Andrea Legati

1.8k total citations
41 papers, 762 citations indexed

About

Andrea Legati is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Andrea Legati has authored 41 papers receiving a total of 762 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 22 papers in Clinical Biochemistry and 8 papers in Genetics. Recurrent topics in Andrea Legati's work include Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (22 papers) and ATP Synthase and ATPases Research (10 papers). Andrea Legati is often cited by papers focused on Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (22 papers) and ATP Synthase and ATPases Research (10 papers). Andrea Legati collaborates with scholars based in Italy, United States and United Kingdom. Andrea Legati's co-authors include Daniele Ghezzi, Alessia Nasca, Eleonora Lamantea, Giovanni Coppola, Anna Ardissone, Isabella Moroni, Barbara Garavaglia, Costanza Lamperti, Roberta R. Lemos and Gaël Nicolas and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and Brain.

In The Last Decade

Andrea Legati

40 papers receiving 760 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrea Legati Italy 17 509 222 128 113 91 41 762
Silvia Di Giandomenico Italy 10 499 1.0× 130 0.6× 62 0.5× 22 0.2× 73 0.8× 11 741
Kenji Nanao Japan 10 220 0.4× 66 0.3× 80 0.6× 90 0.8× 78 0.9× 17 561
Annabelle Chaussenot France 16 634 1.2× 210 0.9× 93 0.7× 101 0.9× 75 0.8× 35 870
Sietske H. Kevelam Netherlands 10 283 0.6× 86 0.4× 83 0.6× 100 0.9× 13 0.1× 11 473
Claudio Bruno Italy 20 833 1.6× 314 1.4× 203 1.6× 66 0.6× 106 1.2× 30 1.3k
Kunqian Ji China 14 503 1.0× 134 0.6× 40 0.3× 39 0.3× 65 0.7× 50 772
Corinne Magdelaine France 15 299 0.6× 35 0.2× 78 0.6× 159 1.4× 28 0.3× 45 749
M. T. Dotti Italy 13 309 0.6× 123 0.6× 45 0.4× 153 1.4× 55 0.6× 38 583
Edoardo Malfatti France 19 867 1.7× 170 0.8× 158 1.2× 78 0.7× 34 0.4× 89 1.1k
Tania Tiepolo Italy 7 840 1.7× 57 0.3× 60 0.5× 61 0.5× 86 0.9× 9 1.1k

Countries citing papers authored by Andrea Legati

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Legati

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Legati

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Legati. A scholar is included among the top collaborators of Andrea Legati 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 Andrea Legati. Andrea Legati 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
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Zupin, Luisa, Eleonora Lamantea, Enrico Baruffini, et al.. (2025). De Novo DNM1L Pathogenic Variant Associated with Lethal Encephalocardiomyopathy—Case Report and Literature Review. International Journal of Molecular Sciences. 26(2). 846–846. 1 indexed citations
3.
Marchet, Silvia, Lorenzo Nanetti, Andrea Legati, et al.. (2024). A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies. Orphanet Journal of Rare Diseases. 19(1). 200–200. 1 indexed citations
4.
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Invernizzi, Federica, Andrea Legati, Nadia Zanetti, et al.. (2023). NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia. Genes. 14(7). 1393–1393. 3 indexed citations
6.
Legati, Andrea & Daniele Ghezzi. (2023). Parkinson’s Disease, Parkinsonisms, and Mitochondria: the Role of Nuclear and Mitochondrial DNA. Current Neurology and Neuroscience Reports. 23(4). 131–147. 9 indexed citations
7.
Tyzack, Giulia E., et al.. (2022). Axonal Length Determines Distinct Homeostatic Phenotypes in Human iPSC Derived Motor Neurons on a Bioengineered Platform. Advanced Healthcare Materials. 11(10). e2101817–e2101817. 10 indexed citations
8.
Neri, Marcella, F. Fortunato, Alessandra Ferlini, et al.. (2022). AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian Patients. The Cerebellum. 22(6). 1313–1319. 1 indexed citations
9.
10.
Legati, Andrea, Nadia Zanetti, Alessia Nasca, et al.. (2021). Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNA. Journal of Molecular Diagnostics. 23(6). 732–741. 26 indexed citations
11.
Peverelli, Lorenzo, Andrea Legati, Eleonora Lamantea, et al.. (2019). New missense variants of NDUFA11 associated with late‐onset myopathy. Muscle & Nerve. 60(2). E11–E14. 8 indexed citations
12.
Catania, Alessia, Andrea Legati, Lorenzo Peverelli, et al.. (2019). Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment. American Journal of Medical Genetics Part A. 179(5). 827–831. 4 indexed citations
13.
Montano, Vincenzo, et al.. (2019). CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions. SHILAP Revista de lepidopterología. 2019. 1–4. 1 indexed citations
14.
Ritelli, Marco, et al.. (2018). GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS. Bioinformatics. 34(17). 3038–3040. 21 indexed citations
15.
Ardissone, Anna, Davide Tonduti, Andrea Legati, et al.. (2018). KARS-related diseases: progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature. Orphanet Journal of Rare Diseases. 13(1). 45–45. 28 indexed citations
16.
Legati, Andrea, Aurelio Reyes, Alessia Nasca, et al.. (2016). New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857(8). 1326–1335. 71 indexed citations
17.
Lemos, Roberta R., Eliana Marisa Ramos, Andrea Legati, et al.. (2015). Update and Mutational Analysis ofSLC20A2: A Major Cause of Primary Familial Brain Calcification. Human Mutation. 36(5). 489–495. 59 indexed citations
18.
Ferrer, Isidró, Andrea Legati, Juan Carlos García‐Moncó, et al.. (2015). Familial Behavioral Variant Frontotemporal Dementia Associated With Astrocyte-Predominant Tauopathy. Journal of Neuropathology & Experimental Neurology. 74(4). 370–379. 34 indexed citations
19.
Moreno, Fermín, Gil D. Rabinovici, Anna Karydas, et al.. (2015). A novel mutation P112H in the TARDBP gene associated with frontotemporal lobar degeneration without motor neuron disease and abundant neuritic amyloid plaques. Acta Neuropathologica Communications. 3(1). 19–19. 49 indexed citations
20.
Ardissone, Anna, Giuseppe Piscosquito, Andrea Legati, et al.. (2015). A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders. Neurology. 84(21). 2193–2195. 52 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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