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.