Frédéric Leprêtre

2.8k total citations · 1 hit paper
47 papers, 1.8k citations indexed

About

Frédéric Leprêtre is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Frédéric Leprêtre has authored 47 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 12 papers in Genetics and 7 papers in Immunology. Recurrent topics in Frédéric Leprêtre's work include Metabolism, Diabetes, and Cancer (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chronic Lymphocytic Leukemia Research (4 papers). Frédéric Leprêtre is often cited by papers focused on Metabolism, Diabetes, and Cancer (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chronic Lymphocytic Leukemia Research (4 papers). Frédéric Leprêtre collaborates with scholars based in France, United Kingdom and United States. Frédéric Leprêtre's co-authors include Philippe Froguel, Christian Dina, Nathalie Vionnet, Cécile Lecœur, Emmanuelle Durand, S. Dupont, Francis Vasseur, El Habib Hani, Sophie Gallina and Stephan Francke and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Frédéric Leprêtre

46 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24

2000 576 citations Nathalie Vionnet, El Habib Hani et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Frédéric Leprêtre France	21	690	473	460	405	244	47	1.8k
Shufang Wu China	27	744 1.1×	208 0.4×	300 0.7×	152 0.4×	178 0.7×	66	1.8k
Helen Imrie United Kingdom	22	376 0.5×	235 0.5×	367 0.8×	446 1.1×	165 0.7×	39	1.6k
Takuya Tomaru Japan	18	558 0.8×	431 0.9×	548 1.2×	122 0.3×	215 0.9×	51	1.4k
Miina K. Öhman United States	20	520 0.8×	431 0.9×	412 0.9×	272 0.7×	459 1.9×	34	1.7k
Luisella Alberti Italy	26	997 1.4×	343 0.7×	192 0.4×	275 0.7×	284 1.2×	41	2.1k
Yan Ge China	26	805 1.2×	190 0.4×	167 0.4×	191 0.5×	233 1.0×	88	1.9k
Genzo Iguchi Japan	28	501 0.7×	657 1.4×	467 1.0×	200 0.5×	337 1.4×	104	2.3k
Junji Fujikura Japan	25	1.0k 1.5×	208 0.4×	440 1.0×	255 0.6×	501 2.1×	53	1.9k
Mads Kjølby Denmark	21	660 1.0×	163 0.3×	248 0.5×	187 0.5×	354 1.5×	46	1.8k
David M. Flavell United Kingdom	18	848 1.2×	121 0.3×	336 0.7×	328 0.8×	134 0.5×	25	1.5k

Countries citing papers authored by Frédéric Leprêtre

Since Specialization

Citations

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

Fields of papers citing papers by Frédéric Leprêtre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frédéric Leprêtre

This figure shows the co-authorship network connecting the top 25 collaborators of Frédéric Leprêtre. A scholar is included among the top collaborators of Frédéric Leprêtre 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 Frédéric Leprêtre. Frédéric Leprêtre 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

Bray, Fabrice, Alain Lescoat, Martin Figeac, et al.. (2025). Immunoglobulins G from Patients with Systemic Sclerosis Modify the Molecular Signatures of Endothelial Cells. RMD Open. 11(1). e004290–e004290. 3 indexed citations

Djouina, Madjid, Christophe Waxin, Frédéric Leprêtre, et al.. (2022). Gene/environment interaction in the susceptibility of Crohn's disease patients to aluminum. The Science of The Total Environment. 850. 158017–158017. 11 indexed citations

Leprêtre, Frédéric, Shéhérazade Sebda, Céline Villenet, et al.. (2022). Detection of residual and chemoresistant leukemic cells in an immune-competent mouse model of acute myeloid leukemia: Potential for unravelling their interactions with immunity. PLoS ONE. 17(4). e0267508–e0267508. 2 indexed citations

Leprêtre, Frédéric, Martin Figeac, Thomas Guerrier, et al.. (2022). A Spontaneous Model of Experimental Autoimmune Encephalomyelitis Provides Evidence of MOG-Specific B Cell Recruitment and Clonal Expansion. Frontiers in Immunology. 13. 755900–755900. 10 indexed citations

Jendoubi, Manel, Thomas Guerrier, Silvia Speca, et al.. (2022). Simple gene signature to assess murine fibroblast polarization. Scientific Reports. 12(1). 11748–11748. 4 indexed citations

Al‐Thuwaini, Tahreer M., et al.. (2020). Co-inherited novel SNPs of the LIPE gene associated with increased carcass dressing and decreased fat-tail weight in Awassi breed. Tropical Animal Health and Production. 52(6). 3631–3638. 9 indexed citations

Leprêtre, Frédéric, Fabienne Escande, Zoulika Kherrouche, et al.. (2018). Optimization of Routine Testing for MET Exon 14 Splice Site Mutations in NSCLC Patients. Journal of Thoracic Oncology. 13(12). 1873–1883. 27 indexed citations

Maillet, Denis, Frédéric Leprêtre, Sylvie Isaac, et al.. (2016). Genomic copy number alterations in 33 malignant peritoneal mesothelioma analyzed by comparative genomic hybridization array. Human Pathology. 55. 72–82. 22 indexed citations

Leblay, Noémie, Frédéric Leprêtre, Nolwenn Le Stang, et al.. (2016). BAP1 Is Altered by Copy Number Loss, Mutation, and/or Loss of Protein Expression in More Than 70% of Malignant Peritoneal Mesotheliomas. Journal of Thoracic Oncology. 12(4). 724–733. 59 indexed citations

10.

Poulain, Stéphanie, Christophe Roumier, Martin Figeac, et al.. (2015). Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia. Clinical Cancer Research. 22(6). 1480–1488. 82 indexed citations

11.

Kuranda, Klaudia, Céline Berthon, Frédéric Leprêtre, et al.. (2011). Expression of CD34 in hematopoietic cancer cell lines reflects tightly regulated stem/progenitor‐like state. Journal of Cellular Biochemistry. 112(5). 1277–1285. 13 indexed citations

12.

Leprêtre, Frédéric, Sélim Corm, Franck E. Nicolini, et al.. (2010). Genomic characterization of Imatinib resistance in CD34+ cell populations from chronic myeloid leukaemia patients. Leukemia Research. 35(4). 448–458. 10 indexed citations

13.

Mutez, Eugénie, Frédéric Leprêtre, Vincent Mouroux, et al.. (2010). Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation. Neurobiology of Aging. 32(10). 1839–1848. 78 indexed citations

14.

Andrieux, Joris, Steven Richebourg, Bénédicte Duban‐Bedu, et al.. (2008). Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delay. European Journal of Medical Genetics. 51(4). 373–381. 11 indexed citations

15.

Andrieux, Joris, Frédéric Leprêtre, Jean‐Marie Cuisset, et al.. (2008). Deletion 18q21.2q21.32 involving TCF4 in a boy diagnosed by CGH-array. European Journal of Medical Genetics. 51(2). 172–177. 22 indexed citations

16.

Leprêtre, Frédéric, Francis Vasseur, Martine Vaxillaire, et al.. (2004). A CD36 nonsense mutation associated with insulin resistance and familial type 2 diabetes. Human Mutation. 24(1). 104–104. 56 indexed citations

17.

Leprêtre, Frédéric, et al.. (2003). Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardation. Cytogenetic and Genome Research. 101(2). 124–129. 15 indexed citations

18.

Leprêtre, Frédéric, et al.. (2001). Molecular and cytogenetic characterisation of a small interstitial <i>de novo</i> 20p13→p12.3 deletion in a patient with severe growth deficit. Cytogenetic and Genome Research. 94(3-4). 142–146. 4 indexed citations

19.

Vionnet, Nathalie, El Habib Hani, S. Dupont, et al.. (2000). Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24. The American Journal of Human Genetics. 67(6). 1470–1480. 576 indexed citations breakdown →

20.

Leprêtre, Frédéric, et al.. (1999). Type 2 diabetes mellitus: association study of five candidate genes in an Indian population of Guadeloupe, genetic contribution of FABP2 polymorphism.. PubMed. 25(2). 150–6. 52 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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