Liao H - Search Results

1

Prevalent and low-frequency null mutations in the filaggrin gene are associated with early-onset and persistent atopic eczema.

Brown SJ, Sandilands A, Zhao Y, Liao H, Relton CL, Meggitt SJ, Trembath RC, Barker JN, Reynolds NJ, Cordell HJ, McLean WH. Brown SJ, et al. Among authors: liao h. J Invest Dermatol. 2008 Jun;128(6):1591-4. doi: 10.1038/sj.jid.5701206. Epub 2007 Dec 20. J Invest Dermatol. 2008. PMID: 18094728 Free article. No abstract available.

2

Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis.

Sandilands A, O'Regan GM, Liao H, Zhao Y, Terron-Kwiatkowski A, Watson RM, Cassidy AJ, Goudie DR, Smith FJ, McLean WH, Irvine AD. Sandilands A, et al. Among authors: liao h. J Invest Dermatol. 2006 Aug;126(8):1770-5. doi: 10.1038/sj.jid.5700459. Epub 2006 Jun 29. J Invest Dermatol. 2006. PMID: 16810297 Free article.

3

Null mutations in the filaggrin gene (FLG) determine major susceptibility to early-onset atopic dermatitis that persists into adulthood.

Barker JN, Palmer CN, Zhao Y, Liao H, Hull PR, Lee SP, Allen MH, Meggitt SJ, Reynolds NJ, Trembath RC, McLean WH. Barker JN, et al. Among authors: liao h. J Invest Dermatol. 2007 Mar;127(3):564-7. doi: 10.1038/sj.jid.5700587. Epub 2006 Sep 21. J Invest Dermatol. 2007. PMID: 16990802 Free article.

4

Filaggrin null alleles are not associated with psoriasis.

Zhao Y, Terron-Kwiatkowski A, Liao H, Lee SP, Allen MH, Hull PR, Campbell LE, Trembath RC, Capon F, Griffiths CE, Burden D, McManus R, Hughes R, Kirby B, Rogers SF, Fitzgerald O, Kane D, Barker JN, Palmer CN, Irvine AD, McLean WH. Zhao Y, et al. Among authors: liao h. J Invest Dermatol. 2007 Aug;127(8):1878-82. doi: 10.1038/sj.jid.5700817. Epub 2007 Apr 5. J Invest Dermatol. 2007. PMID: 17410197 Free article.

5

Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children.

Brown SJ, Relton CL, Liao H, Zhao Y, Sandilands A, McLean WH, Cordell HJ, Reynolds NJ. Brown SJ, et al. Among authors: liao h. Br J Dermatol. 2009 Oct;161(4):884-9. doi: 10.1111/j.1365-2133.2009.09339.x. Epub 2009 Jun 11. Br J Dermatol. 2009. PMID: 19681860 Free PMC article.

6

Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis.

Nomura T, Sandilands A, Akiyama M, Liao H, Evans AT, Sakai K, Ota M, Sugiura H, Yamamoto K, Sato H, Palmer CN, Smith FJ, McLean WH, Shimizu H. Nomura T, et al. Among authors: liao h. J Allergy Clin Immunol. 2007 Feb;119(2):434-40. doi: 10.1016/j.jaci.2006.12.646. J Allergy Clin Immunol. 2007. PMID: 17291859

7

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.

Sandilands A, Terron-Kwiatkowski A, Hull PR, O'Regan GM, Clayton TH, Watson RM, Carrick T, Evans AT, Liao H, Zhao Y, Campbell LE, Schmuth M, Gruber R, Janecke AR, Elias PM, van Steensel MA, Nagtzaam I, van Geel M, Steijlen PM, Munro CS, Bradley DG, Palmer CN, Smith FJ, McLean WH, Irvine AD. Sandilands A, et al. Among authors: liao h. Nat Genet. 2007 May;39(5):650-4. doi: 10.1038/ng2020. Epub 2007 Apr 8. Nat Genet. 2007. PMID: 17417636

8

Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis.

Liao H, Waters AJ, Goudie DR, Aitken DA, Graham G, Smith FJ, Lewis-Jones S, McLean WH. Liao H, et al. J Invest Dermatol. 2007 Dec;127(12):2795-8. doi: 10.1038/sj.jid.5700971. Epub 2007 Jul 26. J Invest Dermatol. 2007. PMID: 17657246 Free article.

9

Filaggrin null mutations and childhood atopic eczema: a population-based case-control study.

Brown SJ, Relton CL, Liao H, Zhao Y, Sandilands A, Wilson IJ, Burn J, Reynolds NJ, McLean WH, Cordell HJ. Brown SJ, et al. Among authors: liao h. J Allergy Clin Immunol. 2008 Apr;121(4):940-46.e3. doi: 10.1016/j.jaci.2008.01.013. Epub 2008 Mar 4. J Allergy Clin Immunol. 2008. PMID: 18313126 Free PMC article.

10

A heterozygous frameshift mutation in the V1 domain of keratin 5 in a family with Dowling-Degos disease.

Liao H, Zhao Y, Baty DU, McGrath JA, Mellerio JE, McLean WH. Liao H, et al. J Invest Dermatol. 2007 Feb;127(2):298-300. doi: 10.1038/sj.jid.5700523. Epub 2006 Aug 17. J Invest Dermatol. 2007. PMID: 16917491 Free article.

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