Wensheng Liu

发表

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia

Zhong-xian Lu, Shaobin Lin, S. Kong, 2019, Molecular genetics & genomic medicine.

The role of tyrosine phosphatase Shp2 in spermatogonial differentiation and spermatocyte meiosis

Zhong-xian Lu, G. Feng, S. Kong, 2019, Asian journal of andrology.

Mutations in ZP4 are associated with abnormal zona pellucida and female infertility

Xiaohong Yan, Zhong-xian Lu, Qicai Liu, 2021, Journal of Clinical Pathology.

Deletion of the tyrosine phosphatase Shp2 in Sertoli cells causes infertility in mice

Wenjie Liu, Zhong-xian Lu, G. Feng, 2015, Scientific Reports.

Biallelic mutations of CFAP58 are associated with multiple morphological abnormalities of the sperm flagella

Yifeng Wang, Y. Sha, Wensheng Liu, 2020, Clinical genetics.

Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice

V. Isachenko, Yifeng Wang, Xiaoyan Liu, 2022, Journal of Medical Genetics.

Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF)

Zhong-xian Lu, Shaobin Lin, S. Kong, 2019, Journal of Medical Genetics.

Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype

Tonghang Guo, Y. Sha, Wensheng Liu, 2019, Clinical genetics.

Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome

V. Isachenko, Yifeng Wang, Jing Chen, 2021, Frontiers in Cell and Developmental Biology.

Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility

R. Wu, Zhong-xian Lu, Fuxing Zhang, 2021, Asian journal of andrology.

A Novel Meiosis-Related lncRNA, Rbakdn, Contributes to Spermatogenesis by Stabilizing Ptbp2

Zhong-xian Lu, Jiancheng Ding, Yingpu Tian, 2021, Frontiers in Genetics.

Pathogenic variants of ATG4D in infertile men with non‐obstructive azoospermia identified using whole‐exome sequencing

Bowen Tang, Xiong Wang, Xiaoyu Yang, 2021, Clinical genetics.

A familial analysis of two brothers with azoospermia caused by maternal 46,Y, t(X; 1) (q28; q21) chromosomal abnormality

Y. Sha, Wensheng Liu, Li-bin Mei, 2020, Andrologia.

Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention

Yaling Tang, Yifeng Wang, Y. Sha, 2020, Journal of Ovarian Research.

CCDC9 is identified as a novel candidate gene of severe asthenozoospermia

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

Biallelic mutations in KATNAL2 cause male infertility due to oligo‐astheno‐teratozoospermia

Zhong-xian Lu, Jing Chen, V. Isachenko, 2021, Clinical genetics.

DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella

Weibing Qin, Yunge Tang, Zhong-xian Lu, 2019, Clinical genetics.

Mutations in DNAH8 contribute to multiple morphological abnormalities of sperm flagella and male infertility.

Y. Sha, Wensheng Liu, Xinzong Zhang, 2021, Acta biochimica et biophysica Sinica.

Homozygous mutation in DNALI1 leads to asthenoteratozoospermia by affecting the inner dynein arms

Weibing Qin, Xiaoming Jiang, Y. Sha, 2023, Frontiers in Endocrinology.

Biallelic mutations in PMFBP1 cause acephalic spermatozoa

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

Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family

Ning Zhang, Xiong Wang, Wensheng Liu, 2019, BMC Medical Genetics.

Author response for "DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella (MMAF)"

Weibing Qin, Yunge Tang, Zhong-xian Lu, 2019 .

TENT5D disruption causes oligoasthenoteratozoospermia and male infertility

Y. Sha, Wensheng Liu, Xiaoli Wei, 2023, Andrology.

Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis

Lin Li, Y. Sha, Wensheng Liu, 2023, EBioMedicine.