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M. Hornak · SciRah

Researcher profile · Semantic Scholar

M. Hornak

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M. Hornak — researcher profile on SciRah

h-index: 9
Works: 27
Citations: 262

Most-cited papers

Incidence and origin of meiotic whole and segmental chromosomal aneuploidies detected by karyomapping.
D. Kubíček, M. Hornak, J. Horák, Rostislav Navratil +3 more
2019Reproductive Biomedicine Online57 citations Open access
Semantic Scholar
Concordance of various chromosomal errors among different parts of the embryo and the value of re-biopsy in embryos with segmental aneuploidies
Rostislav Navratil, J. Horák, M. Hornak, D. Kubíček +4 more
2020Molecular human reproduction45 citations Open access
Semantic Scholar
Frequency of Aneuploidy Related to Age in Porcine Oocytes
M. Hornak, M. Ješeta, P. Musilová, A. Pavlok +4 more
2011PLoS ONE35 citations Open access
Semantic Scholar
Aneuploidy Detection in Pigs Using Comparative Genomic Hybridization: From the Oocytes to Blastocysts
M. Hornak, E. Oráčová, P. Hulínská, L. Urbankova +1 more
2012PLoS ONE26 citations Open access
Semantic Scholar
Development and application of camelid molecular cytogenetic tools.
F. Avila, P. Das, M. Kutzler, E. Owens +5 more
2014Journal of Heredity22 citations Open access
Semantic Scholar
Investigation of Chromosome Aneuploidies in Early Porcine Embryos Using Comparative Genomic Hybridization
M. Hornak, P. Hulínská, P. Musilová, S. Kubíčková +1 more
2009Cytogenetic and Genome Research18 citations
Semantic Scholar
Aneuploidy Detection and mtDNA Quantification in Bovine Embryos with Different Cleavage Onset Using a Next-Generation Sequencing-Based Protocol
M. Hornak, D. Kubíček, P. Brož, P. Hulínská +4 more
2016Cytogenetic and Genome Research13 citations Open access
Semantic Scholar
OneGene PGT: comprehensive preimplantation genetic testing method utilizing next-generation sequencing
M. Hornak, Kateřina Bezděková, D. Kubíček, Rostislav Navratil +5 more
2023Journal of Assisted Reproduction and Genetics11 citations Open access
Semantic Scholar
Different Fusion Configurations of Evolutionarily Conserved Segments in Karyotypes of Potamochoerus porcus and Phacochoerus africanus
P. Musilová, S. Kubíčková, M. Hornak, H. Černohorská +2 more
2010Cytogenetic and Genome Research9 citations
Semantic Scholar
Comprehensive meiotic segregation analysis of a 4-breakpoint t(1;3;6) complex chromosome rearrangement using single sperm array comparative genomic hybridization and FISH.
M. Hornak, M. Vozdová, P. Musilová, P. Přinosilová +4 more
2014Reproductive Biomedicine Online7 citations Open access
Semantic Scholar
Twelve years of assessing the quality of preimplantation genetic testing for monogenic disorders
Z. Deans, A. Biricik, M. De Rycke, G. Harton +5 more
2022Prenatal Diagnosis5 citations Open access
Semantic Scholar
Comparative genomic hybridization in detection of DNA changes in canine lymphomas.
M. Drážovská, K. Šiviková, J. Dianovskỳ, M. Hornak
2017Animal science journal = Nihon chikusan Gakkaiho4 citations
Semantic Scholar
A high incidence of chromosome abnormalities in two-cell stage porcine IVP embryos
M. Hornak, M. Ješeta, Š. Hanuláková, J. Rubes
2015Journal of Applied Genetics4 citations
Semantic Scholar
15. THE INCIDENCE AND ORIGIN OF CHROMOSOME ANEUPLOIDIES IN HIGH QUALITY KARYOMAPPING SNP PROFILES
M. Hornak, J. Horák, D. Kubíček, Rostislav Navratil +4 more
2019Reproductive Biomedicine Online2 citations
Semantic Scholar
Prevalence of Smith–Lemli–Opitz Syndrome Carriers and the Spectrum of DHCR7 Pathogenic Variants in Representative Czech and Hungarian Population Cohorts
E. Kovács, Z. Szűcs, M. Hornak, D. Kubíček +9 more
2026Genes1 citations Open access
Semantic Scholar
Gain of heterozygosity: an embryo-only, single-nucleotide polymorphism-based method to identify meiotic trisomies in preimplantation genetic testing for aneuploidy.
M. Hornak, R. Brozek, P. Musilová, Rostislav Navratil +3 more
2026Reproductive Biomedicine Online1 citations
Semantic Scholar
The incidence and origin of segmental chromosome abnormalities in human IVF embryos detected during PGD and PGS
M. Hornak, J. Horák, D. Kubíček, Rostislav Navratil +3 more
20181 citations
Semantic Scholar
A high incidence of chromosome abnormalities in two-cell stage porcine IVP embryos
M. Hornak, M. Ješeta, Š. Hanuláková, J. Rubes
2015Journal of Applied Genetics1 citations
Semantic Scholar
L26/P-672 Paternal monosomy in PGT: re-biopsy reveals frequent association with segmental aberrations
M. Hornak, D. Blahútová, R. Brozek, M. Pesakova +3 more
2026Human Reproduction0 citations
Semantic Scholar
Reproducibility of different aneuploid findings at second trophectoderm biopsy evaluated by independent NGS platforms
J. Horák, D. Kubíček, Rostislav Navratil, M. Hornak +3 more
2019Reproductive Biomedicine Online0 citations
Semantic Scholar
26. MAJOR FACTORS INVOLVING AN IMPLANTATION RATE OF PGT-A EUPLOID EMBRYOS IN EGG DONATION PROGRAM OVER 35 YEARS
Kateřina Veselá, G. Tauwinklová, L. Hromadová, J. Horák +6 more
2019Reproductive Biomedicine Online0 citations
Semantic Scholar
What can karyomapping teach us about segmental mosaicism and mechanisms of its origin
D. Kubíček, J. Horák, M. Hornak, Rostislav Navratil +2 more
2019Reproductive Biomedicine Online0 citations
Semantic Scholar
Evaluation of chromosomal constitution in choronic villi samples of aborted fetuses after embryo transfers of euploid blastocysts
K. Veselá, J. Horák, V. Vlahova, M. Hornak +7 more
2019Reproductive Biomedicine Online0 citations
Semantic Scholar
10. COMPARISON OF VARIOUS ANEUPLOIDY TYPES AMONG TWO TROPHECTODERM BIOPSIES AND A REST OF THE EMBRYO
Rostislav Navratil, J. Horák, M. Hornak, D. Kubíček +4 more
2019Reproductive Biomedicine Online0 citations
Semantic Scholar
Segmental aneuploidies in PGD cycles for single gene conditions by karyomapping
K. Veselá, M. Hornak, J. Horák, D. Kubíček +6 more
20180 citations
Semantic Scholar
O7 Assessment of 669 embryos and clinical outcome from 113 cycles using array CGH of blastomeres
Kateřina Veselá, M. Hornak, J. Horák, E. Oráčová +4 more
20120 citations
Semantic Scholar
Contents Vol. 129, 2010
P. Rao, Wei-Lin Li, L. Vissers, J. Veltman +46 more
2010Cytogenetic and Genome Research0 citations Open access
Semantic Scholar

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