Modelling mutational and selection pressures on dinucleotides in eukaryotic phyla –selection against CpG and UpA in cytoplasmically expressed RNA and in RNA viruses

by Simmonds, Peter, Xia, Wenjun, Baillie, J Kenneth, McKinnon, Ken
Published 2013

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

by Liu, Fei, Hu, Jiongjiong, Xia, Wenjun, Hao, Lili, Ma, Jing, Ma, Duan, Ma, Zhaoxin
Published 2015

Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss

by Hu, Jiongjiong, Liu, Fei, Xia, Wenjun, Hao, Lili, Lan, Jun, Zhu, Zhenghua, Ye, Jing, Ma, Duan, Ma, Zhaoxin
Published 2016

Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish

by Liu, Fei, Xia, Wenjun, Hu, Jiongjiong, Wang, Yingzhi, Yang, Fan, Sun, Shaoyang, Zhang, Jin, Jiang, Nan, Wang, Huijun, Tian, Weidong, Wang, Xu, Ma, Duan
Published 2015