María Miranda

2.8k total citations
13 papers, 605 citations indexed

About

María Miranda is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, María Miranda has authored 13 papers receiving a total of 605 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 2 papers in Genetics. Recurrent topics in María Miranda's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (4 papers). María Miranda is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (4 papers). María Miranda collaborates with scholars based in United States, Germany and France. María Miranda's co-authors include Nils‐Göran Larsson, Inge Kühl, Aleksandra Filipovska, Arnaud Mourier, Ilian Atanassov, Nadee Nissanka, Carlos T. Moraes, James B. Stewart, Johanna H.K. Kauppila and Siôn L. Williams and has published in prestigious journals such as Nature, Cell and Journal of Clinical Investigation.

In The Last Decade

María Miranda

13 papers receiving 598 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
María Miranda United States 9 542 181 52 50 45 13 605
Jorge Asin-Cayuela Sweden 11 669 1.2× 157 0.9× 48 0.9× 62 1.2× 77 1.7× 16 764
Lukáš Stibůrek Czechia 13 556 1.0× 148 0.8× 35 0.7× 44 0.9× 63 1.4× 15 660
Jorida Çoku United States 12 459 0.8× 204 1.1× 34 0.7× 23 0.5× 37 0.8× 18 525
Mariël A.M. van den Brand Netherlands 12 710 1.3× 292 1.6× 24 0.5× 40 0.8× 40 0.9× 14 796
Devorah Soiferman Israel 10 426 0.8× 173 1.0× 28 0.5× 25 0.5× 49 1.1× 10 531
R. Nair Finland 10 265 0.5× 84 0.5× 28 0.5× 30 0.6× 41 0.9× 12 380
Tegan Stait Australia 6 469 0.9× 125 0.7× 46 0.9× 31 0.6× 77 1.7× 8 561
Nanna Cornelius Denmark 8 423 0.8× 341 1.9× 32 0.6× 22 0.4× 98 2.2× 10 551
Grzegorz J. Stępień France 9 656 1.2× 237 1.3× 36 0.7× 66 1.3× 85 1.9× 12 730
Milena Vukotic Germany 7 645 1.2× 191 1.1× 16 0.3× 26 0.5× 43 1.0× 9 682

Countries citing papers authored by María Miranda

Since Specialization
Citations

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

Fields of papers citing papers by María Miranda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of María Miranda

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

All Works

13 of 13 papers shown
1.
Meisel, Joshua D., Pallavi R. Joshi, María Miranda, et al.. (2025). Mutations in mitochondrial ferredoxin FDX2 suppress frataxin deficiency. Nature. 649(8097). 713–720. 1 indexed citations
2.
Marutani, Eizo, María Miranda, Timothy Durham, et al.. (2025). Hypoxia ameliorates neurodegeneration and movement disorder in a mouse model of Parkinson’s disease. Nature Neuroscience. 28(9). 1858–1867. 1 indexed citations
3.
Meisel, Joshua D., María Miranda, Owen S. Skinner, et al.. (2024). Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism. Cell. 187(3). 659–675.e18. 20 indexed citations
4.
Marutani, Eizo, Masanobu Morita, María Miranda, et al.. (2024). Exclusion of sulfide:quinone oxidoreductase from mitochondria causes Leigh-like disease in mice by impairing sulfide metabolism. Journal of Clinical Investigation. 134(15). 10 indexed citations
5.
Ferreira, Tiago, María Miranda, Rosário Pinto‐Leite, et al.. (2024). Integrated Study of Canine Mammary Tumors Histopathology, Immunohistochemistry, and Cytogenetic Findings. Veterinary Sciences. 11(9). 409–409. 2 indexed citations
6.
Miranda, María, et al.. (2024). Therapeutic hypoxia for mitochondrial disease via enhancement of hemoglobin affinity and inhibition of HIF-2α. Journal of Clinical Investigation. 134(23). 4 indexed citations
7.
Miranda, María, Nina A. Bonekamp, & Inge Kühl. (2022). Starting the engine of the powerhouse: mitochondrial transcription and beyond. Biological Chemistry. 403(8-9). 779–805. 20 indexed citations
8.
Walker, Melissa, et al.. (2021). On the dynamic and even reversible nature of Leigh syndrome: Lessons from human imaging and mouse models. Current Opinion in Neurobiology. 72. 80–90. 12 indexed citations
9.
Jiang, Shan, Camilla Koolmeister, Stefan J. Siira, et al.. (2019). TEFM regulates both transcription elongation and RNA processing in mitochondria. EMBO Reports. 20(6). 56 indexed citations
10.
Bacman, Sandra R., Johanna H.K. Kauppila, Cláudia V. Pereira, et al.. (2018). MitoTALEN reduces mutant mtDNA load and restores tRNAAla levels in a mouse model of heteroplasmic mtDNA mutation. Nature Medicine. 24(11). 1696–1700. 200 indexed citations
11.
Kühl, Inge, María Miranda, Ilian Atanassov, et al.. (2017). Transcriptomic and proteomic landscape of mitochondrial dysfunction reveals secondary coenzyme Q deficiency in mammals. eLife. 6. 162 indexed citations
12.
Kühl, Inge, María Miranda, Viktor Posse, et al.. (2016). POLRMT regulates the switch between replication primer formation and gene expression of mammalian mtDNA. Science Advances. 2(8). e1600963–e1600963. 105 indexed citations
13.
Kaalund, Sanne S., Rikke S. Møller, María Miranda, et al.. (2008). Investigation of 4q‐deletion in two unrelated patients using array CGH. American Journal of Medical Genetics Part A. 146A(18). 2431–2434. 12 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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