Maria Tzetis
- Molecular Biology top 10%
- Pulmonary and Respiratory Medicine top 5%
- Genetics top 5%
- Pediatrics, Perinatology and Child Health top 2%
- Genetics top 2%
- Co-authors
- Emmanuel KanavakisJoanne Traeger‐SynodinosSofia Kitsiou‐TzeliChristina VrettouStavros DoudounakisAspasia TsezouAlexandra EfthymiadouC. Kattamis
- Topics
- Genomic variations and chromosomal abnormalities (25 papers)Cystic Fibrosis Research Advances (22 papers)Prenatal Screening and Diagnostics (14 papers)
- Journals
- SHILAP Revista de lepidopterologíaHuman Molecular GeneticsClinical Chemistry
- Partner nations
- GreeceUnited StatesSwitzerland
In The Last Decade
Maria Tzetis
111 papers receiving 2.3k citations
Peers
Comparison fields: 5 of 120
- Molecular Biology 703
- Pulmonary and Respiratory Medicine 556
- Genetics 424
- Pediatrics, Perinatology and Child Health 411
- Genetics 402
Countries citing papers authored by Maria Tzetis
This map shows the geographic impact of Maria Tzetis'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 Maria Tzetis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Tzetis more than expected).
Fields of papers citing papers by Maria Tzetis
This network shows the impact of papers produced by Maria Tzetis. 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 Maria Tzetis. The network helps show where Maria Tzetis may publish in the future.
Co-authorship network of co-authors of Maria Tzetis
This figure shows the co-authorship network connecting the top 25 collaborators of Maria Tzetis. A scholar is included among the top collaborators of Maria Tzetis 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 Maria Tzetis. Maria Tzetis 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 | 5 | |
| 3 | 8 | |
| 4 | 96 | |
| 5 | 30 | |
| 6 | 15 | |
| 7 | 29 | |
| 8 | 1 | |
| 9 | 13 | |
| 10 | 3 | |
| 11 | 6 | |
| 12 | 13 | |
| 13 | 9 | |
| 14 | 26 | |
| 15 | 19 | |
| 16 | 10 | |
| 17 | 5 | |
| 18 | 60 | |
| 19 | 20 | |
| 20 | 25 |
About Maria Tzetis
Maria Tzetis is a scholar working on Genetics, Genetics and Pediatrics, Perinatology and Child Health, having authored 115 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Cystic Fibrosis Research Advances (22 papers) and Prenatal Screening and Diagnostics (14 papers). The work is most often cited by research in Genetics (402 citations), Hematology (269 citations) and Pediatrics, Perinatology and Child Health (411 citations). Maria Tzetis has collaborated with scholars based in Greece, United States and Switzerland. Frequent co-authors include Emmanuel Kanavakis, Joanne Traeger‐Synodinos, Sofia Kitsiou‐Tzeli, Christina Vrettou, Stavros Doudounakis, Aspasia Tsezou, Alexandra Efthymiadou, C. Kattamis, Emmanouel Kanavakis and Myrto Poulou. Their work appears in journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Clinical Chemistry.
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.