Masoud Zamani Esteki
Masoud Zamani Esteki
Associate professor @MaastrichtUMC+ & @Maastricht University
Verified email at - Homepage
Cited by
Cited by
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
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
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
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
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
J Demeulemeester, P Kumar, EK M°ller, S Nord, DC Wedge, A Peterson, ...
Genome biology 17, 1-15, 2016
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
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
Preimplantation genetic diagnosis guided by single-cell genomics
N Van der Aa, MZ Esteki, JR Vermeesch, T Voet
Genome medicine 5, 1-10, 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
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
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
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 N§ukas, O Žilina, ...
Nature medicine 25 (11), 1699-1705, 2019
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
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
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
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
Endometrial receptivity in women of advanced age: an underrated factor in infertility
ADS Pathare, M Loid, M Saare, SB Gidl÷f, M Zamani Esteki, G Acharya, ...
Human reproduction update 29 (6), 773-793, 2023
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
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
Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities
M Isrie, MZ Esteki, H Peeters, T Voet, J Van Houdt, W Van Paesschen, ...
European journal of medical genetics 58 (4), 205-210, 2015
The system can't perform the operation now. Try again later.
Articles 1–20