Eftychia Dimitriadou

1.2k citations

26 papers · 748 · h-index 15

Impact in

Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting

Papers in

Pediatrics, Perinatology and Child Health 18
- Prenatal Screening and Diagnostics 18
Genetics 14
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 5
- Coagulation, Bradykinin, Polyphosphates, and Angioedema 1

Co-authors: Joris Vermeesch (20 shared papers)Thierry Voet (10 shared papers)Masoud Zamani Esteki (11 shared papers)Martine De Rycke (3 shared papers)Sophie Debrock (9 shared papers)V. Goossens (2 shared papers)Niels van der Aa (3 shared papers)Nathalie Vermeulen (2 shared papers)
Journals: Human Reproduction (4 papers)Nucleic Acids Research (3 papers)Reproductive BioMedicine Online (2 papers)Human Molecular Genetics (1 paper)npj Genomic Medicine (1 paper)
Partner nations: Belgium United States Netherlands

In The Last Decade

Eftychia Dimitriadou

23 papers receiving 721 citations

Peers

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-authors

The 25 scholars most cited alongside Eftychia Dimitriadou, 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 Eftychia Dimitriadou Line = papers co-authored together Eftychia Dimitriadou links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders† Human Reproduction Open ·(unknown), Filipa Carvalho, Céline Moutou, Eftychia Dimitriadou, Jos Dreesen, Carles Giménez, V. Goossens, Georgia Kakourou, Nathalie Vermeulen, Daniela Zuccarello, Martine De Rycke	2020	101
2	Concurrent Whole-Genome Haplotyping and Copy-Number Profiling of Single Cells The American Journal of Human Genetics ·Masoud Zamani Esteki, Eftychia Dimitriadou, Ligia Mateiu, Cindy Melotte, Niels van der Aa, Parveen Kumar, Rakhi Das, Koen Theunis, (unknown), Eric Legius, Yves Moreau, Sophie Debrock, Thomas D’Hooghe, Pieter Verdyck, Martine De Rycke, Karen Sermon, Joris Vermeesch, Thierry Voet	2015	90
3	ESHRE PGT Consortium good practice recommendations for the detection of structural and numerical chromosomal aberrations† Human Reproduction Open ·(unknown), Edith Coonen, Carmen Quiñones Rubio, Dimitra Christopikou, Eftychia Dimitriadou, J. V. Gontar, V. Goossens, Maria Maurer, Francesca Spinella, Nathalie Vermeulen, Martine De Rycke	2020	79
4	Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy Genome Research ·Aspasia Destouni, Masoud Zamani Esteki, Maaike Catteeuw, Olga Tšuiko, Eftychia Dimitriadou, Katrien Smits, Ants Kurg, Andres Salumets, Ann Van Soom, Thierry Voet, Joris Vermeesch	2016	66
5	Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains Nucleic Acids Research ·Niels van der Aa, (unknown), Ligia Mateiu, Masoud Zamani Esteki, Parveen Kumar, Eftychia Dimitriadou, Evelyne Vanneste, Yves Moreau, Joris Vermeesch, Thierry Voet	2013	63
6	Retrotransposon RNA expression and evidence for retrotransposition events in human oocytes Human Molecular Genetics ·Ioannis Georgiou, Dimitrios Noutsopoulos, Eftychia Dimitriadou, Γεώργιος Μαρκόπουλος, A. Apergi, Leandros Lazaros, T. Vaxevanoglou, Konstantinos Pantos, Maria Syrrou, Theodore Tzavaras	2009	58
7	Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M Human Reproduction ·Aspasia Destouni, Eftychia Dimitriadou, Heleen Masset, Sophie Debrock, Cindy Melotte, Kris Van Den Bogaert, Masoud Zamani Esteki, Jia Ding, Thierry Voet, Ellen Denayer, Thomy de Ravel, Eric Legius, Christel Meuleman, Karen Peeraer, Joris Vermeesch	2018	49
8	Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos Human Reproduction ·Eftychia Dimitriadou, Cindy Melotte, Sophie Debrock, Masoud Zamani Esteki, Kris Dierickx, Thierry Voet, Koenraad Devriendt, Thomy de Ravel, Eric Legius, Karen Peeraer, Christel Meuleman, Joris Vermeesch	2017	35
9	Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge European Journal of Human Genetics ·Lore Lannoo, Khaila van Straaten, Jeroen Breckpot, Nathalie Brison, Luc De Catte, Eftychia Dimitriadou, Eric Legius, Hilde Peeters, Ilse Parijs, Olga Tšuiko, Leen Vancoillie, Joris Vermeesch, Griet Van Buggenhout, Kris Van Den Bogaert, Kristel Van Calsteren, Koenraad Devriendt	2022	28
10	Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts Genome biology ·Tine De Coster, Heleen Masset, Olga Tšuiko, Maaike Catteeuw, Yan Zhao, Nicolas Dierckxsens, Ainhoa Larreategui-Aparicio, Eftychia Dimitriadou, Sophie Debrock, Karen Peeraer, Marta de Ruijter‐Villani, Katrien Smits, Ann Van Soom, Joris Vermeesch	2022	25
11	Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing Nucleic Acids Research ·Heleen Masset, Jia Ding, Eftychia Dimitriadou, Amin Ardeshirdavani, Sophie Debrock, Olga Tšuiko, Katrien Smits, Karen Peeraer, Yves Moreau, Thierry Voet, Masoud Zamani Esteki, Joris Vermeesch	2022	24
12	Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA Genetics in Medicine ·Huiwen Che, Darine Villela, Eftychia Dimitriadou, Cindy Melotte, Nathalie Brison, Maria Neofytou, Kris Van Den Bogaert, Olga Tšuiko, Koenraad Devriendt, Eric Legius, Masoud Zamani Esteki, Thierry Voet, Joris Vermeesch	2020	24
13	Single cell segmental aneuploidy detection is compromised by S phase Molecular Cytogenetics ·Eftychia Dimitriadou, Niels van der Aa, (unknown), Thierry Voet, Joris Vermeesch	2014	24
14	Haplotyping-based preimplantation genetic testing reveals parent-of-origin specific mechanisms of aneuploidy formation npj Genomic Medicine ·Olga Tšuiko, Michiel Vanneste, Cindy Melotte, Jia Ding, Sophie Debrock, Heleen Masset, Maire Peters, Andres Salumets, Anne De Leener, Céline Pirard, Candice Kluyskens, Katleen Hostens, Arne van de Vijver, Karen Peeraer, Ellen Denayer, Joris Vermeesch, Eftychia Dimitriadou	2021	22
15	AbnormalDLK1/MEG3imprinting correlates with decreased HERV-K methylation after assisted reproduction and preimplantation genetic diagnosis Stress ·Eftychia Dimitriadou, Dimitrios Noutsopoulos, Γεώργιος Μαρκόπουλος, Angeliki‐Maria Vlaikou, Stefania Mantziou, Joanne Traeger‐Synodinos, Emmanouel Kanavakis, George P. Chrousos, Theodore Tzavaras, Maria Syrrou	2013	15
16	Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents Cytogenetic and Genome Research ·Wolfram Demaerel, Majid Hosseinzadeh, Nayereh Nouri, Maryam Sedghi, Eftychia Dimitriadou, Mansoor Salehi, Hossein Abdali, Mehrdad Memarzadeh, Mahdi Zamani, Joris Vermeesch	2016	14
17	Preclinical workup using long-read amplicon sequencing provides families withde novopathogenic variants access to universal preimplantation genetic testing Human Reproduction ·Olga Tšuiko, Yasmine El Ayeb, Tatjana Jatsenko, Joke Allemeersch, Cindy Melotte, Jia Ding, Sophie Debrock, Karen Peeraer, Arne Vanhie, Anne De Leener, Céline Pirard, Candice Kluyskens, Ellen Denayer, Eric Legius, Joris Vermeesch, Hilde Brems, Eftychia Dimitriadou	2023	9
18	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 ·Bernard Thienpont, Eftychia Dimitriadou, K Theodoropoulos, Jeroen Breckpot, Helen Fryssira, Sophia Kitsiou‐Tzeli, Meropi Tzoufi, Joris Vermeesch, Maria Syrrou, Koenraad Devriendt	2009	6
19	Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome Amplification Methods in molecular biology ·Eftychia Dimitriadou, Masoud Zamani Esteki, Joris Vermeesch	2015	5
20	Primary mediastinal large B‐cell lymphoma is characterized by large‐scale copy‐neutral loss of heterozygosity Genes Chromosomes and Cancer ·Stefania Tuveri, Koen Debackere, Lukas Marcelis, Nicolas Dierckxsens, Jonas Demeulemeester, Eftychia Dimitriadou, Daan Dierickx, Pierre Lefesvre, Karen Deraedt, Carlos Graux, Lucienne Michaux, Jan Cools, Thomas Tousseyn, Joris Vermeesch, Iwona Włodarska	2022	4

About Eftychia Dimitriadou

Eftychia Dimitriadou is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Cancer Research, Molecular Biology and Plant Science, having authored 26 papers that have together received 748 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (12 papers), Cancer Genomics and Diagnostics (5 papers), Genetic Syndromes and Imprinting (5 papers), Chromosomal and Genetic Variations (4 papers), Congenital Anomalies and Fetal Surgery (2 papers), Sarcoma Diagnosis and Treatment (1 paper) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (443 citations), Genetics (232 citations), Public Health, Environmental and Occupational Health (125 citations), Cancer Research (59 citations) and Reproductive Medicine (31 citations). Eftychia Dimitriadou has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Joris Vermeesch, Thierry Voet, Masoud Zamani Esteki, Martine De Rycke, Sophie Debrock, V. Goossens, Niels van der Aa, Nathalie Vermeulen, Olga Tšuiko and Eric Legius. Their work appears in journals such as Human Reproduction, Nucleic Acids Research, Reproductive BioMedicine Online, Human Molecular Genetics and npj Genomic Medicine.

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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Eftychia Dimitriadou

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About Eftychia Dimitriadou

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