Jian-jun Chen

发表

Progressive symmetric erythrokeratodermia: report of a Chinese family and evidence for genetic heterogeneity.

Xuejun Zhang, Wei Huang, Yong Cui, 2004, Journal of dermatological science (Amsterdam).

Identification of a novel locus for progressive symmetric erythrokeratodermia to a 19.02-cM interval at 21q11.2-21q21.2.

Ying Wang, Liangdan Sun, Xuejun Zhang, 2006, The Journal of investigative dermatology.

Identification of a novel mutation in the DSRAD gene in a Chinese pedigree with dyschromatosis symmetrica hereditaria

Jun Wang, Xuejun Zhang, Wei Huang, 2005, Archives of Dermatological Research.

Two novel mutations of the ATP2C1 gene in Chinese families with Hailey-Hailey disease.

Xuejun Zhang, F. Zhou, W. Du, 2006, Journal of dermatological science.

The gene for a rare autosomal dominant form of pompholyx maps to chromosome 18q22.1-18q22.3.

Xuejun Zhang, Wei Huang, F. Zhou, 2006, The Journal of investigative dermatology.

Association of HLA class I alleles with psoriasis vulgaris in southeastern Chinese Hans.

Xuejun Zhang, Yong Cui, Sen Yang, 2003, Journal of dermatological science.

Association of HLA class I alleles with aloplecia areata in Chinese Hans.

Liangdan Sun, Xuejun Zhang, Yong Cui, 2006, Journal of dermatological science.

The genetic concept of vitiligo.

Xuejun Zhang, Jian-jun Chen, Jiang-Bo Liu, 2005, Journal of dermatological science.

Platelet-derived growth factor receptor alpha gene mutations in vitiligo vulgaris.

Liangdan Sun, Xuejun Zhang, Jianjun Liu, 2010, Acta dermato-venereologica.

Evidence for two susceptibility loci on chromosomes 22q12 and 6p21-p22 in Chinese generalized vitiligo families.

Liangdan Sun, Xuejun Zhang, Wei Huang, 2007, The Journal of investigative dermatology.

A novel linkage to generalized vitiligo on 4q13-q21 identified in a genomewide linkage analysis of Chinese families.

Wei Li, Xuejun Zhang, Wei Huang, 2005, American journal of human genetics.

Two frameshift mutations in the RNA-specific adenosine deaminase gene associated with dyschromatosis symmetrica hereditaria.

Xuejun Zhang, Wei Huang, W. Du, 2005, Archives of dermatology.

A novel MGST2 non-synonymous mutation in a Chinese pedigree with psoriasis vulgaris.

Liangdan Sun, Xuejun Zhang, Wei Huang, 2006, The Journal of investigative dermatology.

Five novel mutations of RNA-specific adenosine deaminase gene with dyschromatosis symmetrica hereditaria.

Xuejun Zhang, F. Zhou, W. Du, 2007, Acta dermato-venereologica.

Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH)

Xuejun Zhang, Wei Huang, Sen Yang, 2004, Human mutation.

Follow-up analysis of PSORS9 in 151 Chinese families confirmed the linkage to 4q31-32 and refined the evidence to the families of early-onset psoriasis.

Wei Li, Liangdan Sun, Xuejun Zhang, 2007, The Journal of investigative dermatology.

Identification of the cylindromatosis tumor-suppressor gene responsible for multiple familial trichoepithelioma.

Xuejun Zhang, Wei Huang, Sen Yang, 2004, The Journal of investigative dermatology.

Mutation analysis of the ED1 gene in two Chinese Han families with X-linked hypohidrotic ectodermal dysplasia

Xiao-yan Xiong, Xuejun Zhang, Wei Huang, 2003, Archives of Dermatological Research.

A mutation in the connexin 30 gene in Chinese Han patients with hidrotic ectodermal dysplasia.

Xiao-yan Xiong, Y. Wang, Xuejun Zhang, 2003, Journal of dermatological science.

Identification of a novel PAX6 mutation in a Chinese family with aniridia

Z. Zhong, Jian-jun Chen, Min Liu, 2019, BMC Ophthalmology.

Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's disease

Ru-jing Ren, Gang Wang, E. Dammer, 2019, Neurobiology of Aging.

Identification of Mutations in Myocilin and Beta-1,4-galactosyltransferase 3 Genes in a Chinese Family with Primary Open-angle Glaucoma

D. Ye, R. Liao, Z. Zhong, 2016, Chinese medical journal.