Stefania Bigoni
Impact in
Papers in
- Genetics 19
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 7
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- RNA regulation and disease 5
- RNA modifications and cancer 5
- Co-authors
- Alessandra Ferlini (16 shared papers)Marcella Neri (4 shared papers)Giorgio Pini (5 shared papers)Marco Fichera (2 shared papers)Elisa Calzolari (2 shared papers)Mariangela Lo Giudice (1 shared paper)Olga Calabrese (2 shared papers)Daniela Tropea (3 shared papers)
- Journals
- Neuromuscular Disorders (2 papers)Clinical Neurophysiology (1 paper)European Journal of Human Genetics (1 paper)Orphanet Journal of Rare Diseases (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- ItalyIrelandUnited Kingdom
In The Last Decade
Stefania Bigoni
31 papers receiving 514 citations
Peers
Comparison fields: 5 of 66
- Genetics 255
- Neurology 69
- Cellular and Molecular Neuroscience 105
- Psychiatry and Mental health 82
- Genetics 53
Countries citing papers authored by Stefania Bigoni
This map shows the geographic impact of Stefania Bigoni'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 Stefania Bigoni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefania Bigoni more than expected).
Fields of papers citing papers by Stefania Bigoni
This network shows the impact of papers produced by Stefania Bigoni. 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 Stefania Bigoni. The network helps show where Stefania Bigoni may publish in the future.
Co-authors
The 25 scholars most cited alongside Stefania Bigoni, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 122 | |
| 2 | 2004 | 85 | |
| 3 | 2016 | 42 | |
| 4 | 2016 | 33 | |
| 5 | 2017 | 23 | |
| 6 | 2017 | 21 | |
| 7 | 2018 | 19 | |
| 8 | 2013 | 17 | |
| 9 | 2004 | 15 | |
| 10 | 2015 | 15 | |
| 11 | 2015 | 15 | |
| 12 | 2016 | 13 | |
| 13 | 2020 | 13 | |
| 14 | 2019 | 13 | |
| 15 | 2008 | 12 | |
| 16 | 2021 | 11 | |
| 17 | 2020 | 9 | |
| 18 | 2017 | 9 | |
| 19 | 2023 | 5 | |
| 20 | 2022 | 5 |
About Stefania Bigoni
Stefania Bigoni is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Genetics and Pathology and Forensic Medicine, having authored 33 papers that have together received 520 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Autism Spectrum Disorder Research (5 papers), RNA regulation and disease (5 papers), RNA modifications and cancer (5 papers), Hereditary Neurological Disorders (3 papers) and Neurological diseases and metabolism (3 papers). The work is most often cited by research in Genetics (255 citations), Neurology (69 citations), Cellular and Molecular Neuroscience (105 citations), Psychiatry and Mental health (82 citations) and Genetics (53 citations). Stefania Bigoni has collaborated with scholars based in Italy, Ireland and United Kingdom. Frequent co-authors include Alessandra Ferlini, Marcella Neri, Giorgio Pini, Marco Fichera, Elisa Calzolari, Mariangela Lo Giudice, Olga Calabrese, Daniela Tropea, Davide Mei and Carmen Barba. Their work appears in journals such as Neuromuscular Disorders, Clinical Neurophysiology, European Journal of Human Genetics, Orphanet Journal of Rare Diseases and European 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.