Keyphrases
Atopic Dermatitis
100%
Filaggrin
88%
Gain-of-function mutation
44%
Eczema
37%
Filaggrin mutations
35%
Ichthyosis Vulgaris
33%
Pachyonychia Congenita
29%
Filaggrin Gene
29%
Epidermis
28%
Small Interfering RNA (siRNA)
21%
Atopic Eczema
20%
Skin Barrier
19%
Filaggrin Gene mutation
16%
Keratin
15%
Mutation in the Filaggrin Gene
14%
Psoriasis
14%
Filaggrin null mutations
14%
Stratum Corneum
14%
Asthma
14%
Null mutation
13%
Palmoplantar Keratoderma
13%
Odds Ratio
12%
Epidermolysis Bullosa
12%
Keratinocytes
11%
Allergy
10%
2282del4
10%
Transepidermal Water Loss
10%
R501X
9%
Autosomal Dominant
9%
Natural Moisturizing Factor
9%
Atopic Disease
9%
Food Allergy
9%
FLG mutation
9%
Genotype
9%
Fuchs Endothelial Corneal Dystrophy
8%
Skin Diseases
8%
Null Allele
8%
Susceptibility Loci
8%
Allele-specific
8%
Risk Factors
8%
Singapore Chinese
8%
Confidence Interval
8%
Skin Barrier Function
7%
Predisposing Factors
7%
Genome-wide Association Study
7%
Corneocytes
7%
Autosomal Recessive
6%
Keratin 5
6%
Peanut Allergy
6%
Non-associated
6%
Biochemistry, Genetics and Molecular Biology
Filaggrin
38%
Keratin
30%
Small Interfering RNA
18%
Allele
18%
Genetics
17%
Autosomal Dominant Inheritance
14%
Loss of Function Mutation
13%
Keratinocyte
12%
Missense Mutation
12%
Epidermolysis bullosa
11%
Genomics
10%
Gene Mutation
10%
Autosomal Recessive Inheritance
7%
Genome-Wide Association Study
7%
Exome Sequencing
7%
Candidate Gene
6%
Exon
6%
Genodermatosis
6%
Messenger RNA
6%
N-Terminus
5%
Keratin 12
5%
Molecular Genetics
5%
Clinical Trial
5%
Medicine and Dentistry
Atopic Dermatitis
34%
Filaggrin
29%
Pachyonychia congenita
18%
Diseases
16%
Keratin
15%
Ichthyosis vulgaris
12%
Loss of Function Mutation
9%
Palmoplantar Keratoderma
8%
Dermatosis
7%
Small Interfering RNA
7%
Dermatitis
7%
Autosomal Dominant Inheritance
6%
Skin Water Loss
6%
Disease
6%
Atopy
6%
Missense Mutation
6%
Chemexfoliation
5%
Keratinocyte
5%
Sensitization
5%
Allele
5%
