SNP array-based analyses of unbalanced embryos as a reference to distinguish between balanced translocation carrier and normal blastocysts

Journal of Assisted Reproduction and Genetics

Volumn 33, Issue 8, 2016, Pages 1115-1119

  Treff, Nathan R ^a,b   Thompson, Katherine ^a   Rafizadeh, Michael ^a   Chow, Michael ^a   Morrison, Liza ^a   Tao, Xin ^c   Garnsey, Heather ^c   Reda, Christine V ^a   Metzgar, Talia L ^a   Neal, Shelby ^a   Jalas, Chaim ^c   Scott, Richard T ^a,b   Forman, Eric J ^a,b  

^a REPRODUCTIVE MEDICINE ASSOCIATES OF NEW JERSEY   (United States)

^b ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

^c Foundation for Embryonic Competence   (United States)

Author keywords

Microarray; Preimplantation genetic testing; Reciprocal translocation

Indexed keywords

DNA;

ARTICLE; BIOPSY; BLASTOCYST; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; EMBRYO; FERTILIZATION IN VITRO; GENE AMPLIFICATION; GENOTYPE; HUMAN; KARYOTYPING; MAJOR CLINICAL STUDY; NEWBORN; NIDATION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; CYTOLOGY; DNA MICROARRAY; EMBRYO TRANSFER; GENE TRANSLOCATION; GENETIC SCREENING; GENETICS; IN VITRO FERTILIZATION; MAMMALIAN EMBRYO; PREIMPLANTATION GENETIC DIAGNOSIS; PROCEDURES; VALIDATION STUDY;

BLASTOCYST; EMBRYO IMPLANTATION; EMBRYO TRANSFER; EMBRYO, MAMMALIAN; FERTILIZATION IN VITRO; GENETIC TESTING; GENOTYPE; HUMANS; KARYOTYPING; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; PREIMPLANTATION DIAGNOSIS; TRANSLOCATION, GENETIC;

EID: 84973106798     PISSN: 10580468     EISSN: 15737330     Source Type: Journal    
DOI: 10.1007/s10815-016-0734-0     Document Type: Article

References (13)

1. Tan YQ et al. Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers. Hum Reprod. 2013;28(9):2581–92.
2. van Uum CM et al. SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations. Eur J Hum Genet. 2012;20(9):938–44.
3. Alfarawati S, Fragouli E, Colls P, Wells D. First births after preimplantation genetic diagnosis of structural chromosome abnormalities using comparative genomic hybridization and microarray analysis. Hum Reprod. 2011;26:1560–74.
4. Vanneste E et al. PGD for a complex chromosomal rearrangement by array comparative genomic hybridization. Hum Reprod. 2011;26:941–9.
5. Treff NR et al. Single nucleotide polymorphism microarray-based concurrent screening of 24 chromosome aneuploidy and unbalanced translocations in preimplantation human embryos. Fertil Steril. 2010;95:1606–12. e1601-1602.
6. Forman EJ, Hong KH, Scott RT Jr. Single embryo transfer with aneuploidy screening: same delivery rate, better obstetrical outcome. 61st American College of Obstetricians and Gynecologists Annual Clinical Meeting (2013).
7. Scott Jr RT et al. Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial. Fertil Steril. 2013;100:697–703.
8. Forman EJ et al. In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial. Fertil Steril. 2013;100:100–7. e101.
9. Yang Z et al. 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. Mol Cytogenet. 2012;5:24.
10. Treff NR, Scott Jr RT. Methods for comprehensive chromosome screening of oocytes and embryos: capabilities, limitations, and evidence of validity. J Assist Reprod Genet. 2012;29:381–90.
11. Shamash J et al. Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier’s embryos- preliminary observations of two robertsonian translocation carrier families. J Assist Reprod Genet. 2011;28:77–83.
12. Treff NR, Su J, Tao X, Levy B, Scott Jr RT. Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays. Fertil Steril. 2010;94:2017–21.
13. Treff NR et al. Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier. Fertil Steril. 2011;96:e58–65.