Y. Wen

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.

γ-Secretase Gene Mutations in Familial Acne Inversa

Baoxi Wang, Miao Sun, Bo Liu, 2010, Science.

Nucleic acid‐based non‐invasive prenatal diagnosis of genetic skin diseases: are we ready?

Y. Wen, Yonghui Ma, He Gong, 2013, Experimental dermatology.

Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report.

S. Cichon, M. Nöthen, Y. Wen, 2011, Journal of the American Academy of Dermatology.

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

S. Cichon, M. Nöthen, C. Bodemer, 2009, Nature Genetics.

A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family

Y. Wen, Miao Sun, Yang Luo, 2009, Journal of Human Genetics.

South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin

S. Kežić, Y. Wen, A. Irvine, 2014, The Journal of allergy and clinical immunology.