Medicine and Dentistry
Patient
81%
Retina
59%
Gene
58%
Diseases
52%
Age Related Macular Degeneration
43%
Diagnosis
39%
Mendelian Randomization Analysis
34%
Eye Disease
34%
Genetic Screening
33%
Retinal Disease
32%
Family
30%
Phenotype
29%
Agents Acting on the Eye
25%
Autofluorescence
24%
Child
24%
Visual Impairment
23%
Vision
23%
Development
21%
Retina Disease
20%
Analysis
20%
Examination
19%
Macular Degeneration
17%
Dysplasia
17%
Cells
17%
Exon
16%
Adult
14%
Visual Acuity
14%
Comprehension
14%
Retinal Imaging
14%
Odds Ratio
13%
Exercise
13%
Clinical Genetics
13%
Molecular Diagnosis
12%
Exome Sequencing
12%
Ornithine Oxoacid Aminotransferase
12%
Study Design
11%
Dark Adaptation
11%
Congenital Stationary Night Blindness
11%
Skin
11%
Human
11%
Pediatric Ophthalmology
10%
Spectral Domain Optical Coherence Tomography
10%
Etiology
10%
Retina Degeneration
10%
Ophthalmology
10%
Cataract
9%
Human Phenotype Ontology
9%
Phenome
9%
Health Outcomes
9%
Aptitude
9%
Biochemistry, Genetics and Molecular Biology
Nested Gene
100%
Albinism
65%
Mutation
61%
Retinitis pigmentosa
34%
Mendelian Randomization
34%
Age
34%
Proband
34%
Genetics
33%
Protein
33%
Phenotype
30%
Genetic Screening
23%
Pediatrics
20%
Penetrance
20%
Exome Sequencing
20%
Data Base
19%
Coding
19%
Development
18%
Autosomal Recessive Inheritance
18%
Autophagy
17%
CRISPR/Cas9
17%
Induced Pluripotent Stem Cell
17%
Stem Cell Line
17%
Homozygosity
16%
Human
15%
Electric Potential
13%
Health
13%
DNA Damage
13%
Tyrosinase
12%
Pigmentation
12%
TRPM1
11%
Association
11%
Vision
11%
Introspection
10%
KCNJ13
10%
Potassium Channel
10%
Screening
10%
Allele
10%
Haplotype
10%
Exercise
9%
Aptitude
9%
Genotyping
9%
Skin Pigmentation
9%
Leadership
8%
Videorecording
8%
Crystal
8%
Melanocyte
8%
Lysozyme
8%
Gene Mutation
8%
Melanogenesis
8%
Genome Editing
8%
