Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes

par Wang, Bo, You, Guoling, Fu, Qihua
Publié dans Sci Rep (2017)

Association between ABO Blood Group and Risk of Congenital Heart Disease: A 6-year large cohort study

par Zu, Bailing, You, Guoling, Fu, Qihua, Wang, Jing
Publié dans Sci Rep (2017)

A Novel Multiplex HRM Assay to Detect Clopidogrel Resistance

par Zhang, Lichen, Ma, Xiaowei, You, Guoling, Zhang, Xiaoqing, Fu, Qihua
Publié dans Sci Rep (2017)

Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot

par You, Guoling, Zu, Bailing, Wang, Bo, Fu, Qihua, Li, Fen
Publié dans Front Genet (2020)

Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly

par You, Guoling, Zu, Bailing, Wang, Bo, Wang, Zhigang, Xu, Yunlan, Fu, Qihua
Publié dans Int J Mol Sci (2017)

ARE/SUZ12 dual specifically-regulated adenoviral TK/GCV system for CML blast crisis cells

par Zu, Bailing, Shi, Yi, Xu, Min, You, Guoling, Huang, Zhenglan, Gao, Miao, Feng, Wenli
Publié dans J Exp Clin Cancer Res (2015)

Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting

par Zhang, Xiaoqing, Wang, Bo, Zhang, Lichen, You, Guoling, Palais, Robert A., Zhou, Luming, Fu, Qihua
Publié dans BMC Genomics (2018)

Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing

par Zu, Bailing, Zhang, Xiaoqing, Xu, Yunlan, Xiang, Ying, Wang, Zhigang, Cai, Haiqing, Wang, Bo, You, Guoling, Fu, Qihua
Publié dans Comput Struct Biotechnol J (2021)

SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients

par Liang, Fei, Wang, Bo, Geng, Juan, You, Guoling, Fa, Jingjing, Zhang, Min, Sun, Hunying, Chen, Huiwen, Fu, Qihua, Zhang, Xiaoqing, Zhang, Zhen
Publié dans eLife (2021)

MET mutation causes muscular dysplasia and arthrogryposis

par Zhou, Hang, Lian, Chengjie, Wang, Tingting, Yang, Xiaoming, Xu, Caixia, Su, Deying, Zheng, Shuhui, Huang, Xiangyu, Liao, Zhiheng, Zhou, Taifeng, Qiu, Xianjian, Chen, Yuyu, Gao, Bo, Li, Yongyong, Wang, Xudong, You, Guoling, Fu, Qihua, Gurnett, Christina, Huang, Dongsheng, Su, Peiqiang
Publié dans EMBO Mol Med (2019)