Preimplantation Diagnosis

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  Subject Areas on Research

  • Evidence-Based Care for Couples With Infertility. 
  • High relative deoxyribonucleic acid content of trophectoderm biopsy adversely affects pregnancy outcomes. 
  • Impact of gene patents and licensing practices on access to genetic testing for cystic fibrosis. 
  • Interpretation of noninvasive prenatal testing results following in vitro fertilization and preimplantation genetic testing for aneuploidy. 
  • Pre-implantation genetic testing alters the sex ratio: an analysis of 91,805 embryo transfer cycles. 
  • Preimplantation genetic diagnosis (PGD) for genetic prion disorder due to F198S mutation in the PRNP gene. 
  • Preimplantation genetic diagnosis for inherited neurological disorders. 
  • Preimplantation genetic testing for aneuploidy is cost-effective, shortens treatment time, and reduces the risk of failed embryo transfer and clinical miscarriage. 
  • Quest for a less invasive approach to preimplantation genetic testing remains ongoing. 
  • SNP array-based analyses of unbalanced embryos as a reference to distinguish between balanced translocation carrier and normal blastocysts. 
  • The FMR1 premutation and reproduction. 
  • The impact of contemporary preimplantation genetic screening and diagnosis on the detection of aneuploidy and inherited genetic diseases. 
  • When next-generation sequencing-based preimplantation genetic testing for aneuploidy (PGT-A) yields an inconclusive report: diagnostic results and clinical outcomes after re biopsy.