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Human Genetics|September 21, 2022
Truncation mutations in MYRF underlie primary angle closure glaucomaJiamin Ouyang, Wenmin Sun, Huangxuan Shen, et al.
Plos One|January 31, 2017
Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital CataractsXiaodong Jiao, Shahid Y Khan, Bushra Irum, et al.
Nature Communications|April 8, 2024
Electron paramagnetic resonance as a tool to determine the sodium charge storage mechanism of hard carbonBin Wang, Jack R Fitzpatrick, Adam Brookfield, et al.
Scientific Reports|October 14, 2022
Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucomaBushra Rauf, Shahid Y Khan, Xiaodong Jiao, et al.
Plos One|September 25, 2015
Missense Mutations in CRYAB Are Liable for Recessive Congenital CataractsXiaodong Jiao, Shahid Y Khan, Bushra Irum, et al.
Investigative Ophthalmology & Visual Science|March 14, 2023
The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High MyopiaYi Jiang, Lin Zhou, Yingwei Wang, et al.
Molecular Vision|January 16, 2014
AIPL1 implicated in the pathogenesis of two cases of autosomal recessive retinal degenerationDavid Li, Chongfei Jin, Xiaodong Jiao, et al.
Molecular Vision|November 18, 2006
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani familiesS Amer Riazuddin, Fareeha Zulfiqar, Qingjiong Zhang, et al.
Molecular and Cellular Biochemistry|July 9, 2024
Death associated protein like 1 acts as a novel tumor suppressor in melanoma by increasing the stability of P21 proteinXiaoyan Liu, Xiaojuan Hu, Meiyu Jing, et al.
Molecular Vision|May 2, 2020
Mutations in <i>FYCO1</i> identified in families with congenital cataractsHira Iqbal, Shahid Y Khan, Lin Zhou, et al.
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