Daniela Piga

580 total citations
21 papers, 401 citations indexed

About

Daniela Piga is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Daniela Piga has authored 21 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Daniela Piga's work include Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (9 papers) and ATP Synthase and ATPases Research (7 papers). Daniela Piga is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (9 papers) and ATP Synthase and ATPases Research (7 papers). Daniela Piga collaborates with scholars based in Italy, United Kingdom and United States. Daniela Piga's co-authors include Dario Ronchi, Giacomo P. Comi, Stefania Corti, Nereo Bresolin, Mario Barilani, Andrey Y. Abramov, Alessandro Santini, Lorenza Lazzari, Alessandro Protti and Marta Dossena and has published in prestigious journals such as International Journal of Molecular Sciences, Human Molecular Genetics and Biochimica et Biophysica Acta (BBA) - Bioenergetics.

In The Last Decade

Daniela Piga

19 papers receiving 391 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniela Piga Italy 9 289 79 54 51 42 21 401
Michela Ripolone Italy 13 349 1.2× 67 0.8× 121 2.2× 50 1.0× 43 1.0× 40 526
Peter Schneiderat Germany 13 487 1.7× 190 2.4× 60 1.1× 14 0.3× 32 0.8× 19 598
Xiaoyi Shao China 14 150 0.5× 23 0.3× 47 0.9× 36 0.7× 16 0.4× 26 394
Dina Marek‐Yagel Israel 12 358 1.2× 63 0.8× 29 0.5× 23 0.5× 33 0.8× 26 507
Bénédicte Mousson de Camaret France 16 552 1.9× 298 3.8× 70 1.3× 35 0.7× 29 0.7× 22 652
Sara Scapolan Italy 10 271 0.9× 70 0.9× 43 0.8× 11 0.2× 45 1.1× 11 348
Tim M. Strom Germany 4 173 0.6× 50 0.6× 51 0.9× 16 0.3× 51 1.2× 4 336
Martin Krenn Austria 13 135 0.5× 13 0.2× 86 1.6× 25 0.5× 24 0.6× 36 394
Javier Prieto Spain 8 322 1.1× 30 0.4× 25 0.5× 45 0.9× 20 0.5× 13 390

Countries citing papers authored by Daniela Piga

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Piga

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Piga

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Piga. A scholar is included among the top collaborators of Daniela Piga 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 Daniela Piga. Daniela Piga 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.
Piga, Daniela, Simona Zanotti, Michela Ripolone, et al.. (2024). Association between ZASP/LDB3 Pro26Ser and Inclusion Body Myopathy. International Journal of Molecular Sciences. 25(12). 6547–6547. 1 indexed citations
2.
Piga, Daniela, M. Rimoldi, Francesca Magri, et al.. (2024). Case report: A novel ACTA1 variant in a patient with nemaline rods and increased glycogen deposition. Frontiers in Neurology. 15. 1340693–1340693. 1 indexed citations
3.
Rimoldi, M., Francesca Magri, Michela Ripolone, et al.. (2023). Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant. Frontiers in Genetics. 14. 1278572–1278572. 3 indexed citations
4.
Scarcella, Simone, Laura Dell’Arti, Delia Gagliardi, et al.. (2023). Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation. BMC Neurology. 23(1). 165–165.
5.
Vecchio, Domizia, Letizia Mazzini, Gionata Strigaro, et al.. (2023). Walking Difficulties and Brainstem Dysfunction: a Case Report of Adult Onset Leigh Syndrome. SN Comprehensive Clinical Medicine. 5(1).
6.
Zanotti, Simona, Francesca Magri, Sabrina Salani, et al.. (2023). Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes. International Journal of Molecular Sciences. 24(6). 5551–5551. 7 indexed citations
7.
Manini, Arianna, Leonardo Caporali, Megi Meneri, et al.. (2022). Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions. Frontiers in Genetics. 13. 906667–906667. 5 indexed citations
8.
Fumagalli, Monica, Dario Ronchi, Maria Francesca Bedeschi, et al.. (2022). A novel RRM2B mutation associated with mitochondrial DNA depletion syndrome. Molecular Genetics and Metabolism Reports. 32. 100887–100887. 5 indexed citations
9.
Mauri, Eleonora, Daniela Piga, Alessandra Govoni, et al.. (2021). Early Findings in Neonatal Cases of RYR1–Related Congenital Myopathies. Frontiers in Neurology. 12. 664618–664618. 2 indexed citations
10.
Vecchio, Domizia, Letizia Mazzini, Gionata Strigaro, et al.. (2021). A young male with walking difficulties and subacute brainstem dysfunction: Adult-onset Leigh syndrome. Journal of the Neurological Sciences. 429. 119363–119363. 1 indexed citations
11.
Ronchi, Dario, Leonardo Caporali, Megi Meneri, et al.. (2020). TYMP Variants Result in Late-Onset Mitochondrial Myopathy With Altered Muscle Mitochondrial DNA Homeostasis. Frontiers in Genetics. 11. 860–860. 6 indexed citations
12.
Piga, Daniela, Sabrina Salani, Francesca Magri, et al.. (2019). Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies. Therapeutic Advances in Neurological Disorders. 12. 1278055046–1278055046. 25 indexed citations
13.
Gagliardi, Delia, Eleonora Mauri, Francesca Magri, et al.. (2019). Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature. Frontiers in Neurology. 10. 38–38. 13 indexed citations
14.
Ronchi, Dario, Changwei Liu, Leonardo Caporali, et al.. (2019). Novel mutations in DNA2 associated with myopathy and mtDNA instability. Annals of Clinical and Translational Neurology. 6(9). 1893–1899. 10 indexed citations
15.
Mauri, Eleonora, Robertino Dilena, Dario Ronchi, et al.. (2018). Subclinical Leber’s hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye. BMC Neurology. 18(1). 220–220. 4 indexed citations
16.
Borsani, Oscar, Daniela Piga, Stefania Costa, et al.. (2018). Stormorken Syndrome Caused by a p.R304W STIM1 Mutation: The First Italian Patient and a Review of the Literature. Frontiers in Neurology. 9. 22 indexed citations
17.
Angelova, Plamena R., Mario Barilani, Christopher Lovejoy, et al.. (2017). Mitochondrial dysfunction in Parkinsonian mesenchymal stem cells impairs differentiation. Redox Biology. 14. 474–484. 98 indexed citations
18.
Rizzo, Federica, Dario Ronchi, Sabrina Salani, et al.. (2016). Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neurons. Human Molecular Genetics. 25(19). 4266–4281. 50 indexed citations
19.
Valente, Lucia, Daniela Piga, Eleonora Lamantea, et al.. (2008). Identification of novel mutations in five patients with mitochondrial encephalomyopathy. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1787(5). 491–501. 78 indexed citations
20.
Blasi, Claudia Di, Daniela Piga, Isabella Moroni, et al.. (2005). LAMA2 Gene Analysis in Congenital Muscular Dystrophy. Archives of Neurology. 62(10). 1582–6. 24 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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