Three Novel Variants of CEP290 and CC2D2DA and a Link Between ZNF77 and SHH Signaling Pathway Are Found in Two Meckel-Gruber Syndrome Fetuses

por Hong, Zhidan, He, Xuanyi, Yu, Fang, Liu, Huanyu, Zhang, Xiaoli, Zhang, Yuanzhen
Publicado 2022

Identification of compound heterozygous variants in MSH4 as a novel genetic cause of diminished ovarian reserve

por Wan, Yingjing, Hong, Zhidan, Ma, Binyu, He, Xuanyi, Ma, Ling, Wang, Mei, Zhang, Yuanzhen
Publicado 2023

Downregulation of LHCGR Attenuates COX-2 Expression and Induces Luteinized Unruptured Follicle Syndrome in Endometriosis

por Geng, Ting, Sun, Yifan, Cheng, Lin, Cao, Yuming, Zhang, Ming, Hong, Zhidan, Ma, Ling, Zhang, Yuanzhen
Publicado 2022

MGA-seq: robust identification of extrachromosomal DNA and genetic variants using multiple genetic abnormality sequencing

por Lin, Da, Zou, Yanyan, Li, Xinyu, Wang, Jinyue, Xiao, Qin, Gao, Xiaochen, Lin, Fei, Zhang, Ningyuan, Jiao, Ming, Guo, Yu, Teng, Zhaowei, Li, Shiyi, Wei, Yongchang, Zhou, Fuling, Yin, Rong, Zhang, Siheng, Xing, Lingyu, Xu, Weize, Wu, Xiaofeng, Yang, Bing, Xiao, Ke, Wu, Chengchao, Tao, Yingfeng, Yang, Xiaoqing, Zhang, Jing, Hu, Sheng, Dong, Shuang, Li, Xiaoyu, Ye, Shengwei, Hong, Zhidan, Pan, Yihang, Yang, Yuqin, Sun, Haixiang, Cao, Gang
Publicado 2023