F Miélot

972 total citations
37 papers, 674 citations indexed

About

F Miélot is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, F Miélot has authored 37 papers receiving a total of 674 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Hematology, 12 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in F Miélot's work include Acute Myeloid Leukemia Research (11 papers), Hemoglobinopathies and Related Disorders (8 papers) and Erythrocyte Function and Pathophysiology (6 papers). F Miélot is often cited by papers focused on Acute Myeloid Leukemia Research (11 papers), Hemoglobinopathies and Related Disorders (8 papers) and Erythrocyte Function and Pathophysiology (6 papers). F Miélot collaborates with scholars based in France, Switzerland and United Kingdom. F Miélot's co-authors include Gil Tchernia, Brigitte Bader‐Meunier, J.P. Dommergues, Narla Mohandas, Frédéric Gauthier, Thérèse Cynober, J. M. Lavergne, Stanislas Lyonnet, Jean La Fontaine and Carol Thomas and has published in prestigious journals such as The Lancet, Blood and The Journal of Pediatrics.

In The Last Decade

F Miélot

36 papers receiving 653 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F Miélot France 13 263 165 163 154 113 37 674
Gavivann Veerakul Thailand 14 238 0.9× 163 1.0× 177 1.1× 128 0.8× 68 0.6× 34 744
Kleebsabai Sanpakit Thailand 13 256 1.0× 220 1.3× 101 0.6× 70 0.5× 59 0.5× 57 587
Judith Behrens United Kingdom 10 752 2.9× 219 1.3× 468 2.9× 175 1.1× 117 1.0× 18 1.1k
G. W. Marsh United Kingdom 14 247 0.9× 378 2.3× 59 0.4× 67 0.4× 103 0.9× 25 673
Lyubica Dabich United States 15 278 1.1× 111 0.7× 102 0.6× 34 0.2× 137 1.2× 29 767
Man Updesh Singh Sachdeva India 13 245 0.9× 185 1.1× 107 0.7× 93 0.6× 46 0.4× 118 648
Kyung‐Nam Koh South Korea 14 297 1.1× 91 0.6× 60 0.4× 90 0.6× 95 0.8× 89 660
Axel A. Fauser Germany 15 643 2.4× 103 0.6× 181 1.1× 53 0.3× 53 0.5× 27 978
Rawle M. McIntosh United States 15 127 0.5× 125 0.8× 97 0.6× 70 0.5× 69 0.6× 30 711
Hagit Miskin Israel 12 195 0.7× 190 1.2× 48 0.3× 66 0.4× 77 0.7× 24 455

Countries citing papers authored by F Miélot

Since Specialization
Citations

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

Fields of papers citing papers by F Miélot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F Miélot

This figure shows the co-authorship network connecting the top 25 collaborators of F Miélot. A scholar is included among the top collaborators of F Miélot 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 F Miélot. F Miélot 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.
Parez, N., Marc Dommergues, V. Zupan, et al.. (2000). Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha‐interferon therapy. British Journal of Haematology. 110(2). 420–423. 42 indexed citations
2.
Miélot, F. (1999). CHILDHOOD MYELODYSPLASTIC SYNDROMES. Pediatric Hematology and Oncology. 16(4). 283–284. 2 indexed citations
3.
Schischmanoff, Pierre Olivier, F Miélot, L Leclerc, et al.. (1999). Southeast asian ovalocytosis in white persons. Hemoglobin. 23(1). 47–56. 6 indexed citations
4.
Chiron, Marielle, Thérèse Cynober, F Miélot, Gil Tchernia, & Laure Croisille. (1999). The GEN.S: a fortuitous finding of a routine screening test for hereditary spherocytosis. PubMed. 41(3). 113–116. 21 indexed citations
5.
Miélot, F, Jacqueline Buisine, Éliane Duchayne, et al.. (1998). Myelodysplastic Syndromes In Childhood: Is the FAB Classification Relevant?Report of 81 Children From a French Multicentre Study. Leukemia & lymphoma. 28(5-6). 531–540. 9 indexed citations
6.
Cynober, Thérèse, Brigitte Bader‐Meunier, Frédéric Gauthier, et al.. (1997). Sphérocytose héréditaire. Évolution et intérêt de la splénectomie subtotale. Archives de Pédiatrie. 4(6). 515–520. 7 indexed citations
7.
Bader‐Meunier, Brigitte, Gil Tchernia, Jacqueline Buisine, et al.. (1997). Syndromes myélodysplasiques de l'enfant. Archives de Pédiatrie. 4(6). 561–567. 1 indexed citations
8.
Devictor, Denis, et al.. (1996). Early Pre-B Acute Lymphoblastic Leukemia Presenting as Fulminant Liver Failure. Journal of Pediatric Gastroenterology and Nutrition. 22(1). 103–106. 19 indexed citations
9.
Tchernia, Gil, et al.. (1996). Myelodysplasia in childhood may be a polyclonal disease. PubMed. 38(4). 325–330. 4 indexed citations
10.
Bader‐Meunier, Brigitte, F Miélot, Laure Croisille, et al.. (1994). Refractory anaemia and mitochondrial cytopathy in childhood. British Journal of Haematology. 87(2). 381–385. 38 indexed citations
11.
Miélot, F, et al.. (1993). Acute lymphoblastic leukemia with trisomy 21 constitutional mosaicism. Cancer Genetics and Cytogenetics. 66(1). 70–72. 2 indexed citations
12.
Tchernia, Gil, Frédéric Gauthier, F Miélot, et al.. (1993). Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis. Blood. 81(8). 2014–2020. 54 indexed citations
13.
Bader‐Meunier, Brigitte, Franck Thollot, F Miélot, et al.. (1992). [Regressive myelodysplastic syndromes in children. Committee on Childhood Myelodysplasia of the Society of Pediatric Hematology and Immunology].. PubMed. 49(10). 883–6. 3 indexed citations
14.
Boué, François, Gil Tchernia, G. Tertian, et al.. (1991). Un syndrome d'activation histio-monocytaire peut révéler une maladie lupique. À propos de trois observations. La Revue de Médecine Interne. 12(3). S43–S43. 1 indexed citations
15.
Coulombel, Laure, F. Morinet, F Miélot, et al.. (1989). PARVOVIRUS INFECTION, LEUKAEMIA, AND IMMUNODEFICIENCY. The Lancet. 333(8629). 101–102. 52 indexed citations
16.
Tertian, G., et al.. (1989). Low-dose arabinosyl cytosine therapy of AML may be effective after failure of high or conventional doses.. PubMed. 31(4). 311–3. 3 indexed citations
17.
Coulombel, Laure, Florence Veber, Christine Le Roy, et al.. (1988). Granulopoietic differentiation in long‐term bone marrow cultures from children with congenital neutropenia. American Journal of Hematology. 27(2). 93–98. 10 indexed citations
18.
Miélot, F, et al.. (1987). [Acquired deficiencies in antithrombin III and C protein during treatment with L-asparaginase].. PubMed. 44(3). 161–5.
19.
Tchernia, Gil, F Miélot, Laure Coulombel, & Narla Mohandas. (1981). Characterization of circulating erythroid progenitor cells in human newborn blood.. PubMed. 97(3). 322–31. 12 indexed citations
20.
Lortholary, P, et al.. (1967). [The cytologic development of acute leukemias treated with rubidomycin].. PubMed. 15(19). 945–7. 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.

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