Aurélie Toussaint

469 total citations
5 papers, 149 citations indexed

About

Aurélie Toussaint is a scholar working on Cell Biology, Genetics and Surgery. According to data from OpenAlex, Aurélie Toussaint has authored 5 papers receiving a total of 149 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Cell Biology, 2 papers in Genetics and 1 paper in Surgery. Recurrent topics in Aurélie Toussaint's work include Vitamin D Research Studies (1 paper), Genomics and Rare Diseases (1 paper) and Digestive system and related health (1 paper). Aurélie Toussaint is often cited by papers focused on Vitamin D Research Studies (1 paper), Genomics and Rare Diseases (1 paper) and Digestive system and related health (1 paper). Aurélie Toussaint collaborates with scholars based in France, Tunisia and Belgium. Aurélie Toussaint's co-authors include Anne Houdusse, Fiona Francis, Caroline Elie, Nadia Bahi‐Buisson, Isabelle Souville, Carolyn A. Moores, Pierre Louis Léger, Chérif Beldjord, Karine Poirier and Franck J. Fourniol and has published in prestigious journals such as Blood, Brain and Kidney International.

In The Last Decade

Aurélie Toussaint

5 papers receiving 148 citations

Peers

Aurélie Toussaint

MB

GENET

HEMAT

PPCH

Irén Haltrich Hungary

Syed K. Rafi United States

Francesca Fumagalli Italy

Shanice Beerepoot Netherlands

Johanne Germain France

Mara Cavallin France

Lucia Castiglia Italy

Thomas Smol France

Amira Masri Jordan

Anna Norberg Sweden

Irén Haltrich Hungary

Aurélie Toussaint

103 ×1.5

MB

16 ×0.3

GENET

93 ×2.4

GENET

43 ×1.2

HEMAT

22 ×0.7

PPCH

Citations per year, relative to Aurélie Toussaint Aurélie Toussaint (= 1×) peers Irén Haltrich

Countries citing papers authored by Aurélie Toussaint

Since Specialization

Citations

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

Fields of papers citing papers by Aurélie Toussaint

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurélie Toussaint

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

All Works

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5 of 5 papers shown

1.

Tabibzadeh, Nahid, Michel Daudon, Jean‐Philippe Haymann, et al.. (2017). The Case | Epistasis and urolithiasis. Kidney International. 92(2). 523–524. 2 indexed citations

2.

Silve, Caroline, I. Chabchoub, Aurélie Toussaint, et al.. (2016). Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets. Hormone Research in Paediatrics. 87(1). 23–29. 4 indexed citations

3.

Marty, Caroline, Cécile Saint‐Martin, C. Pecquet, et al.. (2014). Germ-line JAK2 mutations in the kinase domain are responsible for hereditary thrombocytosis and are resistant to JAK2 and HSP90 inhibitors. Blood. 123(9). 1372–1383. 55 indexed citations

4.

Toussaint, Aurélie, Chrystel Leroy, Nathalie Deburgrave, et al.. (2013). Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes. European Journal of Human Genetics. 21(9). 977–987. 14 indexed citations

5.

Bahi‐Buisson, Nadia, Isabelle Souville, Franck J. Fourniol, et al.. (2013). New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum. Brain. 136(1). 223–244. 74 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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