L. Campbell

发表

Multi-ethnic genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

Manuel A. R. Ferreira, M. Jarvelin, C. Gieger, 2015, 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.

Atopic dermatitis and skin disease Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency

S. Kežić, R. Lutter, G. Puppels, 2012 .

Skin barrier function in healthy subjects and patients with atopic dermatitis in relation to filaggrin loss-of-function mutations.

S. Kežić, E. Koster, M. Verberk, 2011, The Journal of investigative dermatology.

The persistence of atopic dermatitis and filaggrin (FLG) mutations in a US longitudinal cohort.

D. Margolis, T. Rebbeck, N. Mitra, 2012, The Journal of allergy and clinical immunology.

Atopic dermatitis and disease severity are the main risk factors for food sensitization in exclusively breastfed infants.

C. Flohr, K. Logan, G. Lack, 2014, The Journal of investigative dermatology.

Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin

J. Kudoh, C. Munro, A. Irvine, 2012, The Journal of investigative dermatology.

Filaggrin loss‐of‐function mutations are associated with early‐onset eczema, eczema severity and transepidermal water loss at 3 months of age

C. Flohr, G. Lack, J. Barker, 2010, The British journal of dermatology.

Association between domestic water hardness, chlorine, and atopic dermatitis risk in early life: A population-based cross-sectional study.

D. Strachan, C. Flohr, K. Logan, 2016, The Journal of allergy and clinical immunology.

Reliability and validity of genotyping filaggrin null mutations.

D. Margolis, T. Rebbeck, N. Mitra, 2013, Journal of dermatological science.

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

C. Gieger, G. Barton, A. Balmain, 2013, The Journal of allergy and clinical immunology.

Heterozygous null alleles in filaggrin contribute to clinical dry skin in young adults and the elderly.

C. Palmer, C. Munro, W. McLean, 2009, The Journal of investigative dermatology.

Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status

C. Greenwood, A. Irvine, F. Rousseau, 2013, The Journal of allergy and clinical immunology.

Loss-of-function mutations in the filaggrin gene lead to reduced level of natural moisturizing factor in the stratum corneum.

S. Kežić, G. Puppels, A. Irvine, 2008, 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.

Filaggrin Null Alleles Are Not Associated with

R. Trembath, F. Capon, D. Kane, 2007 .

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Matti Pirinen, Christian Gieger, Peter Donnelly, 2012 .

Filaggrin breakdown products determine corneocyte conformation in patients with atopic dermatitis

S. Kežić, A. Irvine, M. McAleer, 2015, The Journal of allergy and clinical immunology.

Skin barrier dysfunction measured by transepidermal water loss at 2 days and 2 months predates and predicts atopic dermatitis at 1 year

A. Irvine, L. Campbell, W. McLean, 2015, The Journal of allergy and clinical immunology.

Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity

S. Kežić, A. Irvine, G. O’Regan, 2011, Allergy.

Filaggrin-null mutations are associated with increased maturation markers on Langerhans cells

R. Weller, S. Howie, J. Schwarze, 2016, The Journal of allergy and clinical immunology.

South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin

S. Kežić, Y. Wen, A. Irvine, 2014, The Journal of allergy and clinical immunology.

Filaggrin loss-of-function mutations and atopic dermatitis as risk factors for hand eczema in apprentice nurses: part II of a prospective cohort study

S. Kežić, M. Verberk, L. Campbell, 2013, Contact dermatitis.

Loss-of-Function Mutations in the Gene Encoding Filaggrin Are Not Strongly Associated with Chronic Actinic Dermatitis.

S. Ibbotson, S. Brown, L. Campbell, 2015, The Journal of investigative dermatology.

Impact of atopic dermatitis and loss‐of‐function mutations in the filaggrin gene on the development of occupational irritant contact dermatitis

S. Kežić, S. Weidinger, L. Landeck, 2013, The British journal of 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.

Patients with atopic dermatitis with filaggrin loss‐of‐function mutations show good but lower responses to immunosuppressive treatment

M. Leeflang, S. Kežić, P. Spuls, 2017, The British journal of dermatology.

Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis.

O. Sarig, G. Ast, N. Shomron, 2016, The Journal of investigative dermatology.

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

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

Multi-ethnic genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

David M. Evans, M. Jarvelin, C. Gieger, 2015, Nature Genetics.

Intragenic Copy Number Variation within Filaggrin Contributes to the Risk of Atopic Dermatitis with a Dose-Dependent Effect

S. Kežić, H. Cordell, A. Irvine, 2011, The Journal of investigative dermatology.

Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis.

D. Postma, X. Estivill, G. Koppelman, 2010, The Journal of investigative dermatology.

Wide spectrum of filaggrin‐null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations

M. Tang, J. Common, H. Cordell, 2011, The British journal of dermatology.

A homozygous frameshift mutation in the murine filaggrin gene facilitates enhanced percutaneous allergen priming

A. Shiohama, Takashi Sasaki, N. Shimizu, 2009, Nature Genetics.

Generation and Characterisation of Keratin 7 (K7) Knockout Mice

E. Lane, W. McLean, S. Fleming, 2013, PloS one.

Genetics (AAGC) (2015). Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.

Weidinger, M. Jarvelin, C. Gieger, 2015 .

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.

Raman profiles of the stratum corneum define 3 filaggrin genotype–determined atopic dermatitis endophenotypes

Gerwin J. Puppels, Peter J. Caspers, G. Puppels, 2010, The Journal of allergy and clinical immunology.

Chromosome 11q13.5 variant associated with childhood eczema: An effect supplementary to filaggrin mutations

H. Cordell, A. Irvine, G. O’Regan, 2010, The Journal of allergy and clinical immunology.

Filaggrin genotype does not determine the skin's threshold to UV-induced erythema

S. Ibbotson, A. Dinkova-Kostova, R. Dawe, 2016, The Journal of allergy and clinical immunology.

Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma

L. Tetley, C. Munro, R. Eady, 2009, The British journal of dermatology.

Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis.

O. Sarig, G. Ast, N. Shomron, 2016, The Journal of investigative dermatology.

Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency

S. Kežić, P. Fallon, P. Caspers, 2012, The Journal of allergy and clinical immunology.

Association between domestic water hardness, chlorine, and atopic dermatitis risk in early life: A population-based cross-sectional study.

D. Strachan, K. Logan, G. Lack, 2016, Journal of Allergy and Clinical Immunology.

Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis.

D. Postma, X. Estivill, G. Koppelman, 2010, The Journal of investigative dermatology.