Ri‐Tai Huang

GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot

Yi‐Qing Yang, Lara Gharibeh, Ruogu Li et al. · Human Mutation · 2013 · 87 citations

Life Sciences, Cardiology, Genetics +16

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation

Ri‐Tai Huang, Song Xue, Ying‐Jia Xu et al. · International Journal of Molecular Medicine · 2013 · 62 citations · Full text

Medicine, Cardiology, Genetics +16

A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot

Caixia Lü, Hairong Gong, Xing‐Yuan Liu et al. · International Journal of Molecular Medicine · 2015 · 61 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

Yu‐Min Sun, Jun Wang, Xing‐Biao Qiu et al. · G3 Genes Genomes Genetics · 2016 · 60 citations · Full text

Medicine, Genetics, Molecular Genetics +17

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

Ri‐Tai Huang, Juan Wang, Song Xue et al. · International Journal of Medical Sciences · 2017 · 60 citations · Full text

Medicine, Genetics, Molecular Genetics +17