France Léveillé

505 total citations
6 papers, 297 citations indexed

About

France Léveillé is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Genetics. According to data from OpenAlex, France Léveillé has authored 6 papers receiving a total of 297 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Public Health, Environmental and Occupational Health and 2 papers in Genetics. Recurrent topics in France Léveillé's work include DNA Repair Mechanisms (4 papers), Acute Lymphoblastic Leukemia research (2 papers) and Melanoma and MAPK Pathways (1 paper). France Léveillé is often cited by papers focused on DNA Repair Mechanisms (4 papers), Acute Lymphoblastic Leukemia research (2 papers) and Melanoma and MAPK Pathways (1 paper). France Léveillé collaborates with scholars based in United States, Netherlands and Canada. France Léveillé's co-authors include Hans Joenje, Johan P. de Winter, Martin A. Rooimans, Fré Arwert, Quinten Waisfisz, Jûrgen Steltenpool, Ilja Demuth, Jeff Lightfoot, Kenshi Komatsu and Carola G.M. van Berkel and has published in prestigious journals such as Journal of Biological Chemistry, The American Journal of Human Genetics and Human Mutation.

In The Last Decade

France Léveillé

5 papers receiving 292 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
France Léveillé United States	5	277	99	70	40	34	6	297
Inês Pinheiro Germany	6	429 1.5×	86 0.9×	86 1.2×	37 0.9×	27 0.8×	6	492
Bob Plumb United Kingdom	3	256 0.9×	69 0.7×	164 2.3×	49 1.2×	25 0.7×	3	330
Chantal Stoepker Netherlands	6	312 1.1×	83 0.8×	107 1.5×	34 0.8×	36 1.1×	7	358
Valentina Quarantotti United States	10	362 1.3×	62 0.6×	124 1.8×	32 0.8×	79 2.3×	11	418
Sandra Barral United States	3	306 1.1×	117 1.2×	116 1.7×	30 0.8×	14 0.4×	3	369
Julianne Smith United States	8	387 1.4×	77 0.8×	120 1.7×	30 0.8×	25 0.7×	8	429
Francesco Cucco Italy	9	274 1.0×	29 0.3×	95 1.4×	39 1.0×	34 1.0×	15	343
Evert-Jan Uringa Netherlands	6	287 1.0×	38 0.4×	57 0.8×	35 0.9×	64 1.9×	8	379
Ahlem Amouri Tunisia	9	169 0.6×	51 0.5×	127 1.8×	21 0.5×	13 0.4×	27	257
Katja Kratz Switzerland	7	410 1.5×	84 0.8×	55 0.8×	42 1.1×	43 1.3×	8	460

Countries citing papers authored by France Léveillé

Since Specialization

Citations

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

Fields of papers citing papers by France Léveillé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of France Léveillé

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

All Works

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6 of 6 papers shown

1.

Laramée, Louise, Marieke Rozendaal, Henrique Bittencourt, et al.. (2024). The impact of comparative genomic hybridization/single‐nucleotide polymorphism microarray in risk stratification of pediatric acute lymphoblastic leukemia. Pediatric Blood & Cancer. 71(9). e31129–e31129.

2.

Vairy, Stéphanie, Loubna Jouan, Mélanie Bilodeau, et al.. (2018). Novel PDE10A-BRAF Fusion With Concomitant NF1 Mutation Identified in an Undifferentiated Sarcoma of Infancy With Sustained Response to Trametinib. JCO Precision Oncology. 2(2). 1–13. 5 indexed citations

3.

Ameziane, Najim, Abdellatif Errami, France Léveillé, et al.. (2007). Genetic subtyping of Fanconi anemia by comprehensive mutation screening. Human Mutation. 29(1). 159–166. 48 indexed citations

4.

Léveillé, France, Miriam Ferrer, Annette L. Medhurst, et al.. (2006). The nuclear accumulation of the Fanconi anemia protein FANCE depends on FANCC. DNA repair. 5(5). 556–565. 20 indexed citations

5.

Léveillé, France, Eric Blom, Annette L. Medhurst, et al.. (2004). The Fanconi Anemia Gene Product FANCF Is a Flexible Adaptor Protein. Journal of Biological Chemistry. 279(38). 39421–39430. 49 indexed citations

6.

Winter, Johan P. de, France Léveillé, Carola G.M. van Berkel, et al.. (2000). Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene. The American Journal of Human Genetics. 67(5). 1306–1308. 175 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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