Huijia Chen

The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases

Ildikó Szeverényi, Andrew Cassidy, Cheuk Wang Chung et al. · Human Mutation · 2007 · 370 citations · Full text

Comprehensive Information, Human Genome Variations, Genetics +22

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

Sanja Kežić, Gráinne M. O’Regan, René Lutter et al. · Journal of Allergy and Clinical Immunology · 2012 · 263 citations · Full text

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

Gráinne M. O’Regan, P. M. J. H. Kemperman, Aileen Sandilands et al. · Journal of Allergy and Clinical Immunology · 2010 · 147 citations · Full text

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

Stephan Weidinger, Hansjörg Baurecht, Stefan Wagenpfeil et al. · Journal of Allergy and Clinical Immunology · 2008 · 83 citations · Full text

Medicine, Genetics, Genetic Epidemiology +9

Unique and Recurrent Mutations in the Filaggrin Gene in Singaporean Chinese Patients with Ichthyosis Vulgaris

Huijia Chen, Jean Chin Ching Ho, Aileen Sandilands et al. · Journal of Investigative Dermatology · 2008 · 68 citations · Full text

Recurrent Mutations, Mendelian Disorder, Genetic Disorder +10