Angela Peron
Impact in
- Physiology top 5%
- Tuberous Sclerosis Complex Research
- Histiocytic Disorders and Treatments
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Physiology 22
- Tuberous Sclerosis Complex Research 21
- Histiocytic Disorders and Treatments 4
- Genetics 21
- Genetics and Neurodevelopmental Disorders 12
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 4
- Co-authors
- Aglaia Vignoli (34 shared papers)Maria Paola Canevini (31 shared papers)Francesca La Briola (22 shared papers)Hope Northrup (2 shared papers)Katherine Turner (11 shared papers)Kit Sing Au (1 shared paper)Filippo Ghelma (5 shared papers)Elena Zambrelli (9 shared papers)
- Journals
- American Journal of Medical Genetics Part C Seminars in Medical Genetics (4 papers)Epilepsy & Behavior (3 papers)International Journal of Molecular Sciences (3 papers)Orphanet Journal of Rare Diseases (3 papers)European Journal of Medical Genetics (2 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Angela Peron
52 papers receiving 834 citations
Peers
Comparison fields: 5 of 71
- Physiology 355
- Genetics 308
- Psychiatry and Mental health 101
- Cognitive Neuroscience 92
- Oncology 83
Countries citing papers authored by Angela Peron
This map shows the geographic impact of Angela Peron'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 Angela Peron with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Angela Peron more than expected).
Fields of papers citing papers by Angela Peron
This network shows the impact of papers produced by Angela Peron. 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 Angela Peron. The network helps show where Angela Peron may publish in the future.
Co-authors
The 25 scholars most cited alongside Angela Peron, 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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 67 | |
| 2 | 2018 | 66 | |
| 3 | 2018 | 63 | |
| 4 | 2016 | 38 | |
| 5 | 2018 | 31 | |
| 6 | 2012 | 30 | |
| 7 | 2018 | 29 | |
| 8 | 2016 | 27 | |
| 9 | 2011 | 27 | |
| 10 | 2013 | 27 | |
| 11 | 2018 | 27 | |
| 12 | 2016 | 25 | |
| 13 | 2019 | 25 | |
| 14 | 2018 | 25 | |
| 15 | 2013 | 23 | |
| 16 | 2017 | 23 | |
| 17 | 2020 | 20 | |
| 18 | 2016 | 19 | |
| 19 | 2020 | 17 | |
| 20 | 2017 | 17 |
About Angela Peron
Angela Peron is a scholar working on Physiology, Genetics, Molecular Biology, Psychiatry and Mental health and Genetics, having authored 54 papers that have together received 859 indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (21 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (7 papers), Polyomavirus and related diseases (6 papers), Epilepsy research and treatment (6 papers), Neuroscience and Neuropharmacology Research (4 papers), Histiocytic Disorders and Treatments (4 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Physiology (355 citations), Genetics (308 citations), Psychiatry and Mental health (101 citations), Cognitive Neuroscience (92 citations) and Oncology (83 citations). Angela Peron has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Aglaia Vignoli, Maria Paola Canevini, Francesca La Briola, Hope Northrup, Katherine Turner, Kit Sing Au, Filippo Ghelma, Elena Zambrelli, Katarzyna Kotulska and Massimo Mastrangelo. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, Epilepsy & Behavior, International Journal of Molecular Sciences, 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.