Sofia Kitsiou‐Tzeli
Impact in
-
- Prenatal Screening and Diagnostics
- Neonatal Health and Biochemistry
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomics and Rare Diseases
Papers in
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- Congenital heart defects research 5
- Epigenetics and DNA Methylation 3
- Advanced biosensing and bioanalysis techniques 2
- Genetics 14
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Maria Tzetis (13 shared papers)Emmanuel Kanavakis (13 shared papers)Aspasia Tsezou (7 shared papers)Marios Ioannides (3 shared papers)Philippos C. Patsalis (3 shared papers)Carolina Sismani (3 shared papers)Konstantina Kosma (7 shared papers)Helen Fryssira (3 shared papers)
- Journals
- Molecular Cytogenetics (4 papers)European Journal of Medical Genetics (2 papers)HORMONES (2 papers)The Neurologist (1 paper)Gene (1 paper)
- Partner nations
- GreeceUnited StatesSwitzerland
In The Last Decade
Sofia Kitsiou‐Tzeli
31 papers receiving 506 citations
Peers
Comparison fields: 5 of 65
- Pediatrics, Perinatology and Child Health 142
- Genetics 186
- Genetics 40
- Rheumatology 49
- Molecular Biology 219
Countries citing papers authored by Sofia Kitsiou‐Tzeli
This map shows the geographic impact of Sofia Kitsiou‐Tzeli'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 Sofia Kitsiou‐Tzeli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sofia Kitsiou‐Tzeli more than expected).
Fields of papers citing papers by Sofia Kitsiou‐Tzeli
This network shows the impact of papers produced by Sofia Kitsiou‐Tzeli. 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 Sofia Kitsiou‐Tzeli. The network helps show where Sofia Kitsiou‐Tzeli may publish in the future.
Co-authors
The 25 scholars most cited alongside Sofia Kitsiou‐Tzeli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 62 | |
| 2 | 2008 | 53 | |
| 3 | 2010 | 45 | |
| 4 | 2008 | 36 | |
| 5 | 2018 | 29 | |
| 6 | 2008 | 29 | |
| 7 | 2006 | 27 | |
| 8 | 2009 | 26 | |
| 9 | 2012 | 21 | |
| 10 | 2006 | 18 | |
| 11 | 2011 | 17 | |
| 12 | 2007 | 14 | |
| 13 | 2010 | 14 | |
| 14 | 2012 | 14 | |
| 15 | 2009 | 11 | |
| 16 | 2007 | 10 | |
| 17 | 2008 | 10 | |
| 18 | 2009 | 9 | |
| 19 | 2015 | 9 | |
| 20 | Awareness of prenatal screening for fetal aneuploidy among pregnant women in Greece. | 2015 | 9 |
About Sofia Kitsiou‐Tzeli
Sofia Kitsiou‐Tzeli is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Plant Science, having authored 31 papers that have together received 513 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (5 papers), Prenatal Screening and Diagnostics (4 papers), Chromosomal and Genetic Variations (4 papers), Neonatal Health and Biochemistry (4 papers), Epigenetics and DNA Methylation (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Advanced biosensing and bioanalysis techniques (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (142 citations), Genetics (186 citations), Genetics (40 citations), Rheumatology (49 citations) and Molecular Biology (219 citations). Sofia Kitsiou‐Tzeli has collaborated with scholars based in Greece, United States and Switzerland. Frequent co-authors include Maria Tzetis, Emmanuel Kanavakis, Aspasia Tsezou, Marios Ioannides, Philippos C. Patsalis, Carolina Sismani, Konstantina Kosma, Helen Fryssira, Ariadni Mavrou and Dimitrios Iliopoulos. Their work appears in journals such as Molecular Cytogenetics, European Journal of Medical Genetics, HORMONES, The Neurologist and Gene.
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.