Mélanie Léoné

1.7k total citations
7 papers, 188 citations indexed

About

Mélanie Léoné is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Mélanie Léoné has authored 7 papers receiving a total of 188 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Mélanie Léoné's work include Genomic variations and chromosomal abnormalities (4 papers), BRCA gene mutations in cancer (3 papers) and CRISPR and Genetic Engineering (2 papers). Mélanie Léoné is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), BRCA gene mutations in cancer (3 papers) and CRISPR and Genetic Engineering (2 papers). Mélanie Léoné collaborates with scholars based in France, United States and Spain. Mélanie Léoné's co-authors include Olga M. Sinilnikova, Gilbert Lenoir, Monique Buisson, Rebeca Font, Alain Calender, P. Viladiu, Sylvie Mazoyer, L. Vilardell, Olga Anczuków and F. Xavier Bosch and has published in prestigious journals such as Nucleic Acids Research, Clinical Cancer Research and International Journal of Cancer.

In The Last Decade

Mélanie Léoné

7 papers receiving 184 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mélanie Léoné France	4	120	83	72	37	37	7	188
Saundra Buys United States	3	109 0.9×	83 1.0×	80 1.1×	46 1.2×	48 1.3×	3	192
Despoina Kalfakakou Greece	7	111 0.9×	85 1.0×	42 0.6×	50 1.4×	44 1.2×	12	182
Baptiste Brault France	4	183 1.5×	133 1.6×	116 1.6×	71 1.9×	62 1.7×	5	271
Rebecca Mathew Qatar	8	124 1.0×	125 1.5×	53 0.7×	51 1.4×	35 0.9×	17	245
Angélina Legros France	5	189 1.6×	147 1.8×	124 1.7×	73 2.0×	62 1.7×	9	285
Mara Colombo Italy	10	118 1.0×	156 1.9×	50 0.7×	47 1.3×	36 1.0×	15	250
Tadeusz Dębniak Poland	9	160 1.3×	111 1.3×	69 1.0×	80 2.2×	67 1.8×	14	246
Bryce A. Seifert United States	7	140 1.2×	90 1.1×	82 1.1×	67 1.8×	40 1.1×	15	229
Valentina Zampiga Italy	7	94 0.8×	77 0.9×	29 0.4×	42 1.1×	31 0.8×	20	153
Wendy A. van Zelst-Stams Netherlands	5	53 0.4×	87 1.0×	58 0.8×	72 1.9×	45 1.2×	5	168

Countries citing papers authored by Mélanie Léoné

Since Specialization

Citations

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

Fields of papers citing papers by Mélanie Léoné

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mélanie Léoné

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

Bouras, Ahmed, Mélanie Léoné, Adrien Buisson, et al.. (2023). Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort. Cancers. 15(13). 3420–3420. 3 indexed citations

Bouras, Ahmed, Mélanie Léoné, Valérie Bonadona, et al.. (2021). Identification and Characterization of New Alu Element Insertion in the BRCA1 Exon 14 Associated with Hereditary Breast and Ovarian Cancer. Genes. 12(11). 1736–1736. 4 indexed citations

Léoné, Mélanie, et al.. (2015). Occurrence of a non deleterious gene conversion event in the BRCA1 gene. Genes Chromosomes and Cancer. 54(10). 646–652. 1 indexed citations

Lesecque, Yann, Monique Buisson, Mélanie Léoné, et al.. (2014). Estimation of theRNU2macrosatellite mutation rate byBRCA1mutation tracing. Nucleic Acids Research. 42(14). 9121–9130. 3 indexed citations

Anczuków, Olga, Monique Buisson, Mélanie Léoné, et al.. (2012). BRCA2 Deep Intronic Mutation Causing Activation of a Cryptic Exon: Opening toward a New Preventive Therapeutic Strategy. Clinical Cancer Research. 18(18). 4903–4909. 52 indexed citations

Bonadona, Valérie, Olga M. Sinilnikova, Antonis C. Antoniou, et al.. (2005). Contribution of BRCA1 and BRCA2 germ‐line mutations to the incidence of breast cancer in young women: Results from a prospective population‐based study in France. Genes Chromosomes and Cancer. 43(4). 404–413. 35 indexed citations

Sanjosé, Sílvia de, Mélanie Léoné, Á. Izquierdo, et al.. (2003). Prevalence of BRCA1 and BRCA2 germline mutations in young breast cancer patients: A population‐based study. International Journal of Cancer. 106(4). 588–593. 90 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.

Explore authors with similar magnitude of impact