- Works count
- 629
- Citation count
- 38,949
- H-index
- 88
- i10-index
- 295
Research interests
Publications
The Immunomodulatory Metabolite Itaconate Modifies NLRP3 and Inhibits Inflammasome Activation
Cell Metabolism · 2020 · https://doi.org/10.1016/j.cmet.2020.07.016
Atopic dermatitis
Nature Reviews Disease Primers · 2018 · https://doi.org/10.1038/s41572-018-0001-z
The microbiome in patients with atopic dermatitis
Journal of Allergy and Clinical Immunology · 2018 · https://doi.org/10.1016/j.jaci.2018.11.015
When does atopic dermatitis warrant systemic therapy? Recommendations from an expert panel of the International Eczema Council
Journal of the American Academy of Dermatology · 2017 · https://doi.org/10.1016/j.jaad.2017.06.042
RETRACTED: Skin barrier impairment at birth predicts food allergy at 2 years of age
Journal of Allergy and Clinical Immunology · 2016 · https://doi.org/10.1016/j.jaci.2015.12.1312
Skin microbiome before development of atopic dermatitis: Early colonization with commensal staphylococci at 2 months is associated with a lower risk of atopic dermatitis at 1 year
Journal of Allergy and Clinical Immunology · 2016 · https://doi.org/10.1016/j.jaci.2016.07.029
RETRACTED: Skin barrier dysfunction measured by transepidermal water loss at 2 days and 2 months predates and predicts atopic dermatitis at 1 year
Journal of Allergy and Clinical Immunology · 2015 · https://doi.org/10.1016/j.jaci.2014.12.013
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis
Human Molecular Genetics · 2013 · https://doi.org/10.1093/hmg/ddt317
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting
Nature Genetics · 2013 · https://doi.org/10.1038/ng.2739
Filaggrin Mutations Associated with Skin and Allergic Diseases
New England Journal of Medicine · 2011 · https://doi.org/10.1056/nejmra1011040
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
Nature Genetics · 2010 · https://doi.org/10.1038/ng.694
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
Nature Genetics · 2009 · https://doi.org/10.1038/ng.276
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema
Nature Genetics · 2007 · https://doi.org/10.1038/ng2020
Netherton Syndrome: Disease Expression and Spectrum of SPINK5 Mutations in 21 Families
Journal of Investigative Dermatology · 2002 · https://doi.org/10.1046/j.1523-1747.2002.01603.x
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome
Nature Genetics · 2000 · https://doi.org/10.1038/75977
Current projects
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