Christalena Sofocleous
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 31
- Genetics and Neurodevelopmental Disorders 11
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 9
- Genetic Syndromes and Imprinting 5
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- Muscle Physiology and Disorders 5
- RNA modifications and cancer 4
- Co-authors
- Emmanuel Kanavakis (11 shared papers)Joanne Traeger‐Synodinos (17 shared papers)Maria Tzetis (9 shared papers)Helen Fryssira (8 shared papers)Christina Vrettou (7 shared papers)Sophia Kitsiou‐Tzeli (7 shared papers)Konstantina Kosma (13 shared papers)Ariadni Mavrou (9 shared papers)
- Journals
- Expert Review of Molecular Diagnostics (4 papers)Birth Defects Research Part A Clinical and Molecular Teratology (3 papers)International Journal of Molecular Sciences (3 papers)Pediatric Blood & Cancer (2 papers)European Journal of Paediatric Neurology (2 papers)
- Partner nations
- GreeceUnited StatesSwitzerland
In The Last Decade
Christalena Sofocleous
50 papers receiving 598 citations
Peers
Comparison fields: 5 of 57
- Genetics 289
- Developmental Neuroscience 32
- Genetics 68
- Pediatrics, Perinatology and Child Health 79
- Molecular Biology 252
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-authors
The 25 scholars most cited alongside Christalena Sofocleous, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 54 | |
| 2 | 2010 | 50 | |
| 3 | 2012 | 42 | |
| 4 | 2021 | 38 | |
| 5 | 2005 | 37 | |
| 6 | 2013 | 34 | |
| 7 | 2016 | 30 | |
| 8 | 2022 | 26 | |
| 9 | 2010 | 24 | |
| 10 | 2011 | 24 | |
| 11 | 2023 | 22 | |
| 12 | 2004 | 18 | |
| 13 | 2008 | 17 | |
| 14 | 2017 | 16 | |
| 15 | 2013 | 16 | |
| 16 | 2011 | 15 | |
| 17 | 2020 | 15 | |
| 18 | 2014 | 13 | |
| 19 | 2008 | 12 | |
| 20 | 10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach. | 2008 | 10 |
About Christalena Sofocleous
Christalena Sofocleous is a scholar working on Genetics, Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health and Developmental Neuroscience, having authored 57 papers that have together received 635 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (9 papers), Muscle Physiology and Disorders (5 papers), Autism Spectrum Disorder Research (5 papers), Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (5 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Genetics (289 citations), Developmental Neuroscience (32 citations), Genetics (68 citations), Pediatrics, Perinatology and Child Health (79 citations) and Molecular Biology (252 citations). Christalena Sofocleous has collaborated with scholars based in Greece, United States and Switzerland. Frequent co-authors include Emmanuel Kanavakis, Joanne Traeger‐Synodinos, Maria Tzetis, Helen Fryssira, Christina Vrettou, Sophia Kitsiou‐Tzeli, Konstantina Kosma, Ariadni Mavrou, Kyriaki Kekou and Andreas Pampanos. Their work appears in journals such as Expert Review of Molecular Diagnostics, Birth Defects Research Part A Clinical and Molecular Teratology, International Journal of Molecular Sciences, Pediatric Blood & Cancer and European Journal of Paediatric Neurology.
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.