Medicine and Dentistry
Age
37%
Alternative RNA Splicing
17%
Analysis
20%
Aortic Dissection
17%
Cardiac Magnetic Resonance Imaging
9%
Cardiomyocyte
8%
Cardiomyopathy
69%
Caregiver
8%
Cells
13%
Clinical Method
10%
Diagnosis
10%
Dilated Cardiomyopathy
10%
Diseases
18%
Dissection
20%
Dysplasia
26%
Embryonic Hemoglobin
14%
Family
12%
Female
10%
Gene
77%
Genotype Phenotype Correlation
17%
Haploinsufficiency
24%
Haplotype
9%
Heart Transplantation
8%
Heart Ventricle Arrhythmia
15%
Hospital Mortality
8%
Hypertension
8%
In Silico
13%
Induced Pluripotent Stem Cell
13%
Introspection
17%
Male
10%
Medical Record
10%
Mitogen Activated Protein Kinase 3
17%
Mortality Rate
8%
Neurodevelopmental Disorder
13%
Nonsense Mediated mRNA Decay
8%
Pathogenicity
8%
Patient
68%
Penetrance
8%
Phenotype
97%
Postoperative Complication
8%
Predictor
8%
Promoter Region
8%
Real-Time Polymerase Chain Reaction
8%
Recognition
8%
RNA Sequence
8%
Sex
8%
Skin
8%
Syndrome
14%
Thoracic Aortic Aneurysm
8%
Vascular Disease
17%
Biochemistry, Genetics and Molecular Biology
Age
36%
Allele
17%
Alternative Splicing
17%
Aptitude
5%
BCL11A
17%
Cell Membrane
5%
Cellular Respiration
5%
Chromosome
11%
Contrast
5%
DNA
5%
Drosophila
5%
Dysplasia
25%
Electric Potential
11%
Energy-Dispersive X-Ray Spectroscopy
11%
Exome Sequencing
13%
Extraction
5%
FBN1
7%
Fetal Hemoglobin
5%
Fibroblast
5%
FLNA
17%
Gadolinium
7%
GenBank
5%
Genetic Code
77%
Genetics
31%
Genotype Phenotype Correlation
17%
Geographic Distribution
5%
Haploinsufficiency
23%
Haplotype
9%
HBG1
7%
Introspection
35%
Kinase
17%
Lifespan
5%
Locomotion
5%
Magnetism
7%
Marfan's Syndrome
17%
Mental Retardation
41%
mRNA Expression Level
5%
Mutation
31%
Nerve Cell Plasticity
10%
Nested Gene
77%
Neurotransmission
5%
Orthology
5%
Phenotype
100%
Pregnancy
17%
Promoter Region
5%
Protein
24%
Reduction (Chemistry)
5%
Spectrum
22%
Visibility
5%
Western Blot
5%
Neuroscience
Alternative Splicing
17%
Aneurysm
7%
Cognition
17%
Dependent Personality Disorder
10%
Epilepsy
17%
Exome Sequencing
13%
Gait
5%
Gene Expression
5%
Intellectual Disability
17%
Long-Term Memory
5%
Membrane Transport
5%
Neurite Outgrowth
5%
Neurodevelopmental Disorder
13%
Neuron
11%
Phenotype
17%
Psychopathology
17%
Receptor Tyrosine Kinase
5%
Reference Memory
5%
RNA
5%
Single-Pass Transmembrane Proteins
5%
Synapse
17%
X Chromosome
5%
