Medicine and Dentistry
Disease
100%
Ichthyosis
84%
Atopic Dermatitis
73%
Autosomal Recessive Inheritance
66%
Hair Follicle
62%
Pachyonychia congenita
58%
Palmoplantar Keratoderma
54%
Dermatitis
52%
Pediatrics
49%
Keratin
46%
Hypotrichosis
44%
Capillary Hemangioma
44%
Desmoglein 1
33%
Scalp
30%
Molecular Epidemiology
29%
Epidermolysis Bullosa Dystrophica
29%
B-Cell Lymphoma
29%
P Cadherin
29%
Tinea Capitis
29%
Griseofulvin
29%
Keratinocyte
28%
Terbinafine
27%
Adverse Event
26%
Alopecia Mucinosa
24%
Prevalence
23%
Desmosome
22%
Genetic Disorder
22%
Exome
21%
Cytoskeleton
21%
Exome Sequencing
21%
Psoriasis
19%
Erythroderma
19%
Loss of Function Mutation
19%
Failure to Thrive
19%
Netherton Syndrome
18%
Pruritus
18%
Missense Mutation
17%
Morphogenesis
17%
Cell Adhesion
17%
Cell Surface
17%
Prematurity
16%
Nevus Sebaceous
16%
Cohort Analysis
16%
Ustekinumab
16%
Diagnosis
16%
Genetic Variability
16%
Scar Formation
16%
Exon
16%
Topical Treatment
16%
Cross Sectional Study
14%
Keyphrases
Atopic Dermatitis
68%
Hair Follicle
62%
Pachyonychia Congenita
58%
Epidermolysis Bullosa
58%
Gain-of-function mutation
50%
Autosomal Recessive
50%
Epidermis
46%
Autosomal Recessive Congenital Ichthyosis
44%
P-cadherin
44%
Palmoplantar Keratoderma
43%
Pediatric
40%
Infantile Hemangioma
35%
Epidermolytic Ichthyosis
33%
Epidermal Differentiation
32%
Ocular Complications
31%
Missense Variants
30%
Direct Sequencing
30%
Molecular Epidemiology
29%
Hair Follicle Development
29%
Tinea Capitis
29%
BNT162b2 Vaccine
29%
Griseofulvin
29%
Clinical Features
29%
Terbinafine
27%
Pathogenic Variants
26%
Hypotrichosis
26%
SAM Syndrome
25%
Periocular
25%
Genetic Defects
24%
Whole Exome Sequencing
23%
Ichthyosis
23%
Hair Growth
22%
Alopecia
22%
Keratin Genes
21%
Desmoglein
20%
Metabolic
20%
Quantitative PCR
20%
KRT10
20%
DSG1
19%
Psoriasis
19%
Scalp
19%
Human Hair
19%
KRT16
18%
Nonsyndromic
18%
Desmosome
18%
Skin Biology
18%
Netherton Syndrome
18%
Clinical Efficacy
18%
Disorders of Cornification
17%
Keratinocytes
17%
Biochemistry, Genetics and Molecular Biology
Autosomal Recessive Inheritance
90%
Genetics
77%
Keratin
60%
Epidermolysis bullosa
58%
Cadherin
51%
Keratinocyte
38%
Prevalence
37%
Autosomal Dominant Inheritance
34%
Missense
32%
Cell Adhesion
27%
Desmoglein-1
25%
Exome Sequencing
23%
Downregulation
23%
Desmosome
22%
Cytoskeleton
21%
Exome
19%
Exon
19%
Loss of Function Mutation
18%
Missense Mutation
17%
Phenotypic Heterogeneity
17%
Morphogenesis
17%
Wnt Signaling Pathway
17%
Pigmentation
17%
Surface Property
17%
Genetic Divergence
16%
Protein Modeling
16%
Keratin 17
15%
Notch Signaling Pathway
14%
Desquamation
14%
Founder Effect
14%
Mesenchymal-Epithelial Transition
14%
CARD Domain
14%
Gentamicin
14%
Calpain
14%
Serpin
14%
ABHD5
14%
Haplotype
14%
Keratin 10
14%
MicroRNA
14%
Revertant
14%
Cathepsin B
14%
Arginine Deiminase
14%
Melanogenesis
14%
Transforming Growth Factor
14%
Nonsense Mutation
14%
Protein Catabolism
14%
Western Blot
13%
Cell Junction
13%
Genodermatosis
13%
Real-Time Polymerase Chain Reaction
12%
