Sofìa Kitsiou

543 total citations
25 papers, 260 citations indexed

About

Sofìa Kitsiou is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sofìa Kitsiou has authored 25 papers receiving a total of 260 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 9 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sofìa Kitsiou's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Prenatal Screening and Diagnostics (4 papers). Sofìa Kitsiou is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Prenatal Screening and Diagnostics (4 papers). Sofìa Kitsiou collaborates with scholars based in Greece, Cyprus and Sweden. Sofìa Kitsiou's co-authors include Aspasia Tsezou, Michael B. Petersen, Emmanouil Kanavakis, Elisabeth Blennow, Polyxeni Nicolaidou, D Kaskarélis, Maria Syrrou, Maria Tzetis, Ariadni Mavrou and A Kolialexi and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Postgraduate Medical Journal and European Journal of Human Genetics.

In The Last Decade

Sofìa Kitsiou

24 papers receiving 237 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sofìa Kitsiou Greece 10 155 73 71 48 38 25 260
Frédérique Tihy Canada 11 215 1.4× 146 2.0× 120 1.7× 21 0.4× 25 0.7× 18 384
Eveline Wesby–van Swaay Netherlands 9 177 1.1× 91 1.2× 97 1.4× 25 0.5× 14 0.4× 14 287
Drew Duckett United Kingdom 9 249 1.6× 128 1.8× 142 2.0× 63 1.3× 7 0.2× 23 353
Robert‐Jan Galjaard Netherlands 8 180 1.2× 94 1.3× 179 2.5× 20 0.4× 49 1.3× 10 326
Michiko Ohno Japan 8 142 0.9× 134 1.8× 113 1.6× 37 0.8× 13 0.3× 14 383
Tung‐Yao Chang Taiwan 12 171 1.1× 191 2.6× 104 1.5× 30 0.6× 25 0.7× 35 357
Sandra Peacock United States 9 308 2.0× 207 2.8× 183 2.6× 71 1.5× 40 1.1× 11 489
Patricia Mowery‐Rushton United States 9 167 1.1× 74 1.0× 109 1.5× 35 0.7× 13 0.3× 13 242
Florence Amblard France 10 147 0.9× 75 1.0× 122 1.7× 23 0.5× 20 0.5× 21 276
Nathalie Leporrier France 15 167 1.1× 251 3.4× 153 2.2× 34 0.7× 30 0.8× 24 478

Countries citing papers authored by Sofìa Kitsiou

Since Specialization
Citations

This map shows the geographic impact of Sofìa Kitsiou'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 Sofìa Kitsiou with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sofìa Kitsiou more than expected).

Fields of papers citing papers by Sofìa Kitsiou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sofìa Kitsiou. 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 Sofìa Kitsiou. The network helps show where Sofìa Kitsiou may publish in the future.

Co-authorship network of co-authors of Sofìa Kitsiou

This figure shows the co-authorship network connecting the top 25 collaborators of Sofìa Kitsiou. A scholar is included among the top collaborators of Sofìa Kitsiou 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 Sofìa Kitsiou. Sofìa Kitsiou 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.
Kekou, Kyriaki, Christalena Sofocleous, George Konstantinidis, et al.. (2014). SMA prenatal diagnosis: A modified protocol to help differentiation between deletions and gene conversion. Molecular and Cellular Probes. 29(1). 71–73. 3 indexed citations
2.
Syrigou, Ekaterini, et al.. (2011). Food allergy-related paediatric constipation: the usefulness of atopy patch test. European Journal of Pediatrics. 170(9). 1173–1178. 18 indexed citations
3.
Fretzayas, Andrew, et al.. (2009). Long-term follow-up of a multifocal hepatic mesenchymal hamartoma producing a-fetoprotein. Pediatric Surgery International. 25(4). 381–384. 1 indexed citations
4.
Sofocleous, Christalena, Christina Vrettou, Aspasia Destouni, et al.. (2009). PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol. Reproductive BioMedicine Online. 19(3). 418–425. 3 indexed citations
5.
Dinopoulos, Argirios, et al.. (2009). Coinheritance of Noonan syndrome and Becker muscular dystrophy. Neuromuscular Disorders. 20(1). 61–63. 5 indexed citations
6.
Fretzayas, Andrew, et al.. (2009). The clinical pattern of group C streptococcal pharyngitis in children. Journal of Infection and Chemotherapy. 15(4). 228–232. 15 indexed citations
7.
Sofocleous, Christalena, Sofìa Kitsiou, A Kolialexi, et al.. (2008). 10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.. PubMed. 22(4). 451–5. 9 indexed citations
8.
Psoni, Stavroula, Kyriaki Kekou, Joanne Traeger‐Synodinos, et al.. (2007). Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome. European Journal of Paediatric Neurology. 11(4). 235–239. 3 indexed citations
9.
10.
Mavrou, Ariadni, et al.. (2006). A case of Ehlers Danlos syndrome type VI.. PubMed. 17(3). 291–4. 6 indexed citations
11.
Fretzayas, Andrew, et al.. (2006). UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis. Scandinavian Journal of Infectious Diseases. 38(6-7). 537–540.
12.
Nicolaidou, Polyxeni, et al.. (2005). GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND GILBERT SYNDROME. Pediatric Hematology and Oncology. 22(7). 561–566. 10 indexed citations
13.
Kolialexi, A, George Th. Tsangaris, Sofìa Kitsiou, Emmanouil Kanavakis, & Ariadni Mavrou. (2005). Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies.. PubMed. 25(4). 2979–83. 11 indexed citations
14.
Tsezou, Aspasia, Sofìa Kitsiou, Michael B. Petersen, et al.. (2000). Molecular cytogenetic characterization and origin of two de novo duplication 9p cases. American Journal of Medical Genetics. 91(2). 102–106. 21 indexed citations
15.
Tsezou, Aspasia, Dimitrios Gourgiotis, Angela Pasparaki, et al.. (1999). Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy. Clinical Genetics. 56(6). 441–446. 26 indexed citations
16.
Syrrou, Maria, Ioannis Georgiou, Maria Grigoriadou, et al.. (1998). FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population. Genetic Epidemiology. 15(1). 103–109. 14 indexed citations
17.
Bugge, Merete, Elisabeth Blennow, Michael B. Petersen, et al.. (1996). Tetrasomy 18p de novo: Parental Origin and Different Mechanisms of Formation. European Journal of Human Genetics. 4(3). 160–167. 33 indexed citations
18.
Kitsiou, Sofìa, et al.. (1988). [Polymorphism of restriction fragment length in the detection of the precise status of monosomy 21 in a deformed retarded girl].. PubMed. 36(1-2). 99–102. 1 indexed citations
19.
Kitsiou, Sofìa, et al.. (1987). Complex chromosome rearrangement in a retarded girl with malformations.. PubMed. 30(1). 59–61. 5 indexed citations
20.
Kitsiou, Sofìa, et al.. (1986). Unusual association of XYY chromosomal constitution with colobomas of iris, myopia, increased lipoproteins, mental retardation and convulsions.. PubMed. 29(4). 264–5. 5 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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