Jin‐Lan Chen

A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: Additional support for a CHD locus at distal 13q34 region

Yifeng Yang, Qi Ai, Can Huang et al. · Gene · 2013 · 56 citations

Life Sciences, Genetics, Molecular Genetics +17

Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion

Can Huang, Yifeng Yang, Ni Yin et al. · Gene · 2012 · 36 citations

Medicine, Cardiology, Genetics +15

Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death

Zhiping Tan, Yao Deng, Jin‐Lan Chen et al. · Scientific Reports · 2014 · 30 citations · Full text

Medicine, Cardiology, Genetics +17

Microduplication of 3p25.2 encompassing <i>RAF1</i> associated with congenital heart disease suggestive of Noonan syndrome

Cheng Luo, Yifeng Yang, Bang‐Liang Yin et al. · American Journal of Medical Genetics Part A · 2012 · 29 citations

Life Sciences, Genetics, Molecular Genetics +17

Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11

Jin‐Lan Chen, Tianli Zhao, Jian Wang et al. · Molecular Cytogenetics · 2014 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17