Christalena Sofocleous
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health
- Cognitive Neuroscience
- Genetics
- Co-authors
- Emmanuel KanavakisJoanne Traeger‐SynodinosMaria TzetisHelen FryssiraChristina VrettouSophia Kitsiou‐TzeliAriadni MavrouKonstantina Kosma
- Topics
- Genomic variations and chromosomal abnormalities (10 papers)Genetics and Neurodevelopmental Disorders (7 papers)Genomics and Rare Diseases (6 papers)
- Cited by
- GeneticsDevelopmental Neuroscience
- Partner nations
- GreeceSwitzerlandGermany
In The Last Decade
Christalena Sofocleous
41 papers receiving 449 citations
Peers
Comparison fields: 5 of 59
- Genetics 261
- Molecular Biology 218
- Pediatrics, Perinatology and Child Health 81
- Cognitive Neuroscience 67
- Genetics 48
Countries citing papers authored by Christalena Sofocleous
This map shows the geographic impact of Christalena Sofocleous'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 Christalena Sofocleous with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christalena Sofocleous more than expected).
Fields of papers citing papers by Christalena Sofocleous
This network shows the impact of papers produced by Christalena Sofocleous. 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 Christalena Sofocleous. The network helps show where Christalena Sofocleous may publish in the future.
Co-authorship network of co-authors of Christalena Sofocleous
This figure shows the co-authorship network connecting the top 25 collaborators of Christalena Sofocleous. A scholar is included among the top collaborators of Christalena Sofocleous 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 Christalena Sofocleous. Christalena Sofocleous is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 7 | |
| 2 | 2 | |
| 3 | 0 | |
| 4 | 2 | |
| 5 | 16 | |
| 6 | 1 | |
| 7 | 1 | |
| 8 | 13 | |
| 9 | 2 | |
| 10 | 5 | |
| 11 | 6 | |
| 12 | 3 | |
| 13 | 4 | |
| 14 | 34 | |
| 15 | 4 | |
| 16 | 33 | |
| 17 | 13 | |
| 18 | 22 | |
| 19 | 3 | |
| 20 | 17 |
About Christalena Sofocleous
Christalena Sofocleous is a scholar working on Genetics, Genetics and Developmental Neuroscience, having authored 45 papers that have together received 459 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (6 papers). The work is most often cited by research in Genetics (261 citations), Developmental Neuroscience (31 citations) and Genetics (48 citations). Christalena Sofocleous has collaborated with scholars based in Greece, Switzerland and Germany. Frequent co-authors include Emmanuel Kanavakis, Joanne Traeger‐Synodinos, Maria Tzetis, Helen Fryssira, Christina Vrettou, Sophia Kitsiou‐Tzeli, Ariadni Mavrou, Konstantina Kosma, Kyriaki Kekou and Giles Palmer. Their work appears in journals such as International Journal of Molecular Sciences, Gene and Fertility and Sterility.
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.