Olga Grafakou
- Co-authors
- Beat SteinmannAndrea Superti‐FurgaLambert van den HeuvelKonrad OexleFrans J.M. TrijbelsN. U. BosshardHans H. GoebelJan Smeitink
- Topics
- Metabolism and Genetic Disorders (6 papers)Mitochondrial Function and Pathology (4 papers)Glycogen Storage Diseases and Myoclonus (2 papers)
- Partner nations
- CyprusGreeceNetherlands
In The Last Decade
Olga Grafakou
10 papers receiving 134 citations
Peers
Comparison fields: 5 of 42
- Clinical Biochemistry 73
- Molecular Biology 63
- Physiology 38
- Biochemistry 29
- Epidemiology 17
Countries citing papers authored by Olga Grafakou
This map shows the geographic impact of Olga Grafakou'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 Olga Grafakou with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Olga Grafakou more than expected).
Fields of papers citing papers by Olga Grafakou
This network shows the impact of papers produced by Olga Grafakou. 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 Olga Grafakou. The network helps show where Olga Grafakou may publish in the future.
Co-authorship network of co-authors of Olga Grafakou
This figure shows the co-authorship network connecting the top 25 collaborators of Olga Grafakou. A scholar is included among the top collaborators of Olga Grafakou 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 Olga Grafakou. Olga Grafakou is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 2 | |
| 3 | 0 | |
| 4 | 2 | |
| 5 | 2 | |
| 6 | 5 | |
| 7 | 22 | |
| 8 | 13 | |
| 9 | 15 | |
| 10 | 44 | |
| 11 | Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. | 13 |
| 12 | 18 |
About Olga Grafakou
Olga Grafakou is a scholar working on Clinical Biochemistry, Biochemistry and Rheumatology, having authored 12 papers that have together received 136 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (4 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). The work is most often cited by research in Clinical Biochemistry (73 citations), Biochemistry (29 citations) and Physiology (38 citations). Olga Grafakou has collaborated with scholars based in Cyprus, Greece and Netherlands. Frequent co-authors include Beat Steinmann, Andrea Superti‐Furga, Lambert van den Heuvel, Konrad Oexle, Frans J.M. Trijbels, N. U. Bosshard, Hans H. Goebel, Jan Smeitink, Roel Smeets and Maria Moustaki. Their work appears in journals such as Journal of Inherited Metabolic Disease, Pediatric Pulmonology and European Journal of Pediatrics.
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.