Alessia Nasca

1.2k total citations
27 papers, 605 citations indexed

About

Alessia Nasca is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alessia Nasca has authored 27 papers receiving a total of 605 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 15 papers in Clinical Biochemistry and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alessia Nasca's work include Mitochondrial Function and Pathology (21 papers), Metabolism and Genetic Disorders (15 papers) and ATP Synthase and ATPases Research (11 papers). Alessia Nasca is often cited by papers focused on Mitochondrial Function and Pathology (21 papers), Metabolism and Genetic Disorders (15 papers) and ATP Synthase and ATPases Research (11 papers). Alessia Nasca collaborates with scholars based in Italy, United Kingdom and Germany. Alessia Nasca's co-authors include Daniele Ghezzi, Andrea Legati, Costanza Lamperti, Eleonora Lamantea, Massimo Zeviani, Anna Ardissone, Isabella Moroni, Aurelio Reyes, Federica Invernizzi and Barbara Garavaglia and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Alessia Nasca

26 papers receiving 601 citations

Peers

Alessia Nasca

GENET

CMN

NEURO

Nicole J. Lake United States

Cathy E. Woodward United Kingdom

Lauren Brady Canada

Mazhor Aldosary Saudi Arabia

Akihiko Miyauchi Japan

Sophie Aubert France

Matteo Granatiero Italy

Samira Ait-El-Mkadem France

Elisa Rahikkala Finland

Malavika Hebbar India

Nicole J. Lake United States

Alessia Nasca

578 ×1.1

314 ×1.2

83 ×1.2

GENET

52 ×0.9

CMN

23 ×0.7

NEURO

Citations per year, relative to Alessia Nasca Alessia Nasca (= 1×) peers Nicole J. Lake

Countries citing papers authored by Alessia Nasca

Since Specialization

Citations

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

Fields of papers citing papers by Alessia Nasca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessia Nasca

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

All Works

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20 of 20 papers shown

Nasca, Alessia, et al.. (2025). Late-onset first epileptic seizure and cerebral small vessel disease: role of juxtacortical white matter lesions. Frontiers in Neurology. 15. 1508663–1508663.

Berti, Beatrice, Daniela Verrigni, Alessia Nasca, et al.. (2024). De Novo DNM1L Mutation in a Patient with Encephalopathy, Cardiomyopathy and Fatal Non-Epileptic Paroxysmal Refractory Vomiting. International Journal of Molecular Sciences. 25(14). 7782–7782. 2 indexed citations

Legati, Andrea, et al.. (2024). Investigation in yeast of novel variants in mitochondrial aminoacyl-tRNA synthetases WARS2, NARS2, and RARS2 genes associated with mitochondrial diseases. Human Molecular Genetics. 33(18). 1630–1641. 1 indexed citations

Nasca, Alessia, Eleonora Lamantea, Silvia Marchet, et al.. (2023). Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber’s Hereditary Optic Neuropathy (LHON) Subjects. International Journal of Molecular Sciences. 24(16). 12580–12580. 2 indexed citations

Frascarelli, Chiara, Nadia Zanetti, Alessia Nasca, et al.. (2023). Nanopore long-read next-generation sequencing for detection of mitochondrial DNA large-scale deletions. Frontiers in Genetics. 14. 1089956–1089956. 22 indexed citations

Zambon, Alberto A., Daniele Ghezzi, Cristina Baldoli, et al.. (2023). Expanding the spectrum of neonatal‐onset AIFM1‐associated disorders. Annals of Clinical and Translational Neurology. 10(10). 1844–1853. 1 indexed citations

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

Panteghini, Celeste, Chiara Reale, Alessia Nasca, et al.. (2021). Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson’s disease with brain iron accumulation through pseudo-exon activation. Neurogenetics. 22(4). 347–351. 4 indexed citations

Nasca, Alessia, Ivano Di Meo, Yakov Fellig, et al.. (2021). A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy. Journal of Human Genetics. 66(8). 835–840. 3 indexed citations

10.

Nasca, Alessia, Juliana Heidler, Kyle Thompson, et al.. (2020). Bi‐allelic pathogenic variants in NDUFC2 cause early‐onset Leigh syndrome and stalled biogenesis of complex I. EMBO Molecular Medicine. 12(11). e12619–e12619. 22 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.

Nasca, Alessia, et al.. (2017). Functionally pathogenic EARS2 variants in vitro may not manifest a phenotype in vivo. Neurology Genetics. 3(4). e162–e162. 14 indexed citations

13.

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

14.

Reyes, Aurelio, Laura Melchionda, Alessia Nasca, et al.. (2015). RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy. The American Journal of Human Genetics. 97(1). 186–193. 80 indexed citations

15.

Bee, Leonardo, Alessia Nasca, Filippo Cendron, et al.. (2015). A nonsense mutation of human XRCC 4 is associated with adult‐onset progressive encephalocardiomyopathy. EMBO Molecular Medicine. 7(7). 918–929. 19 indexed citations

16.

Diodato, Daria, Giorgio Tasca, Daniela Verrigni, et al.. (2015). A novel AIFM1 mutation expands the phenotype to an infantile motor neuron disease. European Journal of Human Genetics. 24(3). 463–466. 53 indexed citations

17.

Ardissone, Anna, Federica Invernizzi, Alessia Nasca, et al.. (2015). Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance. SHILAP Revista de lepidopterología. 5. 51–54. 16 indexed citations

18.

Perli, Elena, Carla Giordano, Annalinda Pisano, et al.. (2014). The isolated carboxy‐terminal domain of human mitochondrial leucyl‐ tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells. EMBO Molecular Medicine. 6(2). 169–182. 37 indexed citations

19.

Melchionda, Laura, et al.. (2014). A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions. Frontiers in Genetics. 5. 397–397. 17 indexed citations

20.

Diodato, Daria, Laura Melchionda, Tobias B. Haack, et al.. (2014). VARS2andTARS2Mutations in Patients with Mitochondrial Encephalomyopathies. Human Mutation. 35(8). 983–989. 71 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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