Silvana Beri
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Reading and Literacy Development
Papers in
- Genetics 23
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Congenital heart defects research 6
- Co-authors
- Roberto Giorda (34 shared papers)Orsetta Zuffardi (18 shared papers)Rosario Montirosso (4 shared papers)Livio Provenzi (4 shared papers)María Clara Bonaglia (11 shared papers)Cecilia Marino (6 shared papers)Giorgia Menozzi (4 shared papers)Giorgio Gimelli (8 shared papers)
- Journals
- European Journal of Human Genetics (7 papers)European Journal of Medical Genetics (5 papers)Genes Brain & Behavior (3 papers)Human Mutation (3 papers)Human Genetics (2 papers)
- Partner nations
- ItalyUnited StatesCanada
In The Last Decade
Silvana Beri
34 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 89
- Genetics 436
- Developmental and Educational Psychology 151
- Pediatrics, Perinatology and Child Health 184
- Cognitive Neuroscience 113
- Molecular Biology 363
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-authors
The 25 scholars most cited alongside Silvana Beri, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 100 | |
| 2 | 2016 | 99 | |
| 3 | 2005 | 71 | |
| 4 | 2010 | 65 | |
| 5 | 2016 | 65 | |
| 6 | 2015 | 59 | |
| 7 | 2007 | 55 | |
| 8 | 2010 | 53 | |
| 9 | 2012 | 52 | |
| 10 | 2014 | 48 | |
| 11 | 2010 | 44 | |
| 12 | 2007 | 36 | |
| 13 | 2009 | 31 | |
| 14 | 2014 | 27 | |
| 15 | 2008 | 25 | |
| 16 | 2012 | 24 | |
| 17 | 2008 | 23 | |
| 18 | 2010 | 21 | |
| 19 | 2018 | 20 | |
| 20 | 2009 | 18 |
About Silvana Beri
Silvana Beri is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Developmental and Educational Psychology, having authored 34 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Genetics and Neurodevelopmental Disorders (9 papers), Congenital heart defects research (6 papers), Chromosomal and Genetic Variations (4 papers), Cancer Genomics and Diagnostics (3 papers), Genomics and Rare Diseases (3 papers), Reading and Literacy Development (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Genetics (436 citations), Developmental and Educational Psychology (151 citations), Pediatrics, Perinatology and Child Health (184 citations), Cognitive Neuroscience (113 citations) and Molecular Biology (363 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, Cecilia Marino, Giorgia Menozzi, Giorgio Gimelli, Stefania Gimelli and Francesca Novara. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Genes Brain & Behavior, Human Mutation 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.