Jin Jiang

Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patients.

Renyi Wu, Xiajing Tang, K. Yao, 2007, Molecular vision.

A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family

Renyi Wu, K. Yao, C. Jin, 2008, Molecular vision.

A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family

K. Yao, Jinyu Li, C. Jin, 2010, Molecular vision.

Copy number variations of DNA repair genes and the age-related cataract: Jiangsu Eye Study.

H. Guan, Mei Yang, Yong Yao, 2013, Investigative ophthalmology & visual science.

Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3′ untranslated region

K. Yao, C. Jin, Wei Wang, 2010, Molecular vision.

Sporadic hemangioblastoma of the kidney with PAX2 and focal CD10 expression: report of a case.

Q. Shen, Q. Shi, Bo Yu, 2013, International journal of clinical and experimental pathology.

A novel GJA3 mutation associated with congenital nuclear pulverulent and posterior polar cataract in a chinese family

K. Yao, C. Jin, Wei Wang, 2011, Human mutation.

Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family

K. Xia, Renyi Wu, Xiajing Tang, 2009, Molecular vision.