In silico predicted structural and functional insights of all missense mutations on 2B domain of K1/K10 causing genodermatoses

por Banerjee, Santasree, Wu, Qian, Ying, Yuyi, Li, Yanni, Shirota, Matsuyuki, Neculai, Dante, Li, Chen
Publicado 2016

Familial and genetic association with neurodevelopmental disorders caused by a heterozygous variant in the SRRM2 gene

por Zhang, Tao, Xu, Lei, Zhu, Hongdan, Ying, Yuyi, Ding, Jinlong, Ding, Haigang, Shi, Xiaoliang, He, Yao, Jin, Xin, Xia, Guiyu
Publicado 2023

Fetal Congenital Heart Disease Caused by Compound Heterozygous Mutations in the DNAH9 Gene: A Case Report

por Zhang, Tao, Yuan, Hua, Zhu, Hongdan, Ying, Yuyi, Ding, Jinlong, Ding, Haigang, Shi, Xiaoliang, He, Yao, Pan, Haitao, Zhong, Yongxing
Publicado 2022

KVarPredDB: a database for predicting pathogenicity of missense sequence variants of keratin genes associated with genodermatoses

por Ying, Yuyi, Lu, Lu, Banerjee, Santasree, Xu, Lizhen, Zhao, Qiang, Wu, Hao, Li, Ruiqi, Xu, Xiao, Yu, Hua, Neculai, Dante, Xi, Yongmei, Yang, Fan, Qin, Jiale, Li, Chen
Publicado 2020