Yaran Wen
Baylor Genetics(US)
Publications by Year
Research Areas
Hair Growth and Disorders, Wnt/β-catenin signaling in development and cancer, Skin and Cellular Biology Research, melanin and skin pigmentation, Developmental Biology and Gene Regulation
Most-Cited Works
- → γ-Secretase Gene Mutations in Familial Acne Inversa(2010)445 cited
- → Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis(2009)212 cited
- → Copy-Number Mutations on Chromosome 17q24.2-q24.3 in Congenital Generalized Hypertrichosis Terminalis with or without Gingival Hyperplasia(2009)85 cited
- → South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin(2013)77 cited
- → Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia(2010)38 cited
- → Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report(2010)17 cited
- → A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family(2009)15 cited
- → Strong association of the SNP rs17822931 with wet earwax and bromhidrosis in a Chinese family(2013)6 cited
- → Nucleic acid‐based non‐invasive prenatal diagnosis of genetic skin diseases: are we ready?(2013)6 cited
- [Allgrove syndrome in the mainland of China: clinical report and mutation analysis].(2007)