Zoe Golder

693 total citations
18 papers, 448 citations indexed

About

Zoe Golder is a scholar working on Molecular Biology, Cell Biology and Epidemiology. According to data from OpenAlex, Zoe Golder has authored 18 papers receiving a total of 448 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 4 papers in Cell Biology and 2 papers in Epidemiology. Recurrent topics in Zoe Golder's work include Mitochondrial Function and Pathology (6 papers), Ion Transport and Channel Regulation (4 papers) and Zebrafish Biomedical Research Applications (4 papers). Zoe Golder is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Ion Transport and Channel Regulation (4 papers) and Zebrafish Biomedical Research Applications (4 papers). Zoe Golder collaborates with scholars based in United Kingdom, Portugal and United States. Zoe Golder's co-authors include Stéphane Berghmans, Frances M. Richards, Paul Butler, W. Alderton, Angeleen Fleming, Fiona E. Karet, Paul Goldsmith, Neil J. Ingham, Iain Gardner and Elizabeth E. Norgett and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Zoe Golder

16 papers receiving 442 citations

Peers

Zoe Golder

HTM

PHARM

PHYSI

Koki Kawaguchi Japan

Reiko Kawase Japan

Anne-Lee Gustafson Sweden

Takehiko Oka Japan

Helen Garside United Kingdom

Lynn T. Frame United States

Edwin M. Labut United States

Donglai Sheng China

R Lüllmann-Rauch Germany

Timm Schreiber Germany

Koki Kawaguchi Japan

Zoe Golder

174 ×0.7

119 ×0.8

54 ×0.9

HTM

11 ×0.3

PHARM

28 ×0.9

PHYSI

Citations per year, relative to Zoe Golder Zoe Golder (= 1×) peers Koki Kawaguchi

Countries citing papers authored by Zoe Golder

Since Specialization

Citations

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

Fields of papers citing papers by Zoe Golder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zoe Golder

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

All Works

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18 of 18 papers shown

Golder, Zoe, Stephen P. Burr, Malwina Prater, et al.. (2025). Ubiquitin-mediated mitophagy regulates the inheritance of mitochondrial DNA mutations. Science. 390(6769). 156–163.

Kremer, Laura S., et al.. (2025). The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagy. Science Advances. 11(46). eaea4660–eaea4660.

Rosenberger, Florian A., Kai Chang, Fynn M. Hansen, et al.. (2024). Preventing excessive autophagy protects from the pathology of mtDNA mutations in Drosophila melanogaster. Nature Communications. 15(1). 10719–10719. 3 indexed citations

Murley, Alexander G., Yu Nie, Zoe Golder, et al.. (2023). High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob Disease. Neurology Genetics. 9(1). e200054–e200054. 2 indexed citations

Nie, Yu, Alexander G. Murley, Zoe Golder, et al.. (2022). Heteroplasmic mitochondrial DNA mutations in frontotemporal lobar degeneration. Acta Neuropathologica. 143(6). 687–695. 12 indexed citations

Calabrese, Claudia, et al.. (2021). Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissues. Nucleic Acids Research. 49(22). 12757–12768. 25 indexed citations

Wei, Wei, Michael J. Keogh, Juvid Aryaman, et al.. (2018). Frequency and signature of somatic variants in 1461 human brain exomes. Genetics in Medicine. 21(4). 904–912. 16 indexed citations

Gómez-Durán, Aurora, Yufeng Xu, Zoe Golder, et al.. (2018). mtDNA polymorphic variants as metabolic hubs. Neuromuscular Disorders. 28. S35–S36. 1 indexed citations

Kullar, Peter, Aurora Gómez-Durán, Payam A. Gammage, et al.. (2017). Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family. Brain. 141(1). 55–62. 16 indexed citations

10.

Golder, Zoe & Fiona E. Karet. (2016). Extra-renal locations of the a4 subunit of H+ATPase. BMC Cell Biology. 17(1). 27–27. 3 indexed citations

11.

Golder, Zoe, et al.. (2015). Renal peroxiredoxin 6 interacts with anion exchanger 1 and plays a novel role in pH homeostasis. Kidney International. 89(1). 105–112. 16 indexed citations

12.

Su, Ya, Rafia S. Al‐Lamki, Katherine G. Blake-Palmer, et al.. (2014). Physical and Functional Links between Anion Exchanger-1 and Sodium Pump. Journal of the American Society of Nephrology. 26(2). 400–409. 10 indexed citations

13.

Norgett, Elizabeth E., Zoe Golder, Beatriz Lorente-Cánovas, et al.. (2012). Atp6v0a4 knockout mouse is a model of distal renal tubular acidosis with hearing loss, with additional extrarenal phenotype. Proceedings of the National Academy of Sciences. 109(34). 13775–13780. 49 indexed citations

14.

Lorente-Cánovas, Beatriz, Neil J. Ingham, Elizabeth E. Norgett, et al.. (2012). Mice deficient in the H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear. Disease Models & Mechanisms. 6(2). 434–42. 37 indexed citations

15.

Alderton, W., Stéphane Berghmans, Paul Butler, et al.. (2010). Accumulation and metabolism of drugs and CYP probe substrates in zebrafish larvae. Xenobiotica. 40(8). 547–557. 94 indexed citations

16.

Berghmans, Stéphane, Paul Butler, Paul Goldsmith, et al.. (2008). Zebrafish based assays for the assessment of cardiac, visual and gut function — potential safety screens for early drug discovery. Journal of Pharmacological and Toxicological Methods. 58(1). 59–68. 150 indexed citations

17.

Berghmans, Stéphane, Teresa P. Barros, Zoe Golder, et al.. (2008). Zebrafish: The future of in vivo safety pharmacology screening. Journal of Pharmacological and Toxicological Methods. 58(2). 177–178. 1 indexed citations

18.

Goldsmith, Paul, Zoe Golder, Stéphane Berghmans, et al.. (2007). GBR12909 Possesses Anticonvulsant Activity in Zebrafish and Rodent Models of Generalized Epilepsy but Cardiac Ion Channel Effects Limit Its Clinical Utility. Pharmacology. 79(4). 250–258. 13 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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