Biblio
A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination. Hum Reprod. 2024.
. Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia. Mol Hum Reprod. 2024.
Extended application of PGT-M strategies for small pathogenic CNVs. J Assist Reprod Genet. 2024.
Advances in the study of DNA damage and repair in mammalian oocytes. Yi Chuan. 2023;45(5):379-394.
. Biallelic mutations in cause male infertility with severe MMAF and NOA. J Med Genet. 2023.
Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility. Hum Reprod. 2023.
. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Hum Reprod. 2023.
. Conventional IVF is feasible in preimplantation genetic testing for aneuploidy. J Assist Reprod Genet. 2023.
Defects in phospholipase C zeta cause polyspermy and low fertilization after conventional IVF: not just ICSI failure. Asian J Androl. 2023.
. DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice. Signal Transduct Target Ther. 2023;8(1):26.
. The effect of carrier characteristics and female age on preimplantation genetic testing results of blastocysts from Robertsonian translocation carriers. J Assist Reprod Genet. 2023.
. Embryo development, pregnancy and live birth outcomes following IVF treatment were not compromised during the COVID-19 pandemic. J Assist Reprod Genet. 2023.
. Evaluation of genetic risk of apparently balanced chromosomal rearrangement carriers by breakpoint characterization. J Assist Reprod Genet. 2023.
. Histone acetyltransferase KAT2A modulates neural stem cell differentiation and proliferation by inducing degradation of the transcription factor PAX6. J Biol Chem. 2023:103020.
Live birth after letrozole-stimulated cycles versus hormone replacement treatment cycles for the first frozen embryo transfer in women with polycystic ovary syndrome: protocol for a multicentre randomised controlled trial. BMJ Open. 2023;13(8):e072021.
. Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression. Cell Discov. 2023;9(1):87.
Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192. HGG Adv. 2023:100256.
Navigation of Knowledge: the Impact of COVID-19 on Pregnancy-a Bibliometric Analysis. Reprod Sci. 2023.
. Novel biallelic ASTL variants are associated with polyspermy and female infertility: A successful live birth following ICSI treatment. Gene. 2023:147745.
. Novel homozygous variants in cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella. Front Cell Dev Biol. 2023;11:1184331.
Novel mutations in lead to female infertility with oocyte maturation arrest. Yi Chuan. 2023;45(6):514-525.
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