Keyphrases
Pedigree
100%
Exome Sequencing
75%
Retinal Degeneration
54%
Exome
52%
Genome Analysis
44%
Sequence Variants
40%
Consanguineous
40%
Inherited Retinal Degeneration
40%
Whole Exome Sequencing
40%
Causal mutation
35%
Cardiac Surgery
33%
Frailty
33%
Frail Elderly
33%
Binocular Interaction
33%
Indel
33%
Rapid Identification
33%
Activity-dependent
33%
Retinol-binding Protein 4 (RBP4)
33%
Needle-like
33%
Cortical Representation
33%
Visual Experience
33%
Retinal Dystrophy
33%
Genotype-phenotype Association
33%
Network Meta-analysis
33%
Neuronal Circuits
33%
Spinal Anesthesia
33%
Intrinsic Mechanism
33%
Post-dural Puncture Headache
33%
Optical Response
33%
Atraumatic
33%
Developmental Abnormality
33%
Respirator
33%
Contralateral Eye
33%
Safety Concerns
33%
Cortical Maps
33%
Genetic Analysis
33%
COVID-19 Pandemic
33%
Quantitative Evaluation
33%
Quality of Vision
33%
Variant Filtering
33%
Pakistani
33%
Cerebral Cortex
33%
Novel mutation
33%
Canonical Model
33%
Mouse Visual Cortex
33%
Binocular
33%
Visual Deprivation
33%
Protection Level
33%
Evaluation Method
33%
Cause of Disease
33%
Biochemistry, Genetics and Molecular Biology
Pedigree
100%
Exome
85%
Exome Sequencing
75%
Indel
33%
Retinol Binding Protein 4
33%
Genotyping
33%
Genetics
33%
Filtration
33%
Retinitis pigmentosa
25%
RPE65
19%
Vitamin A
16%
USH2A
15%
Autosomal Recessive Inheritance
12%
PDE6B
12%
Photosynthetic Pigment
12%
Dideoxynucleotide Sequencing
10%
Visual Field
8%
Vitamin A Deficiency
8%
Visual Acuity
8%
Allele
8%
Transthyretin
8%
Genetic Disorder
8%
Retinol
8%
Metabolic Pathway
8%
Single-Nucleotide Polymorphism
8%
Next Generation Sequencing
8%
Homozygosity
8%
ABCA4
8%
Absorption
8%
Photoreceptor Cell
8%
Messenger RNA
8%
Haplotype Map
6%
CNGB1
6%
GUCY2D
6%
Reference Database
6%
