Keyphrases
Type 2 Diabetes Mellitus (T2DM)
92%
Genome-wide Association Study
88%
Meta-analysis
60%
Peroxisome Proliferator-activated Receptor
35%
Coronary Artery Disease
30%
Genotype
29%
Odds Ratio
26%
Scotland
26%
Single nucleotide Polymorphism
26%
Common Variants
26%
Diabetes
25%
Tayside
24%
Asthma
21%
Obesity
21%
European Ancestry
20%
Genetic Variants
20%
Genetic Architecture
20%
Body Mass Index
18%
Diabetes Genetics
18%
Type 2 Diabetes Risk
18%
Statins
17%
Asthma Exacerbation
17%
Blood Pressure
17%
Scottish
16%
Polymorphism
15%
Filaggrin
14%
Confidence Interval
14%
Lipids
13%
Metformin
13%
Heart Failure
13%
Type 2 Diabetic Patients
13%
SNP
12%
Inhaled Corticosteroids
12%
Susceptibility Loci
12%
Neuropathic Pain
12%
Genetic Risk
12%
Rare Variants
12%
Gain-of-function mutation
12%
Eczema
11%
Genetic Variation
11%
Genome-wide Association Analysis
11%
Hemoglobin A1c (HbA1c)
11%
Diversity Arrays Technology (DArT)
11%
Older Adults
11%
Diabetes Susceptibility
11%
Genetic Loci
10%
Insulin Resistance
10%
Risk Factors
10%
Atopic Dermatitis
10%
Hazard Ratio
10%
Biochemistry, Genetics and Molecular Biology
Genome-Wide Association Study
100%
Genetics
85%
Allele
58%
Genetic Divergence
46%
Genotyping
37%
Single-Nucleotide Polymorphism
31%
Single Nucleotide Polymorphism
27%
Genomics
23%
Genetic Architecture
22%
Genome Wide Association Study
21%
Body Mass
21%
Blood Pressure
17%
Exome
17%
Genetic Risk
16%
Lipid
16%
Genetic Determinism
16%
Peroxisome Proliferator-Activated Receptor
15%
Statin
15%
Gene Locus
14%
Haplotype
14%
Genetic Variation
13%
Rare Variant
12%
Polygenic Score
12%
Insulin Resistance
12%
Mendelian Randomization
11%
Candidate Gene
11%
Sample Size
10%
Minor Allele Frequency
10%
Genetic Association
10%
Gene Expression
9%
Filaggrin
9%
Blood Lipids
8%
Pharmacogenetics
8%
Triglyceride
8%
Lipid Level
8%
Cytochrome P450
7%
Exome Sequencing
7%
Cohort Study
7%
Gene Frequency
7%
Peroxisome
6%
Agonist
6%
Amino Acids
6%
Blood Plasma
6%
HDL-Cholesterol
6%
Cell Function
6%
Missense
6%
Glucose Level
5%
Systolic Blood Pressure
5%
Pharmacogenomics
5%
Pleiotropy
5%