Clinical application of next-generation sequencing in preimplantation genetic diagnosis cycles for Robertsonian and reciprocal translocations

Detection and quantitation of chromosomal mosaicism in human blastocysts using copy number variation sequencing

(2016) Tida Ruttanajit et al.   PRENATAL DIAGNOSIS

The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities

(2015) Na Li et al.   Journal of Genetics and Genomics

Validation of a semiconductor next-generation sequencing-based protocol for preimplantation genetic diagnosis of reciprocal translocations

(2015) S. Bono et al.   PRENATAL DIAGNOSIS

The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryos

(2015) Junmei Fan et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Validation of Copy Number Variation Sequencing for Detecting Chromosome Imbalances in Human Preimplantation Embryos1

(2014) Li Wang et al.   BIOLOGY OF REPRODUCTION

Validation of multiple annealing and looping-based amplification cycle sequencing for 24-chromosome aneuploidy screening of cleavage-stage embryos

(2014) Jin Huang et al.   FERTILITY AND STERILITY

Development and validation of a next-generation sequencing–based protocol for 24-chromosome aneuploidy screening of embryos

(2014) Francesco Fiorentino et al.   FERTILITY AND STERILITY

A PGD Pregnancy Achieved by Embryo Copy Number Variation Sequencing with Confirmation by Non-Invasive Prenatal Diagnosis

(2014) Hui Wang et al.   Journal of Genetics and Genomics

Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation

(2014) Dagan Wells et al.   JOURNAL OF MEDICAL GENETICS

Copy Number Variation Sequencing for Comprehensive Diagnosis of Chromosome Disease Syndromes

(2014) Desheng Liang et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing

(2014) Yueqiu Tan et al.   GigaScience

Massively Parallel Sequencing for Chromosomal Abnormality Testing in Trophectoderm Cells of Human Blastocysts1

(2013) XuYang Yin et al.   BIOLOGY OF REPRODUCTION

Maternal Mosaicism Is a Significant Contributor to Discordant Sex Chromosomal Aneuploidies Associated with Noninvasive Prenatal Testing

(2013) Y. Wang et al.   CLINICAL CHEMISTRY

24-chromosome copy number analysis: a comparison of available technologies

(2013) Alan H. Handyside   FERTILITY AND STERILITY

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing

(2013) Desheng Liang et al.   PRENATAL DIAGNOSIS

Preimplantation Genetic Diagnosis for Aneuploidy and Translocations Using Array Comparative Genomic Hybridization

(2012) Santiago Munne   CURRENT GENOMICS

Genetic Factors as a Cause of Miscarriage

(2012) N. Suzumori et al.   CURRENT MEDICINAL CHEMISTRY

Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos

(2011) Thierry Voet et al.   HUMAN MUTATION

PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization

(2011) F. Fiorentino et al.   HUMAN REPRODUCTION

Fast and accurate long-read alignment with Burrows–Wheeler transform

(2010) Heng Li et al.   BIOINFORMATICS

Single nucleotide polymorphism microarray–based concurrent screening of 24-chromosome aneuploidy and unbalanced translocations in preimplantation human embryos

(2010) Nathan R. Treff et al.   FERTILITY AND STERILITY

Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses

(2009) Jill Fischer et al.   FERTILITY AND STERILITY

Chromosome instability is common in human cleavage-stage embryos

(2009) Evelyne Vanneste et al.   NATURE MEDICINE