Biochemistry, Genetics and Molecular Biology
Mutation
100%
Nested Gene
79%
Age
75%
Protein
40%
Genome-Wide Association Study
39%
Autosomal Dominant Inheritance
34%
Association
30%
Tumor Necrosis Factors
27%
Glycosylation
27%
Whole Genome Sequencing
27%
HTRA1
27%
Transcriptome
27%
Immunoglobulin G
27%
USH2A
27%
Visual Field
12%
Computer Model
12%
Genetics
11%
Polysaccharides
10%
TIMP3
10%
Membrane
10%
Mouse
10%
Hearing
9%
Genetic Screening
9%
Proband
8%
Spectrum
8%
Missense Mutation
8%
Introspection
7%
Sample Size
6%
Genetic Association
6%
Gene Locus
6%
Genetic Divergence
6%
MMP9
6%
Gene Expression
6%
MGAT3
5%
FUT8
5%
Transcription Factor
5%
Glycosyltransferase
5%
Regulatory Mechanism
5%
RUNX1
5%
SMARCB1
5%
IKZF1
5%
Fucosyltransferase
5%
Medicine and Dentistry
Retina Degeneration
81%
Patient
55%
Age
36%
Autosomal Dominant Inheritance
34%
Protein
34%
Therapeutic Procedure
31%
Macular Degeneration
30%
Tumor Necrosis Factor
27%
Pathology
27%
Case Report
27%
Whole Genome Sequencing
27%
Complement Component C1q
27%
Syndrome
27%
Cornea
27%
Retina
21%
Photoreceptor
18%
Hearing Impairment
13%
Visual Field
12%
Visual Impairment
12%
In Silico
12%
Retinal Pigment Epithelium
11%
Age Related Macular Degeneration
11%
Family
11%
Atrophy
11%
Bruch Membrane
10%
Assessment
9%
Diagnosis
9%
Genetic Screening
9%
Missense Mutation
8%
Collagen Type 1
8%
Analysis
7%
Nyctalopia
7%
Retina Dystrophy
7%
Combination Therapy
6%
Agents Acting on the Eye
6%
In Vitro
6%
Motivation
5%
Visual Field Test
5%
Retina Disease
5%
Corneal Keratocyte
5%
Pigment
5%
Optical Coherence Tomography
5%
Neuroscience
Retinal Degeneration
54%
Protein
34%
Complement Component C1q
27%
Tumor Necrosis Factor Alpha
27%
Cornea
27%
Gene
16%
Choroid
13%
Retinal Pigment Epithelium
11%
Collagen Type 1
8%
Bruch's Membrane
6%
In Vitro
6%
