Berardo Rinaldi
- Molecular Biology
- Genetics
- Pathology and Forensic Medicine
- Pediatrics, Perinatology and Child Health
- Epidemiology
- Co-authors
- Maria Francesca BedeschiOrsetta ZuffardiLivia GaravelliPalma FinelliRoberta VillaSabrina GiglioAnnalisa VetroEdoardo Errichiello
- Topics
- Genomic variations and chromosomal abnormalities (11 papers)Genomics and Rare Diseases (9 papers)Genetics and Neurodevelopmental Disorders (7 papers)
In The Last Decade
Berardo Rinaldi
21 papers receiving 167 citations
Peers
Comparison fields: 5 of 51
- Molecular Biology 99
- Genetics 90
- Pathology and Forensic Medicine 32
- Pediatrics, Perinatology and Child Health 15
- Epidemiology 12
Countries citing papers authored by Berardo Rinaldi
This map shows the geographic impact of Berardo Rinaldi'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 Berardo Rinaldi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Berardo Rinaldi more than expected).
Fields of papers citing papers by Berardo Rinaldi
This network shows the impact of papers produced by Berardo Rinaldi. 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 Berardo Rinaldi. The network helps show where Berardo Rinaldi may publish in the future.
Co-authorship network of co-authors of Berardo Rinaldi
This figure shows the co-authorship network connecting the top 25 collaborators of Berardo Rinaldi. A scholar is included among the top collaborators of Berardo Rinaldi 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 Berardo Rinaldi. Berardo Rinaldi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 1 | |
| 3 | 2 | |
| 4 | 4 | |
| 5 | 1 | |
| 6 | 1 | |
| 7 | 0 | |
| 8 | 2 | |
| 9 | 2 | |
| 10 | 2 | |
| 11 | 5 | |
| 12 | 12 | |
| 13 | 0 | |
| 14 | 0 | |
| 15 | 8 | |
| 16 | 3 | |
| 17 | 10 | |
| 18 | 14 | |
| 19 | 4 | |
| 20 | 4 |
About Berardo Rinaldi
Berardo Rinaldi is a scholar working on Genetics, Pathology and Forensic Medicine and Developmental Neuroscience, having authored 26 papers that have together received 170 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). The work is most often cited by research in Genetics (90 citations), Pathology and Forensic Medicine (32 citations) and Molecular Biology (99 citations). Berardo Rinaldi has collaborated with scholars based in Italy, France and Denmark. Frequent co-authors include Maria Francesca Bedeschi, Orsetta Zuffardi, Livia Garavelli, Palma Finelli, Roberta Villa, Sabrina Giglio, Annalisa Vetro, Edoardo Errichiello, Hugo de Jonge and Patrizia Morbini. Their work appears in journals such as PLoS Genetics, The Journal of Pathology and Human Genetics.
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.