Tian Y, Li M, Yang J, Chen H, Lu D
Arch Gynecol Obstet. 2024; 309(5):1787-1799.
PMID: 38376520
DOI: 10.1007/s00404-024-07370-z.
Jager R
Int J Mol Sci. 2022; 23(13).
PMID: 35806097
PMC: 9267064.
DOI: 10.3390/ijms23137090.
Volozonoka L, Miskova A, Gailite L
Int J Mol Sci. 2022; 23(9).
PMID: 35563216
PMC: 9102663.
DOI: 10.3390/ijms23094819.
Desai S, Mangoli V
J Obstet Gynaecol India. 2021; 70(6):417-424.
PMID: 33417648
PMC: 7758391.
DOI: 10.1007/s13224-020-01383-9.
Rothschild J
J Gen Fam Med. 2020; 21(3):37-47.
PMID: 32489755
PMC: 7260159.
DOI: 10.1002/jgf2.321.
Preimplantation Genetic Testing: Its Evolution, Where Are We Today?.
Parikh F, Athalye A, Naik N, Naik D, Sanap R, Madon P
J Hum Reprod Sci. 2019; 11(4):306-314.
PMID: 30787513
PMC: 6333033.
DOI: 10.4103/jhrs.JHRS_132_18.
Coexisting genomic aberrations associated with lymph node metastasis in breast cancer.
Bao L, Qian Z, Lyng M, Wang L, Yu Y, Wang T
J Clin Invest. 2018; 128(6):2310-2324.
PMID: 29558370
PMC: 5983317.
DOI: 10.1172/JCI97449.
Preimplantation genetic diagnosis/screening by comprehensive molecular testing.
Kurahashi H, Kato T, Miyazaki J, Nishizawa H, Nishio E, Furukawa H
Reprod Med Biol. 2017; 15(1):13-19.
PMID: 29259418
PMC: 5715840.
DOI: 10.1007/s12522-015-0216-6.
Tripolar mitosis and partitioning of the genome arrests human preimplantation development in vitro.
Ottolini C, Kitchen J, Xanthopoulou L, Gordon T, Summers M, Handyside A
Sci Rep. 2017; 7(1):9744.
PMID: 28851957
PMC: 5575028.
DOI: 10.1038/s41598-017-09693-1.
A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns.
Zhang Y, Cheung Y, Su W
Sci Rep. 2017; 7(1):9666.
PMID: 28851906
PMC: 5575355.
DOI: 10.1038/s41598-017-09139-8.
nbCNV: a multi-constrained optimization model for discovering copy number variants in single-cell sequencing data.
Zhang C, Cai H, Huang J, Song Y
BMC Bioinformatics. 2016; 17:384.
PMID: 27639558
PMC: 5027123.
DOI: 10.1186/s12859-016-1239-7.
Reanalysis of human blastocysts with different molecular genetic screening platforms reveals significant discordance in ploidy status.
Tortoriello D, Dayal M, Beyhan Z, Yakut T, Keskintepe L
J Assist Reprod Genet. 2016; 33(11):1467-1471.
PMID: 27423662
PMC: 5125143.
DOI: 10.1007/s10815-016-0766-5.
Preimplantation genetic screening 2.0: the theory.
Geraedts J, Sermon K
Mol Hum Reprod. 2016; 22(8):839-44.
PMID: 27256482
PMC: 4986416.
DOI: 10.1093/molehr/gaw033.
High Performance DNA Probes for Perinatal Detection of Numerical Chromosome Aberrations.
Lemke K, Weier J, Weier H, Lawin-OBrien A
Adv Tech Biol Med. 2016; 3(3).
PMID: 26855976
PMC: 4739796.
DOI: 10.4172/2379-1764.1000155.
Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing.
Tan Y, Yin X, Zhang S, Jiang H, Tan K, Li J
Gigascience. 2015; 3(1):30.
PMID: 25685330
PMC: 4326468.
DOI: 10.1186/2047-217X-3-30.
Application of next-generation sequencing technology in forensic science.
Yang Y, Xie B, Yan J
Genomics Proteomics Bioinformatics. 2014; 12(5):190-7.
PMID: 25462152
PMC: 4411420.
DOI: 10.1016/j.gpb.2014.09.001.
Oligonucleotide arrays vs. metaphase-comparative genomic hybridisation and BAC arrays for single-cell analysis: first applications to preimplantation genetic diagnosis for Robertsonian translocation carriers.
Ramos L, Rey J, Daina G, Garcia-Aragones M, Armengol L, Fernandez-Encinas A
PLoS One. 2014; 9(11):e113223.
PMID: 25415307
PMC: 4240610.
DOI: 10.1371/journal.pone.0113223.
Current status of comprehensive chromosome screening for elective single-embryo transfer.
Wu M, Chao K, Chen C, Chang L, Chen S, Yang Y
Obstet Gynecol Int. 2014; 2014:581783.
PMID: 24991216
PMC: 4058795.
DOI: 10.1155/2014/581783.
Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization.
Munne S
Curr Genomics. 2013; 13(6):463-70.
PMID: 23448851
PMC: 3426780.
DOI: 10.2174/138920212802510457.
Population-scale analysis of human microsatellites reveals novel sources of exonic variation.
McIver L, McCormick J, Martin A, Fondon 3rd J, Garner H
Gene. 2013; 516(2):328-34.
PMID: 23274653
PMC: 3815531.
DOI: 10.1016/j.gene.2012.12.068.