Biochemistry, Genetics and Molecular Biology
Allele
15%
Autofluorescence
8%
Autosomal Dominant Inheritance
19%
Candidate Gene
18%
Clinical Trial
5%
Cohort Study
5%
CYP1B1
7%
Endophenotype
6%
Exome
7%
Exome Sequencing
6%
Exon
9%
Eye Development
6%
Gene Linkage
10%
Gene Locus
13%
Genetic Architecture
6%
Genetic Association
6%
Genetic Correlation
8%
Genetic Counseling
8%
Genetic Determinism
7%
Genetic Divergence
21%
Genetic Risk
7%
Genetic Screening
10%
Genetics
100%
Genome Wide Association Study
15%
Genome-Wide Association Study
52%
Genomics
12%
Genotyping
12%
Haplotype
18%
Intraocular Pressure
39%
Leber Hereditary Optic Neuropathy
27%
Mendelian Randomization
9%
Microperimetry
6%
Microsatellite Marker
6%
Mitochondrial DNA
9%
Mitochondrial Genome
6%
MYOC
9%
Optineurin
7%
Pedigree
38%
Penetrance
18%
Photosynthetic Pigment
7%
Polygenic Score
15%
Prevalence
25%
Proband
10%
Rare Variant
9%
Retinal Ganglion Cell
6%
Single Nucleotide Polymorphism
12%
Single-Nucleotide Polymorphism
15%
Twin Study
8%
Visual Field
9%
Vitamin D
9%
Medicine and Dentistry
Age Related Macular Degeneration
6%
Agents Acting on the Eye
15%
Autofluorescence
16%
Biometry
7%
Cataract
14%
Clinical Trial
6%
Cohort Analysis
8%
Congenital Cataract
6%
Diseases
32%
Eye Disease
16%
Eye Examination
6%
Eye Injury
10%
Family History
6%
Gene Linkage
6%
Gene Locus
6%
Genetic Risk
6%
Genome Wide Association Study
25%
Glaucoma
53%
Heritability
9%
Intraocular Pressure
13%
Keratoconus
9%
Leber Hereditary Optic Neuropathy
14%
Meta-Analysis
13%
Myocilin
11%
Obstructive Sleep Apnea
6%
Odds Ratio
11%
Open Angle Glaucoma
23%
Ophthalmology
6%
Optic Disc
7%
Optic Nerve
7%
Optical Coherence Tomography
11%
Pediatrics
14%
Pedigree
10%
Placebo
11%
Prevalence
24%
Pterygium
8%
Randomized Controlled Trial
6%
Refractive Error
33%
Retina Disease
7%
Retinal Blood Vessel
5%
Retinal Nerve Fiber Layer
11%
Retinitis pigmentosa
5%
Retinopathy
5%
Scotoma
5%
Single Nucleotide Polymorphism
8%
Spectral Domain Optical Coherence Tomography
6%
Sun Exposure
12%
Twin Study
5%
Visual Acuity
11%
Visual Impairment
13%
Neuroscience
Age-Related Macular Degeneration
5%
Endophenotype
5%
Gene Locus
5%
Genome-Wide Association Study
19%
Glaucoma
69%
Haplotype
5%
Intraocular Pressure
22%
Meta-Analysis
7%
Myocilin
11%
Myopia
22%
Nerve Fiber
7%
Open-Angle Glaucoma
56%
Ophthalmic Disorder
5%
Optic Nerve
10%
Optic Neuropathy
16%
Refractive Error
16%
Retinal Disease
9%
Retinal Ganglion Cell
5%
Single-Nucleotide Polymorphism
5%
Stem Cell
6%