Olga Tšuiko

1.1k total citations
30 papers, 583 citations indexed

About

Olga Tšuiko is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Olga Tšuiko has authored 30 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Pediatrics, Perinatology and Child Health, 18 papers in Genetics and 8 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Olga Tšuiko's work include Prenatal Screening and Diagnostics (23 papers), Genetic Syndromes and Imprinting (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Olga Tšuiko is often cited by papers focused on Prenatal Screening and Diagnostics (23 papers), Genetic Syndromes and Imprinting (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Olga Tšuiko collaborates with scholars based in Belgium, Finland and United States. Olga Tšuiko's co-authors include Joris Vermeesch, Andres Salumets, Ants Kurg, Thierry Voet, Tatjana Jatsenko, Pascal Borry, Eftychia Dimitriadou, Katrien Smits, Masoud Zamani Esteki and Ann Van Soom and has published in prestigious journals such as Nucleic Acids Research, Scientific Reports and Genome Research.

In The Last Decade

Olga Tšuiko

27 papers receiving 574 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Olga Tšuiko Belgium 16 353 227 218 195 94 30 583
N.-N. Goodall United States 7 467 1.3× 227 1.0× 223 1.0× 145 0.7× 60 0.6× 14 548
María Vera-Rodríguez Spain 9 387 1.1× 232 1.0× 162 0.7× 239 1.2× 80 0.9× 14 564
D Babariya United Kingdom 6 449 1.3× 209 0.9× 187 0.9× 136 0.7× 65 0.7× 15 505
Christian S. Ottolini United Kingdom 14 468 1.3× 262 1.2× 270 1.2× 247 1.3× 98 1.0× 28 683
Elia Fernandez Gallardo Belgium 6 263 0.7× 195 0.9× 105 0.5× 161 0.8× 91 1.0× 10 406
Susan Gitlin United States 11 482 1.4× 334 1.5× 168 0.8× 146 0.7× 232 2.5× 12 715
Michelle Merrill United States 6 331 0.9× 164 0.7× 295 1.4× 261 1.3× 68 0.7× 8 629
Minyue Ma China 9 188 0.5× 126 0.6× 128 0.6× 153 0.8× 48 0.5× 18 347
Vanessa Peinado Spain 16 566 1.6× 326 1.4× 241 1.1× 216 1.1× 152 1.6× 22 719
Katerina Chatzimeletiou Greece 14 343 1.0× 412 1.8× 109 0.5× 210 1.1× 327 3.5× 52 703

Countries citing papers authored by Olga Tšuiko

Since Specialization
Citations

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

Fields of papers citing papers by Olga Tšuiko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olga Tšuiko

This figure shows the co-authorship network connecting the top 25 collaborators of Olga Tšuiko. A scholar is included among the top collaborators of Olga Tšuiko 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 Olga Tšuiko. Olga Tšuiko 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.
Jatsenko, Tatjana, Thierry Voet, Olga Tšuiko, et al.. (2025). Origin and development of uniparental and polyploid blastomeres. iScience. 28(5). 112337–112337. 1 indexed citations
2.
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).
3.
Vermeesch, Joris, et al.. (2024). Polygenic embryo screening: quo vadis?. Journal of Assisted Reproduction and Genetics. 41(7). 1719–1726. 4 indexed citations
4.
Zhao, Yan, Olga Tšuiko, S. Demyda‐Peyrás, et al.. (2024). Genome-wide equine preimplantation genetic testing enabled by simultaneous haplotyping and copy number detection. Scientific Reports. 14(1). 2003–2003. 4 indexed citations
5.
Vermeesch, Joris, Taneli Raivio, Arne Vanhie, et al.. (2024). Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screening. Reproductive BioMedicine Online. 49(3). 104294–104294. 6 indexed citations
6.
7.
Vermeesch, Joris, et al.. (2023). Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores. European Journal of Human Genetics. 31(10). 1133–1138. 17 indexed citations
8.
Zhao, Yan, et al.. (2023). Simultaneous genome-wide haplotyping and copy number detection enabling PGT-A and PGT-M testing in equine in vitro produced embryos. Journal of Equine Veterinary Science. 125. 104642–104642.
9.
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
10.
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
11.
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
12.
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
13.
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
14.
Tšuiko, Olga, Elia Fernandez Gallardo, Thierry Voet, & Joris Vermeesch. (2020). PREIMPLANTATION GENETIC TESTING: Single-cell technologies at the forefront of PGT and embryo research. Reproduction. 160(5). A19–A31. 11 indexed citations
15.
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
16.
Tšuiko, Olga, Tatjana Jatsenko, Parameswaran Grace Lalitkumar, et al.. (2018). A speculative outlook on embryonic aneuploidy: Can molecular pathways be involved?. Developmental Biology. 447(1). 3–13. 31 indexed citations
17.
18.
Jatsenko, Tatjana, Olev Poolamets, Olga Tšuiko, et al.. (2018). Chromosomal scan of single sperm cells by combining fluorescence-activated cell sorting and next-generation sequencing. Journal of Assisted Reproduction and Genetics. 36(1). 91–97. 15 indexed citations
19.
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
20.
Tšuiko, Olga, Margit Nõukas, Olga Žilina, et al.. (2016). Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases. Human Reproduction. 31(8). 1913–1925. 41 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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