2022
An Incidental Detection of a Cryptic Complex Chromosome Rearrangement Found During NGS Based PGT-SR: A Case Report
Özer L, Aktuna S, Unsal E, Baltaci A, Baltaci V. An Incidental Detection of a Cryptic Complex Chromosome Rearrangement Found During NGS Based PGT-SR: A Case Report. Journal Of Reproduction & Infertility 2022, 23: 303-309. PMID: 36452189, PMCID: PMC9674458, DOI: 10.18502/jri.v23i4.10817.Peer-Reviewed Original ResearchPreimplantation genetic testingIVF studiesHealthy boysGenetic testingIVF treatment cyclesIVF attemptsIVF centerCase reportIncidental detectionSpontaneous abortionDifferent IVF centresHigh riskFertilization failureTreatment cyclesComplex chromosome rearrangementPGT-SRNext-generation sequencingReproductive failureHealthy embryosStructural chromosomal rearrangementsSitu hybridizationCopy number variationsBoysChromosomal breakpointsNormal phenotype
2019
69. IMPROVED IVF SUCCESS OF COMBINED PGT-M AND PGT-A APPLICATIONS
Unsal E, Aktuna S, Aydin M, Ozer L, Baltacı V. 69. IMPROVED IVF SUCCESS OF COMBINED PGT-M AND PGT-A APPLICATIONS. Reproductive BioMedicine Online 2019, 39: e69-e70. DOI: 10.1016/j.rbmo.2019.04.122.Peer-Reviewed Original ResearchPreimplantation genetic testingSingle gene disordersEuploid embryosTrophectoderm biopsySpontaneous miscarriage rateGene disordersMiscarriage rateWhole genome amplification technologySpontaneous miscarriageCarrier patientsPregnancy rateIVF successHigh riskPatient's requestDisorder patientsAverage agePatientsPregnancy ratioEmbryo transferNext-generation sequencing technologiesGenetic testingGeneration sequencing technologyChromosome screeningDisordersGenetic conditions