C. Goh

Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin

J. Kudoh, C. Munro, A. Irvine, 2012, The Journal of investigative dermatology.

Identification and characterization of the gene responsible for the matted mouse phenotype

C. Goh, 2013 .

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

C. Gieger, G. Barton, A. Balmain, 2013, The Journal of allergy and clinical immunology.

Filaggrin null mutations are not a protective factor for acne vulgaris.

M. Tang, E. Lane, J. Common, 2011, The Journal of investigative dermatology.

Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting

O. Sarig, N. Shomron, M. Simpson, 2013, Nature Genetics.

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma

G. Barton, M. Akiyama, H. Shimizu, 2012, Nature Genetics.

Wide spectrum of filaggrin‐null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations

M. Tang, J. Common, H. Cordell, 2011, The British journal of dermatology.

Human reconstructed skin xenografts on mice to model skin physiology.

Li Fang Koh, J. Common, G. Salgado, 2017, Differentiation; research in biological diversity.