Medicine and Dentistry
Patient
100%
Diagnosis
28%
Best Corrected Visual Acuity
28%
Age
28%
Phenotype
24%
Diseases
22%
Optical Coherence Tomography
21%
Electroretinography
21%
Therapeutic Procedure
18%
Onset Age
18%
Gene
18%
Autofluorescence
17%
Retinitis pigmentosa
17%
Inpatient
16%
Retinopathy
14%
Visual Acuity
14%
Dystrophy
13%
Prevalence
13%
Syndrome
13%
Glaucoma
12%
Hypoplasia
12%
Incidence
12%
Atropine
12%
Maculopathy
11%
Visual Impairment
10%
Child
10%
Follow up
10%
High Myopia
9%
Cataract Surgery
9%
Myopia
9%
Retina Dystrophy
9%
Cohen Syndrome
9%
Retrospective Cohort Study
8%
Cells
8%
Symptom
8%
Morphology
8%
Vision
7%
Life
7%
Optical Coherence Tomography
7%
Whole Genome Sequencing
6%
Assessment
6%
Combination Therapy
6%
Autosomal Recessive Inheritance
6%
Photoreceptor
6%
Retinal Pigment Epithelium
6%
Biological Marker
6%
Diagnostic Error
6%
Deterioration
6%
Inflammatory Disorder
6%
Sex
6%
Biochemistry, Genetics and Molecular Biology
Nested Gene
42%
Age
26%
Genetics
23%
Atropine
14%
Electroretinography
13%
Electric Potential
13%
Incidence
12%
Length
10%
GUCY2D
10%
Exome Sequencing
10%
Best Corrected Visual Acuity
9%
Prevalence
9%
Mouse
8%
Whole Genome Sequencing
6%
Cohort Study
6%
Phenotype
6%
Autosomal Recessive Inheritance
6%
Time
6%
Mutation
6%
Genome-Wide Association Study
6%
Inheritance
6%
YAP1
6%
Sex
6%
Retinitis pigmentosa
5%