Stefania Bigoni
Impact in
Papers in
- Genetics 20
- Genetics and Neurodevelopmental Disorders 11
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 6
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- Congenital heart defects research 4
- Co-authors
- Marcella Neri (4 shared papers)Alessandra Ferlini (16 shared papers)Marco Fichera (2 shared papers)Giorgio Pini (5 shared papers)Elisa Calzolari (2 shared papers)Olga Calabrese (2 shared papers)Mariangela Lo Giudice (1 shared paper)Daniela Tropea (3 shared papers)
- Journals
- Neuromuscular Disorders (2 papers)Clinical Neurophysiology (1 paper)Biomedicines (1 paper)Hormone Research in Paediatrics (1 paper)Neurology (1 paper)
- Partner nations
- ItalyIrelandUnited Kingdom
In The Last Decade
Stefania Bigoni
33 papers receiving 544 citations
Peers
Comparison fields: 5 of 66
- Genetics 237
- Neurology 66
- Cellular and Molecular Neuroscience 113
- Genetics 56
- Psychiatry and Mental health 65
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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 123 | |
| 2 | 2004 | 96 | |
| 3 | 2016 | 44 | |
| 4 | 2016 | 34 | |
| 5 | 2017 | 23 | |
| 6 | 2017 | 21 | |
| 7 | 2018 | 19 | |
| 8 | 2013 | 19 | |
| 9 | 2019 | 16 | |
| 10 | 2004 | 16 | |
| 11 | 2015 | 16 | |
| 12 | 2015 | 15 | |
| 13 | 2020 | 15 | |
| 14 | 2016 | 14 | |
| 15 | 2008 | 14 | |
| 16 | 2021 | 11 | |
| 17 | 2020 | 9 | |
| 18 | 2017 | 9 | |
| 19 | 2023 | 8 | |
| 20 | 2022 | 5 |
About Stefania Bigoni
Stefania Bigoni is a scholar working on Genetics, Molecular Biology, Genetics, Cognitive Neuroscience and Pathology and Forensic Medicine, having authored 34 papers that have together received 555 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers), Congenital heart defects research (4 papers), Neurological diseases and metabolism (3 papers), Hereditary Neurological Disorders (3 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Autism Spectrum Disorder Research (3 papers). The work is most often cited by research in Genetics (237 citations), Neurology (66 citations), Cellular and Molecular Neuroscience (113 citations), Genetics (56 citations) and Psychiatry and Mental health (65 citations). Stefania Bigoni has collaborated with scholars based in Italy, Ireland and United Kingdom. Frequent co-authors include Marcella Neri, Alessandra Ferlini, Marco Fichera, Giorgio Pini, Elisa Calzolari, Olga Calabrese, Mariangela Lo Giudice, Daniela Tropea, Carla Marini and Elena Cellini. Their work appears in journals such as Neuromuscular Disorders, Clinical Neurophysiology, Biomedicines, Hormone Research in Paediatrics and Neurology.
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.