Sofìa Kitsiou

543 citations
25 papers · 260 · h-index 10

Impact in

    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Estrogen and related hormone effects
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Prenatal Screening and Diagnostics

Papers in

    • Genomic variations and chromosomal abnormalities 8
    • Genetics and Neurodevelopmental Disorders 5
    • Genomics and Rare Diseases 3
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
    • Genetic Syndromes and Imprinting 2
    • RNA modifications and cancer 3

Sofìa Kitsiou

24 papers receiving 237 citations

Peers

Sofìa Kitsiou
Comparison fields: 5 of 56
  • Genetics 155
  • Pediatrics, Perinatology and Child Health 73
  • Gastroenterology 11
  • Endocrine and Autonomic Systems 11
  • Pharmacy 8
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Citations per field
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Citations per year

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-authors

The 25 scholars most cited alongside Sofìa Kitsiou, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sofìa Kitsiou Line = papers co-authored together Sofìa Kitsiou links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1 199633
2 200731
3 197929
4 199926
5 200021
6 201118
7 200915
8 199814
9
Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies.
200511
10 200510
11
10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.
20089
12
A case of Ehlers Danlos syndrome type VI.
20066
13 20095
14
Unusual association of XYY chromosomal constitution with colobomas of iris, myopia, increased lipoproteins, mental retardation and convulsions.
19865
15
Complex chromosome rearrangement in a retarded girl with malformations.
19875
16
Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
20065
17 20093
18 20073
19 20143
20 19942

About Sofìa Kitsiou

Sofìa Kitsiou is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Plant Science, having authored 25 papers that have together received 260 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers), Prenatal Screening and Diagnostics (4 papers), Chromosomal and Genetic Variations (4 papers), RNA modifications and cancer (3 papers), Genomics and Rare Diseases (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (155 citations), Pediatrics, Perinatology and Child Health (73 citations), Gastroenterology (11 citations), Endocrine and Autonomic Systems (11 citations) and Pharmacy (8 citations). Sofìa Kitsiou has collaborated with scholars based in Greece, Cyprus and Sweden. Frequent co-authors include Aspasia Tsezou, Michael B. Petersen, Emmanouil Kanavakis, Maria Syrrou, D Kaskarélis, Elisabeth Blennow, Polyxeni Nicolaidou, A Kolialexi, Ανδρέας Παμπάνος and Ariadni Mavrou. Their work appears in journals such as Genetic Epidemiology, Postgraduate Medical Journal, European Journal of Human Genetics, American Journal of Obstetrics and Gynecology and The Breast.

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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