Zhiying Su

发表

A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF).

Ping Li, Li-bin Mei, Yan-Wei Sha, 2017, Gene.

Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype

Shaobin Lin, Y. Sha, Xianjing Huang, 2020, Journal of Human Genetics.

Loss‐of‐function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype

Xiong Wang, Y. Sha, Xing-shen Zhu, 2020, Clinical genetics.

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

C. Yin, Shaobin Lin, Ping Li, 2018, Gene.

DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella

Shaobin Lin, Y. Sha, Xianjing Huang, 2019, Annals of human genetics.

Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.

Ping Li, Zhiyong Ji, Li-bin Mei, 2018, Gene.

DNAH6 is a novel candidate gene associated with sperm head anomaly

X. Xu, C. Yin, C. Wang, 2018, Andrologia.

Two novel biallelic mutations in PSMC3IP in a patient affected by premature ovarian insufficiency.

Yanru Huang, Xuemei He, Ping Li, 2021, Molecular medicine reports.

CCDC9 is identified as a novel candidate gene of severe asthenozoospermia

Xiong Wang, Shaobin Lin, Jing Chen, 2019, Systems biology in reproductive medicine.

TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family.

C. Yin, Xiong Wang, Chengrong Wang, 2018, Gene.

Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing

Shaobin Lin, Ping Li, Xianjing Huang, 2018, Systems Biology in Reproductive Medicine.

Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China.

Shaobin Lin, Yulin Zhou, Ping Li, 2018, Gene.

Biallelic mutations in PMFBP1 cause acephalic spermatozoa

Xiong Wang, S. Kong, Jing Chen, 2018, Clinical genetics.

Turner syndrome with Xp deletions and rare endometrial abnormalities

Jing Chen, Yanru Huang, Xuemei He, 2021, Medicine.

Two novel biallelic mutations in PSMC3IP in a Chinese patient affected by primary ovarian insufficiency: case report and review of the literature

Yanru Huang, Xuemei He, Ping Li, 2020 .

Patients with multiple morphological abnormalities of the sperm flagella harbouring CFAP44 or CFAP43 mutations have a good pregnancy outcome following intracytoplasmic sperm injection

Xiong Wang, H. Bao, Ping Li, 2018, Andrologia.