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

por Wang, Bo, You, Guoling, Fu, Qihua
Publicado 2017

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

por Zu, Bailing, You, Guoling, Fu, Qihua, Wang, Jing
Publicado 2017

A Novel Multiplex HRM Assay to Detect Clopidogrel Resistance

por Zhang, Lichen, Ma, Xiaowei, You, Guoling, Zhang, Xiaoqing, Fu, Qihua
Publicado 2017

Sexual difference of small RNA expression in Tetralogy of Fallot

por Wang, Bo, Shi, Guocheng, Zhu, Zhongqun, Chen, Huiwen, Fu, Qihua
Publicado 2018

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

por You, Guoling, Zu, Bailing, Wang, Bo, Fu, Qihua, Li, Fen
Publicado 2020

A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease

por Zhang, Xiaoqing, Wang, Jian, Wang, Bo, Chen, Sun, Fu, Qihua, Sun, Kun
Publicado 2016

Molecular Characteristic and Virulence Gene Profiles of Community-Associated Methicillin-Resistant Staphylococcus aureus Isolates from Pediatric Patients in Shanghai, China

por Wang, Xing, Li, Xia, Liu, Wei, Huang, Weichun, Fu, Qihua, Li, Min
Publicado 2016

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

por You, Guoling, Zu, Bailing, Wang, Bo, Wang, Zhigang, Xu, Yunlan, Fu, Qihua
Publicado 2017

Molecular Characteristics of Community-Associated Staphylococcus aureus Isolates From Pediatric Patients With Bloodstream Infections Between 2012 and 2017 in Shanghai, China

por Wang, Xing, Liu, Qian, Zhang, He, Li, Xia, Huang, Weichun, Fu, Qihua, Li, Min
Publicado 2018

Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle

por Zhang, Xingyu, Wang, Bo, You, Guoling, Xiang, Ying, Fu, Qihua, Yu, Yongguo, Zhang, Xiaoqing
Publicado 2021

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

por Zhang, Xiaoqing, Wang, Bo, Zhang, Lichen, You, Guoling, Palais, Robert A., Zhou, Luming, Fu, Qihua
Publicado 2018

A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease

por Zhang, Xiaoqing, Xu, Yuejuan, Liu, Deyuan, Geng, Juan, Chen, Sun, Jiang, Zhengwen, Fu, Qihua, Sun, Kun
Publicado 2015

Investigation of Somatic NKX2-5 Mutations in Chinese Children with Congenital Heart Disease

por Zheng, Jiayi, Li, Fen, Liu, Jinfen, Xu, Zhiwei, Zhang, Haibo, Fu, Qihua, Wang, Jian, Sun, Kun
Publicado 2015

Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing

por Xie, Huilin, Zhang, Erge, Hong, Nanchao, Fu, Qihua, Li, Fen, Chen, Sun, Yu, Yu, Sun, Kun
Publicado 2018

Hemodynamic Effects of A Simplified Venturi Conduit for Fontan Circulation: A Pilot, In Silico Analysis

por Zhu, Fang, Shi, Guocheng, Wen, Chen, Zhang, Qian, Fu, Qihua, Liu, Jinlong, Zhu, Zhongqun, Chen, Huiwen
Publicado 2020

FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically

por Zhang, Xingyu, Gao, Yunqian, Zhang, Xiaoping, Zhang, Xiaoqing, Xiang, Ying, Fu, Qihua, Wang, Bo, Xu, Zhuoming
Publicado 2021

Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies

por Lu, Yibo, Zhou, Yiyang, Guo, Jing, Qi, Ming, Lin, Yuwan, Zhang, Xingyu, Xiang, Ying, Fu, Qihua, Wang, Bo
Publicado 2023

Novel Mutations in the SCNN1A Gene Causing Pseudohypoaldosteronism Type 1

por Wang, Jian, Yu, Tingting, Yin, Lei, Li, Jing, Yu, Li, Shen, Ye, Yu, Yongguo, Shen, Yongnian, Fu, Qihua
Publicado 2013

Heterogeneous spectrum of EXT gene mutations in Chinese patients with hereditary multiple osteochondromas

por Li, Yuchan, Wang, Jian, Tang, Jingyan, Wang, Zhigang, Han, Bingqiang, Li, Niu, Yu, Tingting, Chen, Yulin, Fu, Qihua
Publicado 2018

HBprem: A database of transcription, translation, and posttranscriptional and posttranslational modifications in hepatoblastoma

por Song, Hang, Bian, Zhixuan, Mao, Siwei, Zhu, Jiabei, Zhang, Yue, Gu, Song, Yin, Minzhi, Fu, Qihua, Pan, Qiuhui
Publicado 2020