Biochemistry, Genetics and Molecular Biology
Mutation
100%
Nested Gene
57%
Exome Sequencing
34%
Phenotype
25%
Somatic Mutation
14%
Development
13%
Association
13%
Spectrum
12%
Sample
11%
Aldosterone
11%
Sequencing
11%
Exome
10%
Missense Mutation
10%
Mental Retardation
9%
Genome-Wide Association Study
9%
Mouse
8%
Mutant
7%
Immunoglobulin A
7%
Comprehension
7%
Germline
7%
Allele
7%
Age
7%
DNA Methylation
6%
KCNJ5
6%
Calcium Channel
6%
Transcriptome
6%
Potassium Channel
6%
C-Terminus
6%
Loss of Heterozygosity
6%
Histone
6%
Regulatory Mechanism
6%
Molecule
6%
CACNA1H
5%
Speech and Language
5%
CHD3
5%
E2F1
5%
Gain of Function Mutation
5%
Lysosomal Storage Disease
5%
Loss of Function Mutation
5%
Candidate Gene
5%
Autosomal Recessive Inheritance
5%
Proband
5%
Medicine and Dentistry
Patient
30%
Gene
26%
Disease
13%
Syndrome
12%
Diagnosis
12%
Analysis
11%
Exome Sequencing
11%
Mutant
10%
Development
9%
Phenotype
9%
Primary Hyperaldosteronism
7%
Lung Adenocarcinoma
7%
Combination Therapy
7%
Cells
7%
Family
6%
Follow up
6%
Association
5%
Gain of Function Mutation
5%
CACNA1H
5%
Cerebral Hemorrhage
5%
Liver Polycystic Disease
5%
Alzheimer's Disease
5%
Polycystin 1
5%
Age
5%
Base
5%
Exome
5%
Hypertension
5%
Neoplasm
5%
Somatic Mutation
5%
