Xiang Wang

发表

Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome

Mohan Liu, Ying Shen, Xueguang Zhang, 2020, Journal of Assisted Reproduction and Genetics.

CYP11A1 Upregulation Leads to Trophoblast Oxidative Stress and Fetal Neurodevelopmental Toxicity That can be Rescued by Vitamin D

Qun Sun, A. Dinnyés, G. He, 2021, Frontiers in Molecular Biosciences.

A novel missense mutation in GREB1L identified in a three-generation family with renal hypodysplasia/aplasia-3

Jiaojiao Zhou, Ying Shen, Xiang Wang, 2022, Orphanet Journal of Rare Diseases.

A novel homozygous CFAP65 mutation in humans causes male infertility with multiple morphological abnormalities of the sperm flagella

Ying Shen, Xueguang Zhang, Xiang Wang, 2019, Clinical genetics.

Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella

L. Tang, Weiyu Li, Xiaoyu Yang, 2019, Nature Communications.

Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings

Hongqian Liu, Ying Shen, Xueguang Zhang, 2020, Human Genomics.

A novel splice site variant in ANOS1 gene leads to Kallmann syndrome in three siblings.

Ying Shen, Xueguang Zhang, Xiang Wang, 2020, Gene.

Sequencing of the ZMYND15 gene in a cohort of infertile Chinese men reveals novel mutations in patients with teratozoospermia

Ying Shen, Xiang Wang, Yuting Wen, 2022, Journal of Medical Genetics.

A homozygous RNF220 mutation leads to male infertility with small-headed sperm.

Zhun Xiao, Ying Shen, Xueguang Zhang, 2019, Gene.

Novel variations in TENT5D lead to teratozoospermia in infertile patients.

Chuan Jiang, Ying Shen, Xiang Wang, 2024, Andrology.

Identification of nonfunctional PABPC1L causing oocyte maturation abnormalities and early embryonic arrest in female primary infertility

Mohan Liu, Chuan Jiang, Yanting Yang, 2023, Clinical genetics.