Zhengfeng Xu

Clinical application of massively parallel sequencing‐based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors

Wei Wang, Jinghui Ren, Yali Li et al. · Prenatal Diagnosis · 2012 · 235 citations · Full text

Medicine, Genetics, Obstetrics +17

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach

Zirui Dong, Jun Zhang, Ping Hu et al. · Genetics in Medicine · 2016 · 227 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Functional variant in microRNA-196a2 contributes to the susceptibility of congenital heart disease in a Chinese population

Jing Xu, Zhibin Hu, Zhengfeng Xu et al. · Human Mutation · 2009 · 132 citations

Medicine, Genetics, Molecular Genetics +15

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing

Sheng‐Pei Chen, Tze Kin Lau, Chunlei Zhang et al. · Prenatal Diagnosis · 2013 · 131 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations

Zhibin Hu, Yongyong Shi, Xuming Mo et al. · Nature Genetics · 2013 · 105 citations

Life Sciences, Genetics, Molecular Genetics +15