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Page 1
ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis.
Chourabi M, Liew MS, Lim S, H'mida-Ben Brahim D, Boussofara L, Dai L, Wong PM, Foo JN, Sriha B, Robinson KS, Denil S, Common JE, Mamaï O, Ben Khalifa Y, Bollen M, Liu J, Denguezli M, Bonnard C, Saad A, Reversade B. Chourabi M, et al. Among authors: foo jn. J Invest Dermatol. 2018 Feb;138(2):291-300. doi: 10.1016/j.jid.2017.08.045. Epub 2017 Sep 28. J Invest Dermatol. 2018. PMID: 28964717 Free article.
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: foo jn. PLoS One. 2014 Feb 3;9(2):e87250. doi: 10.1371/journal.pone.0087250. eCollection 2014. PLoS One. 2014. PMID: 24498303 Free PMC article.
CHCHD2 and Parkinson's disease.
Foo JN, Liu J, Tan EK. Foo JN, et al. Lancet Neurol. 2015 Jul;14(7):681-2. doi: 10.1016/S1474-4422(15)00098-8. Lancet Neurol. 2015. PMID: 26067114 Free article. No abstract available.
GWAS reveal novel IgA nephropathy risk loci.
Foo JN, Liu J, Yu XQ. Foo JN, et al. Oncotarget. 2015 Jun 30;6(18):15738-9. doi: 10.18632/oncotarget.4632. Oncotarget. 2015. PMID: 26119152 Free PMC article. No abstract available.
136 results