Benjamin O’Callaghan

657 total citations
11 papers, 162 citations indexed

About

Benjamin O’Callaghan is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Benjamin O’Callaghan has authored 11 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Neurology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Benjamin O’Callaghan's work include Parkinson's Disease Mechanisms and Treatments (4 papers), Mitochondrial Function and Pathology (3 papers) and Autophagy in Disease and Therapy (2 papers). Benjamin O’Callaghan is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (4 papers), Mitochondrial Function and Pathology (3 papers) and Autophagy in Disease and Therapy (2 papers). Benjamin O’Callaghan collaborates with scholars based in United Kingdom, United States and India. Benjamin O’Callaghan's co-authors include Henry Houlden, Annet M. Bosch, Hélène Plun‐Favreau, John Hardy, Roope Männikkö, Ian J. White, Rahul Phadke, Emma Matthews, Sunaina Surana and Umbertina Conti Reed and has published in prestigious journals such as Brain, Neurology and The Journal of Physiology.

In The Last Decade

Benjamin O’Callaghan

11 papers receiving 162 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benjamin O’Callaghan United Kingdom 7 81 59 35 30 29 11 162
Karit Reinson Estonia 8 122 1.5× 80 1.4× 36 1.0× 16 0.5× 29 1.0× 14 198
Lance H. Rodan United States 5 72 0.9× 27 0.5× 31 0.9× 19 0.6× 10 0.3× 8 127
Michele Sacchini Italy 6 66 0.8× 37 0.6× 15 0.4× 27 0.9× 53 1.8× 11 162
Faïza Bensemain France 6 76 0.9× 28 0.5× 29 0.8× 19 0.6× 9 0.3× 6 152
Omar Hikmat Norway 9 234 2.9× 128 2.2× 37 1.1× 13 0.4× 18 0.6× 20 281
Anne‐Laure Bédat‐Millet France 7 128 1.6× 79 1.3× 28 0.8× 19 0.6× 13 0.4× 11 176
Koujyu Katayama Japan 7 296 3.7× 191 3.2× 29 0.8× 39 1.3× 25 0.9× 9 385
Alejandra Darling Spain 8 78 1.0× 16 0.3× 45 1.3× 42 1.4× 10 0.3× 18 177
India Butler South Africa 3 276 3.4× 211 3.6× 38 1.1× 19 0.6× 29 1.0× 5 320
Jingli Shan China 7 62 0.8× 41 0.7× 16 0.5× 12 0.4× 22 0.8× 7 98

Countries citing papers authored by Benjamin O’Callaghan

Since Specialization
Citations

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

Fields of papers citing papers by Benjamin O’Callaghan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benjamin O’Callaghan. 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 Benjamin O’Callaghan. The network helps show where Benjamin O’Callaghan may publish in the future.

Co-authorship network of co-authors of Benjamin O’Callaghan

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

All Works

11 of 11 papers shown
1.
Chung, Chih-Yao, Benjamin O’Callaghan, M Madej, et al.. (2025). Metabolic remodeling in hiPSC-derived myofibers carrying the m.3243A>G mutation. Stem Cell Reports. 20(4). 102448–102448. 1 indexed citations
2.
O’Callaghan, Benjamin, et al.. (2024). Common genetic risk for Parkinson's disease and dysfunction of the endo-lysosomal system. Philosophical Transactions of the Royal Society B Biological Sciences. 379(1899). 20220517–20220517. 6 indexed citations
3.
Esteras, Noemí, et al.. (2024). KAT8 compound inhibition inhibits the initial steps of PINK1-dependant mitophagy. Scientific Reports. 14(1). 11721–11721. 2 indexed citations
4.
Reynolds, Regina H., Benjamin O’Callaghan, Sonia García-Ruiz, et al.. (2023). The non-specific lethal complex regulates genes and pathways genetically linked to Parkinson’s disease. Brain. 146(12). 4974–4987. 2 indexed citations
5.
O’Callaghan, Benjamin, John Hardy, & Hélène Plun‐Favreau. (2023). PINK1: From Parkinson’s disease to mitophagy and back again. PLoS Biology. 21(6). e3002196–e3002196. 13 indexed citations
6.
Nascimento, Filipe, Ian J. White, Roisin Sullivan, et al.. (2023). Pathophysiology of Dyt1- Tor1a dystonia in mice is mediated by spinal neural circuit dysfunction. Science Translational Medicine. 15(694). eadg3904–eadg3904. 18 indexed citations
7.
Wu, Zhiyi, et al.. (2020). The startle disease mutation α1S270T predicts shortening of glycinergic synaptic currents. The Journal of Physiology. 598(16). 3417–3438. 2 indexed citations
8.
Hostettler, Isabel C., Benjamin O’Callaghan, Enrico Bugiardini, et al.. (2020). ANGPTL6 Genetic Variants Are an Underlying Cause of Familial Intracranial Aneurysms. Neurology. 96(6). e947–e955. 7 indexed citations
9.
Gayathri, Santhalingam, Benjamin O’Callaghan, Stéphanie Efthymiou, et al.. (2020). Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance. European Journal of Neurology. 28(3). 945–954. 7 indexed citations
10.
O’Callaghan, Benjamin, Annet M. Bosch, & Henry Houlden. (2019). An update on the genetics, clinical presentation, and pathomechanisms of human riboflavin transporter deficiency. Journal of Inherited Metabolic Disease. 42(4). 598–607. 78 indexed citations
11.
Zanoteli, Edmar, R. Scalco, Umbertina Conti Reed, et al.. (2018). A novelATP1A2mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. Brain. 141(12). 3308–3318. 26 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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