Elisa Fassone

1.3k total citations
19 papers, 880 citations indexed

About

Elisa Fassone is a scholar working on Molecular Biology, Clinical Biochemistry and Neurology. According to data from OpenAlex, Elisa Fassone has authored 19 papers receiving a total of 880 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 2 papers in Neurology. Recurrent topics in Elisa Fassone's work include Mitochondrial Function and Pathology (16 papers), ATP Synthase and ATPases Research (11 papers) and Metabolism and Genetic Disorders (11 papers). Elisa Fassone is often cited by papers focused on Mitochondrial Function and Pathology (16 papers), ATP Synthase and ATPases Research (11 papers) and Metabolism and Genetic Disorders (11 papers). Elisa Fassone collaborates with scholars based in Italy, United Kingdom and United States. Elisa Fassone's co-authors include Shamima Rahman, Jan‐Willem Taanman, Andreina Bordoni, Nereo Bresolin, Maurizio Moggio, Dario Ronchi, Stefania Corti, Giacomo P. Comi, Francesco Fortunato and Costanza Lamperti and has published in prestigious journals such as Oncogene, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

In The Last Decade

Elisa Fassone

19 papers receiving 873 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisa Fassone Italy 13 705 365 132 75 70 19 880
Andrea Legati Italy 17 509 0.7× 222 0.6× 113 0.9× 62 0.8× 35 0.5× 41 762
Daniel Beltrán-Valero de Bernabé United States 14 743 1.1× 360 1.0× 63 0.5× 138 1.8× 49 0.7× 16 972
Emanuela Bottani Italy 14 585 0.8× 247 0.7× 43 0.3× 137 1.8× 91 1.3× 25 810
Christoph Korenke Germany 14 343 0.5× 329 0.9× 195 1.5× 178 2.4× 26 0.4× 21 757
Manuèle Miné France 17 362 0.5× 105 0.3× 150 1.1× 49 0.7× 29 0.4× 27 612
Kunqian Ji China 14 503 0.7× 134 0.4× 39 0.3× 117 1.6× 115 1.6× 50 772
Ginat Narkis Israel 14 528 0.7× 101 0.3× 72 0.5× 62 0.8× 88 1.3× 23 836
Johan Van Hove United States 10 531 0.8× 290 0.8× 30 0.2× 119 1.6× 20 0.3× 17 733
Nicole J. Lake United States 9 578 0.8× 314 0.9× 23 0.2× 47 0.6× 30 0.4× 17 668
Gunter Scharer United States 17 616 0.9× 583 1.6× 46 0.3× 108 1.4× 25 0.4× 29 1.1k

Countries citing papers authored by Elisa Fassone

Since Specialization
Citations

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

Fields of papers citing papers by Elisa Fassone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Fassone

This figure shows the co-authorship network connecting the top 25 collaborators of Elisa Fassone. A scholar is included among the top collaborators of Elisa Fassone 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 Elisa Fassone. Elisa Fassone is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Wedatilake, Yehani, Elisa Fassone, Christopher A. Powell, et al.. (2016). TRNT1 deficiency: clinical, biochemical and molecular genetic features. Orphanet Journal of Rare Diseases. 11(1). 90–90. 54 indexed citations
2.
Fassone, Elisa, et al.. (2016). The pleiotropic effects of decanoic acid treatment on mitochondrial function in fibroblasts from patients with complex I deficient Leigh syndrome. Journal of Inherited Metabolic Disease. 39(3). 415–426. 44 indexed citations
3.
Fassone, Elisa, Yehani Wedatilake, Catherine DeVile, et al.. (2013). Treatable Leigh-like encephalopathy presenting in adolescence. BMJ Case Reports. 2013. bcr2013200838–bcr2013200838. 42 indexed citations
4.
Marega, Carla, S. Spataro, Elisa Fassone, Isabella Camurati, & Antonio Marigo. (2013). Self‐welding 1‐butene/ethylene copolymers from metallocene catalysts: Structure, morphology, and mechanical properties. Journal of Applied Polymer Science. 131(8). 4 indexed citations
5.
Yao, Zhi, Aleck W.E. Jones, Elisa Fassone, et al.. (2012). PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutations. Oncogene. 32(20). 2592–2600. 35 indexed citations
6.
Fassone, Elisa & Shamima Rahman. (2012). Complex I deficiency: clinical features, biochemistry and molecular genetics. Journal of Medical Genetics. 49(9). 578–590. 233 indexed citations
7.
Ronchi, Dario, Andreina Bordoni, Mafalda Rizzuti, et al.. (2011). Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation. Biochemical and Biophysical Research Communications. 412(2). 245–248. 12 indexed citations
8.
Ronchi, Dario, Elisa Fassone, Andreina Bordoni, et al.. (2011). Two novel mutations in PEO1 (Twinkle) gene associated with chronic external ophthalmoplegia. Journal of the Neurological Sciences. 308(1-2). 173–176. 6 indexed citations
9.
Fassone, Elisa, Jan‐Willem Taanman, Iain P. Hargreaves, et al.. (2011). Mutations in the mitochondrial complex I assembly factor NDUFAF1 cause fatal infantile hypertrophic cardiomyopathy. Journal of Medical Genetics. 48(10). 691–697. 50 indexed citations
10.
Pitceathly, Robert D. S., Elisa Fassone, Jan‐Willem Taanman, et al.. (2011). Kearns–Sayre syndrome caused by defective R1/p53R2 assembly. Journal of Medical Genetics. 48(9). 610–617. 28 indexed citations
11.
Ronchi, Dario, Monica Sciacco, Andreina Bordoni, et al.. (2011). The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment. European Journal of Human Genetics. 20(3). 357–360. 3 indexed citations
12.
Pitceathly, Robert D. S., Elisa Fassone, Jan‐Willem Taanman, et al.. (2011). P53 Kearns-Sayre syndrome caused by defective R1/p53R2 assembly. Neuromuscular Disorders. 21(9). S21–S21. 23 indexed citations
13.
Fassone, Elisa, Jan‐Willem Taanman, Michael I. Sadowski, et al.. (2011). Kearns-Sayre syndrome caused by defective R1/p53R2 assembly. 2. 2 indexed citations
14.
Fassone, Elisa, et al.. (2011). A novel homozygous deletion in NDUFS4 causes complex I deficient Leigh syndrome. Mitochondrion. 11(4). 656–656. 1 indexed citations
15.
Fassone, Elisa, Andrew Duncan, Jan‐Willem Taanman, et al.. (2010). FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy. Human Molecular Genetics. 19(24). 4837–4847. 78 indexed citations
16.
Lamperti, Costanza, Valeria Lucchini, Dario Ronchi, et al.. (2010). Mitochondrial Respiratory Chain Dysfunction in Muscle From Patients With Amyotrophic Lateral Sclerosis. Archives of Neurology. 67(7). 849–54. 114 indexed citations
17.
Ronchi, Dario, Andreina Bordoni, Elisa Fassone, et al.. (2010). The m.12316G>A mutation in the mitochondrial tRNALeu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment. Journal of the Neurological Sciences. 292(1-2). 107–110. 1 indexed citations
18.
Fonzo, Alessio Di, Dario Ronchi, Tiziana Lodi, et al.. (2009). The Mitochondrial Disulfide Relay System Protein GFER Is Mutated in Autosomal-Recessive Myopathy with Cataract and Combined Respiratory-Chain Deficiency. The American Journal of Human Genetics. 84(5). 594–604. 114 indexed citations
19.
Ronchi, Dario, Andreina Bordoni, Elisa Fassone, et al.. (2009). Mitochondrial DNA G8363A mutation in the tRNALys gene: Clinical, biochemical and pathological study. Journal of the Neurological Sciences. 281(1-2). 85–92. 36 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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