Sara Osimani

473 total citations
5 papers, 35 citations indexed

About

Sara Osimani is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Sara Osimani has authored 5 papers receiving a total of 35 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Pediatrics, Perinatology and Child Health and 1 paper in Molecular Biology. Recurrent topics in Sara Osimani's work include Genetic Syndromes and Imprinting (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Prenatal Screening and Diagnostics (2 papers). Sara Osimani is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Prenatal Screening and Diagnostics (2 papers). Sara Osimani collaborates with scholars based in Italy, France and United States. Sara Osimani's co-authors include Isabelle Husson, Laurence Perrin, Sandrine Passemard, Isabelle Marey, Monique Elmaleh, Mirella Filocamo, Chloé Quēlin, Olivier Delalande, Alain Verloès and Maria Rosaria Licenziati and has published in prestigious journals such as PEDIATRICS, Frontiers in Pediatrics and Journal of Endocrinological Investigation.

In The Last Decade

Sara Osimani

4 papers receiving 34 citations

Peers

Sara Osimani
Cecilia E Kim United States
Sara Osimani
Citations per year, relative to Sara Osimani Sara Osimani (= 1×) peers Cecilia E Kim

Countries citing papers authored by Sara Osimani

Since Specialization
Citations

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

Fields of papers citing papers by Sara Osimani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Osimani

This figure shows the co-authorship network connecting the top 25 collaborators of Sara Osimani. A scholar is included among the top collaborators of Sara Osimani 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 Sara Osimani. Sara Osimani 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.
Grugni, Graziano, Sarah Bocchini, Antonino Crinò, et al.. (2023). Multicentric Italian case–control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome. Journal of Endocrinological Investigation. 46(7). 1397–1406.
2.
Licenziati, Maria Rosaria, Dario Bacchini, Antonino Crinò, et al.. (2022). The Hyperphagia Questionnaire: Insights From a Multicentric Validation Study in Individuals With Prader Willi Syndrome. Frontiers in Pediatrics. 10. 829486–829486. 4 indexed citations
3.
Grugni, Graziano, Paolo Marzullo, Maurizio Delvecchio, et al.. (2020). Stimulated GH levels during the transition phase in Prader–Willi syndrome. Journal of Endocrinological Investigation. 44(7). 1465–1474. 4 indexed citations
4.
Biran, Valérie, Marie Bornes, Azzedine Aboura, et al.. (2011). A Long-term Competent Chimeric Immune System in a Dizygotic Dichorionic Twin. PEDIATRICS. 128(2). e458–e463. 7 indexed citations
5.
Osimani, Sara, Isabelle Husson, Sandrine Passemard, et al.. (2010). Craniosynostosis: A rare complication of pycnodysostosis. European Journal of Medical Genetics. 53(2). 89–92. 20 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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