Mathyer ME, Quiggle AM, Wong XFCC, Denil SLIJ, Kumar MG, Ciliberto HM, Bayliss SJ, Common JE, de Guzman Strong C. Tiled array-based sequencing identifies enrichment of loss-of-function variants in the highly homologous filaggrin gene in African American children with severe atopic dermatitis. Exp Dermatol. 2018 May 23. doi: 10.1111/exd.13691
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Fuentes I, Guttmann-Gruber C, Ling Tay AS, Hofbauer JP, Denil SLIJ, Reichelt J, Palisson F, Common JEA, South AP. Reduced microbial diversity is a feature of recessive dystrophic epidermolysis bullosa involved skin and wounds. J Invest Dermatol. 2018 May 10. pii: S0022-202X(18)31963-8. doi: 10.1016/j.jid.2018.04.026
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Pigors M, Common JEA, Wong XFCC, Malik S, Scott CA, Tabarra N, Liany H, Liu J, Limviphuvadh V, Maurer-Stroh S, Tang MB, Lench N, Margolis DJ, van Heel DA, Mein CA, Novak N, Baurecht H, Weidinger S, McLean WHI, Irvine AD, O'Toole EA, Simpson MA, Kelsell DP. Exome sequencing and rare variant analysis reveals multiple filaggrin mutations in Bangladeshi atopic eczema families and additional risk genes. J Invest Dermatol. 2018 May 29. pii: S0022-202X(18)31990-0. doi: 10.1016/j.jid.2018.05.013
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Kheng LH, Rahim AB, Leo VI, Shatarupa D, Lim TC, Uemura T, Igarashi K, Common J, Vardy LA. Polyamine regulator AMD1 promotes cell migration in epidermal wound healing. J Invest Dermatol. 2018 Jun 12. pii: S0022-202X(18)32058-X. doi: 10.1016/j.jid.2018.05.029
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Kong HH, Andersson B, Clavel T, Common JE, Jackson SA, Olson ND, Segre JA, Traidl-Hoffmann C. Performing Skin Microbiome Research: A Method to the Madness. J Invest Dermatol. 2017 Jan 4. pii: S0022-202X(16)32621-5. doi:
10.1016/j.jid.2016.10.033.
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Kumar D, Puan KJ, Andiappan AK, Lee B, Westerlaken GH, Haase D, Melchiotti R, Li Z, Yusof N, Lum J, Koh G, Foo S, Yeong J, Alves AC, Pekkanen J, Sun LD, Irwanto A, Fairfax BP, Naranbhai V, Common JE, Tang M, Chuang CK, Jarvelin MR, Knight JC, Zhang X, Chew FT, Prabhakar S, Jianjun L, Wang Y, Zolezzi F, Poidinger M, Lane EB, Meyaard L, Rötzschke O. A functional SNP associated with atopic dermatitis controls cell type-specific methylation of the VSTM1 gene locus. Genome Med. 2017 Feb 20;9(1):18. doi: 10.1186/s13073-017-0404-6
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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. ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis. J Invest Dermatol. 2017 Sep 27. pii: S0022-202X(17)32982-2. doi: 10.1016/j.jid.2017.08.045
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Salgado G, Ng YZ, Koh LF, Goh CSM, Common JE. Human reconstructed skin
xenografts on mice to model skin physiology. Differentiation. 2017 Sep
14;98:14-24. doi: 10.1016/j.diff.2017.09.004.
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Wong XFCC, Denil SLIJ, Foo JN, Chen H, Tay ASL, Haines RL, Tang MBY, McLean WHI, Sandilands A, Smith FJD, Lane EB, Liu J, Common JEA. Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants. J Allergy Clin Immunol. 2017 Oct 19. pii: S0091-6749(17)31588-9. doi: 10.1016/j.jaci.2017.10.001.
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Tan TS, Ng YZ, Badowski C, Dang T, Common JE, Lacina L, Szeverényi I, Lane EB. Assays to Study Consequences of Cytoplasmic Intermediate Filament Mutations: The Case of Epidermal Keratins. Methods Enzymol. 2016;568:219-53. doi: 10.1016/bs.mie.2015.09.030.
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Kern Rei Chng, Angeline Su Ling Tay, Chenhao Li, Amanda Hui Qi Ng, Jingjing Wang, Bani Kaur Suri, Sri Anusha Matta, Naomi McGovern, Baptiste Janela, Xuan Fei Colin C. Wong, Yang Yie Sio, Bijin Veonice Au, Andreas Wilm, Paola Florez De Sessions, Thiam Chye Lim, Mark Boon Yang Tang, Florent Ginhoux, John E. Connolly, E. Birgitte Lane, Fook Tim Chew, John E. A. Common & Niranjan Nagarajan. Whole metagenome profiling reveals skin microbiome-dependent susceptibility to atopic dermatitis flare. Nature Microbiology 2016;1:16106. doi:10.1038/nmicrobiol.2016.106
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Odell ID, Flavell RA. Microbiome: Ecology of eczema. Nat Microbiol. 2016 Aug
26;1(9):16135. doi: 10.1038/nmicrobiol.2016.135
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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. Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria. PLoS One. 2014 Feb 3;9(2):e87250. doi: 10.1371/journal.pone.0087250. eCollection 2014. PubMed PMID: 24498303; PubMed Central PMCID: PMC3911924.
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Pan J, Yung Chan S, Common JE, Amini S, Miserez A, Birgitte Lane E, Kang L. Fabrication of a 3D hair follicle-like hydrogel by soft lithography. J Biomed Mater Res A. 2013 Nov;101(11):3159-69. doi: 10.1002/jbm.a.34628. Epub 2013 Mar 30. PubMed PMID: 23554315.
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Dreesen O, Chojnowski A, Ong PF, Zhao TY, Common JE, Lunny D, Lane EB, Lee SJ, Vardy LA, Stewart CL, Colman A. Lamin B1 fluctuations have differential effects on cellular proliferation and senescence. J Cell Biol. 2013 Mar 4;200(5):605-17. doi: 10.1083/jcb.201206121. Epub 2013 Feb 25. PubMed PMID: 23439683; PubMed Central PMCID: PMC3587829.
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Sundaram GM, Common JE, Gopal FE, Srikanta S, Lakshman K, Lunny DP, Lim TC, Tanavde V, Lane EB, Sampath P. 'See-saw' expression of microRNA-198 and FSTL1 from a single transcript in wound healing. Nature. 2013 Mar 7;495(7439):103-6. doi: 10.1038/nature11890.
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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. Validation of GWAS loci for atopic dermatitis in a Singapore Chinese population. J Invest Dermatol. 2012 May;132(5):1505-7. doi: 10.1038/jid.2011.471. Epub 2012 Feb 9. PubMed PMID: 22318392.
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Cai SC, Chen H, Koh WP, Common JE, van Bever HP, McLean WH, Lane EB, Giam YC, Tang MB. Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitis. Br J Dermatol. 2012 Jan;166(1):200-3. doi: 10.1111/j.1365-2133.2011.10541.x. Epub 2011 Nov 17. PubMed PMID: 21790526.
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Canning CA, Chan JS, Common JE, Lane EB, Jones CM. Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos. Dev Dyn. 2011 Aug;240(8):1958-63. doi: 10.1002/dvdy.22683. PubMed PMID: 21761481.
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Common JE, Brown SJ, Haines RL, Goh CS, Chen H, Balakrishnan A, Munro CS, Tan AW, Tan HH, Tang MB, Lane EB. Filaggrin null mutations are not a protective factor for acne vulgaris. J Invest Dermatol. 2011 Jun;131(6):1378-80. doi: 10.1038/jid.2011.23. Epub 2011 Feb 17. PubMed PMID: 21326297; PubMed Central PMCID: PMC3094589.
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Chen H, Common JE, Haines RL, Balakrishnan A, Brown SJ, Goh CS, Cordell HJ, Sandilands A, Campbell LE, Kroboth K, Irvine AD, Goh DL, Tang MB, van Bever HP, Giam YC, McLean WH, Lane EB. Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations. Br J Dermatol. 2011 Jul;165(1):106-14. doi: 10.1111/j.1365-2133.2011.10331.x. PubMed PMID: 21428977.
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Chong KL, Common JE, Lane EB, Goh BK. A novel mutation in the kinase domain of KIT in an Indian family with a mild piebaldism phenotype. J Dermatol Sci. 2010 Sep;59(3):206-9. doi: 10.1016/j.jdermsci.2010.06.009. Epub 2010 Jul 8. PubMed PMID: 20688482.
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Neoh CY, Chen H, Ng SK, Lane EB, Common JE. A rare connexin 26 mutation in a patient with a forme fruste of keratitis-ichthyosis-deafness (KID) syndrome. Int J Dermatol. 2009 Oct;48(10):1078-81. PubMed PMID: 19785089.
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Van Bever H, Lane B, Common J. Gene defects and allergy. BMJ. 2009 Jul 9;339:b1203. doi: 10.1136/bmj.b1203. PubMed PMID: 19589814.
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Goh BK, Common JE, Gan WH, Kumarasinghe P. A case of dermatopathia pigmentosa reticularis with wiry scalp hair and digital fibromatosis resulting from a recurrent KRT14 mutation. Clin Exp Dermatol. 2009 Apr;34(3):340-3. doi: 10.1111/j.1365-2230.2008.02950.x. Epub 2008 Nov 24. PubMed PMID: 19040520.
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Szeverenyi I, Cassidy AJ, Chung CW, Lee BT, Common JE, Ogg SC, Chen H, Sim SY, Goh WL, Ng KW, Simpson JA, Chee LL, Eng GH, Li B, Lunny DP, Chuon D, Venkatesh A, Khoo KH, McLean WH, Lim YP, Lane EB. The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases. Hum Mutat. 2008 Mar;29(3):351-60. PubMed PMID: 18033728.
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Harper LJ, Piper K, Common J, Fortune F, Mackenzie IC. Stem cell patterns in cell lines derived from head and neck squamous cell carcinoma. J Oral Pathol Med. 2007 Nov;36(10):594-603. PubMed PMID: 17944752.
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Common JE, O'Toole EA, Leigh IM, Thomas A, Griffiths WA, Venning V, Grabczynska S, Peris Z, Kansky A, Kelsell DP. Clinical and genetic heterogeneity of erythrokeratoderma variabilis. J Invest Dermatol. 2005 Nov;125(5):920-7. PubMed PMID: 16297190.
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Di WL, Gu Y, Common JE, Aasen T, O'Toole EA, Kelsell DP, Zicha D. Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis. J Cell Sci. 2005 Apr 1;118(Pt 7):1505-14. Epub 2005 Mar 15. PubMed PMID: 15769851.
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Common JE, Bitner-Glindzicz M, O'Toole EA, Barnes MR, Jenkins L, Forge A, Kelsell DP. Specific loss of connexin 26 expression in ductal sweat gland epithelium associated with the deletion mutation del(GJB6-D13S1830). Clin Exp Dermatol. 2005 Nov;30(6):688-93. PubMed PMID: 16197390.
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Common JE, Di WL, Davies D, Kelsell DP. Further evidence for heterozygote advantage of GJB2 deafness mutations: a link with cell survival. J Med Genet. 2004 Jul;41(7):573-5. PubMed PMID: 15235031; PubMed Central PMCID: PMC1735824.
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Common JE, Di WL, Davies D, Galvin H, Leigh IM, O'Toole EA, Kelsell DP. Cellular mechanisms of mutant connexins in skin disease and hearing loss. Cell Commun Adhes. 2003 Jul-Dec;10(4-6):347-51. PubMed PMID: 14681040.
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Common JE, Becker D, Di WL, Leigh IM, O'Toole EA, Kelsell DP. Functional studies of human skin disease- and deafness-associated connexin 30 mutations. Biochem Biophys Res Commun. 2002 Nov 15;298(5):651-6. PubMed PMID: 12419304.
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Di WL, Monypenny J, Common JE, Kennedy CT, Holland KA, Leigh IM, Rugg EL, Zicha D, Kelsell DP. Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations. Hum Mol Genet. 2002 Aug 15;11(17):2005-14. PubMed PMID: 12165562.
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Rugg EL, Common JE, Wilgoss A, Stevens HP, Buchan J, Leigh IM, Kelsell DP. Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography. Br J Dermatol. 2002 Jun;146(6):952-7. PubMed PMID: 12072061.
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Di WL, Common JE, Kelsell DP. Connexin 26 expression and mutation analysis in epidermal disease. Cell Commun Adhes. 2001;8(4-6):415-8. PubMed PMID: 12064628.
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