Françoise Auriol

568 total citations
10 papers, 227 citations indexed

About

Françoise Auriol is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Françoise Auriol has authored 10 papers receiving a total of 227 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Françoise Auriol's work include Genetic Syndromes and Imprinting (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Regulation of Appetite and Obesity (2 papers). Françoise Auriol is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Regulation of Appetite and Obesity (2 papers). Françoise Auriol collaborates with scholars based in France, United States and Germany. Françoise Auriol's co-authors include Jean‐Pierre Salles, M. Tauber, Catherine Molinas, Sanaa Eddiry, Éric Bieth, Dorothée Cailley, F. Lorenzini, Véronique Gaston, Benoı̂t Arveiler and Alexandre Buffet and has published in prestigious journals such as BMC Cancer, Genetics in Medicine and Journal of the American Society of Echocardiography.

In The Last Decade

Françoise Auriol

9 papers receiving 223 citations

Peers

Françoise Auriol
Fernanda A. Correa Brazil
Everlayny F. Costalonga Brazil
Maria Maniati-Christidi Greece
Dinesh Giri United Kingdom
Kitiwan Rojnueangnit Thailand
H. G. Dörr Germany
Kirsten Seale Australia
Lea Velsher Canada
Viviane C. Campos Brazil
Thipwimol Tim‐Aroon Thailand
Fernanda A. Correa Brazil
Françoise Auriol
Citations per year, relative to Françoise Auriol Françoise Auriol (= 1×) peers Fernanda A. Correa

Countries citing papers authored by Françoise Auriol

Since Specialization
Citations

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

Fields of papers citing papers by Françoise Auriol

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Auriol

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

All Works

10 of 10 papers shown
1.
2.
Eddiry, Sanaa, Gwénaëlle Diene, Catherine Molinas, et al.. (2021). SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome. Genetics in Medicine. 23(9). 1664–1672. 12 indexed citations
3.
Revet, Alexis, Agnès Suc, Françoise Auriol, et al.. (2021). Peritraumatic distress predicts prolonged grief disorder symptom severity after the death of a parent in children and adolescents. European journal of psychotraumatology. 12(1). 1936916–1936916. 7 indexed citations
4.
Batut, Aurélie, Jérôme Sales de Gauzy, Françoise Auriol, et al.. (2020). Ghrelin uses the GHS-R1a/Gi/cAMP pathway and induces differentiation only in mature osteoblasts. This ghrelin pathway is impaired in AIS patients. Biochemistry and Biophysics Reports. 24. 100782–100782. 4 indexed citations
5.
Hascoët, Sébastien, Khaled Hadeed, Clément Karsenty, et al.. (2018). Feasibility, Safety and Accuracy of Echocardiography-Fluoroscopy Imaging Fusion During Percutaneous Atrial Septal Defect Closure in Children. Journal of the American Society of Echocardiography. 31(11). 1229–1237. 11 indexed citations
6.
Papadopoulos, Theofilos, Audrey Casemayou, Eric Neau, et al.. (2017). Systems biology combining human- and animal-data miRNA and mRNA data identifies new targets in ureteropelvic junction obstruction. BMC Systems Biology. 11(1). 31–31. 14 indexed citations
7.
Abbo, Olivier, Marion Taurand, Paul Monsarrat, et al.. (2016). Comparison between pediatric and adult adipose mesenchymal stromal cells. Cytotherapy. 19(3). 395–407. 10 indexed citations
8.
Tauber, M., Françoise Auriol, Isabelle Gennero, et al.. (2015). Muscle and bone impairment in children with Marfan syndrome: correlation with age and FBN1 genotype. Bone Abstracts. 5 indexed citations
9.
Bieth, Éric, Sanaa Eddiry, Véronique Gaston, et al.. (2014). Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome. European Journal of Human Genetics. 23(2). 252–255. 126 indexed citations
10.
Tauber, M., et al.. (2004). Hyperghrelinemia Is a Common Feature of Prader-Willi Syndrome and Pituitary Stalk Interruption: A Pathophysiological Hypothesis. Hormone Research in Paediatrics. 62(1). 49–54. 38 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