Matteo Bertelli

3.6k total citations
183 papers, 2.2k citations indexed

About

Matteo Bertelli is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Matteo Bertelli has authored 183 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 40 papers in Genetics and 30 papers in Oncology. Recurrent topics in Matteo Bertelli's work include Retinal Development and Disorders (29 papers), Lymphatic System and Diseases (25 papers) and Retinal Diseases and Treatments (18 papers). Matteo Bertelli is often cited by papers focused on Retinal Development and Disorders (29 papers), Lymphatic System and Diseases (25 papers) and Retinal Diseases and Treatments (18 papers). Matteo Bertelli collaborates with scholars based in Italy, Türkiye and United States. Matteo Bertelli's co-authors include Tommaso Beccari, K Dhuli, Stefano Paolacci, Elena Manara, Aysha Karim Kiani, Sandro Michelini, Paolo Enrico Maltese, Astrit Dautaj, K Donato and Giuseppina Matera and has published in prestigious journals such as SHILAP Revista de lepidopterología, Analytical Biochemistry and Scientific Reports.

In The Last Decade

Matteo Bertelli

174 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matteo Bertelli Italy 24 696 396 274 271 246 183 2.2k
Jun Tang China 33 896 1.3× 304 0.8× 131 0.5× 204 0.8× 122 0.5× 108 3.7k
Wen Lu China 24 684 1.0× 287 0.7× 282 1.0× 176 0.6× 143 0.6× 102 2.2k
Santiago Rodrı́guez United Kingdom 27 871 1.3× 220 0.6× 796 2.9× 168 0.6× 181 0.7× 88 3.2k
Eunok Im South Korea 36 1.5k 2.2× 369 0.9× 371 1.4× 490 1.8× 110 0.4× 108 3.8k
Tanja Maier Germany 28 974 1.4× 412 1.0× 164 0.6× 574 2.1× 93 0.4× 65 2.5k
Óscar Fraile-Martínez Spain 26 867 1.2× 341 0.9× 115 0.4× 267 1.0× 217 0.9× 117 2.4k
Mingming Liu China 29 1.2k 1.7× 236 0.6× 97 0.4× 308 1.1× 168 0.7× 220 3.3k
Jun Nishihira Japan 48 1.5k 2.2× 473 1.2× 226 0.8× 290 1.1× 253 1.0× 202 6.5k
Philip M. Cummins Ireland 29 1.3k 1.8× 264 0.7× 140 0.5× 347 1.3× 75 0.3× 64 3.0k
D.R. Glick United States 10 1.8k 2.6× 427 1.1× 119 0.4× 199 0.7× 175 0.7× 21 4.1k

Countries citing papers authored by Matteo Bertelli

Since Specialization
Citations

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

Fields of papers citing papers by Matteo Bertelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matteo Bertelli

This figure shows the co-authorship network connecting the top 25 collaborators of Matteo Bertelli. A scholar is included among the top collaborators of Matteo Bertelli 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 Matteo Bertelli. Matteo Bertelli 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.
2.
Cannarella, Rossella, Rosita A. Condorelli, Andrea Bernini, et al.. (2023). Genetic Analysis of Patients with Congenital Hypogonadotropic Hypogonadism: A Case Series. International Journal of Molecular Sciences. 24(8). 7428–7428. 3 indexed citations
3.
Micheletti, Cristian, Maria Chiara Medori, G Bonetti, et al.. (2023). Effects of Carob Extract on the Intestinal Microbiome and Glucose Metabolism: A Systematic Review and Meta-Analysis.. PubMed. 174(Suppl 2(6)). 169–172. 2 indexed citations
4.
Donato, K, Alejandro Macchia, G Bonetti, et al.. (2023). Reduction of nitrosamines in cigarette smoke vapors through a filter functionalized with polyphenols from olive tree.. PubMed. 174(Suppl 2(6)). 126–141. 1 indexed citations
5.
Bonetti, G, Giuseppe Marceddu, K Dhuli, et al.. (2023). AKR1C1 and hormone metabolism in lipedema pathogenesis: a computational biology approach.. PubMed. 27(6 Suppl). 137–147. 3 indexed citations
6.
Ceccarini, Maria Rachele, Irene Chiesa, Francesca Ripanti, et al.. (2023). Electrospun Nanofibrous UV Filters with Bidirectional Actuation Properties Based on Salmon Sperm DNA/Silk Fibroin for Biomedical Applications. ACS Omega. 8(41). 38233–38242. 3 indexed citations
7.
Maltese, Paolo Enrico, Maria Cristina Savastano, Matteo Bertelli, et al.. (2023). Retinitis Pigmentosa Associated with EYS Gene Mutations: Disease Severity Staging and Central Retina Atrophy. Diagnostics. 13(5). 850–850. 4 indexed citations
8.
Cristofoli, Francesca, Paolo Enrico Maltese, G Bonetti, et al.. (2023). MAGI-ACMG: Algorithm for the Classification of Variants According to ACMG and ACGS Recommendations. Genes. 14(8). 1600–1600. 7 indexed citations
9.
Parravano, Mariacristina, Eliana Costanzo, Matteo Bertelli, et al.. (2022). Multimodal Study of PRPH2 Gene-Related Retinal Phenotypes. Diagnostics. 12(8). 1851–1851. 10 indexed citations
10.
Missaglia, Sara, et al.. (2021). Imbalance between Expression of FOXC2 and Its lncRNA in Lymphedema-Distichiasis Caused by Frameshift Mutations. Genes. 12(5). 650–650. 4 indexed citations
11.
Falsini, Benedetto, Maria Cristina Savastano, Angelo Maria Minnella, et al.. (2021). USH2A-Related Retinitis Pigmentosa: Staging of Disease Severity and Morpho-Functional Studies. Diagnostics. 11(2). 213–213. 10 indexed citations
12.
Cristofoli, Francesca, Giulia Guerri, Roberta Maia de Castro Romanelli, et al.. (2021). Variant Selection and Interpretation: An Example of Modified VarSome Classifier of ACMG Guidelines in the Diagnostic Setting. Genes. 12(12). 1885–1885. 9 indexed citations
13.
Marino, Valerio, et al.. (2021). Impaired Ca2+ Sensitivity of a Novel GCAP1 Variant Causes Cone Dystrophy and Leads to Abnormal Synaptic Transmission Between Photoreceptors and Bipolar Cells. International Journal of Molecular Sciences. 22(8). 4030–4030. 5 indexed citations
14.
Cannarella, Rossella, Vincenza Precone, Giulia Guerri, et al.. (2020). Clinical Evaluation of a Custom Gene Panel as a Tool for Precision Male Infertility Diagnosis by Next-Generation Sequencing. Life. 10(10). 242–242. 8 indexed citations
15.
Michelini, Sandro, Syed Hussain Basha, Juraj Krajčovič, et al.. (2020). TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema. International Journal of Molecular Sciences. 21(18). 6780–6780. 12 indexed citations
16.
Temel, Şehime Gülsün, Mahmut Çerkez Ergören, Elena Manara, et al.. (2020). Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann–Rautenstrauch syndrome. European Journal of Human Genetics. 28(12). 1675–1680. 7 indexed citations
17.
Michelini, Sandro, Bruno Amato, Elena Manara, et al.. (2020). Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema. Genes. 11(11). 1361–1361. 4 indexed citations
18.
Compagna, Rita, Bruno Amato, Syed Hussain Basha, et al.. (2020). Mutations in the ARAP3 Gene in Three Families with Primary Lymphedema Negative for Mutations in Known Lymphedema-Associated Genes. International Journal of Genomics. 2020. 1–9.
19.
Marino, Valerio, Elisa Oppici, Paolo Enrico Maltese, et al.. (2018). A novel p.(Glu111Val) missense mutation in GUCA1A associated with cone-rod dystrophy leads to impaired calcium sensing and perturbed second messenger homeostasis in photoreceptors. Human Molecular Genetics. 27(24). 4204–4217. 27 indexed citations
20.
Montesano, Giovanni, et al.. (2018). Comparison of 5-year progression of retinitis pigmentosa involving the posterior pole among siblings by means of SD-OCT: a retrospective study. BMC Ophthalmology. 18(1). 153–153. 14 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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