Roberta Polli
Impact in
- Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 20
- Genetics and Neurodevelopmental Disorders 18
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 4
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- Chromatin Remodeling and Cancer 3
- Congenital heart defects research 2
- Co-authors
- Alessandra Murgia (31 shared papers)Maddalena Martella (7 shared papers)Stefano Sartori (10 shared papers)Cinzia Vinanzi (6 shared papers)Emanuela Leonardi (9 shared papers)Marilena Vecchi (4 shared papers)Eva Orzan (3 shared papers)Franco Zacchello (4 shared papers)
- Journals
- Journal of Child Neurology (2 papers)Neurology (1 paper)Journal of Medical Genetics (1 paper)Neuropsychologia (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- ItalyUnited StatesSpain
In The Last Decade
Roberta Polli
31 papers receiving 878 citations
Peers
Comparison fields: 5 of 67
- Sensory Systems 165
- Genetics 475
- Cognitive Neuroscience 170
- Molecular Biology 414
- Endocrine and Autonomic Systems 38
Countries citing papers authored by Roberta Polli
This map shows the geographic impact of Roberta Polli'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 Roberta Polli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberta Polli more than expected).
Fields of papers citing papers by Roberta Polli
This network shows the impact of papers produced by Roberta Polli. 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 Roberta Polli. The network helps show where Roberta Polli may publish in the future.
Co-authors
The 25 scholars most cited alongside Roberta Polli, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 216 | |
| 2 | 1999 | 127 | |
| 3 | 2014 | 85 | |
| 4 | 2009 | 61 | |
| 5 | 2000 | 57 | |
| 6 | 2009 | 33 | |
| 7 | 2006 | 30 | |
| 8 | 1999 | 30 | |
| 9 | 2011 | 23 | |
| 10 | 2006 | 23 | |
| 11 | 2018 | 20 | |
| 12 | 2014 | 18 | |
| 13 | 1996 | 16 | |
| 14 | 2012 | 16 | |
| 15 | 2021 | 15 | |
| 16 | 2020 | 15 | |
| 17 | 2006 | 15 | |
| 18 | 2020 | 14 | |
| 19 | 2014 | 14 | |
| 20 | 2017 | 13 |
About Roberta Polli
Roberta Polli is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Sensory Systems and Cancer Research, having authored 32 papers that have together received 899 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (7 papers), Autism Spectrum Disorder Research (6 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers), Genomics and Rare Diseases (4 papers), Chromatin Remodeling and Cancer (3 papers), Congenital heart defects research (2 papers) and Vestibular and auditory disorders (2 papers). The work is most often cited by research in Sensory Systems (165 citations), Genetics (475 citations), Cognitive Neuroscience (170 citations), Molecular Biology (414 citations) and Endocrine and Autonomic Systems (38 citations). Roberta Polli has collaborated with scholars based in Italy, United States and Spain. Frequent co-authors include Alessandra Murgia, Maddalena Martella, Stefano Sartori, Cinzia Vinanzi, Emanuela Leonardi, Marilena Vecchi, Eva Orzan, Franco Zacchello, Elisa Bettella and Elif Acar Arslan. Their work appears in journals such as Journal of Child Neurology, Neurology, Journal of Medical Genetics, Neuropsychologia and European Journal of Human 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.