Jing Liu

发表

Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract

M. Hayden, Xiangyin Kong, H. Eiberg, 2002, Nature Genetics.

Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis

X. Liu, S. Blanton, Zhengmao Hu, 2019, Genetics in Medicine.

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

Zhu Chen, Xiangyin Kong, G. Fu, 2001, Nature Genetics.

The gamma S-crystallin gene is mutated in autosomal recessive cataract in mouse.

Xiangyin Kong, Q. Xie, L. Bu, 2002, Genomics.

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Pieter J. de Jong, Saeed Bohlega, Jing Liu, 1998, Nature Genetics.

Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families

Yong Feng, Jing Liu, Shu-shan Sang, 2019, Front. Genet..

A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract.

Xiangyin Kong, L. Bu, Yiping Jin, 2003, Molecular vision.

A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review.

X. Liu, Yong Feng, Jing Liu, 2019, Gene.

Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.

X. Liu, D. Yan, Yong Feng, 2019, Human molecular genetics.

GJB2 mutations are rare in probands with hearing loss in Chinese assortative mating families.

Jing Liu, Siqing Fu, Jiashu Dong, 2014, International journal of pediatric otorhinolaryngology.

Mutation Analysis of PAX6 in a Chinese Family and a Patient with a Presumed Sporadic Case of Congenital Aniridia

Xu Ma, Jing Liu, Y. Jie, 2011, Ophthalmic Research.

Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation.

Yong Feng, Jing Liu, L. Mei, 2021, Stem cell research.