Periklis Makrythanasis
- Co-authors
- Stylianos E. AntonarakisFederico SantoniMichel GuipponiMaria TzetisHanan HamamyEmmanuel KanavakisHelen FryssiraArmand Bottani
- Topics
- Genomic variations and chromosomal abnormalities (15 papers)Genomics and Rare Diseases (12 papers)Genetics and Neurodevelopmental Disorders (7 papers)
- Cited by
- GeneticsMolecular Biology
- Partner nations
- SwitzerlandGreeceUnited States
In The Last Decade
Periklis Makrythanasis
55 papers receiving 787 citations
Peers
Comparison fields: 5 of 89
- Molecular Biology 402
- Genetics 278
- Pulmonary and Respiratory Medicine 111
- Surgery 99
- Cancer Research 83
Countries citing papers authored by Periklis Makrythanasis
This map shows the geographic impact of Periklis Makrythanasis'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 Periklis Makrythanasis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Periklis Makrythanasis more than expected).
Fields of papers citing papers by Periklis Makrythanasis
This network shows the impact of papers produced by Periklis Makrythanasis. 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 Periklis Makrythanasis. The network helps show where Periklis Makrythanasis may publish in the future.
Co-authorship network of co-authors of Periklis Makrythanasis
This figure shows the co-authorship network connecting the top 25 collaborators of Periklis Makrythanasis. A scholar is included among the top collaborators of Periklis Makrythanasis 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 Periklis Makrythanasis. Periklis Makrythanasis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 3 | |
| 3 | 16 | |
| 4 | 3 | |
| 5 | 13 | |
| 6 | 19 | |
| 7 | 17 | |
| 8 | 14 | |
| 9 | 41 | |
| 10 | 5 | |
| 11 | 26 | |
| 12 | 11 | |
| 13 | 31 | |
| 14 | 16 | |
| 15 | 3 | |
| 16 | 6 | |
| 17 | 32 | |
| 18 | 19 | |
| 19 | 6 | |
| 20 | 23 |
About Periklis Makrythanasis
Periklis Makrythanasis is a scholar working on Genetics, Genetics and Molecular Biology, having authored 58 papers that have together received 798 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Genomics and Rare Diseases (12 papers) and Genetics and Neurodevelopmental Disorders (7 papers). The work is most often cited by research in Genetics (278 citations), Genetics (82 citations) and Molecular Biology (402 citations). Periklis Makrythanasis has collaborated with scholars based in Switzerland, Greece and United States. Frequent co-authors include Stylianos E. Antonarakis, Federico Santoni, Michel Guipponi, Maria Tzetis, Hanan Hamamy, Emmanuel Kanavakis, Helen Fryssira, Armand Bottani, Samia A. Temtamy and Ghada A. Otaify. Their work appears in journals such as Nature Communications, PLoS ONE and International Journal of Molecular Sciences.
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.