Luisa Iommarini

4.7k total citations
53 papers, 1.6k citations indexed

About

Luisa Iommarini is a scholar working on Molecular Biology, Cancer Research and Clinical Biochemistry. According to data from OpenAlex, Luisa Iommarini has authored 53 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 17 papers in Cancer Research and 14 papers in Clinical Biochemistry. Recurrent topics in Luisa Iommarini's work include Mitochondrial Function and Pathology (41 papers), ATP Synthase and ATPases Research (25 papers) and Cancer, Hypoxia, and Metabolism (15 papers). Luisa Iommarini is often cited by papers focused on Mitochondrial Function and Pathology (41 papers), ATP Synthase and ATPases Research (25 papers) and Cancer, Hypoxia, and Metabolism (15 papers). Luisa Iommarini collaborates with scholars based in Italy, United States and France. Luisa Iommarini's co-authors include Anna Maria Porcelli, Giuseppe Gasparre, Ivana Kurelac, Anna Ghelli, Valério Carelli, Michela Rugolo, Francisca Díaz, Maria Antonietta Calvaruso, Christine M. Betts and G. Cara Romeo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Applied and Environmental Microbiology.

In The Last Decade

Luisa Iommarini

51 papers receiving 1.6k citations

Peers

Luisa Iommarini

PHYSI

ONCOL

Hezhi Fang China

Laura Hulea Canada

Katherine Mattaini United States

Paulo A. Gameiro United States

Loredana Moro Italy

Amit Sharma Germany

Hélène Simonnet France

Brian P. Fiske United States

Sergei Chetyrkin United States

Hiroki Sawa Japan

Hezhi Fang China

Luisa Iommarini

996 ×0.8

303 ×0.6

260 ×1.0

147 ×1.2

PHYSI

99 ×1.0

ONCOL

Citations per year, relative to Luisa Iommarini Luisa Iommarini (= 1×) peers Hezhi Fang

Countries citing papers authored by Luisa Iommarini

Since Specialization

Citations

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

Fields of papers citing papers by Luisa Iommarini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luisa Iommarini

This figure shows the co-authorship network connecting the top 25 collaborators of Luisa Iommarini. A scholar is included among the top collaborators of Luisa Iommarini 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 Luisa Iommarini. Luisa Iommarini 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

Bigi, Alessandra, Cristina Cecchi, Manuela Sollazzo, et al.. (2025). Human astrocytes from healthy individuals and Alzheimer’s patients respond differently to Aβ1–42 oligomers, triggering distinct paths of reactivity and senescence. Mechanisms of Ageing and Development. 228. 112116–112116.

Luise, Monica De, Carla Bini, Guido Pelletti, et al.. (2024). The landscape of rare mitochondrial DNA variants in sudden cardiac death: A potential role for ATP synthase. Heliyon. 11(1). e41592–e41592.

Musiani, Francesco, et al.. (2022). New Insights on Rotenone Resistance of Complex I Induced by the m.11778G>A/MT-ND4 Mutation Associated with Leber’s Hereditary Optic Neuropathy. Molecules. 27(4). 1341–1341. 5 indexed citations

Pirone, Daniele, Lisa Miccio, Vittorio Bianco, et al.. (2022). 3D imaging lipidometry in single cell by in-flow holographic tomography. Opto-Electronic Advances. 6(1). 220048–220048. 20 indexed citations

D’Angelo, Luigi, Monica De Luise, Ivana Kurelac, et al.. (2021). NDUFS3 depletion permits complex I maturation and reveals TMEM126A/OPA7 as an assembly factor binding the ND4-module intermediate. Cell Reports. 35(3). 109002–109002. 21 indexed citations

Strobbe, Daniela, Leonardo Caporali, Luisa Iommarini, et al.. (2018). Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases. Neurobiology of Disease. 114. 129–139. 20 indexed citations

Iommarini, Luisa, Anna Maria Porcelli, Giuseppe Gasparre, & Ivana Kurelac. (2017). Non-Canonical Mechanisms Regulating Hypoxia-Inducible Factor 1 Alpha in Cancer. Frontiers in Oncology. 7. 286–286. 176 indexed citations

Girolimetti, Giulia, Flora Guerra, Luisa Iommarini, et al.. (2017). Platinum-induced mitochondrial DNA mutations confer lower sensitivity to paclitaxel by impairing tubulin cytoskeletal organization. Human Molecular Genetics. 26(15). 2961–2974. 21 indexed citations

Porcelli, Anna Maria, Maria Antonietta Calvaruso, Luisa Iommarini, et al.. (2016). A unique combination of rare mitochondrial ribosomal RNA variants affects the kinetics of complex I assembly. The International Journal of Biochemistry & Cell Biology. 75. 117–122. 2 indexed citations

10.

Zaffagnini, Mirko, Simona Fermani, Matteo Calvaresi, et al.. (2015). Tuning Cysteine Reactivity and Sulfenic Acid Stability by Protein Microenvironment in Glyceraldehyde-3-Phosphate Dehydrogenases of Arabidopsis thaliana. Antioxidants and Redox Signaling. 24(9). 502–517. 30 indexed citations

11.

Iommarini, Luisa, Susana Peralta, Alessandra Torraco, & Francisca Díaz. (2015). Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function. Mitochondrion. 22. 96–118. 18 indexed citations

12.

Musicco, Clara, Antonella Cormio, Maria Antonietta Calvaruso, et al.. (2014). Analysis of the mitochondrial proteome of cybrid cells harbouring a truncative mitochondrial DNA mutation in respiratory complex I. Molecular BioSystems. 10(6). 1313–1319. 7 indexed citations

13.

Ghelli, Anna, Maria Antonietta Calvaruso, Luisa Iommarini, et al.. (2013). The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes. Human Molecular Genetics. 22(11). 2141–2151. 36 indexed citations

14.

Bartoletti‐Stella, Anna, Erminia Mariani, Ivana Kurelac, et al.. (2013). Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. Cell Death and Disease. 4(6). e663–e663. 46 indexed citations

15.

Iommarini, Luisa, Ivana Kurelac, Mariantonietta Capristo, et al.. (2013). Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment. Human Molecular Genetics. 23(6). 1453–1466. 80 indexed citations

16.

Gasparre, Giuseppe, Ivana Kurelac, Mariantonietta Capristo, et al.. (2011). A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1 , an Oncojanus Function. Cancer Research. 71(19). 6220–6229. 81 indexed citations

17.

Ghelli, Anna, Anna Maria Porcelli, Claudia Zanna, et al.. (2009). The Background of Mitochondrial DNA Haplogroup J Increases the Sensitivity of Leber's Hereditary Optic Neuropathy Cells to 2,5-Hexanedione Toxicity. PLoS ONE. 4(11). e7922–e7922. 77 indexed citations

18.

Srivastava, Sarika, Francisca Díaz, Luisa Iommarini, et al.. (2009). PGC-1α/β induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders. Human Molecular Genetics. 18(10). 1805–1812. 87 indexed citations

19.

Carelli, Valério, Pascal Reynier, Maria Lucia Valentino, et al.. (2008). Opa1 Mutations Induce Mitochondrial Dna Instability and Optic Atrophy Plus Phenotypes. Investigative Ophthalmology & Visual Science. 49(13). 5388–5388. 3 indexed citations

20.

Gasparre, Giuseppe, Luisa Iommarini, Anna Maria Porcelli, et al.. (2008). An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. Human Mutation. 30(3). 391–396. 44 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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