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

Por Wang, Bo, You, Guoling, Fu, Qihua
Publicado no Sci Rep (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 no Sci Rep (2017)

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 no PLoS One (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 no Front Microbiol (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 no Int J Mol Sci (2017)

MAMLD1 gene mutation in the incidence of hypospadias in the Chinese population

Por Zhuang Likai, Bai Ming, Zhou Wei, Yu Yongguo, Wang Jian, Fu Qihua, Sun Jie
Publicado em 2014-01-01

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 no BMC Genomics (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 no Int J Med Sci (2015)

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 em 2013

Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype

Por LI, NIU, DING, YU, YU, TINGTING, LI, JUAN, SHEN, YONGNIAN, WANG, XIUMIN, FU, QIHUA, SHEN, YIPING, HUANG, XIAODONG, WANG, JIAN
Publicado no Exp Ther Med (2016)

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

Por Xu, Yuejuan, Fang, Shaohai, Zhang, Erge, Pu, Tian, Cao, Ruixue, Fu, Qihua, Li, Fen, Chen, Sun, Sun, Kun, Xu, Rang
Publicado no Sci Rep (2017)

The Fas/Fas Ligand Death Receptor Pathway Contributes to Phenylalanine-Induced Apoptosis in Cortical Neurons

Por Huang, Xiaodong, Lu, Zhaohui, Lv, Zhongwei, Yu, Tingting, Yang, Peirong, Shen, Yongnian, Ding, Yu, Fu, Da, Zhang, Xiaoping, Fu, Qihua, Yu, Yongguo
Publicado em 2013

Screening for Coding Variants in FTO and SH2B1 Genes in Chinese Patients with Obesity

Por Zheng, Zhaojing, Hong, Li, Huang, Xiaodong, Yang, Peirong, Li, Juan, Ding, Yu, Yao, Ru-en, Geng, Juan, Shen, Yongnian, Shen, Yiping, Fu, Qihua, Yu, Yongguo
Publicado em 2013

Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield

Por Geng, Juan, Picker, Jonathan, Zheng, Zhaojing, Zhang, Xiaoqing, Wang, Jian, Hisama, Fuki, Brown, David W, Mullen, Mary P, Harris, David, Stoler, Joan, Seman, Ann, Miller, David T, Fu, Qihua, Roberts, Amy E, Shen, Yiping
Publicado no BMC Genomics (2014)

A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal

Por Wang, Jian, Yu, Tingting, Wang, Zhigang, Ohte, Satoshi, Yao, Ru-en, Zheng, Zhaojing, Geng, Juan, Cai, Haiqing, Ge, Yihua, Li, Yuchan, Xu, Yunlan, Zhang, Qinghua, Gusella, James F, Fu, Qihua, Pregizer, Steven, Rosen, Vicki, Shen, Yiping
Publicado no J Bone Miner Res (2015)