A. M. Bardelli

435 total citations
23 papers, 265 citations indexed

About

A. M. Bardelli is a scholar working on Molecular Biology, Ophthalmology and Cell Biology. According to data from OpenAlex, A. M. Bardelli has authored 23 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Ophthalmology and 5 papers in Cell Biology. Recurrent topics in A. M. Bardelli's work include Metabolism and Genetic Disorders (3 papers), Skin and Cellular Biology Research (2 papers) and Mitochondrial Function and Pathology (2 papers). A. M. Bardelli is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Skin and Cellular Biology Research (2 papers) and Mitochondrial Function and Pathology (2 papers). A. M. Bardelli collaborates with scholars based in Italy, Russia and United States. A. M. Bardelli's co-authors include Antonio Federico, Paolo Galluzzi, Ignazio Maria Vallone, Carlo Venturi, Theodora Hadjistilianou, Matteo Vanni, R. Frezzotti, Laura Barberi, Carla Battisti and Maria Teresa Dotti and has published in prestigious journals such as Radiology, The American Journal of Cardiology and Human Mutation.

In The Last Decade

A. M. Bardelli

21 papers receiving 242 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. M. Bardelli Italy 10 116 75 73 46 39 23 265
Leslie A. Bard United States 10 249 2.1× 40 0.5× 68 0.9× 151 3.3× 149 3.8× 11 480
Chongfei Jin China 13 239 2.1× 20 0.3× 99 1.4× 159 3.5× 14 0.4× 22 361
Sarah S. Alousi United States 11 229 2.0× 115 1.5× 17 0.2× 11 0.2× 7 0.2× 13 355
Céline Bürer Switzerland 10 170 1.5× 15 0.2× 71 1.0× 20 0.4× 151 3.9× 16 342
Silvia Lechner Austria 6 106 0.9× 61 0.8× 95 1.3× 15 0.3× 6 0.2× 8 221
Rungnapa Ittiwut Thailand 10 85 0.7× 23 0.3× 83 1.1× 6 0.1× 27 0.7× 26 213
Kimberly A. Neely United States 10 100 0.9× 15 0.2× 33 0.5× 150 3.3× 8 0.2× 16 257
Natalie Krassikoff United States 10 153 1.3× 15 0.2× 163 2.2× 9 0.2× 15 0.4× 13 333
Arum Oh South Korea 7 109 0.9× 30 0.4× 91 1.2× 6 0.1× 18 0.5× 18 247
J Gärtner Germany 10 73 0.6× 32 0.4× 18 0.2× 167 3.6× 12 0.3× 47 289

Countries citing papers authored by A. M. Bardelli

Since Specialization
Citations

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

Fields of papers citing papers by A. M. Bardelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. M. Bardelli. 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 A. M. Bardelli. The network helps show where A. M. Bardelli may publish in the future.

Co-authorship network of co-authors of A. M. Bardelli

This figure shows the co-authorship network connecting the top 25 collaborators of A. M. Bardelli. A scholar is included among the top collaborators of A. M. Bardelli 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 A. M. Bardelli. A. M. Bardelli 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.
Galluzzi, Paolo, Carlo Venturi, Alfonso Cerase, et al.. (2001). Coats Disease: Smaller Volume of the Affected Globe. Radiology. 221(1). 64–69. 19 indexed citations
2.
Meloni, Ilaria, Pietro Rubegni, G. De Aloe, et al.. (2001). Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11. Human Mutation. 18(1). 85–85. 37 indexed citations
3.
Rubegni, Pietro, et al.. (2000). Mitral valve prolapse in healthy relatives of patients with familial pseudoxanthoma elasticum. The American Journal of Cardiology. 85(10). 1268–1271. 14 indexed citations
4.
Galluzzi, Paolo, et al.. (1999). MRI of Wolfram syndrome (DIDMOAD). Neuroradiology. 41(10). 729–731. 33 indexed citations
5.
Battisti, Carla, et al.. (1998). Schnyder corneal crystalline dystrophy: Description of a new family with evidence of abnormal lipid storage in skin fibroblasts. American Journal of Medical Genetics. 75(1). 35–39. 36 indexed citations
6.
Dotti, M. T., A. M. Bardelli, Nicola De Stefano, et al.. (1993). Optic Atrophy in Marinesco-Sjögren Syndrome: An Additional Ocular Feature: Report of three Cases in two Families. Ophthalmic Paediatrics and Genetics. 14(1). 5–7. 13 indexed citations
7.
Mastrangelo, Domenico, et al.. (1989). Analysis of 75 cases and proposal for a new model of oncogenesis and tumor growth kinetics. Ophthalmic Paediatrics and Genetics. 10(3). 161–171. 3 indexed citations
8.
Bardelli, A. M., et al.. (1989). Congenital and developmental cataracts and multimalformation syndromes. Ophthalmic Paediatrics and Genetics. 10(4). 293–298. 8 indexed citations
9.
Bardelli, A. M. & Theodora Hadjistilianou. (1989). Buphthalmos and progressive elephantiasis in neurofibromatosis: A report of three cases. Ophthalmic Paediatrics and Genetics. 10(4). 279–286. 6 indexed citations
10.
Federico, Antonio, L. Manneschi, Mario Meloni, et al.. (1988). Histochemical, ultrastructural and biochemical study of muscle mitochondria in Leber's hereditary optic atrophy. Journal of Inherited Metabolic Disease. 11(S2). 193–197. 8 indexed citations
11.
Federico, Antonio, et al.. (1987). Electrocardiographic abnormalities in Leber's hereditary optic atrophy. Journal of Inherited Metabolic Disease. 10(S2). 256–259. 5 indexed citations
12.
Fois, A., M. Cioni, R. Frezzotti, et al.. (1986). Presentation of the data of the Italian registry for oculocutaneous tyrosinaemia. Journal of Inherited Metabolic Disease. 9(S2). 262–264. 20 indexed citations
13.
Dotti, M. T., Alessandro Rossi, N. Rizzuto, et al.. (1985). Atypical Phenotype of Refsum’s Disease: Clinical, Biochemical, Neurophysiological and Pathological Study. European Neurology. 24(2). 85–93. 8 indexed citations
14.
Bardelli, A. M., Theodora Hadjistilianou, & Laura Barberi. (1985). Aicardi's syndrome. Ophthalmic Paediatrics and Genetics. 5(3). 141–144. 1 indexed citations
15.
Bardelli, A. M., et al.. (1985). Ocular manifestations in Kniest syndrome, Smith-Lemli-Opitz syndrome, Hallermann-Streiff-François syndrome, Rubinstein-Taybi syndrome and median cleft face syndrome. Ophthalmic Paediatrics and Genetics. 6(1-2). 103–107. 14 indexed citations
16.
Bardelli, A. M., et al.. (1985). Leber's optic neuritis. Ophthalmic Paediatrics and Genetics. 5(3). 133–140. 2 indexed citations
17.
Frezzotti, R., et al.. (1984). The pars plana approach in two cases of persistent hyperplastic primary vitreous (PHPV). Ophthalmic Paediatrics and Genetics. 4(2). 107–110. 11 indexed citations
18.
Giuffrè, R, et al.. (1983). Anterior optic pathways gliomas. The dilemma of treatment.. PubMed. 26(1). 61–72. 7 indexed citations
19.
20.
Bardelli, A. M., et al.. (1977). Familial Tyrosinaemia with Eye and Skin Lesions. Ophthalmologica. 175(1). 5–9. 12 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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