Single-cell paired-end genome sequencing reveals structural variation per cell cycle T Voet, P Kumar, P Van Loo, SL Cooke, J Marshall, ML Lin, ... Nucleic acids research 41 (12), 6119-6138, 2013 | 174 | 2013 |
Concurrent whole-genome haplotyping and copy-number profiling of single cells MZ Esteki, E Dimitriadou, L Mateiu, C Melotte, N Van der Aa, P Kumar, ... The American Journal of Human Genetics 96 (6), 894-912, 2015 | 154 | 2015 |
Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations C Robberecht, T Voet, MZ Esteki, BA Nowakowska, JR Vermeesch Genome research 23 (3), 411-418, 2013 | 131 | 2013 |
Genome stability of bovine in vivo-conceived cleavage-stage embryos is higher compared to in vitro-produced embryos O Tšuiko, M Catteeuw, M Zamani Esteki, A Destouni, O Bogado Pascottini, ... Human reproduction 32 (11), 2348-2357, 2017 | 102 | 2017 |
Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy A Destouni, MZ Esteki, M Catteeuw, O Tšuiko, E Dimitriadou, K Smits, ... Genome research 26 (5), 567-578, 2016 | 100 | 2016 |
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing J Demeulemeester, P Kumar, EK Møller, S Nord, DC Wedge, A Peterson, ... Genome biology 17, 1-15, 2016 | 90 | 2016 |
EBV-positive and EBV-negative posttransplant diffuse large B cell lymphomas have distinct genomic and transcriptomic features JF Ferreiro, J Morscio, D Dierickx, P Vandenberghe, O Gheysens, ... American Journal of Transplantation 16 (2), 414-425, 2016 | 90 | 2016 |
Preimplantation genetic diagnosis guided by single-cell genomics N Van der Aa, MZ Esteki, JR Vermeesch, T Voet Genome medicine 5, 1-10, 2013 | 74 | 2013 |
Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains N Van der Aa, J Cheng, L Mateiu, MZ Esteki, P Kumar, E Dimitriadou, ... Nucleic acids research 41 (6), e66-e66, 2013 | 74 | 2013 |
Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing H Masset, M Zamani Esteki, E Dimitriadou, J Dreesen, S Debrock, ... Human Reproduction 34 (8), 1608-1619, 2019 | 60 | 2019 |
Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M A Destouni, E Dimitriadou, H Masset, S Debrock, C Melotte, ... Human Reproduction 33 (12), 2302-2311, 2018 | 60 | 2018 |
Endometrial receptivity in women of advanced age: an underrated factor in infertility ADS Pathare, M Loid, M Saare, SB Gidlöf, M Zamani Esteki, G Acharya, ... Human reproduction update 29 (6), 773-793, 2023 | 57 | 2023 |
In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages M Zamani Esteki, T Viltrop, O Tšuiko, A Tiirats, M Koel, M Nõukas, O Žilina, ... Nature medicine 25 (11), 1699-1705, 2019 | 57 | 2019 |
Noninvasive prenatal test results indicative of maternal malignancies: a nationwide genetic and clinical follow-up study CJ Heesterbeek, SM Aukema, RJH Galjaard, EMJ Boon, MI Srebniak, ... Journal of Clinical Oncology 40 (22), 2426-2435, 2022 | 51 | 2022 |
Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos E Dimitriadou, C Melotte, S Debrock, MZ Esteki, K Dierickx, T Voet, ... Human Reproduction 32 (3), 687-697, 2017 | 49 | 2017 |
Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA H Che, D Villela, E Dimitriadou, C Melotte, N Brison, M Neofytou, ... Genetics in Medicine 22 (5), 962-973, 2020 | 33 | 2020 |
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing H Masset, J Ding, E Dimitriadou, A Ardeshirdavani, S Debrock, O Tšuiko, ... Nucleic acids research 50 (11), e63-e63, 2022 | 31 | 2022 |
Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss R Essers, IN Lebedev, A Kurg, EA Fonova, SJC Stevens, RM Koeck, ... Nature Medicine 29 (12), 3233-3242, 2023 | 30 | 2023 |
Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practice SCEH Sallevelt, APA Stegmann, B de Koning, C Velter, A Steyls, ... Genetics in Medicine 23 (6), 1125-1136, 2021 | 29 | 2021 |
How to analyse a single blastomere? Application of whole-genome technologies: micro-arrays and next generation sequencing P Kumar, M Zamani Esteki, N Van der Aa, T Voet Cambridge University Press, 2013 | 21* | 2013 |