Elisabetta Pelo

809 total citations
36 papers, 480 citations indexed

About

Elisabetta Pelo is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Elisabetta Pelo has authored 36 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 11 papers in Genetics and 8 papers in Ophthalmology. Recurrent topics in Elisabetta Pelo's work include Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). Elisabetta Pelo is often cited by papers focused on Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). Elisabetta Pelo collaborates with scholars based in Italy, United Kingdom and Australia. Elisabetta Pelo's co-authors include Elena Di Gianantonio, Romano Tenconi, Isabella Mammi, Francesca Torricelli, Ilaria Passerini, Andrea Sodi, Francesco Testa, Stanislao Rizzo, Francesca Simonelli and Sandro Banfi and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Bioinformatics.

In The Last Decade

Elisabetta Pelo

32 papers receiving 463 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabetta Pelo Italy 11 216 88 80 62 52 36 480
Qing Tian China 12 230 1.1× 258 2.9× 22 0.3× 55 0.9× 45 0.9× 34 604
Natalie Hauser United States 13 293 1.4× 54 0.6× 228 2.9× 17 0.3× 51 1.0× 26 562
Viviana Cordeddu Italy 13 775 3.6× 197 2.2× 203 2.5× 30 0.5× 37 0.7× 22 995
Siddharth Banka United Kingdom 18 339 1.6× 37 0.4× 480 6.0× 40 0.6× 42 0.8× 55 991
Dominique Leboeuf Canada 14 250 1.2× 26 0.3× 48 0.6× 74 1.2× 13 0.3× 23 498
James D. Weisfeld‐Adams United States 14 284 1.3× 19 0.2× 90 1.1× 20 0.3× 52 1.0× 27 663
Almundher Al‐Maawali Oman 14 312 1.4× 26 0.3× 142 1.8× 7 0.1× 31 0.6× 55 605
Steven Rostad United States 14 173 0.8× 34 0.4× 28 0.3× 18 0.3× 155 3.0× 26 553
Go Hun Seo South Korea 11 256 1.2× 26 0.3× 204 2.5× 21 0.3× 26 0.5× 82 527
Jana M. Mitchell United States 10 457 2.1× 28 0.3× 62 0.8× 8 0.1× 32 0.6× 11 688

Countries citing papers authored by Elisabetta Pelo

Since Specialization
Citations

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

Fields of papers citing papers by Elisabetta Pelo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabetta Pelo

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabetta Pelo. A scholar is included among the top collaborators of Elisabetta Pelo 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 Elisabetta Pelo. Elisabetta Pelo 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.
Giansanti, Fabrizio, Dario Giorgio, Andrea Sodi, et al.. (2024). Myopic Macular Hole and Detachment after Gene Therapy in Atypical RPE65 Retinal Dystrophy: A Case Report. Genes. 15(7). 879–879. 1 indexed citations
2.
Bagnoli, Silvia, Giulia Giacomucci, Alessandra Govoni, et al.. (2023). The Frequency of Intermediate Alleles in Patients with Cerebellar Phenotypes. The Cerebellum. 23(3). 1135–1145.
3.
Baroncini, Anna, Olga Calabrese, Marco Colotto, et al.. (2022). Knowledge and attitude of general pratictioners towards direct-to-consumer genomic tests: a survey conducted in Italy. SHILAP Revista de lepidopterología. 12(4). 2 indexed citations
4.
Karali, Marianthi, Francesco Testa, Valentina Di Iorio, et al.. (2022). Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy. Scientific Reports. 12(1). 20815–20815. 41 indexed citations
5.
Mucciolo, Dario Pasquale, Dario Giorgio, Ilaria Passerini, et al.. (2021). Choroidal Vascularity Index in CHM Carriers. Frontiers in Ophthalmology. 1. 755058–755058. 2 indexed citations
6.
Sodi, Andrea, Sandro Banfi, Francesco Testa, et al.. (2021). RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy. Orphanet Journal of Rare Diseases. 16(1). 257–257. 25 indexed citations
7.
Coltro, Giacomo, Francesco Mannelli, Federica Vergoni, et al.. (2020). Extramedullary blastic transformation of primary myelofibrosis in the form of disseminated myeloid sarcoma: a case report and review of the literature. Clinical and Experimental Medicine. 20(2). 313–320. 6 indexed citations
8.
Bartalucci, Niccolò, Francesco Mannelli, Elisa Contini, et al.. (2019). THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS. Haematologica. 104. 12–12. 1 indexed citations
9.
Murro, Vittoria, Dario Pasquale Mucciolo, Andrea Sodi, et al.. (2019). En face OCT in choroideremia. Ophthalmic Genetics. 40(6). 514–520. 6 indexed citations
10.
Magi, Alberto, Davide Bolognini, Niccolò Bartalucci, et al.. (2019). Nano-GLADIATOR: real-time detection of copy number alterations from nanopore sequencing data. Bioinformatics. 35(21). 4213–4221. 13 indexed citations
11.
Terlizzi, Vito, Antonella Miriam Di Lullo, Marika Comegna, et al.. (2018). S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 2–2. 18 indexed citations
12.
Mazzarotto, Francesco, Francesca Girolami, Beatrice Boschi, et al.. (2018). Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center. Genetics in Medicine. 21(2). 284–292. 51 indexed citations
13.
Sodi, Andrea, Ilaria Passerini, Daniela Bacherini, et al.. (2018). CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease. Ophthalmic Genetics. 39(6). 699–705. 6 indexed citations
14.
Mazzarotto, Francesco, Francesca Girolami, Beatrice Boschi, et al.. (2018). Two decades of genetic testing in hypertrophic cardiomyopathy in a single center: The additive value of extended next-generation sequencing panels lies in the early diagnosis of metabolic mimics. Vascular Pharmacology. 103-105. 63–63. 1 indexed citations
15.
Tarquini, Roberto, Federico Perfetto, Franco Bergesio, et al.. (2007). A new ATTR Phe64Ile mutation with late-onset multiorgan involvement. Amyloid. 14(4). 289–292. 1 indexed citations
16.
Romanelli, Roberto Giulio, Tullio Barni, Mario Maggi, et al.. (2003). Expression and Function of Gonadotropin-releasing Hormone (GnRH) Receptor in Human Olfactory GnRH-secreting Neurons. Journal of Biological Chemistry. 279(1). 117–126. 58 indexed citations
17.
Pelo, Elisabetta, M Ciaccheri, Gabriele Castelli, et al.. (2002). Familial amyloid polyneuropathy with genetic anticipation associated to a gly47glu transthyretin variant in an Italian kindred. Amyloid. 9(1). 35–41. 14 indexed citations
18.
Borsini, Walter, et al.. (2002). Anderson-Fabry disease with cerebrovascular complications in two Italian families. Neurological Sciences. 23(2). 49–53. 22 indexed citations
19.
Torricelli, Francesca, Fabio Martinelli, Elisabetta Pelo, et al.. (2001). Anderson-Fabry Disease: Molecular Analysis and Clinical Manifestations in Three Italian Families. Contributions to nephrology. 216–222. 1 indexed citations
20.
Marziliano, Nicola, et al.. (2000). Melting Temperature Assay for a UGT1A Gene Variant in Gilbert Syndrome. Clinical Chemistry. 46(3). 423–425. 18 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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