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Validation of GWAS loci for atopic dermatitis in a Singapore Chinese population.
Andiappan AK, Foo JN, Choy MW, Chen H, Common JE, Tang MB, van Bever HP, Giam YC, Suri BK, Ramani A, Nilkanth PP, Lane EB, Wang de Y, Chew FT, Liu J. Andiappan AK, et al. Among authors: common je. J Invest Dermatol. 2012 May;132(5):1505-7. doi: 10.1038/jid.2011.471. Epub 2012 Feb 9. J Invest Dermatol. 2012. PMID: 22318392 Free article. No abstract available.
Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.
Liu H, Li Y, Hung KK, Wang N, Wang C, Chen X, Sheng D, Fu X, See K, Foo JN, Low H, Liany H, Irwan ID, Liu J, Yang B, Chen M, Yu Y, Yu G, Niu G, You J, Zhou Y, Ma S, Wang T, Yan X, Goh BK, Common JE, Lane BE, Sun Y, Zhou G, Lu X, Wang Z, Tian H, Cao Y, Chen S, Liu Q, Liu J, Zhang F. Liu H, et al. Among authors: common je. PLoS One. 2014 Feb 3;9(2):e87250. doi: 10.1371/journal.pone.0087250. eCollection 2014. PLoS One. 2014. PMID: 24498303 Free PMC article.
Filaggrin null mutations are not a protective factor for acne vulgaris.
Common JE, Brown SJ, Haines RL, Goh CS, Chen H, Balakrishnan A, Munro CS, Tan AW, Tan HH, Tang MB, Lane EB. Common JE, et al. J Invest Dermatol. 2011 Jun;131(6):1378-80. doi: 10.1038/jid.2011.23. Epub 2011 Feb 17. J Invest Dermatol. 2011. PMID: 21326297 Free PMC article. No abstract available.
A case of erythrokeratoderma variabilis without mutations in connexin 31.
Ishida-Yamamoto A, Kelsell D, Common J, Houseman MJ, Hashimoto M, Shibaki H, Asano K, Takahashi H, Hashimoto Y, Senshu T, Leigh IM, Iizuka H. Ishida-Yamamoto A, et al. Br J Dermatol. 2000 Dec;143(6):1283-7. doi: 10.1046/j.1365-2133.2000.03902.x. Br J Dermatol. 2000. PMID: 11122035
Gene defects and allergy.
Van Bever H, Lane B, Common J. Van Bever H, et al. BMJ. 2009 Jul 9;339:b1203. doi: 10.1136/bmj.b1203. BMJ. 2009. PMID: 19589814 No abstract available.
74 results