Keyphrases
Retinal Dystrophy
100%
Retinitis pigmentosa
67%
CRB1
61%
Visual Acuity
51%
Clinical Characteristics
46%
Genetic Characteristics
46%
Clinical Genetics
46%
Leber Congenital Amaurosis
38%
Best-corrected Visual Acuity
32%
Histopathological Examination
30%
Clinical Trials
30%
Histopathological Features
30%
Clock Genes
30%
Age of Onset
28%
Functional Annotation
27%
Retinal pigment Epithelium
25%
Phenotypic Characteristics
25%
Cone-rod Dystrophy
24%
Electroretinography
24%
Spectral Domain Optical Coherence Tomography (SD-OCT)
20%
Late-onset
20%
Older Patients
20%
Haploinsufficiency
20%
Missense Variants
20%
Follow-up Time
19%
Genetic Isolate
19%
Medical Records
18%
Severe Phenotype
17%
Choroid Plexus
17%
Choroid Plexus Epithelial Cells
17%
Genotype-phenotype Correlation
16%
Gene Expression
16%
Macular Dystrophy
16%
Photoreceptor
15%
RPGR Gene
15%
Retinal Organoids
15%
Rho-associated
15%
SLC16A1
15%
Gene Expression Profile
15%
Monocarboxylate Transporter 1 (MCT1)
15%
Phenotypic Spectrum
15%
Lactate Transport
15%
Mutant Mice
15%
Human Iris
15%
Mouse Eye
15%
CRB1 mutation
15%
Comparative Gene Expression
15%
Natural History
15%
Cas9 Protein
15%
RPE65
15%
Medicine and Dentistry
Retina Dystrophy
92%
Visual Acuity
58%
Retinitis pigmentosa
54%
Leber Congenital Amaurosis
38%
Best Corrected Visual Acuity
38%
Clinical Trial
38%
Cone Rod Dystrophy
34%
Clinical Genetics
33%
Photoreceptor
30%
Electroretinography
27%
Spectral Domain Optical Coherence Tomography
24%
Central Retina
22%
Visual Field
21%
Medical Record
19%
Retina Degeneration
18%
Visual Impairment
17%
Genotype Phenotype Correlation
16%
Anticipation
15%
Clinical Observation
15%
Choroid Plexus
15%
Cross Sectional Study
15%
Choroideremia
15%
Photoreceptor Outer Segment
15%
Rhythm
15%
Genetic Trait
15%
Phagocytosis
15%
Circadian Rhythm
15%
Retinoschisis
15%
Iris
15%
Maculopathy
15%
Exon
15%
Retinal Imaging
14%
Disease Course
14%
Diseases
14%
Autofluorescence
12%
Ophthalmoscopy
11%
Cone Dystrophy
10%
Autosomal Recessive Inheritance
10%
Fundus Photography
10%
Retinal Pigment Epithelium
10%
Histopathology
10%
Indel Mutation
10%
Clinical Finding
10%
Cohort Analysis
10%
Optical Coherence Tomography
10%
Low Vision
9%
Disorientation
8%
Medical History
7%
Clinical Examination
6%
Retrospective Cohort Study
6%
Biochemistry, Genetics and Molecular Biology
Retinitis pigmentosa
32%
Genetics
30%
Gene Expression
30%
Missense
30%
Photosynthetic Pigment
30%
Medical Record
27%
Animal Model
25%
Best Corrected Visual Acuity
24%
Photoreceptor Cell
21%
Haploinsufficiency
20%
Leber's Congenital Amaurosis
20%
Visual Acuity
20%
Electroretinography
17%
SLC16A1
15%
Genetic Trait
15%
CRISPR/Cas9
15%
Blood Cerebrospinal Fluid Barrier
15%
Eye Development
15%
Maturation
15%
Pigmentation
15%
Stem Cell
15%
Retinal
15%
RPE65
15%
Humor
15%
Exon
12%
Genotype Phenotype Correlation
12%
Maculopathy
10%
Indel
10%
Cohort Study
10%
Homeodomain
10%
Knowledge Base
9%
Knockout Rat
7%
SCN4B
7%
SIX1
7%
CDKN2B
7%
KCNA5
7%
SLC4A4
7%
Embryonic Stem Cell
6%
GLUT1
5%
Supernatant
5%
Monocarboxylate Transporter
5%
Chemical Oxygen Demand
5%
Phototransduction
5%
Opsin
5%
Retina Development
5%
