Hualei Luo

Pathogenicity analysis of variations and prenatal diagnosis in a hereditary coagulation factor XIII deficiency family

Li Liu, Weiying Jiang, Yonghua Wang, 2018, Hematology.

Quantification of human embryonic ζ-globin chains in Southeast Asian deletion (--SEA) carriers

Yuhua Ye, Xiangmin Xu, Zhe Ren, 2022, Journal of clinical pathology.

Identification of a novel SUOX pathogenic variants as the cause of isolated sulfite oxidase deficiency in a Chinese pedigree

Weiying Jiang, Jie Xie, Hualei Luo, 2021, Molecular genetics & genomic medicine.

Effects of Nicotinamide on Cervical Cancer-Derived Fibroblasts: Evidence for Therapeutic Potential

Weiying Jiang, Hualei Luo, Reem N Hassan, 2020, Cancer management and research.

Novel recessive PDZD7 biallelic mutations associated with hereditary hearing loss in a Chinese pedigree.

Weiying Jiang, Jie Xie, Hualei Luo, 2019, Gene.

Clinical and genetic features of retinoschisis in 120 families with RS1 mutations

Shi-qiang Li, Wenmin Sun, Panfeng Wang, 2021, British Journal of Ophthalmology.

Spectrum-frequency and genotype-phenotype analysis of rhodopsin variants.

Xueshan Xiao, Shi-qiang Li, Wenmin Sun, 2020, Experimental eye research.

Effects of Nicotinamide on Cervical Cancer-Derived Fibroblasts: Evidence for Therapeutic Potential

Weiying Jiang, Hualei Luo, Wei Jiang, 2020 .