Ruizhi Liu

Evaluation of the post-implantation development of mouse embryos derived from round spermatid injection.

[Clinical analysis of 87 cases of testicular tumor].

[Mutation of the KAL1 gene in 30 male patients with idiopathic hypogonadotropic hypogonadism].

Male infertility in Northeast China: a cytogenetic study of 135 patients with non-obstructive azoospermia and severe oligozoospermia.

Analysis of Y chromosome microdeletion in 1738 infertile men from northeastern China.

The impact of semen quality, occupational exposure to environmental factors and lifestyle on recurrent pregnancy loss.

[Clinical and cytogenetic analysis of 45,X/46,XY individuals].

[Molecular genetic mechanisms of teratozoospermia].

Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testing.

Influence of genetic abnormalities on semen quality and male fertility: A four-year prospective study.

Synergistic effects of eukaryotic co-expression plasmid-based STAT3-specific siRNA and LKB1 on ovarian cancer in vitro and in vivo.

[Predictive value of abnormal second-trimester maternal serum triple screening markers for adverse pregnancy outcomes].

Association Between Dosage Frequency and the Treatment Outcomes of Sildenafil in Young and Middle-aged Men With Erectile Dysfunction: A Chinese, Multicenter, Observational Study.

Complete Azoospermia Factor b Deletion of Y Chromosome in an Infertile Male With Severe Oligoasthenozoospermia: Case Report and Literature Review.

Biological and biomechanical analysis of two types of mesenchymal stem cells for intervention in chemotherapy-induced ovarian dysfunction.

Molecular microdeletion analysis of infertile men with karyotypic Y chromosome abnormalities.

BMP6 Downregulates GDNF Expression Through SMAD1/5 and ERK1/2 Signaling Pathways in Human Granulosa-Lutein Cells.

A novel stopgain mutation c.G992A (p.W331X) in TACR3 gene was identified in nonobstructive azoospermia by targeted next-generation sequencing.

Androgen receptor gene mutations are associated with male infertility in Northeast China: Clinical features and identification of two novel mutations.

Intraoperative assessment of tubules in predicting microdissection testicular sperm extraction outcome in men with Sertoli cell-only syndrome.

Association of single nucleotide polymorphism c.673C>A/p.Gln225Lys in SEPT12 gene with spermatogenesis failure in male idiopathic infertility in Northeast China.

BMP6 increases TGF-β1 production by up-regulating furin expression in human granulosa-lutein cells.

Association of gene polymorphisms with asthenozoospermia in Northeast Chinese patients.

Re-evaluation of the value of sperm morphology in classical fertilization in a Northeastern Chinese population.

Targeted Next-Generation Sequencing Identifies Novel Sequence Variations of Genes Associated with Nonobstructive Azoospermia in the Han Population of Northeast China.

Identification of KISS1R gene mutations in disorders of non-obstructive azoospermia in the northeast population of China.

High frequency of Y chromosome microdeletions in male infertility patients with 45,X/46,XY mosaicism.

Reproductive outcomes of 3 infertile males with XYY syndrome: Retrospective case series and literature review.

Prenatal diagnosis of a de novo tetrasomy 15q24.3-25.3: Case report and literature review.

A novel frameshift mutation in ubiquitin-specific protease 26 gene in a patient with severe oligozoospermia.

CHD7 missense variants and clinical characteristics of Chinese males with infertility.

Case report: A non-obstructive azoospermia patient with heat shock factor-2 mutation.

The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis.

Xp;Yq Unbalanced Translocation with Pseudoautosomal Region Aberrations in a Natural Two-Generation Transmission.

Clinical Application of Chromosomal Microarray Analysis in Pregnant Women with Advanced Maternal Age and Fetuses with Ultrasonographic Soft Markers.

Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature.

[Retracted] Synergistic effects of eukaryotic co‑expression plasmid‑based STAT3‑specific siRNA and LKB1 on ovarian cancer and .

BMP6 increases CD68 expression by up-regulating CTGF expression in human granulosa-lutein cells.

Molecular cytogenetic characterization of 1q42.3q44 deletion and 8q24.3 duplication in a fetus with single umbilical artery and ventricular septal defects.

Molecular cytogenetic characterization of 2q deletion and Xq duplication associated with nasal bone dysplasia in prenatal diagnosis: A case report and literature review.

Associations of sex hormone levels with body mass index (BMI) in men: a cross-sectional study using quantile regression analysis.

Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review.

Incidence and risk factors for early pregnancy loss in women with first pregnancy undergoing in vitro fertilization-embryo transfer.

[Family analysis of a child with Short-rib polydactyly syndrome type III due to variant of DYNC2H1 gene].

The Association Between Self-Reported Household Renovation and Semen Parameters Among Infertile Men: A Cross-Sectional Study.

Nomogram for predicting the risk of preterm birth in women undergoing in vitro fertilization cycles.

Identification and verification of potential biomarkers in sertoli cell-only syndrome via bioinformatics analysis.

Ultrasensitive electrochemical detection and inhibition evaluation of DNA methyltransferase based on cascade strand displacement amplification.

Effects of histones related to sperm chromatin on embryo development and ART outcomes.