Fabienne Danton

1.1k total citations
5 papers, 612 citations indexed

About

Fabienne Danton is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Fabienne Danton has authored 5 papers receiving a total of 612 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 3 papers in Genetics. Recurrent topics in Fabienne Danton's work include Genetic Syndromes and Imprinting (3 papers), Epigenetics and DNA Methylation (3 papers) and Prenatal Screening and Diagnostics (3 papers). Fabienne Danton is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Epigenetics and DNA Methylation (3 papers) and Prenatal Screening and Diagnostics (3 papers). Fabienne Danton collaborates with scholars based in France, Australia and Belgium. Fabienne Danton's co-authors include Christine Gicquel, Virginie Steunou, Sylvie Rossignol, Yves Le Bouc, Irène Netchine, Nathalie Thibaud, Sylvie Cabrol, Martine Le Merrer, Lydie Bürglen and Anne‐Marie Bertrand and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Human Mutation.

In The Last Decade

Fabienne Danton

5 papers receiving 589 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fabienne Danton France 4 537 519 394 38 22 5 612
Nathalie Thibaud France 9 869 1.6× 813 1.6× 574 1.5× 76 2.0× 25 1.1× 10 969
Lukas Soellner Germany 12 480 0.9× 356 0.7× 348 0.9× 68 1.8× 24 1.1× 22 609
Lucy Bowden United Kingdom 6 440 0.8× 562 1.1× 273 0.7× 20 0.5× 11 0.5× 9 647
Marie Watkins United Kingdom 5 286 0.5× 320 0.6× 181 0.5× 8 0.2× 29 1.3× 6 377
Álex Martín-Trujillo Spain 10 251 0.5× 313 0.6× 202 0.5× 5 0.1× 38 1.7× 11 392
R Gracia Spain 7 250 0.5× 234 0.5× 63 0.2× 129 3.4× 9 0.4× 8 353
Oluwakemi Lokulo‐Sodipe United Kingdom 7 263 0.5× 163 0.3× 111 0.3× 57 1.5× 3 0.1× 12 312
Tomoko Fuke Japan 10 245 0.5× 202 0.4× 141 0.4× 15 0.4× 10 0.5× 15 282
A. Nyström Sweden 7 237 0.4× 268 0.5× 163 0.4× 38 1.0× 3 0.1× 8 345
Susanne Fricke‐Otto Germany 10 174 0.3× 194 0.4× 83 0.2× 115 3.0× 3 0.1× 15 299

Countries citing papers authored by Fabienne Danton

Since Specialization
Citations

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

Fields of papers citing papers by Fabienne Danton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabienne Danton

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

All Works

5 of 5 papers shown
1.
Cunat, Séverine, et al.. (2019). PF500 A NEW FTL GENE MUTATION RESPONSIBLE FOR HYPOFERRITINEMIA WITHOUT IRON DEFICIENCY. HemaSphere. 3(S1). 203–203. 1 indexed citations
2.
Alame, Mélissa, et al.. (2016). Implementation of a Reliable Next-Generation Sequencing Strategy for Molecular Diagnosis of Dystrophinopathies. Journal of Molecular Diagnostics. 18(5). 731–740. 15 indexed citations
3.
4.
5.
Gicquel, Christine, Sylvie Rossignol, Sylvie Cabrol, et al.. (2005). Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nature Genetics. 37(9). 1003–1007. 379 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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2026