Roberto Giorda
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 57
- Genomic variations and chromosomal abnormalities 32
- Genetics and Neurodevelopmental Disorders 25
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- Congenital heart defects research 14
- RNA Research and Splicing 9
- Co-authors
- Orsetta Zuffardi (39 shared papers)María Clara Bonaglia (30 shared papers)Silvana Beri (34 shared papers)Massimo Trucco (11 shared papers)Cecilia Marino (26 shared papers)Renato Borgatti (23 shared papers)Massimo Molteni (22 shared papers)Roberto Ciccone (17 shared papers)
- Journals
- European Journal of Human Genetics (12 papers)Human Genetics (7 papers)European Journal of Medical Genetics (7 papers)Human Mutation (5 papers)Journal of Medical Genetics (4 papers)
- Partner nations
- ItalyUnited StatesCanada
In The Last Decade
Roberto Giorda
156 papers receiving 5.2k citations
Peers
Comparison fields: 5 of 134
- Genetics 2.0k
- Pediatrics, Perinatology and Child Health 714
- Developmental and Educational Psychology 457
- Immunology 669
- Molecular Biology 1.9k
Countries citing papers authored by Roberto Giorda
This map shows the geographic impact of Roberto Giorda'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 Roberto Giorda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberto Giorda more than expected).
Fields of papers citing papers by Roberto Giorda
This network shows the impact of papers produced by Roberto Giorda. 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 Roberto Giorda. The network helps show where Roberto Giorda may publish in the future.
Co-authors
The 25 scholars most cited alongside Roberto Giorda, 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 161 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 302 | |
| 2 | 2001 | 242 | |
| 3 | 1990 | 208 | |
| 4 | 2002 | 187 | |
| 5 | 1999 | 182 | |
| 6 | 2005 | 154 | |
| 7 | 2016 | 110 | |
| 8 | 2007 | 108 | |
| 9 | 2003 | 103 | |
| 10 | 1991 | 102 | |
| 11 | 2008 | 96 | |
| 12 | 2019 | 95 | |
| 13 | 2009 | 87 | |
| 14 | 1996 | 83 | |
| 15 | 2010 | 82 | |
| 16 | 2005 | 76 | |
| 17 | 2011 | 75 | |
| 18 | 2006 | 74 | |
| 19 | 2016 | 70 | |
| 20 | 2010 | 70 |
About Roberto Giorda
Roberto Giorda is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Developmental and Educational Psychology, having authored 161 papers that have together received 5.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (32 papers), Genetics and Neurodevelopmental Disorders (25 papers), Congenital heart defects research (14 papers), Chromosomal and Genetic Variations (13 papers), Reading and Literacy Development (13 papers), Child and Adolescent Psychosocial and Emotional Development (12 papers), Infant Development and Preterm Care (12 papers) and RNA Research and Splicing (9 papers). The work is most often cited by research in Genetics (2.0k citations), Pediatrics, Perinatology and Child Health (714 citations), Developmental and Educational Psychology (457 citations), Immunology (669 citations) and Molecular Biology (1.9k citations). Roberto Giorda has collaborated with scholars based in Italy, United States and Canada. Frequent co-authors include Orsetta Zuffardi, María Clara Bonaglia, Silvana Beri, Massimo Trucco, Cecilia Marino, Renato Borgatti, Massimo Molteni, Roberto Ciccone, Giorgio Gimelli and Livio Provenzi. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, European Journal of Medical Genetics, Human Mutation and Journal of Medical 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.