S. Yang

S. Yang, W. Fei, W. Zhai, 2018, Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging.

The genetic epidemiology of tinea versicolor in China

F. Xiao, S. Xu, X. Zhang, 2007, Mycoses.

Refined localization of a punctate palmoplantar keratoderma gene to a 5·06‐cM region at 15q22.2–15q22.31

F. Xiao, X. Zhang, Y. Cui, 2005, The British journal of dermatology.

Identification of a locus for porokeratosis palmaris et plantaris disseminata to a 6·9‐cM region at chromosome 12q24·1–24·2

X. Zhang, S. Yang, L. Bu, 2003, The British journal of dermatology.

A new glycine substitution mutation in the COL7A1 gene in a Chinese family with dominant dystrophic epidermolysis bullosa

S. Yang, Y. Song, M. Li, 2003, Clinical and experimental dermatology.

Childhood psoriasis: a study of 277 patients from China

Liangdan Sun, W. Du, F. Xiao, 2007, Journal of the European Academy of Dermatology and Venereology : JEADV.

Follow‐up analysis of 180 Chinese Han families: identification of a novel locus for psoriasis at 2p22.3–11.2

Liangdan Sun, W. Du, F. Xiao, 2008, The British journal of dermatology.

Genetic heterogeneity in acrokeratosis verruciformis of Hopf

X. Zhang, Y. Cui, S. Yang, 2006, Clinical and experimental dermatology.

Liquid chromatography–tandem mass spectrometry is effective for analysis of ergosterol in fungal‐infected nails

S. Yang, Y. Li, Waimun Ho, 2019, Clinical and experimental dermatology.

Marie Unna hereditary hypotrichosis: report of a Chinese family and evidence for genetic heterogeneity

F. Xiao, Y. Cui, S. Yang, 2004, Clinical and experimental dermatology.

The genetic epidemiology of alopecia areata in China

X. Zhang, S. Yang, Q. Yang, 2004, The British journal of dermatology.

Association of HLA haplotype with alopecia areata in Chinese Hans

D. Ye, F. Zhou, F. Xiao, 2006, Journal of the European Academy of Dermatology and Venereology : JEADV.

Clinical profiles of vitiligo in China: an analysis of 3742 patients

W. Du, X. Zhang, S. Yang, 2005, Clinical and experimental dermatology.

Two novel frame‐shift mutations of ATP2A2 gene in Chinese patients with Darier's disease

C. Quan, X. Zhang, S. Yang, 2008, Journal of the European Academy of Dermatology and Venereology : JEADV.

Epidermal Differentiation Complex Yields a Secret: Mutations in the Cornification Protein Filaggrin Underlie Ichthyosis Vulgaris

S. Yang, M. Gao, A. Sandilands, 2006 .

Multiple variants in 5q31.1 are associated with systemic lupus erythematosus susceptibility and subphenotypes in the Han Chinese population

X. Zuo, D. Morris, F. Zhou, 2017, The British journal of dermatology.

Integrative analyses reveal biological pathways and key genes in psoriasis

L. Sun, Hui Li, Liangdan Sun, 2017, The British journal of dermatology.

Influence of mizolastine on antigen‐induced activation of signalling pathways in murine mast cells

B. Chen, D. Wang, Wei Zhou, 2006, Clinical and experimental dermatology.

A novel deletion mutation in the LPAR6 gene underlies autosomal recessive woolly hair with hypotrichosis

F. Zhou, S. Yang, M. Gao, 2013, Clincal and Experimental Dermatology.

Association of UBASH3A gene polymorphism and atopic dermatitis in the Chinese Han population

Liangdan Sun, F. Zhou, F. Xiao, 2017, Genes and Immunity.

The familial risk of acne vulgaris in Chinese Hans – a case‐control study

C. Quan, L. Sun, S. Xu, 2007, Journal of the European Academy of Dermatology and Venereology : JEADV.

Association between the PD1.3A/G polymorphism of the PDCD1 gene and systemic lupus erythematosus in European populations: a meta‐analysis

F. Xiao, X. Zhang, S. Yang, 2009, Journal of the European Academy of Dermatology and Venereology : JEADV.

A novel missense mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma.

F. Zhou, C. Quan, S. Yang, 2008, Journal of dermatological science.

Two novel CYLD gene mutations in Chinese families with trichoepithelioma and a literature review of 16 families with trichoepithelioma reported in China

F. Xiao, L. Sun, X. Zhang, 2005, The British journal of dermatology.

A novel frameshift mutation of the EDA1 gene in a Chinese Han family with X‐linked hypohidrotic ectodermal dysplasia

F. Zhou, F. Xiao, C. Quan, 2009, Clinical and experimental dermatology.

A novel GJB3 (Cx31) missense mutation in a Chinese patient with erythrokeratodermia variabilis

F. Zhou, L. Sun, X. Zhang, 2011, Journal of the European Academy of Dermatology and Venereology : JEADV.

Gene–gene interactions in IL23/Th17 pathway contribute to psoriasis susceptibility in Chinese Han population

X. Zuo, Sen Yang, X. Yin, 2013, Journal of the European Academy of Dermatology and Venereology : JEADV.

Refined localization of dyschromatosis symmetrica hereditaria gene to a 9·4‐cM region at 1q21–22 and a literature review of 136 cases reported in China

X. Zhang, Y. Cui, S. Yang, 2004, The British journal of dermatology.

One novel and two recurrent mutations in the keratin 5 gene identified in Chinese patients with epidermolysis bullosa simplex

F. Zhou, C. Quan, Y. Cui, 2009, Clinical and experimental dermatology.

Genome‐wide association study identifies three novel susceptibility loci for systemic lupus erythematosus in Han Chinese

X. Zuo, Y. Sheng, S. Yang, 2018, The British journal of dermatology.

Gene–gene interactions between HLA‐C, ERAP1, TNFAIP3 and TRAF3IP2 and the risk of psoriasis in the Chinese Han population

L. Sun, X. Yin, X. Zhang, 2013, The British journal of dermatology.

Familial progressive hyperpigmentation and hypopigmentation without KITLG mutation

X. Zuo, S. Yang, G. Chen, 2016, Clincal and Experimental Dermatology.

Association between the PD1.3A/G polymorphism of the PDCD1 gene and systemic lupus erythematosus in European populations: a meta‐analysis

F. Xiao, X. Zhang, S. Yang, 2009, Journal of the European Academy of Dermatology and Venereology : JEADV.