Wang W, Dai J, Hu X, He W, Gu Y, Wan Z
Hum Genet. 2025; .
PMID: 39969580
DOI: 10.1007/s00439-025-02728-y.
Liu X, Zhang Q, Cao K, Li J, Gao Y, Xu P
Clin Kidney J. 2025; 18(1):sfae356.
PMID: 39802589
PMC: 11719030.
DOI: 10.1093/ckj/sfae356.
Wu Z, Liang T, Liu Y, Ding X, Shu D
Front Genet. 2024; 15:1389461.
PMID: 39175751
PMC: 11338862.
DOI: 10.3389/fgene.2024.1389461.
Lian M, Tan V, Taguchi R, Zhao M, Phang G, Tan A
Int J Mol Sci. 2024; 25(15).
PMID: 39125643
PMC: 11311680.
DOI: 10.3390/ijms25158073.
Volk M, Writzl K, Veble A, Jaklic H, Teran N, Prosenc B
Balkan J Med Genet. 2024; 26(2):5-10.
PMID: 38482262
PMC: 10932602.
DOI: 10.2478/bjmg-2023-0017.
Preimplantation Genetic Testing for Genetic Diseases: Limits and Review of Current Literature.
Giuliano R, Maione A, Vallefuoco A, Sorrentino U, Zuccarello D
Genes (Basel). 2023; 14(11).
PMID: 38003038
PMC: 10671162.
DOI: 10.3390/genes14112095.
Robust preimplantation genetic testing of the common F8 Inv22 pathogenic variant of severe hemophilia A using a highly polymorphic multi-marker panel encompassing the paracentric inversion.
Nguyen M, Nguyen T, Nguyen D, Nguyen T, Nguyen K, Ngo V
Thromb J. 2023; 21(1):108.
PMID: 37864173
PMC: 10588207.
DOI: 10.1186/s12959-023-00552-w.
Establishment of linkage phase, using Oxford Nanopore Technologies, for preimplantation genetic testing of Coffin-Lowry syndrome with a mutation.
Wen X, Du J, Li Z, Liu N, Huo J, Li J
Front Genet. 2023; 14:1169868.
PMID: 37779904
PMC: 10538565.
DOI: 10.3389/fgene.2023.1169868.
Conventional outcome reporting per IVF cycle/embryo transfer may systematically underestimate chances of success for women undergoing ART: relevant biases in registries, epidemiological studies, and guidelines.
Griesinger G, Larsson P
Hum Reprod Open. 2023; 2023(2):hoad018.
PMID: 37250429
PMC: 10214861.
DOI: 10.1093/hropen/hoad018.
Preimplantation genetic testing and child health: a national register-based study.
Ginstrom Ernstad E, Hanson C, Wanggren K, Thurin-Kjellberg A, Hulthe Soderberg C, Syk Lundberg E
Hum Reprod. 2023; 38(4):739-750.
PMID: 36749096
PMC: 10068295.
DOI: 10.1093/humrep/dead021.
Combined Preimplantation Genetic Testing for Genetic Kidney Disease: Genetic Risk Identification, Assisted Reproductive Cycle, and Pregnancy Outcome Analysis.
Xiao M, Shi H, Rao J, Xi Y, Zhang S, Wu J
Front Med (Lausanne). 2022; 9:936578.
PMID: 35783601
PMC: 9247246.
DOI: 10.3389/fmed.2022.936578.
Using affected embryos to establish linkage phase in preimplantation genetic testing for thalassemia.
Ou Z, Deng Y, Liang Y, Chen Z, Sun L
Reprod Biol Endocrinol. 2022; 20(1):75.
PMID: 35490243
PMC: 9055750.
DOI: 10.1186/s12958-022-00948-9.
Evaluating the application value of NGS-based PGT-A by screening cryopreserved MDA products of embryos from PGT-M cycles with known transfer outcomes.
Shen X, Chen D, Ding C, Xu Y, Fu Y, Cai B
J Assist Reprod Genet. 2022; 39(6):1323-1331.
PMID: 35275308
PMC: 9174381.
DOI: 10.1007/s10815-022-02447-7.
Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment.
Chen H, Lin P, Chiang Y, Huang W, Lin C, Ma G
Diagnostics (Basel). 2021; 11(12).
PMID: 34943631
PMC: 8700639.
DOI: 10.3390/diagnostics11122395.
Preimplantation Genetic Diagnosis for DEB by Detecting a Novel Family-Specific COL7A1 Mutation in Vietnam.
Trieutien S, Vu Van T, Tran Ngoc Thao M, Trinh The S, Tran Van K, Nguyen Thanh T
Appl Clin Genet. 2021; 14:467-472.
PMID: 34916826
PMC: 8668251.
DOI: 10.2147/TACG.S344107.
Next-generation sequence-based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism.
Hu X, He W, Zhang S, Luo K, Gong F, Dai J
Mol Genet Genomic Med. 2021; 9(5):e1662.
PMID: 33942572
PMC: 8172198.
DOI: 10.1002/mgg3.1662.
Preimplantation Genetic Testing of Multiple Endocrine Neoplasia Type 2A.
Hansen A, Sonderberg Roos L, Lossl K, Godballe C, Mathiesen J
Front Endocrinol (Lausanne). 2020; 11:572151.
PMID: 33178136
PMC: 7592389.
DOI: 10.3389/fendo.2020.572151.
Preimplantation genetic testing for aneuploidies (abnormal number of chromosomes) in in vitro fertilisation.
Cornelisse S, Zagers M, Kostova E, Fleischer K, van Wely M, Mastenbroek S
Cochrane Database Syst Rev. 2020; 9:CD005291.
PMID: 32898291
PMC: 8094272.
DOI: 10.1002/14651858.CD005291.pub3.
Haplotyping by linked-read sequencing (HLRS) of the genetic disease carriers for preimplantation genetic testing without a proband or relatives.
Li Q, Mao Y, Li S, Du H, He W, He J
BMC Med Genomics. 2020; 13(1):117.
PMID: 32819358
PMC: 7441613.
DOI: 10.1186/s12920-020-00766-1.
A whole-genome sequencing-based novel preimplantation genetic testing method for de novo mutations combined with chromosomal balanced translocations.
Yuan P, Xia J, Ou S, Liu P, Du T, Zheng L
J Assist Reprod Genet. 2020; 37(10):2525-2533.
PMID: 32783137
PMC: 7550397.
DOI: 10.1007/s10815-020-01921-4.