Sofia Kitsiou‐Tzeli

1.1k total citations
31 papers, 513 citations indexed

About

Sofia Kitsiou‐Tzeli is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sofia Kitsiou‐Tzeli has authored 31 papers receiving a total of 513 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sofia Kitsiou‐Tzeli's work include Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (5 papers) and Neonatal Health and Biochemistry (4 papers). Sofia Kitsiou‐Tzeli is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (5 papers) and Neonatal Health and Biochemistry (4 papers). Sofia Kitsiou‐Tzeli collaborates with scholars based in Greece, United States and Switzerland. Sofia Kitsiou‐Tzeli's co-authors include Maria Tzetis, Emmanuel Kanavakis, Aspasia Tsezou, Philippos C. Patsalis, Marios Ioannides, Carolina Sismani, Konstantina Kosma, Ariadni Mavrou, Helen Fryssira and Dimitrios Iliopoulos and has published in prestigious journals such as Gene, Fertility and Sterility and Journal of the Neurological Sciences.

In The Last Decade

Sofia Kitsiou‐Tzeli

31 papers receiving 506 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sofia Kitsiou‐Tzeli Greece 14 219 186 142 62 54 31 513
Ariadna González‐del Angel Mexico 13 182 0.8× 169 0.9× 84 0.6× 37 0.6× 37 0.7× 65 420
María Juliana Ballesta‐Martínez Spain 14 308 1.4× 274 1.5× 82 0.6× 29 0.5× 33 0.6× 33 569
Patrick Beaulieu Canada 13 343 1.6× 116 0.6× 101 0.7× 25 0.4× 41 0.8× 27 594
B Ibarra Mexico 16 152 0.7× 246 1.3× 147 1.0× 36 0.6× 26 0.5× 74 628
Agnieszka Stembalska Poland 13 329 1.5× 125 0.7× 54 0.4× 47 0.8× 128 2.4× 47 512
Julie Richer Canada 13 202 0.9× 399 2.1× 89 0.6× 46 0.7× 40 0.7× 34 670
Takeki Hirano Japan 14 170 0.8× 238 1.3× 92 0.6× 97 1.6× 31 0.6× 28 549
Irene Yam China 11 218 1.0× 203 1.1× 256 1.8× 58 0.9× 28 0.5× 20 581
Mahmoud Aarabi United States 11 196 0.9× 207 1.1× 214 1.5× 29 0.5× 12 0.2× 20 541
Jian‐Pei Fang China 14 269 1.2× 93 0.5× 99 0.7× 35 0.6× 95 1.8× 87 733

Countries citing papers authored by Sofia Kitsiou‐Tzeli

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Sofia Kitsiou‐Tzeli

This figure shows the co-authorship network connecting the top 25 collaborators of Sofia Kitsiou‐Tzeli. A scholar is included among the top collaborators of Sofia Kitsiou‐Tzeli 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 Sofia Kitsiou‐Tzeli. Sofia Kitsiou‐Tzeli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Poulou, Myrto, et al.. (2018). Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA. Journal of the Neurological Sciences. 395. 95–105. 29 indexed citations
2.
Tzetis, Maria, Konstantina Kosma, Maria Braoudaki, et al.. (2016). Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases. Meta Gene. 8. 37–43. 4 indexed citations
3.
Kitsiou‐Tzeli, Sofia & Maria Tzetis. (2016). Maternal epigenetics and fetal and neonatal growth. Current Opinion in Endocrinology Diabetes and Obesity. 24(1). 43–46. 62 indexed citations
4.
5.
Sofocleous, Christalena, et al.. (2013). Screening of UBE3A gene in patients referred for Angelman Syndrome. European Journal of Paediatric Neurology. 17(4). 366–373. 4 indexed citations
6.
Megremis, Spyridon, Andromachi Mitsioni, Sofia Kitsiou‐Tzeli, et al.. (2013). Novel and known nephrin gene (NPHS1) mutations in two Greek cases with congenital nephrotic syndrome including a complex genotype. Journal of Genetics. 92(3). 577–581. 1 indexed citations
7.
Kitsiou‐Tzeli, Sofia, et al.. (2013). Microduplication 3q13.2q13.31 identified in a male with dysmorphic features and multiple congenital anomalies. American Journal of Medical Genetics Part A. 164(3). 666–670. 4 indexed citations
8.
Παπαθανασίου, Ιωάννα, et al.. (2011). hTERT regulation by NF-κB and c-myc in irradiated HER2-positive breast cancer cells. International Journal of Radiation Biology. 87(6). 609–621. 17 indexed citations
9.
Manolakos, Emmanouil, Catherine Sarri, Annalisa Vetro, et al.. (2011). Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy. Molecular Cytogenetics. 4(1). 11–11. 4 indexed citations
10.
Iliopoulos, Dimitrios, et al.. (2010). Survivin regulation by HER2 through NF-κB and c-myc in irradiated breast cancer cells. Journal of Cellular and Molecular Medicine. 15(7). 1542–1550. 45 indexed citations
11.
Kitsiou‐Tzeli, Sofia, et al.. (2010). Knowledge and Attitudes towards Prenatal Diagnostic Procedures among Pregnant Women in Greece. Fetal Diagnosis and Therapy. 27(3). 149–155. 14 indexed citations
12.
Tsezou, Aspasia, et al.. (2009). Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population. Genetic Testing. 0(0). 3971321277–3971321277. 9 indexed citations
13.
Tsezou, Aspasia, et al.. (2009). Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population. Genetic Testing and Molecular Biomarkers. 13(1). 143–146. 26 indexed citations
14.
Kitsiou‐Tzeli, Sofia, Emmanouil Manolakos, Nadezda Kosyakova, et al.. (2009). Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male. Molecular Cytogenetics. 2(1). 1–1. 11 indexed citations
15.
Attilakos, Achilleas, et al.. (2008). Acute acalculous cholecystitis in children with Epstein–Barr virus infection: a role for Gilbert's syndrome?. International Journal of Infectious Diseases. 13(4). e161–e164. 36 indexed citations
16.
Galani, Angeliki, et al.. (2008). Sex-reversed phenotype in association with two novel mutations c.2494delA and c.T3004C in the ligand-binding domain of the androgen receptor gene. Fertility and Sterility. 90(5). 2008.e1–2008.e4. 10 indexed citations
17.
Tsezou, Aspasia, et al.. (2007). Genetic Polymorphisms in the UGT1A1 Gene and Breast Cancer Risk in Greek Women. Genetic Testing. 11(3). 303–306. 10 indexed citations
18.
Kitsiou‐Tzeli, Sofia, Carolina Sismani, George Koumbaris, et al.. (2007). Distal del(4) (q33) syndrome: Detailed clinical presentation and molecular description with array-CGH. European Journal of Medical Genetics. 51(1). 61–67. 14 indexed citations
19.
Kitsiou‐Tzeli, Sofia, Carolina Sismani, Marios Ioannides, et al.. (2006). Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion. European Journal of Medical Genetics. 50(1). 73–78. 18 indexed citations
20.
Kitsiou‐Tzeli, Sofia, et al.. (2006). Short stature and dysmorphology associated with defects in the SHOX gene. HORMONES. 5(2). 107–118. 27 indexed citations

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.

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