Simone Gana
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Blood disorders and treatments
Papers in
- Genetics 18
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 3
- Genetic and Kidney Cyst Diseases 3
- Congenital Ear and Nasal Anomalies 2
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- RNA modifications and cancer 3
- Renal and related cancers 2
- Co-authors
- Enza Maria Valente (14 shared papers)Pierangelo Veggiotti (3 shared papers)Orsetta Zuffardi (3 shared papers)Roberto Ciccone (3 shared papers)Elena Rossi (4 shared papers)Cesare Danesino (2 shared papers)Katie Plunkett (1 shared paper)Giuseppe Micieli (1 shared paper)
- Journals
- European Journal of Paediatric Neurology (2 papers)Journal of Medical Genetics (2 papers)Brain and Development (2 papers)Frontiers in Genetics (1 paper)Human Mutation (1 paper)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Simone Gana
30 papers receiving 273 citations
Peers
Comparison fields: 5 of 58
- Genetics 149
- Developmental Biology 6
- Pediatrics, Perinatology and Child Health 35
- Developmental Neuroscience 7
- Molecular Biology 115
Countries citing papers authored by Simone Gana
This map shows the geographic impact of Simone Gana'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 Simone Gana with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone Gana more than expected).
Fields of papers citing papers by Simone Gana
This network shows the impact of papers produced by Simone Gana. 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 Simone Gana. The network helps show where Simone Gana may publish in the future.
Co-authors
The 25 scholars most cited alongside Simone Gana, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2022 | 52 | |
| 2 | 2012 | 34 | |
| 3 | 2015 | 22 | |
| 4 | 2021 | 20 | |
| 5 | 2013 | 19 | |
| 6 | 2011 | 17 | |
| 7 | 2011 | 13 | |
| 8 | 2019 | 9 | |
| 9 | 2021 | 9 | |
| 10 | 2021 | 8 | |
| 11 | 2010 | 8 | |
| 12 | 2020 | 7 | |
| 13 | 2019 | 7 | |
| 14 | Early onset of a nasal perivascular epithelioid cell neoplasm not related to tuberous sclerosis complex. | 2012 | 7 |
| 15 | 2020 | 6 | |
| 16 | 2021 | 5 | |
| 17 | 2021 | 5 | |
| 18 | 2020 | 4 | |
| 19 | 2024 | 4 | |
| 20 | 2013 | 4 |
About Simone Gana
Simone Gana is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 35 papers that have together received 278 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Genomics and Rare Diseases (3 papers), Genetic and Kidney Cyst Diseases (3 papers), RNA modifications and cancer (3 papers), Renal and related cancers (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Genetics (149 citations), Developmental Biology (6 citations), Pediatrics, Perinatology and Child Health (35 citations), Developmental Neuroscience (7 citations) and Molecular Biology (115 citations). Simone Gana has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Enza Maria Valente, Pierangelo Veggiotti, Orsetta Zuffardi, Roberto Ciccone, Elena Rossi, Cesare Danesino, Katie Plunkett, Giuseppe Micieli, Erika Della Mina and Weimin Bi. Their work appears in journals such as European Journal of Paediatric Neurology, Journal of Medical Genetics, Brain and Development, Frontiers in Genetics and Human Mutation.
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.