Ying Shen

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 7

Top Topics

Hepatitis C Virus

Polycystic Ovary Syndrome

Top Venues

Molecular genetics & genomic medicine

Journal of assisted reproduction and genetics

Human reproduction (Oxford, England)

Human molecular genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Siyu Dai, Mohan Liu, Man Liu, Chuan Jiang, Yanting Yang, Huifeng Han, Yihong Yang, Xiaohui Jiang, Ying Shen
Population-based genetic analysis in infertile men reveals novel mutations of ADAD family members in patients with impaired spermatogenesis. Human molecular genetics (2023)
Mohan Liu, Jinhui Li, Chuan Jiang, Yanning Zhou, Yongkang Sun, Yihong Yang, Ying Shen
A novel homozygous mutation in DNAJB13-a gene associated with the sperm axoneme-leads to teratozoospermia. Journal of assisted reproduction and genetics 39 (3) (2022)
Lingling Xing, Ying Shen, Xiang Wei, Yuan Luo, Yan Yang, Haipeng Liu, Hongqian Liu
Long-read Oxford nanopore sequencing reveals a de novo case of complex chromosomal rearrangement involving chromosomes 2, 7, and 13. Molecular genetics & genomic medicine 10 (9) (2022)
Yaqian Li, Chuan Jiang, Xueguang Zhang, Mohan Liu, Yongkang Sun, Yihong Yang, Ying Shen
The effect of a novel LRRC6 mutation on the flagellar ultrastructure in a primary ciliary dyskinesia patient. Journal of assisted reproduction and genetics 38 (3) (2021)
Yaqian Li, Yan Wang, Yuting Wen, Tao Zhang, Xiaodong Wang, Chuan Jiang, Rui Zheng, Fan Zhou, Daijuan Chen, Yihong Yang, Ying Shen
Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects. Human reproduction (Oxford, England) (2021)
Yihong Yang, Chuan Jiang, Xueguang Zhang, Xue Liu, Jinghong Li, Xiaoyong Qiao, Hongqian Liu, Ying Shen
Loss-of-function mutation in DNAH8 induces asthenoteratospermia associated with multiple morphological abnormalities of the sperm flagella. Clinical genetics 98 (4) (2020)
Mohan Liu, Xueguang Zhang, Hongqian Liu, Ying Shen
A 17q24.3 duplication identified in a large Chinese family with brachydactyly-anonychia. Molecular genetics & genomic medicine 8 (9) (2020)