G., et al.. (1989). Hemoglobin Hekinan [α227(B8)Glu→Aspβ2] Detected in Guyana. Hemoglobin. 13(4). 397–402. 9 indexed citations
16.
Mérault, G., J. Garin, Claire Poyart, et al.. (1986). Hemoglobin La Desiradb αA2β2129 (H7) Ala → Val: A New Unstable Hemoglobin. Hemoglobin. 10(6). 593–605. 15 indexed citations
17.
Mérault, G., C. Saint‐Martin, N. Arous, et al.. (1985). Hemoglobin Roseau‐Pointe a Pitre α2β290 (F6) Glu → Gly: a new hemoglobin variant with slight instability and low oxygen affinity. FEBS Letters. 184(1). 10–13. 10 indexed citations
18.
Mazat, Jean‐Pierre, et al.. (1982). Kinetic Anticooperativity in Pre‐Steady‐State Formation of Tryptophanyl Adenylate by Tryptophanyl‐tRNA Synthetase from Beef Pancreas. European Journal of Biochemistry. 128(2-3). 389–398. 18 indexed citations
19.
Mérault, G., Pierre‐Vincent Graves, Bernard Labouesse, & Julie Labouesse. (1978). Influence of Magnesium on the Steady‐State‐Derived Order of Substrate Addition and Product Release in tRNA Trp Aminoacylation by Beef Pancreas Tryptophan: tRNA Ligase. European Journal of Biochemistry. 87(3). 541–550. 34 indexed citations
20.
Dorizzi, Mireille, G. Mérault, Michel Fournier, et al.. (1977). Aminoacylation of tRNATrpfrom beef liver, yeast and E. coli by beef pancreas tryptopban-tRNA ligase. Stoichiometry of tRNATrpbinding. Nucleic Acids Research. 4(1). 31–42. 19 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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