Eftychia Dimitriadou

1.2k total citations
26 papers, 715 citations indexed

About

Eftychia Dimitriadou is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Eftychia Dimitriadou has authored 26 papers receiving a total of 715 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Pediatrics, Perinatology and Child Health, 19 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Eftychia Dimitriadou's work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (17 papers) and Genetic Syndromes and Imprinting (6 papers). Eftychia Dimitriadou is often cited by papers focused on Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (17 papers) and Genetic Syndromes and Imprinting (6 papers). Eftychia Dimitriadou collaborates with scholars based in Belgium, United States and Netherlands. Eftychia Dimitriadou's co-authors include Joris Vermeesch, Thierry Voet, Masoud Zamani Esteki, Martine De Rycke, Niels van der Aa, Sophie Debrock, V. Goossens, Jie Cheng, Nathalie Vermeulen and Olga Tšuiko and has published in prestigious journals such as Nucleic Acids Research, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Eftychia Dimitriadou

23 papers receiving 689 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eftychia Dimitriadou Belgium	15	488	315	251	175	92	26	715
R. Prates United States	7	536 1.1×	321 1.0×	148 0.6×	181 1.0×	52 0.6×	13	615
Masoud Zamani Esteki Netherlands	13	350 0.7×	290 0.9×	286 1.1×	185 1.1×	103 1.1×	34	727
L. Spizzichino Italy	8	652 1.3×	394 1.3×	166 0.7×	216 1.2×	52 0.6×	12	759
Dehua Cheng China	12	307 0.6×	300 1.0×	242 1.0×	162 0.9×	67 0.7×	44	618
Yvonne K. Kwok China	13	300 0.6×	285 0.9×	216 0.9×	36 0.2×	51 0.6×	25	563
Diego Marín United States	14	285 0.6×	151 0.5×	294 1.2×	212 1.2×	37 0.4×	27	602
Andrea Nuccitelli Italy	10	446 0.9×	256 0.8×	104 0.4×	104 0.6×	23 0.3×	16	593
Celia Donaghue United Kingdom	14	437 0.9×	479 1.5×	155 0.6×	44 0.3×	68 0.7×	16	629
Pingyuan Xie China	13	196 0.4×	151 0.5×	182 0.7×	93 0.5×	32 0.3×	36	388

Countries citing papers authored by Eftychia Dimitriadou

Since Specialization

Citations

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

Fields of papers citing papers by Eftychia Dimitriadou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eftychia Dimitriadou

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

All Works

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20 of 20 papers shown

Tšuiko, Olga, Tatjana Jatsenko, Eftychia Dimitriadou, et al.. (2025). Long-read whole-genome sequencing-based concurrent haplotyping and aneuploidy profiling of single cells. Nucleic Acids Research. 53(6).

Lannoo, Lore, Ellen Denayer, Liesbeth Gilissen, et al.. (2024). Preimplantation genetic testing for hereditary angioedema as a potential dominant cost-effective intervention. The Journal of Allergy and Clinical Immunology In Practice. 13(3). 711–714.e3.

Dimitriadou, Eftychia, et al.. (2024). Exploring attitudes and experiences with reproductive genetic carrier screening among couples seeking medically assisted reproduction: a longitudinal survey study. Journal of Assisted Reproduction and Genetics. 41(2). 451–464.

Tšuiko, Olga, Tatjana Jatsenko, Joke Allemeersch, et al.. (2023). Preclinical workup using long-read amplicon sequencing provides families withde novopathogenic variants access to universal preimplantation genetic testing. Human Reproduction. 38(3). 511–519. 9 indexed citations

Debackere, Koen, Lukas Marcelis, Nicolas Dierckxsens, et al.. (2022). Primary mediastinal large B‐cell lymphoma is characterized by large‐scale copy‐neutral loss of heterozygosity. Genes Chromosomes and Cancer. 61(10). 603–615. 3 indexed citations

Lannoo, Lore, Jeroen Breckpot, Nathalie Brison, et al.. (2022). Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge. European Journal of Human Genetics. 30(12). 1323–1330. 25 indexed citations

Tšuiko, Olga, Yan Zhao, Nicolas Dierckxsens, et al.. (2022). Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts. Genome biology. 23(1). 201–201. 22 indexed citations

Ding, Jia, Eftychia Dimitriadou, Amin Ardeshirdavani, et al.. (2022). Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing. Nucleic Acids Research. 50(11). e63–e63. 23 indexed citations

Tšuiko, Olga, Cindy Melotte, Jia Ding, et al.. (2021). Haplotyping-based preimplantation genetic testing reveals parent-of-origin specific mechanisms of aneuploidy formation. npj Genomic Medicine. 6(1). 81–81. 21 indexed citations

10.

Carvalho, Filipa, Céline Moutou, Eftychia Dimitriadou, et al.. (2020). ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders†. Human Reproduction Open. 2020(3). hoaa018–hoaa018. 99 indexed citations

11.

Che, Huiwen, Eftychia Dimitriadou, Cindy Melotte, et al.. (2020). Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA. Genetics in Medicine. 22(5). 962–973. 21 indexed citations

12.

Esteki, Masoud Zamani, Cindy Melotte, Edith Coonen, et al.. (2019). Agilent Technologies OnePGT solution: External verification on both blastomere and trophectoderm biopsies. Reproductive BioMedicine Online. 38. e11–e12. 1 indexed citations

13.

Destouni, Aspasia, Eftychia Dimitriadou, Sophie Debrock, et al.. (2018). Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M. Human Reproduction. 33(12). 2302–2311. 45 indexed citations

14.

Destouni, Aspasia, Masoud Zamani Esteki, Olga Tšuiko, et al.. (2016). Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy. Genome Research. 26(5). 567–578. 64 indexed citations

15.

Hosseinzadeh, Majid, Maryam Sedghi, Eftychia Dimitriadou, et al.. (2016). Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents. Cytogenetic and Genome Research. 148(1). 1–5. 13 indexed citations

16.

Dimitriadou, Eftychia, Masoud Zamani Esteki, & Joris Vermeesch. (2015). Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome Amplification. Methods in molecular biology. 1347. 197–219. 5 indexed citations

17.

Esteki, Masoud Zamani, Eftychia Dimitriadou, Ligia Mateiu, et al.. (2015). Concurrent Whole-Genome Haplotyping and Copy-Number Profiling of Single Cells. The American Journal of Human Genetics. 96(6). 894–912. 87 indexed citations

18.

Dimitriadou, Eftychia, Γεώργιος Μαρκόπουλος, Joanne Traeger‐Synodinos, et al.. (2013). AbnormalDLK1/MEG3imprinting correlates with decreased HERV-K methylation after assisted reproduction and preimplantation genetic diagnosis. Stress. 16(6). 689–697. 14 indexed citations

19.

Thienpont, Bernard, Eftychia Dimitriadou, Jeroen Breckpot, et al.. (2009). Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1. European Journal of Medical Genetics. 52(6). 393–397. 6 indexed citations

20.

Georgiou, Ioannis, Eftychia Dimitriadou, Γεώργιος Μαρκόπουλος, et al.. (2009). Retrotransposon RNA expression and evidence for retrotransposition events in human oocytes. Human Molecular Genetics. 18(7). 1221–1228. 54 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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