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Journal of Molecular Medicine (Berlin, Germany)|June 21, 2022
Identification of KANSL1 as a novel pathogenic gene for developmental dysplasia of the hipXiaowen Xu, Xinying Bi, Jing Wang, et al.Molecular Genetics & Genomic Medicine|February 26, 2022
Identification of a novel heterozygous SOX9 variant in a Chinese family with congenital heart diseaseLi Gong, Chunyan Wang, Haiyang Xie, et al.Bioscience Reports|November 30, 2018
Mutations in EPAS1 in congenital heart disease in TibetansHong Pan, Qiuhong Chen, Shenggui Qi, et al.Bioscience Reports|October 19, 2018
Application of a deep convolutional neural network in the diagnosis of neonatal ocular fundus hemorrhageBinbin Wang, Li Xiao, Yang Liu, et al.Cardiology in the Young|November 6, 2014
A novel variation of GDF3 in Chinese Han children with a broad phenotypic spectrum of non-syndromic CHDsJianmin Xiao, Guanyang Kang, Jing Wang, et al.Journal of Ovarian Research|April 22, 2020
NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigreeLin Li, Fan Feng, Minying Zhao, et al.Andrologia|August 6, 2022
Novel compound heterozygous variants of DNAH17 in a Chinese infertile man with multiple morphological abnormalities of sperm flagellaZhonglin Liu, Chunyan Wang, Feng Ni, et al.Gene|July 27, 2025
A potentially pathogenic KDM5C variant in X-linked high myopiaJianping Zhang, Yijia Zhao, Tengyan Li, et al.Genetic Testing and Molecular Biomarkers|December 28, 2018
Carrying the T Allele of the SNP rs574344, an eQTL of GSTM1, Contributes to Longevity in the Han Chinese PopulationYunxia Zhang, Siyang Zhang, Dongjing Yan, et al.Journal of Ovarian Research|June 20, 2018
Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiencyBeili Chen, Lin Li, Jing Wang, et al.Pageof 4