Dandan Shang

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Yaran Wen, Yang Liu, Yiming Xu et al. · Nature Genetics · 2009 · 208 citations

Inhibitory Upstream Orf, Genetic Disorder, Natural Sciences +8

Mutations of the<i>EPHA2</i>receptor tyrosine kinase gene cause autosomal dominant congenital cataract

Tianxiao Zhang, Rui Hua, Wei Xiao et al. · Human Mutation · 2009 · 101 citations · Full text

Human Ccs, Developmental Biology, Ocular Disease +13

X-Linked Congenital Hypertrichosis Syndrome Is Associated with Interchromosomal Insertions Mediated by a Human-Specific Palindrome near SOX3

Hongwen Zhu, Dandan Shang, Miao Sun et al. · The American Journal of Human Genetics · 2011 · 89 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +11

Copy-Number Mutations on Chromosome 17q24.2-q24.3 in Congenital Generalized Hypertrichosis Terminalis with or without Gingival Hyperplasia

Miao Sun, Ning Li, Dong Wu et al. · The American Journal of Human Genetics · 2009 · 85 citations · Full text

Gingival Hyperplasia, Cytogenetics, Medicine +9

A novel <i>RAB39B</i> gene mutation in X‐linked juvenile parkinsonism with basal ganglia calcification

Changhe Shi, Shuyu Zhang, Zhi-hua Yang et al. · Movement Disorders · 2016 · 43 citations