Hong-duo Chen

The Msi1-mTOR pathway drives the pathogenesis of mammary and extramammary Paget’s disease

Zhengquan Yu, Yiqiang Zhao, B. Andersen, 2020, Cell Research.

Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH)

Xuejun Zhang, Wei Huang, Sen Yang, 2004, Human mutation.

Recessive congenital methemoglobinemia caused by a rare mechanism: maternal uniparental heterodisomy with segmental isodisomy of a chromosome 22.

D. Niu, Yu-Hsiu Huang, Yung-Hsiu Lu, 2012, Blood cells, molecules & diseases.

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

Yang Liu, Sen Yang, Miao Sun, 2009, Nature Genetics.

The use of high resolution melting analysis to detect Fabry mutations in heterozygous females via dry bloodspots.

Jan-Gowth Chang, Hong-Duo Chen, D. Niu, 2012, Clinica chimica acta; international journal of clinical chemistry.

Presence of Human Papillomavirus DNA and Expression of L‐Fucose Moiety in Some Vulvar Intraepithelial Lesions and Vulvar Squamous Cell Carcinoma

Xinghua Gao, Hong-duo Chen, Xin-yuan Wu, 1997, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].