Qihua Fu

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

Juan Geng, Jonathan Picker, Zhaojing Zheng et al. · BMC Genomics · 2014 · 99 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Xiaoqing Zhang, Yuejuan Xu, Deyuan Liu et al. · BMC Genomics · 2015 · 60 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Jian Wang, Tingting Yu, Zhigang Wang et al. · Journal of Bone and Mineral Research · 2015 · 34 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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

Zhaohui Lu, Zhongwei Lv, Tingting Yu et al. · PLoS ONE · 2013 · 33 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

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

Xingyu Zhang, Yun‐Qian Gao, Xiaoping Zhang et al. · Frontiers in Cell and Developmental Biology · 2021 · 32 citations · Full text

Life Sciences, Cardiology, Genetics +15