| P50 | author | Xavier Vendrell | Q93023395 |
| P2093 | author name string | M J Escribà | |
| P2860 | cites work | Confined placental mosaicism | Q24517911 |
| | Coadaptation and conflict, misconception and muddle, in the evolution of genomic imprinting | Q27006276 |
| | Mouse model of chromosome mosaicism reveals lineage-specific depletion of aneuploid cells and normal developmental potential | Q27321241 |
| | Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates | Q28603618 |
| | The "omics" of human male infertility: integrating big data in a systems biology approach | Q31031878 |
| | A single trophectoderm biopsy at blastocyst stage is mathematically unable to determine embryo ploidy accurately enough for clinical use | Q33612541 |
| | Maternal control of early mouse development | Q33710885 |
| | Waves of early transcriptional activation and pluripotency program initiation during human preimplantation development | Q33818101 |
| | Cis and trans effects of human genomic variants on gene expression. | Q33881197 |
| | Dynamic changes in gene expression during human early embryo development: from fundamental aspects to clinical applications | Q34131722 |
| | Chromosomal mosaicism in human preimplantation embryos: a systematic review | Q34181395 |
| | The effect of interspecific oocytes on demethylation of sperm DNA. | Q34336525 |
| | The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans | Q34411991 |
| | Pathway to totipotency: lessons from germ cells | Q34585032 |
| | The molecular foundations of the maternal to zygotic transition in the preimplantation embryo | Q34806720 |
| | The maternal-to-zygotic transition: a play in two acts | Q34998975 |
| | Reprogramming the genome to totipotency in mouse embryos | Q35034392 |
| | Genomic imprinting, action, and interaction of maternal and fetal genomes | Q35699423 |
| | Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation Development | Q35817114 |
| | Variation in human meiotic recombination | Q35918568 |
| | The paradox of longer sperm telomeres in older men's testes: a birth-cohort effect caused by transgenerational telomere erosion in the female germline | Q36555830 |
| | An evolutionary view of human recombination | Q36673942 |
| | The abbreviated pluripotent cell cycle. | Q36886887 |
| | Transgenerational genetic effects | Q37038020 |
| | Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease | Q37187461 |
| | Transgenerational genetic effects on phenotypic variation and disease risk | Q37379485 |
| | Review: Parent-offspring conflict and the control of placental function | Q37966277 |
| | Chromatin-linked determinants of zygotic genome activation | Q38042377 |
| | The ever growing complexity of placental epigenetics - role in adverse pregnancy outcomes and fetal programming | Q38055922 |
| | Enhancer biology and enhanceropathies | Q38193691 |
| | Totipotency and lineage segregation in the human embryo. | Q38201989 |
| | Somatic mosaicism and disease. | Q38220901 |
| | Genetic modifiers and oligogenic inheritance | Q38511788 |
| | Genomic imprinting in the human placenta | Q38597288 |
| | Chromosomal instability in mammalian pre-implantation embryos: potential causes, detection methods, and clinical consequences | Q38641797 |
| | Mosaicism in Preimplantation Human Embryos: When Chromosomal Abnormalities Are the Norm | Q38689280 |
| | The subcortical maternal complex: multiple functions for one biological structure? | Q38831289 |
| | Sperm epigenetics in the study of male fertility, offspring health, and potential clinical applications | Q38903360 |
| | Dynamic Role of trans Regulation of Gene Expression in Relation to Complex Traits | Q41881274 |
| | Genome-wide methylation patterns in normal and uniparental early mouse embryos | Q43829638 |
| | Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases. | Q44523764 |
| | The unique transcriptome through day 3 of human preimplantation development | Q46086301 |
| | Correlation between aneuploidy, apoptotic markers and DNA fragmentation in spermatozoa from normozoospermic patients. | Q46436987 |
| | Non-invasive imaging of human embryos before embryonic genome activation predicts development to the blastocyst stage | Q46697212 |
| | Epigenetics: ambiguities and implications | Q47620325 |
| | Human female meiosis revised: new insights into the mechanisms of chromosome segregation and aneuploidies from advanced genomics and time-lapse imaging. | Q47624886 |
| | Kinetics of the early development of uniparental human haploid embryos | Q47906017 |
| | Causes and consequences of chromosome segregation error in preimplantation embryos | Q50132809 |
| | Placental Defects: An Epigenetic Perspective. | Q52593482 |
| | Chromosome instability is common in human cleavage-stage embryos. | Q53398239 |
| | Mitochondria and the death of oocytes | Q59075483 |
| | Human gene expression first occurs between the four- and eight-cell stages of preimplantation development | Q59084361 |
| | Chaos in the embryo | Q83787832 |
| P433 | issue | 3 | |
| P304 | page(s) | 363-369 | |
| P577 | publication date | 2018-11-12 | |
| P1433 | published in | Journal of Assisted Reproduction and Genetics | Q15755113 |
| P1476 | title | The model of "genetic compartments": a new insight into reproductive genetics | |
| P478 | volume | 36 | |