Sanaa Eddiry

508 total citations
12 papers, 246 citations indexed

About

Sanaa Eddiry is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Sanaa Eddiry has authored 12 papers receiving a total of 246 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Sanaa Eddiry's work include Genetic Syndromes and Imprinting (8 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Epigenetics and DNA Methylation (3 papers). Sanaa Eddiry is often cited by papers focused on Genetic Syndromes and Imprinting (8 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Epigenetics and DNA Methylation (3 papers). Sanaa Eddiry collaborates with scholars based in France, United States and Germany. Sanaa Eddiry's co-authors include Jean‐Pierre Salles, M. Tauber, Catherine Molinas, Éric Bieth, Françoise Auriol, Dorothée Cailley, F. Lorenzini, Véronique Gaston, Jérôme Cavaillé and Benoı̂t Arveiler and has published in prestigious journals such as International Journal of Obesity, Molecular Psychiatry and Genetics in Medicine.

In The Last Decade

Sanaa Eddiry

12 papers receiving 240 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sanaa Eddiry France 7 181 159 38 31 24 12 246
Françoise Auriol France 7 138 0.8× 128 0.8× 24 0.6× 31 1.0× 36 1.5× 10 227
Yuji Oto Japan 12 212 1.2× 128 0.8× 66 1.7× 6 0.2× 58 2.4× 29 331
Elly Brokamp United States 6 132 0.7× 62 0.4× 25 0.7× 19 0.6× 13 0.5× 9 177
Yoko Hiraki Japan 10 131 0.7× 97 0.6× 22 0.6× 11 0.4× 21 0.9× 17 219
Heinz‐Erich Wichmann Germany 6 160 0.9× 131 0.8× 49 1.3× 15 0.5× 16 0.7× 6 321
Andrea M. Lewis United States 9 100 0.6× 102 0.6× 33 0.9× 13 0.4× 24 1.0× 18 233
Magdalena Bartnik Poland 10 168 0.9× 140 0.9× 56 1.5× 13 0.4× 8 0.3× 23 266
Rani Sachdev Australia 7 110 0.6× 137 0.9× 30 0.8× 8 0.3× 20 0.8× 26 237
Dena R. Matalon United States 7 96 0.5× 91 0.6× 11 0.3× 12 0.4× 11 0.5× 18 172
Solveig Heide France 8 94 0.5× 88 0.6× 49 1.3× 9 0.3× 12 0.5× 17 187

Countries citing papers authored by Sanaa Eddiry

Since Specialization
Citations

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

Fields of papers citing papers by Sanaa Eddiry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sanaa Eddiry

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

All Works

12 of 12 papers shown
1.
Bacchetta, Justine, et al.. (2024). Survey on vitamin D supplementation in children in France: Evaluation of real-life practices following the new 2022 French recommendations. Archives de Pédiatrie. 32(1). 4–11. 2 indexed citations
2.
Salles, Juliette, Sanaa Eddiry, Emmanuelle Lacassagne, et al.. (2024). Differential DNA methylation in iPSC-derived dopaminergic neurons: a step forward on the role of SNORD116 microdeletion in the pathophysiology of addictive behavior in Prader-Willi syndrome. Molecular Psychiatry. 29(9). 2742–2752. 1 indexed citations
3.
Collet, Corinne, Isabelle Gennero, Sanaa Eddiry, et al.. (2022). Diagnostic yield of bone fragility gene panel sequencing in children and young adults referred for idiopathic primary osteoporosis at a single regional reference centre. Bone Reports. 16. 101176–101176. 11 indexed citations
4.
Linglart, Agnès, Aurélie Portefaix, Aurélia Bertholet‐Thomas, et al.. (2022). X-linked hypophosphatemia, obesity and arterial hypertension: data from the XLH21 study. Pediatric Nephrology. 38(3). 697–704. 6 indexed citations
5.
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
6.
Salles, Juliette, Sanaa Eddiry, Emmanuelle Lacassagne, et al.. (2021). Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory. Clinical Epigenetics. 13(1). 159–159. 9 indexed citations
7.
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
8.
Salles, Juliette, Emmanuelle Lacassagne, Sanaa Eddiry, et al.. (2020). What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders?. Molecular Psychiatry. 26(1). 51–59. 24 indexed citations
9.
Burnett, Lisa C., Charles A. LeDuc, Carlos R. Sulsona, et al.. (2016). Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS. Stem Cell Research. 17(3). 526–530. 22 indexed citations
10.
Cadoudal, Thomas, Gwénaëlle Diene, Coralie Sengenès, et al.. (2014). Impairment of Adipose Tissue in Prader-Willi Syndrome Rescued by GH Treatment. 82. 1 indexed citations
11.
Cadoudal, Thomas, Marie Buléon, Coralie Sengenès, et al.. (2014). Impairment of adipose tissue in Prader–Willi syndrome rescued by growth hormone treatment. International Journal of Obesity. 38(9). 1234–1240. 28 indexed citations
12.
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

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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