Publications by authors named "Yaran Wen"

Claim this Profile
S
Strong association of the SNP rs17822931 with wet earwax and bromhidrosis in a Chinese family.
Dandan Shang, Xue Zhang, Miao Sun, Yang Wei, Yaran Wen

J Genet· July 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin.
Fatemah Thawer-Esmail, Ivone Jakasa, Gail Todd, Yaran Wen, Sara J Brown

J Allergy Clin Immunol· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Nucleic acid-based non-invasive prenatal diagnosis of genetic skin diseases: are we ready?
Yonghui Ma, He Gong, Yaran Wen

Exp Dermatol· June 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report.
Silke Redler, Roland Kruse, Sibylle Eigelshoven, Sandra Hanneken, Melanie Refke, Yaran Wen

J Am Acad Dermatol· April 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia.
Carol Clericuzio, Karine Harutyunyan, Weidong Jin, Robert P Erickson, Alan D Irvine, Yaran Wen

Am J Med Genet A· February 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Gamma-secretase gene mutations in familial acne inversa.
Baoxi Wang, Wei Yang, Wen Wen, Jing Sun, Bin Su, Yaran Wen

Science· November 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family.
Dan Lv, Yang Luo, Wei Yang, Lihua Cao, Yaran Wen

J Hum Genet· July 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia.
Miao Sun, Ning Li, Wu Dong, Zugen Chen, Qing Liu, Yaran Wen

Am J Hum Genet· June 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
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, Yiwei Zhao, Rui Hua

Nat Genet· February 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Allgrove syndrome in the mainland of China: clinical report and mutation analysis].
Chun-xiu Gong, Ya-ran Wen, Xiu-li Zhao, Chang Su, Bing-yan Cao

Zhonghua Er Ke Za Zhi· June 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis