Giuseppe Barrano
Impact in
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
-
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 7
- Genetics and Neurodevelopmental Disorders 3
- Genetic and Kidney Cyst Diseases 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Francesco Brancati (3 shared papers)Enza Maria Valente (3 shared papers)Bruno Dallapiccola (4 shared papers)Enrico Bertini (2 shared papers)Eugen Boltshauser (2 shared papers)Elisa Fazzi (1 shared paper)Suguna Rani Krishnaswami (1 shared paper)Emanuele Bellacchio (1 shared paper)
- Journals
- Epilepsia (1 paper)Gene (1 paper)Nature Genetics (1 paper)Movement Disorders (1 paper)International Journal of Molecular Sciences (1 paper)
- Partner nations
- ItalySwitzerlandUnited States
In The Last Decade
Giuseppe Barrano
11 papers receiving 435 citations
Peers
Comparison fields: 5 of 48
- Genetics 311
- Pediatrics, Perinatology and Child Health 95
- Ophthalmology 42
- Molecular Biology 310
- Neurology 54
Countries citing papers authored by Giuseppe Barrano
This map shows the geographic impact of Giuseppe Barrano'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 Giuseppe Barrano with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giuseppe Barrano more than expected).
Fields of papers citing papers by Giuseppe Barrano
This network shows the impact of papers produced by Giuseppe Barrano. 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 Giuseppe Barrano. The network helps show where Giuseppe Barrano may publish in the future.
Co-authors
The 25 scholars most cited alongside Giuseppe Barrano, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 291 | |
| 2 | 2008 | 50 | |
| 3 | 2006 | 29 | |
| 4 | 2009 | 29 | |
| 5 | 2012 | 11 | |
| 6 | 2016 | 11 | |
| 7 | 2011 | 6 | |
| 8 | 2020 | 5 | |
| 9 | 2018 | 5 | |
| 10 | 2023 | 4 | |
| 11 | 2021 | 1 |
About Giuseppe Barrano
Giuseppe Barrano is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Neurology, having authored 11 papers that have together received 442 indexed citations. Recurring topics across this work include Fetal and Pediatric Neurological Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic and Kidney Cyst Diseases (2 papers), Neurological disorders and treatments (2 papers), Genetic Neurodegenerative Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Williams Syndrome Research (1 paper) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Genetics (311 citations), Pediatrics, Perinatology and Child Health (95 citations), Ophthalmology (42 citations), Molecular Biology (310 citations) and Neurology (54 citations). Giuseppe Barrano has collaborated with scholars based in Italy, Switzerland and United States. Frequent co-authors include Francesco Brancati, Enza Maria Valente, Bruno Dallapiccola, Enrico Bertini, Eugen Boltshauser, Elisa Fazzi, Suguna Rani Krishnaswami, Emanuele Bellacchio, Loredana Boccone and Marco Castori. Their work appears in journals such as Epilepsia, Gene, Nature Genetics, Movement Disorders and International Journal of Molecular Sciences.
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.