Wilson H.Y. Lo

Association between genetic variation of <i>CACNA1H</i> and childhood absence epilepsy

Yucai Chen, Jianjun Lu, Hong Pan et al. · Annals of Neurology · 2003 · 374 citations · Full text

DSPP mutation in dentinogenesis imperfecta Shields type II

Xiaohai Zhang, Jun Zhao, Changfu Li et al. · Nature Genetics · 2001 · 368 citations

Developmental Anomaly, Genetic Disorder, Genetics +5

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 in HOXD13 Underlie Syndactyly Type V and a Novel Brachydactyly-Syndactyly Syndrome

Xiuli Zhao, Miao Sun, Jin Zhao et al. · The American Journal of Human Genetics · 2007 · 105 citations · Full text

Novel Brachydactyly-syndactyly Syndrome, Genetic Disorder, Genetics +4

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