Angela Peron

1.9k total citations
54 papers, 827 citations indexed

About

Angela Peron is a scholar working on Genetics, Physiology and Molecular Biology. According to data from OpenAlex, Angela Peron has authored 54 papers receiving a total of 827 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 22 papers in Physiology and 18 papers in Molecular Biology. Recurrent topics in Angela Peron's work include Tuberous Sclerosis Complex Research (21 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Polyomavirus and related diseases (11 papers). Angela Peron is often cited by papers focused on Tuberous Sclerosis Complex Research (21 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Polyomavirus and related diseases (11 papers). Angela Peron collaborates with scholars based in Italy, United States and United Kingdom. Angela Peron's co-authors include Aglaia Vignoli, Maria Paola Canevini, Francesca La Briola, Hope Northrup, Katherine Turner, Kit Sing Au, Filippo Ghelma, Elena Zambrelli, Massimo Mastrangelo and Katarzyna Kotulska and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Angela Peron

52 papers receiving 803 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Angela Peron Italy 18 365 344 261 139 127 54 827
Francesca La Briola Italy 17 294 0.8× 288 0.8× 153 0.6× 132 0.9× 165 1.3× 39 715
Kira A. Dies United States 15 553 1.5× 392 1.1× 361 1.4× 156 1.1× 228 1.8× 26 1.2k
Jamie K. Capal United States 12 156 0.4× 340 1.0× 115 0.4× 146 1.1× 84 0.7× 29 523
Eric A. M. Hennekam Netherlands 11 200 0.5× 96 0.3× 408 1.6× 163 1.2× 54 0.4× 14 957
Celeste Bento Portugal 16 279 0.8× 173 0.5× 178 0.7× 19 0.1× 234 1.8× 46 777
Paolo Curatolo Italy 13 120 0.3× 128 0.4× 110 0.4× 73 0.5× 59 0.5× 37 639
Mercédes Pineda Spain 18 278 0.8× 368 1.1× 499 1.9× 16 0.1× 84 0.7× 29 1.0k
Jean‐Baptiste Rivière Canada 18 575 1.6× 79 0.2× 591 2.3× 34 0.2× 101 0.8× 36 1.2k
Alexandra Afenjar France 16 621 1.7× 55 0.2× 521 2.0× 36 0.3× 69 0.5× 42 1.0k
Jennifer L. Ingram United States 10 124 0.3× 193 0.6× 109 0.4× 40 0.3× 142 1.1× 10 633

Countries citing papers authored by Angela Peron

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Angela Peron

This figure shows the co-authorship network connecting the top 25 collaborators of Angela Peron. A scholar is included among the top collaborators of Angela Peron based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Angela Peron. Angela Peron is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bacci, Giacomo Maria, Sara Bargiacchi, Michel Pâques, et al.. (2024). Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights. Scientific Reports. 14(1). 15454–15454. 1 indexed citations
2.
Spagnoli, Carlotta, Stefano Giuseppe Caraffi, A Cavalli, et al.. (2024). Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. International Journal of Molecular Sciences. 25(2). 1248–1248. 9 indexed citations
3.
Barbato, Alessandro, Michele Sacchini, Sara Bargiacchi, et al.. (2024). Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature. Endocrine Connections. 13(10). 2 indexed citations
4.
Capra, Anna Paola, Silvana Briuglia, Chiara Baldo, et al.. (2021). 8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature. Genes. 12(5). 652–652. 12 indexed citations
5.
Fladrowski, Carla, et al.. (2021). Beyond the Guidelines: How We Can Improve Healthcare for People With Tuberous Sclerosis Complex Around the World. Pediatric Neurology. 123. 77–84. 10 indexed citations
6.
Peron, Angela, et al.. (2020). PIGW‐related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literature. American Journal of Medical Genetics Part A. 182(6). 1477–1482. 8 indexed citations
7.
Peron, Angela, Francesca Novara, Francesca La Briola, et al.. (2020). Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotype. American Journal of Medical Genetics Part A. 182(4). 823–828. 11 indexed citations
8.
Pezzani, Lidia, Lucia Mauri, Angelo Selicorni, et al.. (2020). Aortic dilation in Sotos syndrome: An underestimated feature?. American Journal of Medical Genetics Part A. 182(7). 1819–1823. 6 indexed citations
9.
Saletti, Veronica, Katherine Turner, Angela Peron, et al.. (2020). The TAND checklist: a useful screening tool in children with tuberous sclerosis and neurofibromatosis type 1. Orphanet Journal of Rare Diseases. 15(1). 237–237. 14 indexed citations
10.
Peron, Angela, et al.. (2020). Electro-clinical and neurodevelopmental outcome in six children with early diagnosis of tuberous sclerosis complex and role of the genetic background. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 46(1). 36–36. 4 indexed citations
11.
Peron, Angela, Aglaia Vignoli, Francesca La Briola, et al.. (2018). Deep phenotyping of patients with Tuberous Sclerosis Complex and no mutation identified in TSC1 and TSC2. European Journal of Medical Genetics. 61(7). 403–410. 26 indexed citations
12.
Manara, Renzo, Davide Brotto, Maria Federica Pelizza, et al.. (2018). Rhinencephalon changes in tuberous sclerosis complex. Neuroradiology. 60(8). 813–820. 4 indexed citations
13.
Vignoli, Aglaia, Gaia Donata Oggioni, Giovanni De Maria, et al.. (2017). Lennox–Gastaut syndrome in adulthood: Long-term clinical follow-up of 38 patients and analysis of their recorded seizures. Epilepsy & Behavior. 77. 73–78. 23 indexed citations
14.
Marco, Fabiano Di, Silvia Terraneo, Gianluca Imeri, et al.. (2017). Lymphangioleiomyomatosis, multifocal micronodular pneumocyte hyperplasia, and sarcoidosis: more pathological findings in the same chest CT, or a single pathological pathway?. BMC Pulmonary Medicine. 17(1). 107–107. 4 indexed citations
15.
Vignoli, Aglaia, Francesca La Briola, Angela Peron, et al.. (2017). Dramatic relapse of seizures after everolimus withdrawal. European Journal of Paediatric Neurology. 22(1). 203–206. 16 indexed citations
16.
Ronzoni, Luisa, Antonio Novelli, Giulia Brisighelli, et al.. (2016). 2q33.1q34 Deletion in a Girl with Brain Anomalies and Anorectal Malformation. Cytogenetic and Genome Research. 150(1). 23–28. 2 indexed citations
17.
Marco, Fabiano Di, Silvia Terraneo, Gianluca Imeri, et al.. (2016). Women with TSC: Relationship between Clinical, Lung Function and Radiological Features in a Genotyped Population Investigated for Lymphangioleiomyomatosis. PLoS ONE. 11(5). e0155331–e0155331. 18 indexed citations
18.
Vignoli, Aglaia, Elena Lesma, Rosa Maria Alfano, et al.. (2015). Glioblastoma multiforme in a child with tuberous sclerosis complex. American Journal of Medical Genetics Part A. 167(10). 2388–2393. 12 indexed citations
19.
Ronzoni, Luisa, Angela Peron, Vera Bianchi, et al.. (2015). Molecular cytogenetic characterization of a 2q35‐q37 duplication and a 4q35.1‐q35.2 deletion in two cousins: A genotype–phenotype analysis. American Journal of Medical Genetics Part A. 167(7). 1551–1559. 4 indexed citations
20.
Vignoli, Aglaia, Francesca La Briola, Angela Peron, et al.. (2011). Medical care of adolescents and women with Rett syndrome: An Italian study. American Journal of Medical Genetics Part A. 158A(1). 13–18. 27 indexed citations

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.

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