Silvana Beri
- Genetics top 5%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 5%
- Developmental and Educational Psychology top 5%
- Cognitive Neuroscience top 10%
- Co-authors
- Roberto GiordaOrsetta ZuffardiRosario MontirossoLivio ProvenziMaría Clara BonagliaGiorgio GimelliGiorgia MenozziCecilia Marino
- Topics
- Genomic variations and chromosomal abnormalities (14 papers)Genetics and Neurodevelopmental Disorders (10 papers)Congenital heart defects research (5 papers)
- Partner nations
- ItalyUnited StatesCanada
In The Last Decade
Silvana Beri
34 papers receiving 997 citations
Peers
Comparison fields: 5 of 91
- Genetics 473
- Molecular Biology 397
- Pediatrics, Perinatology and Child Health 232
- Developmental and Educational Psychology 161
- Cognitive Neuroscience 130
Countries citing papers authored by Silvana Beri
This map shows the geographic impact of Silvana Beri'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 Silvana Beri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Silvana Beri more than expected).
Fields of papers citing papers by Silvana Beri
This network shows the impact of papers produced by Silvana Beri. 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 Silvana Beri. The network helps show where Silvana Beri may publish in the future.
Co-authorship network of co-authors of Silvana Beri
This figure shows the co-authorship network connecting the top 25 collaborators of Silvana Beri. A scholar is included among the top collaborators of Silvana Beri 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 Silvana Beri. Silvana Beri is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 96 | |
| 2 | 5 | |
| 3 | 58 | |
| 4 | 14 | |
| 5 | 47 | |
| 6 | 24 | |
| 7 | 14 | |
| 8 | 3 | |
| 9 | 6 | |
| 10 | 6 | |
| 11 | Refining the phenotype associated with MEF2C haploinsufficiency | 4 |
| 12 | 65 | |
| 13 | 42 | |
| 14 | 21 | |
| 15 | 18 | |
| 16 | 55 | |
| 17 | 100 | |
| 18 | 37 | |
| 19 | 14 | |
| 20 | 14 |
About Silvana Beri
Silvana Beri is a scholar working on Genetics, Developmental and Educational Psychology and Endocrine and Autonomic Systems, having authored 34 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Genetics (473 citations), Developmental and Educational Psychology (161 citations) and Pediatrics, Perinatology and Child Health (232 citations). Silvana Beri has collaborated with scholars based in Italy, United States and Canada. Frequent co-authors include Roberto Giorda, Orsetta Zuffardi, Rosario Montirosso, Livio Provenzi, María Clara Bonaglia, Giorgio Gimelli, Giorgia Menozzi, Cecilia Marino, Stefania Gimelli and Francesca Novara. Their work appears in journals such as PLoS ONE, Child Development and Neuroscience & Biobehavioral Reviews.
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.