Zhiming Li
Zhongshan, China
Last Updated: 09/26/2026
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Found 11 publications
Paternal age and sperm DNA fragmentation independently affect embryonic ploidy but not euploid embryo implantation potential.
Journal: Frontiers in endocrinology
Published: May 14, 2026
Comparative study of noninvasive chromosomal screening using blastocyst culture media: frozen-thawed embryos outperform fresh embryos.
Journal: Frontiers in endocrinology
Published: April 09, 2026
Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.
Journal: Frontiers in genetics
Published: March 17, 2026
Effectiveness of preimplantation genetic testing for aneuploidy in improving clinical and neonatal outcomes for patients with recurrent pregnancy loss.
Journal: Frontiers in endocrinology
Published: August 21, 2025
Influencing factors and clinical significance of mosaic embryos in preimplantation genetic testing.
Journal: Journal of assisted reproduction and genetics
Published: June 05, 2025
Evaluation of day 5 versus day 6 blastocyst biopsy in preimplantation genetic testing: clinical and neonatal outcomes.
Journal: Frontiers in endocrinology
Published: December 12, 2024
Clinical phenotype and genetic analysis of patients with severe oligoasthenospermia carrying heterozygous SOHLH1 c.346-1G>A mutation.
Journal: Frontiers in genetics
Published: November 20, 2024
Feasibility of preimplantation genetic testing for aneuploidy on frozen-thawed embryos following conventional IVF insemination.
Journal: Frontiers in endocrinology
Published: May 30, 2024
Establishment of linkage phase, using Oxford Nanopore Technologies, for preimplantation genetic testing of Coffin-Lowry syndrome with a de novo RPS6KA3 mutation.
Journal: Frontiers in genetics
Published: February 20, 2023
Prenatal diagnosis of Bardet‑Biedl syndrome due to novel variants in the BBS10 gene in a fetus with multiple anomalies: A case report.
Journal: Experimental and therapeutic medicine
Published: June 27, 2022
Next-generation sequencing reveals a case of Norrie disease in a child with bilateral ocular malformation.
Journal: Frontiers in genetics
Published: February 06, 2022
Showing 1-11 of 11
Last Updated: 09/26/2026