Yaran Wen

发表

γ-Secretase Gene Mutations in Familial Acne Inversa

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

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.

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.

Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia.

Miao Sun, Xin Li, Lin He, 2009, American journal of human genetics.

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

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

Strong association of the SNP rs17822931 with wet earwax and bromhidrosis in a Chinese family

D. Shang, Xue Zhang, M. Sun, 2013, Journal of 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.

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.

Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia

S. Plon, R. Erickson, A. Irvine, 2011, American journal of medical genetics. Part A.

Strong association of the SNP rs17822931 with wet earwax and bromhidrosis in a Chinese family

Miao Sun, D. Shang, Yaran Wen, 2013, Journal Genetika.

γ-Secretase Gene Mutations in Familial Acne Inversa

Yan Shen, Miao Sun, D. Ma, 2010, Science.

Erratum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis (Nature Genetics (2009) 41 (228-233))

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