| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1080/14737159.2017.1325736 |
| P698 | PubMed publication ID | 28459185 |
| P50 | author | Rebecca L Gould | Q87963158 |
| P2093 | author name string | Darren K Griffin | |
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| The Sequence of the Human Genome | Q22065842 | ||
| Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances | Q37273694 | ||
| PGD for monogenic disorders: aspects of molecular biology. | Q37356384 | ||
| Quantitative decision-making in preimplantation genetic (aneuploidy) screening (PGS). | Q37459231 | ||
| Four-hour quantitative real-time polymerase chain reaction-based comprehensive chromosome screening and accumulating evidence of accuracy, safety, predictive value, and clinical efficacy | Q38064612 | ||
| PGD for cystic fibrosis patients and couples at risk of an additional genetic disorder combined with 24-chromosome aneuploidy testing. | Q38092458 | ||
| 24-chromosome copy number analysis: a comparison of available technologies | Q38133070 | ||
| Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification | Q38484837 | ||
| Development and validation of concurrent preimplantation genetic diagnosis for single gene disorders and comprehensive chromosomal aneuploidy screening without whole genome amplification | Q38816982 | ||
| 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 | ||
| What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium Steering Committee | Q39904266 | ||
| Live birth after polar body array comparative genomic hybridization prediction of embryo ploidy-the future of IVF? | Q39925981 | ||
| Preimplantation genetic screening to improve in vitro fertilization pregnancy rates: a prospective randomized controlled trial | Q40146578 | ||
| Genome screening by comparative genomic hybridization | Q40879187 | ||
| Karyomapping allows preimplantation genetic diagnosis of a de-novo deletion undetectable using conventional PGD technology | Q41600011 | ||
| Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nuclei | Q42136601 | ||
| In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial | Q44232985 | ||
| Preimplantation genetic screening for aneuploidy of embryos after in vitro fertilization in women aged at least 35 years: a prospective randomized trial | Q44316456 | ||
| Preimplantation genetic haplotyping: 127 diagnostic cycles demonstrating a robust, efficient alternative to direct mutation testing on single cells | Q44460882 | ||
| Successful hematopoietic stem cell transplantation for Fanconi anemia from an unaffected HLA-genotype-identical sibling selected using preimplantation genetic diagnosis | Q44592660 | ||
| Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease | Q45802005 | ||
| Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders | Q48595572 | ||
| A prospective randomized controlled trial of preimplantation genetic screening in the "good prognosis" patient | Q48738473 | ||
| Preimplantation aneuploidy testing for infertile patients of advanced maternal age: a randomized prospective trial | Q48741471 | ||
| Live births following Karyomapping of human blastocysts: experience from clinical application of the method. | Q50877952 | ||
| Array CGH analysis shows that aneuploidy is not related to the number of embryos generated. | Q51346563 | ||
| Preimplantation genetic screening does not improve delivery rate in women under the age of 36 following single-embryo transfer. | Q51678170 | ||
| Successful umbilical cord blood transplantation for Fanconi anemia using preimplantation genetic diagnosis for HLA-matched donor. | Q52085650 | ||
| Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease. | Q52858843 | ||
| Development and validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of embryos. | Q53063194 | ||
| Validation of microarray comparative genomic hybridization for comprehensive chromosome analysis of embryos. | Q53293819 | ||
| Chromosome instability is common in human cleavage-stage embryos. | Q53398239 | ||
| Prospectively randomized controlled trial of PGS in IVF/ICSI patients with poor implantation. | Q53431315 | ||
| What next for preimplantation genetic screening (PGS)? Experience with blastocyst biopsy and testing for aneuploidy. | Q53472614 | ||
| Preimplantation genetic diagnosis | Q56337915 | ||
| A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms | Q28203288 | ||
| Preimplantation diagnosis for Fanconi anemia combined with HLA matching | Q28203871 | ||
| Proof of principle and first cases using preimplantation genetic haplotyping--a paradigm shift for embryo diagnosis | Q28250334 | ||
| Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors | Q29618818 | ||
| Chromosome abnormalities in human embryos | Q33546940 | ||
| Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis | Q33970561 | ||
| The ESHRE PGD Consortium: 10 years of data collection | Q34161543 | ||
| Preimplantation genetic diagnosis: state of the art 2011. | Q34199663 | ||
| Origins and rates of aneuploidy in human blastomeres | Q34242703 | ||
| Clinical experience with preimplantation diagnosis of sex by dual fluorescent in situ hybridization | Q34316456 | ||
| Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification | Q34321635 | ||
| Singling out genetic disorders and disease | Q34334104 | ||
| Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro | Q34477384 | ||
| Molecular diagnostics in preimplantation genetic diagnosis | Q34516018 | ||
| Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing | Q35079130 | ||
| Characterization of the human cumulus cell transcriptome during final follicular maturation and ovulation. | Q35158295 | ||
| Karyomapping-a comprehensive means of simultaneous monogenic and cytogenetic PGD: comparison with standard approaches in real time for Marfan syndrome | Q35186890 | ||
| Diagnosis of sex in preimplantation embryos by fluorescent in situ hybridisation | Q35188087 | ||
| Concurrent whole-genome haplotyping and copy-number profiling of single cells | Q35759080 | ||
| Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study | Q36112761 | ||
| Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization. | Q36186429 | ||
| Allele dropout in polar bodies and blastomeres. | Q36267646 | ||
| Preimplantation genetic diagnosis of inherited cancer: familial adenomatous polyposis coli | Q36268525 | ||
| Chromosome abnormalities and their relationship to morphology and development of human embryos | Q36396448 | ||
| Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses | Q36435251 | ||
| What's new in karyotyping? The move towards array comparative genomic hybridisation (CGH). | Q36764556 | ||
| Elucidating the origin of chromosomal aberrations in IVF embryos by preimplantation genetic analysis | Q37051737 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 611-621 | |
| P577 | publication date | 2017-05-15 | |
| P1433 | published in | Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare | Q15756305 |
| P1476 | title | Karyomapping and how is it improving preimplantation genetics? | |
| P478 | volume | 17 |
| Q49912258 | Importance of embryo aneuploidy screening in preimplantation genetic diagnosis for monogenic diseases using the karyomap gene chip | cites work | P2860 |
Search more.