Eszter Dombi

662 total citations
19 papers, 425 citations indexed

About

Eszter Dombi is a scholar working on Molecular Biology, Epidemiology and Clinical Biochemistry. According to data from OpenAlex, Eszter Dombi has authored 19 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Epidemiology and 6 papers in Clinical Biochemistry. Recurrent topics in Eszter Dombi's work include Mitochondrial Function and Pathology (11 papers), Autophagy in Disease and Therapy (7 papers) and Metabolism and Genetic Disorders (6 papers). Eszter Dombi is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Autophagy in Disease and Therapy (7 papers) and Metabolism and Genetic Disorders (6 papers). Eszter Dombi collaborates with scholars based in United Kingdom, United States and Norway. Eszter Dombi's co-authors include Joanna Poulton, Heather Mortiboys, Janet Carver, Carl Fratter, Alan Diot, Chunyan Liao, Tim Child, Karl Morten, Diana Nguyen and Shiori Sekine and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Eszter Dombi

19 papers receiving 425 citations

Peers

Eszter Dombi

MB

EPIDE

IMMUN

CB

NEURO

Natalia E. Sejbuk United States

Andrew R. Haynes United Kingdom

Marc Kästle Germany

Erin L. Lousberg Australia

Lingxia Li China

Jieli Wu China

Anusha Angajala United States

Α. Gravanis Greece

Yoshihiro Takamura Japan

Natalia E. Sejbuk United States

Eszter Dombi

268 ×0.9

MB

49 ×0.5

EPIDE

52 ×0.7

IMMUN

40 ×0.6

CB

29 ×0.7

NEURO

Citations per year, relative to Eszter Dombi Eszter Dombi (= 1×) peers Natalia E. Sejbuk

Countries citing papers authored by Eszter Dombi

Since Specialization

Citations

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

Fields of papers citing papers by Eszter Dombi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eszter Dombi

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

All Works

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19 of 19 papers shown

1.

Dombi, Eszter, Val Millar, Janet Carver, et al.. (2024). Nucleoside supplements as treatments for mitochondrial DNA depletion syndrome. Frontiers in Cell and Developmental Biology. 12. 1260496–1260496. 5 indexed citations

2.

Luzwick, Jessica W., Eszter Dombi, Sunetra Roy, et al.. (2021). MRE11-dependent instability in mitochondrial DNA fork protection activates a cGAS immune signaling pathway. Science Advances. 7(51). eabf9441–eabf9441. 29 indexed citations

3.

Liu, Yiting, Xiaoping Huang, Diana Nguyen, et al.. (2020). Loss of CHCHD2 and CHCHD10 activates OMA1 peptidase to disrupt mitochondrial cristae phenocopying patient mutations. Human Molecular Genetics. 29(9). 1547–1567. 51 indexed citations

4.

Dragovic, Rebecca, Eszter Dombi, Ginny Mounce, et al.. (2019). In vitro decidualisation of human endometrial stromal cells is enhanced by seminal fluid extracellular vesicles. Journal of Extracellular Vesicles. 8(1). 1565262–1565262. 53 indexed citations

5.

Cooke, William R., Adam P. Cribbs, Wei Zhang, et al.. (2019). Maternal circulating syncytiotrophoblast-derived extracellular vesicles contain biologically active 5’-tRNA halves. Biochemical and Biophysical Research Communications. 518(1). 107–113. 27 indexed citations

6.

Diot, Alan, Thomas Agnew, Jeremy Sanderson, et al.. (2018). Validating the RedMIT/GFP-LC3 Mouse Model by Studying Mitophagy in Autosomal Dominant Optic Atrophy Due to the OPA1Q285STOP Mutation. Frontiers in Cell and Developmental Biology. 6. 103–103. 9 indexed citations

7.

Bendorius, Mykolas, Indira Neeli, Fengjuan Wang, et al.. (2018). The Mitochondrion-lysosome Axis in Adaptive and Innate Immunity: Effect of Lupus Regulator Peptide P140 on Mitochondria Autophagy and NETosis. Frontiers in Immunology. 9. 2158–2158. 21 indexed citations

8.

Ladds, Emma, Andrea Whitney, Eszter Dombi, et al.. (2018). De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity. Neurology Genetics. 4(4). e258–e258. 27 indexed citations

9.

White, Benjamin, et al.. (2017). Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers. SHILAP Revista de lepidopterología. Volume 10. 163–175. 12 indexed citations

10.

Fang, Evandro Fei, Konstantinos Palikaras, Nuo Sun, et al.. (2017). In Vitro and In Vivo Detection of Mitophagy in Human Cells, C. Elegans, and Mice. Journal of Visualized Experiments. 26 indexed citations

11.

Fratter, Carl, Eszter Dombi, Janet Carver, et al.. (2017). Mitochondrial disease and lipid storage myopathy due to mutation in CHCHD10 or DNM1L and disordered mitochondrial dynamics. Neuromuscular Disorders. 27. S21–S21. 1 indexed citations

12.

Fang, Evandro Fei, Konstantinos Palikaras, Nuo Sun, et al.. (2017). In Vitro and In Vivo Detection of Mitophagy in Human Cells, C. Elegans, and Mice. Journal of Visualized Experiments. 3 indexed citations

13.

Dombi, Eszter, Heather Mortiboys, & Joanna Poulton. (2017). Modulating Mitophagy in Mitochondrial Disease. Current Medicinal Chemistry. 25(40). 5597–5612. 72 indexed citations

14.

Diot, Alan, Karl Morten, Eszter Dombi, et al.. (2017). Acute nutritional stress during pregnancy affects placental efficiency, fetal growth and adult glucose homeostasis. Oncotarget. 8(65). 109478–109486. 4 indexed citations

15.

Liao, Chien‐Chang, Carl Fratter, Janet Carver, et al.. (2017). Defects in mitochondrial DNA (mtDNA) replication cause mtDNA depletion, increased mtDNA turnover and increased mitophagy. Neuromuscular Disorders. 27. S23–S24. 1 indexed citations

16.

Brady, Stefen, Alan Diot, Eszter Dombi, et al.. (2016). Metformin-induced deafness in mitochondrial disease. Neuromuscular Disorders. 26. S178–S178. 1 indexed citations

17.

Dombi, Eszter, Alan Diot, Karl Morten, et al.. (2016). The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy. Neurology. 86(20). 1921–1923. 28 indexed citations

18.

Diot, Alan, Eszter Dombi, Chunyan Liao, et al.. (2016). Modulating mitochondrial quality in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy children. Biochemical Society Transactions. 44(4). 1091–1100. 19 indexed citations

19.

Diot, Alan, Chunyan Liao, Eszter Dombi, et al.. (2015). A novel quantitative assay of mitophagy: Combining high content fluorescence microscopy and mitochondrial DNA load to quantify mitophagy and identify novel pharmacological tools against pathogenic heteroplasmic mtDNA. Pharmacological Research. 100. 24–35. 36 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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