Elena Piozzi

589 total citations
26 papers, 373 citations indexed

About

Elena Piozzi is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Elena Piozzi has authored 26 papers receiving a total of 373 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Ophthalmology and 7 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Elena Piozzi's work include melanin and skin pigmentation (5 papers), Corneal Surgery and Treatments (4 papers) and Glaucoma and retinal disorders (4 papers). Elena Piozzi is often cited by papers focused on melanin and skin pigmentation (5 papers), Corneal Surgery and Treatments (4 papers) and Glaucoma and retinal disorders (4 papers). Elena Piozzi collaborates with scholars based in Italy, United States and Belgium. Elena Piozzi's co-authors include Adriano Magli, Luigi Capasso, Raimondo Forte, Alessandra Longo, Franz Wilhelm Baruffaldi Preis, Silvana Penco, Lucia Mauri, Emanuela Manfredini, Luca Vaienti and Paola Primignani and has published in prestigious journals such as Gene, Medicine and Cancers.

In The Last Decade

Elena Piozzi

24 papers receiving 353 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elena Piozzi Italy 11 181 112 85 81 47 26 373
Rocco Plateroti Italy 12 116 0.6× 144 1.3× 71 0.8× 81 1.0× 31 0.7× 23 369
Mahshad Darvish-Zargar Canada 7 68 0.4× 126 1.1× 69 0.8× 83 1.0× 52 1.1× 13 292
Hideki Fukuoka Japan 10 110 0.6× 61 0.5× 78 0.9× 57 0.7× 10 0.2× 32 280
Katy C. Liu United States 11 90 0.5× 198 1.8× 51 0.6× 90 1.1× 10 0.2× 15 341
Mustafa Özsütçü Türkiye 14 215 1.2× 362 3.2× 207 2.4× 38 0.5× 47 1.0× 43 561
Nilay Yüksel Türkiye 10 164 0.9× 220 2.0× 108 1.3× 31 0.4× 32 0.7× 43 365
Tuomo Puustjärvi Finland 14 158 0.9× 393 3.5× 99 1.2× 78 1.0× 12 0.3× 28 535
Sigrid Roters Germany 17 499 2.8× 529 4.7× 141 1.7× 78 1.0× 29 0.6× 50 736
Fatih Ulaş Türkiye 12 210 1.2× 351 3.1× 57 0.7× 55 0.7× 17 0.4× 47 431
Catherine J. Choi United States 10 71 0.4× 100 0.9× 41 0.5× 92 1.1× 18 0.4× 36 333

Countries citing papers authored by Elena Piozzi

Since Specialization
Citations

This map shows the geographic impact of Elena Piozzi'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 Elena Piozzi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elena Piozzi more than expected).

Fields of papers citing papers by Elena Piozzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elena Piozzi. 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 Elena Piozzi. The network helps show where Elena Piozzi may publish in the future.

Co-authorship network of co-authors of Elena Piozzi

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Piozzi. A scholar is included among the top collaborators of Elena Piozzi 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 Elena Piozzi. Elena Piozzi 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.
Arrigoni, Filippo, Daniela Redaelli, R. Salati, et al.. (2022). Congenital isolated unilateral third nerve palsy in children: the diagnostic contribution of high-resolution MR imaging. Neuroradiology. 65(4). 865–870.
2.
Lepore, Domenico, Marco H. Ji, Gui‐Shuang Ying, et al.. (2021). Early angiographic signs of retinopathy of prematurity requiring treatment. Eye. 35(11). 3094–3101. 5 indexed citations
3.
Longo, Alessandra, et al.. (2018). Ocular features in mucopolysaccharidosis: diagnosis and treatment. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 44(S2). 125–125. 36 indexed citations
4.
Filippi, Luca, et al.. (2018). Propranolol eye drops in patients with corneal neovascularization. Medicine. 97(45). e13002–e13002. 6 indexed citations
5.
Allegrini, Davide, Giovanni Montesano, Paolo Fogagnolo, et al.. (2017). Transient Esotropia in the Child: Case Report and Review of the Literature. Case Reports in Ophthalmology. 8(1). 259–264. 3 indexed citations
6.
Gazzola, Riccardo, Elena Piozzi, Luca Vaienti, & Franz Wilhelm Baruffaldi Preis. (2017). Therapeutic Algorithm for Congenital Ptosis Repair with Levator Resection and Frontalis Suspension: Results and Literature Review. Seminars in Ophthalmology. 33(4). 454–460. 17 indexed citations
7.
Mauri, Lucia, Emanuela Manfredini, Alessandra Longo, et al.. (2016). Clinical evaluation and molecular screening of a large consecutive series of albino patients. Journal of Human Genetics. 62(2). 277–290. 16 indexed citations
8.
Primignani, Paola, Davide Allegrini, Emanuela Manfredini, et al.. (2016). Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations. Ophthalmic Genetics. 37(3). 307–313. 6 indexed citations
9.
Pasutto, Francesca, Lucia Mauri, Bernt Popp, et al.. (2015). Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld–Rieger syndrome and glaucoma. Gene. 568(1). 76–80. 7 indexed citations
10.
Straniero, Letizia, Valeria Rimoldi, Giulia Soldà, et al.. (2015). Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites. Journal of Human Genetics. 60(9). 467–471. 5 indexed citations
11.
Tang, Sunny X., Brett W. Davies, Edward J. Wladis, et al.. (2015). Pediatric Idiopathic Orbital Inflammation: Clinical Features of 30 Cases. Ophthalmic Plastic and Reconstructive Surgery. 32(4). 270–274. 24 indexed citations
12.
13.
Allegrini, Davide, Alessandro Autelitano, Paolo Fogagnolo, et al.. (2015). Lens opacities in glycogenoses type I and III. Canadian Journal of Ophthalmology. 50(6). 480–484. 3 indexed citations
14.
Mauri, Lucia, Alessandra Franzoni, Livia Garavelli, et al.. (2014). SOX2, OTX2 and PAX6 analysis in subjects with anophthalmia and microphthalmia. European Journal of Medical Genetics. 58(2). 66–70. 15 indexed citations
15.
Rimoldi, Valeria, Letizia Straniero, Rosanna Asselta, et al.. (2013). Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II. Gene. 537(1). 79–84. 15 indexed citations
16.
Mauri, Lucia, Alessandra Longo, Elena Piozzi, et al.. (2013). SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other European studies. Gene. 533(1). 398–402. 7 indexed citations
17.
Francesco, Sonia De, Paolo Galluzzi, Alessandra Longo, et al.. (2012). 13q Deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twins. European Journal of Ophthalmology. 22(5). 857–860. 3 indexed citations
18.
Spanò, Andrea, et al.. (2005). Surgical approach in a rare case of coloboma–choristoma. British Journal of Plastic Surgery. 58(5). 732–735. 5 indexed citations
19.
Manoukian, Siranoush, John A. Crolla, M. Testi, et al.. (2005). Bilateral preaxial polydactyly in a WAGR syndrome patient. American Journal of Medical Genetics Part A. 134A(4). 426–429. 4 indexed citations
20.
Pantaleoni, Chiara, Stefano D’Arrigo, Elena Piozzi, et al.. (2001). Papillitis as an onset sign of Leber's hereditary optic neuropathy: a case report. Brain and Development. 23(2). 125–127.

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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