| review article | Q7318358 |
| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1016058152 |
| P356 | DOI | 10.1007/S10815-016-0750-0 |
| P932 | PMC publication ID | 5010808 |
| P698 | PubMed publication ID | 27272212 |
| P2093 | author name string | Guoping Fan | |
| Kevin Huang | |||
| Bo Lv | |||
| Lina Lu | |||
| Zhigang Xue | |||
| Xianmin Zhu | |||
| P2860 | cites work | Genome-wide detection of single-nucleotide and copy-number variations of a single human cell | Q24602999 |
| mRNA-Seq whole-transcriptome analysis of a single cell | Q28240611 | ||
| Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing | Q28281877 | ||
| High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays | Q29615979 | ||
| Comprehensive human genome amplification using multiple displacement amplification | Q29618737 | ||
| Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances | Q32168348 | ||
| Cytogenetic analysis of human blastocysts with the use of FISH, CGH and aCGH: scientific data and technical evaluation | Q33767726 | ||
| Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates | Q33897131 | ||
| Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications | Q34044255 | ||
| The use of morphokinetics as a predictor of embryo implantation | Q34206864 | ||
| Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification | Q34321635 | ||
| Genetic programs in human and mouse early embryos revealed by single-cell RNA sequencing | Q34360246 | ||
| Integrated genome and transcriptome sequencing of the same cell | Q34458660 | ||
| G&T-seq: parallel sequencing of single-cell genomes and transcriptomes | Q34473774 | ||
| Oligonucleotide arrays vs. metaphase-comparative genomic hybridisation and BAC arrays for single-cell analysis: first applications to preimplantation genetic diagnosis for Robertsonian translocation carriers | Q34557302 | ||
| Morphokinetic analysis of cleavage stage embryos and its relationship to aneuploidy in a retrospective time-lapse imaging study | Q34962670 | ||
| Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing | Q35079130 | ||
| Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study. | Q35150481 | ||
| Karyomapping-a comprehensive means of simultaneous monogenic and cytogenetic PGD: comparison with standard approaches in real time for Marfan syndrome | Q35186890 | ||
| Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles | Q35357388 | ||
| Calibrating genomic and allelic coverage bias in single-cell sequencing | Q35603470 | ||
| Application of next-generation sequencing for 24-chromosome aneuploidy screening of human preimplantation embryos | Q35748155 | ||
| Morphokinetic parameters using time-lapse technology and day 5 embryo quality: a prospective cohort study. | Q35938114 | ||
| Medium-based noninvasive preimplantation genetic diagnosis for human α-thalassemias-SEA | Q36009063 | ||
| Healthy Baby Born to a Robertsonian Translocation Carrier following Next-Generation Sequencing-Based Preimplantation Genetic Diagnosis: A Case Report | Q36156557 | ||
| Spontaneous abortions are reduced after preconception diagnosis of translocations | Q36267654 | ||
| Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses | Q36435251 | ||
| Whole genome amplification from a single cell: implications for genetic analysis | Q37081188 | ||
| Could time-lapse embryo imaging reduce the need for biopsy and PGS? | Q37214109 | ||
| Preimplantation genetic screening (PGS) with Comparative genomic hybridization (CGH) following day 3 single cell blastomere biopsy markedly improves IVF outcomes while lowering multiple pregnancies and miscarriages. | Q37300095 | ||
| Live birth following serial vitrification of embryos and PGD for fragile X syndrome in a patient with the premutation and decreased ovarian reserve | Q37429884 | ||
| The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts | Q37621739 | ||
| Preimplantation genetic diagnosis at 20 years | Q37767191 | ||
| Four-hour quantitative real-time polymerase chain reaction-based comprehensive chromosome screening and accumulating evidence of accuracy, safety, predictive value, and clinical efficacy | Q38064612 | ||
| The evolving role of genetics in reproductive medicine | Q38184774 | ||
| Impact of blastocyst biopsy and comprehensive chromosome screening technology on preimplantation genetic screening: a systematic review of randomized controlled trials | Q38323403 | ||
| Clinical applications of preimplantation genetic testing | Q38362074 | ||
| First pregnancies after preconception diagnosis of translocations of maternal origin | Q38502909 | ||
| Development and validation of an accurate quantitative real-time polymerase chain reaction-based assay for human blastocyst comprehensive chromosomal aneuploidy screening | Q39395214 | ||
| Comprehensive chromosome screening alters traditional morphology-based embryo selection: a prospective study of 100 consecutive cycles of planned fresh euploid blastocyst transfer | Q39409658 | ||
| Sequential comprehensive chromosome analysis on polar bodies, blastomeres and trophoblast: insights into female meiotic errors and chromosomal segregation in the preimplantation window of embryo development. | Q39520963 | ||
| Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses | Q39617282 | ||
| Live birth after polar body array comparative genomic hybridization prediction of embryo ploidy-the future of IVF? | Q39925981 | ||
| Dynamic transcriptional symmetry-breaking in pre-implantation mammalian embryo development revealed by single-cell RNA-seq | Q40513230 | ||
| Fluorescent PCR: a new technique for PGD of sex and single-gene defects | Q41020182 | ||
| Routine use of next-generation sequencing for preimplantation genetic diagnosis of blastomeres obtained from embryos on day 3 in fresh in vitro fertilization cycles | Q41522343 | ||
| Karyomapping allows preimplantation genetic diagnosis of a de-novo deletion undetectable using conventional PGD technology | Q41600011 | ||
| Successful implantation and live birth of a healthy boy after triple biopsy and double vitrification of oocyte-embryo-blastocyst | Q41601318 | ||
| Genomic DNA in human blastocoele fluid | Q41604547 | ||
| No evidence of association between blastocyst aneuploidy and morphokinetic assessment in a selected population of poor-prognosis patients: a longitudinal cohort study. | Q41627714 | ||
| Single-cell RNA-Seq profiling of human preimplantation embryos and embryonic stem cells | Q42774013 | ||
| Defining the three cell lineages of the human blastocyst by single-cell RNA-seq. | Q42777328 | ||
| Embryonic DNA sampling without biopsy: the beginnings of non-invasive PGD? | Q43706565 | ||
| Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success | Q44700452 | ||
| Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts | Q44738977 | ||
| Pregnancy after embryo biopsy and coamplification of DNA from X and Y chromosomes | Q44844443 | ||
| Increased IVF pregnancy rates after microarray preimplantation genetic diagnosis due to parental translocations | Q44936428 | ||
| Blastocentesis: a source of DNA for preimplantation genetic testing. Results from a pilot study | Q45240908 | ||
| FISH reanalysis of inner cell mass and trophectoderm samples of previously array-CGH screened blastocysts shows high accuracy of diagnosis and no major diagnostic impact of mosaicism at the blastocyst stage. | Q45785591 | ||
| PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization | Q46450703 | ||
| Morphological and cytogenetic assessment of cleavage and blastocyst stage embryos | Q46790679 | ||
| Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders | Q48595572 | ||
| Genome analyses of single human oocytes | Q48612112 | ||
| Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial | Q48623792 | ||
| Kinetic markers of human embryo quality using time-lapse recordings of IVF/ICSI-fertilized oocytes | Q48739327 | ||
| Validation of multiple annealing and looping-based amplification cycle sequencing for 24-chromosome aneuploidy screening of cleavage-stage embryos. | Q50630585 | ||
| Live births following Karyomapping of human blastocysts: experience from clinical application of the method. | Q50877952 | ||
| Non-invasive pre-implantation genetic diagnosis of X-linked disorders. | Q51116164 | ||
| A cautionary note against embryo aneuploidy risk assessment using time-lapse imaging. | Q51122861 | ||
| Blastocoel fluid from differentiated blastocysts harbors embryonic genomic material capable of a whole-genome deoxyribonucleic acid amplification and comprehensive chromosome microarray analysis. | Q52941113 | ||
| Development and validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of embryos. | Q53063194 | ||
| Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier. | Q54372768 | ||
| Polymerase chain reaction-based detection of chromosomal imbalances on embryos: the evolution of preimplantation genetic diagnosis for chromosomal translocations. | Q54440551 | ||
| Clinical application of comprehensive chromosomal screening at the blastocyst stage | Q57779161 | ||
| Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer | Q58862246 | ||
| Fluorescent in-situ hybridization to interphase nuclei of human preimplantation embryos with X and Y chromosome specific probes | Q67947889 | ||
| Preimplantation genetic diagnosis. In situ hybridization as a tool for analysis | Q68089002 | ||
| Genetic diagnosis using polymerase chain reaction and fluorescent in-situ hybridization analysis of biopsied cells from both the cleavage and blastocyst stages of individual cultured human preimplantation embryos | Q72223940 | ||
| Diagnosis of major chromosome aneuploidies in human preimplantation embryos | Q72347419 | ||
| Chromosome mosaicism in human embryos | Q72365258 | ||
| Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions | Q74268825 | ||
| Single nucleotide polymorphism microarray-based concurrent screening of 24-chromosome aneuploidy and unbalanced translocations in preimplantation human embryos | Q82691847 | ||
| Single-gene testing combined with single nucleotide polymorphism microarray preimplantation genetic diagnosis for aneuploidy: a novel approach in optimizing pregnancy outcome | Q82817515 | ||
| Successful pregnancies after application of array-comparative genomic hybridization in PGS-aneuploidy screening | Q82954172 | ||
| First births after preimplantation genetic diagnosis of structural chromosome abnormalities using comparative genomic hybridization and microarray analysis | Q83743387 | ||
| Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes | Q84785638 | ||
| ESHRE PGD consortium best practice guidelines for amplification-based PGD | Q85239160 | ||
| P433 | issue | 9 | |
| P304 | page(s) | 1129-1134 | |
| P577 | publication date | 2016-06-07 | |
| P1433 | published in | Journal of Assisted Reproduction and Genetics | Q15755113 |
| P1476 | title | Recent advances in preimplantation genetic diagnosis and screening | |
| P478 | volume | 33 |
| Q33874456 | De Novo Paternal FBN1 Mutation Detected in Embryos Before Implantation. |
| Q97066893 | Improved clinical outcomes of preimplantation genetic testing for aneuploidy using MALBAC-NGS compared with MDA-SNP array |
| Q48251264 | Mapping allele with resolved carrier status of Robertsonian and reciprocal translocation in human preimplantation embryos. |
| Q64061836 | Recent developments in genetic/genomic medicine |
| Q90029418 | The current state of sickle cell trait: implications for reproductive and genetic counseling |
| Q94189769 | The current state of sickle cell trait: implications for reproductive and genetic counseling |
| Q42398268 | The expanding and contracting roles of the genome in regulation of the ovarian reserve |
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