Yiwei Zhao

发表

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Yang Liu, Sen Yang, Miao Sun, 2009, Nature Genetics.

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

Colin N A Palmer, Robert Gruber, C. Palmer, 2007, Nature Genetics.

Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk.

C. Strobl, N. Klopp, T. Illig, 2008, The Journal of allergy and clinical immunology.

Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

S. Cichon, M. Nöthen, C. Bodemer, 2009, Nature Genetics.

Filaggrin mutations are a major predisposing factor in childhood-onset adult-persistent atopic dermatitis

R. Trembath, N. Reynolds, J. Barker, 2006 .

Analysis of the individual and aggregate genetic contributions of previously identified SPINK 5 , KLK 7 and FLG polymorphisms to eczema risk

C. Strobl, N. Klopp, T. Illig, 2015 .

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

D. Goudie, Yiwei Zhao, A. Irvine, 2006, The Journal of investigative dermatology.

Filaggrin null alleles are not associated with psoriasis.

R. McManus, C. Palmer, R. Trembath, 2007, The Journal of investigative dermatology.

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

C. Palmer, R. Trembath, N. Reynolds, 2007, The Journal of investigative dermatology.

Atopic dermatitis and skin disease Filaggrin null mutations and childhood atopic eczema : A population-based case-control study

H. Cordell, C. Relton, I. Wilson, 2022 .

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

J. McGrath, Yiwei Zhao, W. McLean, 2007, The Journal of investigative dermatology.

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

H. Cordell, R. Trembath, C. Relton, 2008, The Journal of investigative dermatology.

Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

Colin N A Palmer, Ann Sergeant, Hans Bisgaard, 2006, Nature Genetics.

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris

S. Bale, D. Goudie, C. Munro, 2006, Nature Genetics.

Filaggrin null mutations are associated with increased asthma severity in children and young adults.

Colin N A Palmer, C. Palmer, Yiwei Zhao, 2007, The Journal of allergy and clinical immunology.

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy

C. Wijmenga, G. Roberts, H. Cordell, 2011, The Journal of allergy and clinical immunology.

Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations.

N. Klopp, T. Illig, J. Ring, 2006, The Journal of allergy and clinical immunology.

The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study.

M. Pembrey, G. Smith, C. Palmer, 2008, The Journal of allergy and clinical immunology.

Statins downregulate K6a promoter activity: a possible therapeutic avenue for pachyonychia congenita.

Yiwei Zhao, W. McLean, Ulrike Gartner, 2011, The Journal of investigative dermatology.

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

H. Cordell, C. Relton, N. Reynolds, 2009, The British journal of dermatology.

Erratum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis (Nature Genetics (2009) 41 (228-233))

S. Cichon, M. Nöthen, C. Bodemer, 2009 .

Filaggrin loss‐of‐function variants are associated with atopic comorbidity in pediatric inflammatory bowel disease

H. Drummond, E. Nimmo, J. Satsangi, 2009, Inflammatory bowel diseases.