Roberto Giorda
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 64
- Genomic variations and chromosomal abnormalities 33
- Genetics and Neurodevelopmental Disorders 32
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- Congenital heart defects research 14
- RNA Research and Splicing 9
- Co-authors
- Orsetta Zuffardi (38 shared papers)María Clara Bonaglia (29 shared papers)Silvana Beri (34 shared papers)Massimo Trucco (11 shared papers)Cecilia Marino (26 shared papers)Renato Borgatti (22 shared papers)Massimo Molteni (22 shared papers)Roberto Ciccone (16 shared papers)
- Journals
- European Journal of Human Genetics (12 papers)European Journal of Medical Genetics (7 papers)Human Genetics (7 papers)Human Mutation (5 papers)The Journal of Immunology (4 papers)
- Partner nations
- ItalyUnited StatesCanada
In The Last Decade
Roberto Giorda
154 papers receiving 4.9k citations
Peers
Comparison fields: 5 of 132
- Genetics 2.0k
- Pediatrics, Perinatology and Child Health 765
- Developmental and Educational Psychology 469
- Immunology 668
- Cognitive Neuroscience 552
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 157 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 288 | |
| 2 | 2001 | 225 | |
| 3 | 1990 | 199 | |
| 4 | 1999 | 174 | |
| 5 | 2002 | 160 | |
| 6 | 2005 | 107 | |
| 7 | 2007 | 100 | |
| 8 | 1991 | 100 | |
| 9 | 2016 | 96 | |
| 10 | 2003 | 94 | |
| 11 | 2019 | 89 | |
| 12 | 1996 | 79 | |
| 13 | 2010 | 76 | |
| 14 | 2008 | 75 | |
| 15 | 2005 | 71 | |
| 16 | 2011 | 70 | |
| 17 | 2009 | 68 | |
| 18 | 2006 | 68 | |
| 19 | 2010 | 65 | |
| 20 | 2016 | 63 |
About Roberto Giorda
Roberto Giorda is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Psychology and Developmental and Educational Psychology, having authored 157 papers that have together received 5.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (33 papers), Genetics and Neurodevelopmental Disorders (32 papers), Child and Adolescent Psychosocial and Emotional Development (17 papers), Reading and Literacy Development (16 papers), Infant Development and Preterm Care (14 papers), Congenital heart defects research (14 papers), Chromosomal and Genetic Variations (13 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 (765 citations), Developmental and Educational Psychology (469 citations), Immunology (668 citations) and Cognitive Neuroscience (552 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, European Journal of Medical Genetics, Human Genetics, Human Mutation and The Journal of Immunology.
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.