Catherine Metaxotou

402 total citations
35 papers, 334 citations indexed

About

Catherine Metaxotou is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Catherine Metaxotou has authored 35 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pediatrics, Perinatology and Child Health, 13 papers in Genetics and 12 papers in Molecular Biology. Recurrent topics in Catherine Metaxotou's work include Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (7 papers) and Muscle Physiology and Disorders (5 papers). Catherine Metaxotou is often cited by papers focused on Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (7 papers) and Muscle Physiology and Disorders (5 papers). Catherine Metaxotou collaborates with scholars based in Greece, United States and Vietnam. Catherine Metaxotou's co-authors include Ariadni Mavrou, Stylianos E. Antonarakis, N. Matsaniotis, D. Trichopoulos, A Kolialexi, Paul C. Watkins, Achyut S. Patel, Smita Kittur, Kyriaki Kekou and Penny Panagiotopoulou and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Annals of the New York Academy of Sciences and Journal of Medical Genetics.

In The Last Decade

Catherine Metaxotou

34 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Catherine Metaxotou Greece 12 188 140 130 66 36 35 334
Friedel Wenzel Switzerland 11 164 0.9× 145 1.0× 136 1.0× 24 0.4× 26 0.7× 21 341
Mauricette Jamar Belgium 10 160 0.9× 72 0.5× 79 0.6× 43 0.7× 53 1.5× 17 268
F. R. Sergovich Canada 13 348 1.9× 172 1.2× 232 1.8× 60 0.9× 20 0.6× 20 548
Rina Schmidt United States 12 257 1.4× 109 0.8× 164 1.3× 74 1.1× 32 0.9× 20 430
A. Caine United Kingdom 7 252 1.3× 118 0.8× 124 1.0× 71 1.1× 10 0.3× 9 363
Chiara Palka Italy 10 210 1.1× 136 1.0× 255 2.0× 36 0.5× 95 2.6× 34 468
Jiansheng Xie China 8 190 1.0× 142 1.0× 129 1.0× 29 0.4× 59 1.6× 33 341
Carole Goumy France 11 185 1.0× 100 0.7× 125 1.0× 51 0.8× 26 0.7× 36 324
Drew Duckett United Kingdom 9 249 1.3× 128 0.9× 142 1.1× 63 1.0× 11 0.3× 23 353
Jack H. Jung Canada 13 208 1.1× 83 0.6× 218 1.7× 61 0.9× 25 0.7× 19 411

Countries citing papers authored by Catherine Metaxotou

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Metaxotou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Metaxotou

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Metaxotou. A scholar is included among the top collaborators of Catherine Metaxotou 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 Catherine Metaxotou. Catherine Metaxotou 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.
Mavrou, Ariadni, et al.. (2003). Identification of Fetal Nucleated Red Blood Cells in the Maternal Circulation during Pregnancy Using Anti-Hemoglobin-ε Antibody. Fetal Diagnosis and Therapy. 18(5). 309–313. 11 indexed citations
2.
Akel, Salem, Aggeliki Kοlialexi, Ariadni Mavrou, et al.. (2000). Evaluation at single cell level of residual Philadelphia negative hemopoietic stem cells in chronic phase CML patients. Cancer Genetics and Cytogenetics. 122(2). 93–100. 4 indexed citations
3.
Thomaidis, Loretta, et al.. (1999). Cohen syndrome: two new cases in siblings. European Journal of Pediatrics. 158(10). 838–841. 6 indexed citations
4.
Mavrou, Ariadni, A Kolialexi, Yun‐Ling Zheng, Catherine Metaxotou, & Diana W. Bianchi. (1999). Improved Specificity of NRBC Detection in Chorionic Villus Sample Supernatant Fluids Using Anti-Zeta and Anti-Epsilon Monoclonal Antibodies. Fetal Diagnosis and Therapy. 14(5). 291–295. 14 indexed citations
5.
Mavrou, Ariadni, et al.. (1999). Screening for minor changes in the distal part of the human dystrophin gene in Greek DMD/BMD patients. European Journal of Human Genetics. 7(2). 179–187. 7 indexed citations
6.
Mavrou, Ariadni, Catherine Metaxotou, & D. Trichopoulos. (1998). Awareness and use of prenatal diagnosis among Greek women: a national survey.. PubMed. 18(4). 349–55. 14 indexed citations
7.
Metaxotou, Catherine, et al.. (1998). 3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype. Human Mutation. 11(S1). S209–S212. 3 indexed citations
8.
Mavrou, Ariadni, Catherine Metaxotou, & D. Trichopoulos. (1998). Awareness and use of prenatal diagnosis among Greek women: a national survey. Prenatal Diagnosis. 18(4). 349–355. 12 indexed citations
9.
Kolialexi, A, A Mavrou, George Th. Tsangaris, et al.. (1998). Chromosome fragility and predisposition to childhood malignancies.. PubMed. 18(4A). 2359–64. 2 indexed citations
10.
Metaxotou, Catherine, et al.. (1997). Prenatal diagnosis services in Greece.. PubMed. 5 Suppl 1. 39–41. 2 indexed citations
11.
Mavrou, Ariadni, Yun‐Ling Zheng, A Kolialexi, Catherine Metaxotou, & Diana W. Bianchi. (1997). Fetal nucleated erythrocytes (NRBCS) in chorionic villus sample supernatant fluids: an additional source of fetal material for karyotype confirmation. Prenatal Diagnosis. 17(7). 643–649. 3 indexed citations
12.
Mavrou, Ariadni, et al.. (1991). Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece. American Journal of Medical Genetics. 38(2-3). 437–439. 7 indexed citations
13.
Mavrou, Ariadni, Maria Syrrou, Sotiris Youroukos, et al.. (1988). Martin‐Bell syndrome in Greece, with report of another 47,XXY fragile X patient. American Journal of Medical Genetics. 31(4). 735–739. 10 indexed citations
14.
Metaxotou, Catherine, et al.. (1987). Prenatal diagnosis of chromosomal abnormalities from chorionic biopsy samples: Improved success rate using a modified direct method. Prenatal Diagnosis. 7(7). 461–469. 4 indexed citations
15.
Xanthou, M, et al.. (1984). DETECTION OF DONOR'S LYMPHOCYTES IN THE PERIPHERAL BLOOD OF NEONATES FOLLOWING EXCHANGE-TRANSFUSION. Pediatric Research. 18. 268A–268A. 1 indexed citations
16.
Metaxotou, Catherine, D. Ikkos, Penny Panagiotopoulou, et al.. (1983). A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation. Clinical Genetics. 24(5). 380–383. 23 indexed citations
17.
Metaxotou, Catherine, et al.. (1981). A de novo interstitial deletion of band q21 on chromosome 6.. PubMed. 24(3). 170–1. 21 indexed citations
18.
Metaxotou, Catherine, et al.. (1981). Parental chromosome translocations and fetal loss.. PubMed. 58(4). 456–8. 13 indexed citations
19.
Metaxotou, Catherine, et al.. (1981). Trisomy 3 mosaicism in a live‐born infant. Clinical Genetics. 19(1). 37–40. 14 indexed citations
20.
Metaxotou, Catherine, et al.. (1978). Polymorphism of chromosome 9 in 600 Greek subjects.. PubMed. 30(1). 85–9. 23 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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