Medicine & Life Sciences
Parkinson Disease
100%
Genome-Wide Association Study
83%
Genes
74%
Genome
73%
Single Nucleotide Polymorphism
66%
Exome
59%
Meta-Analysis
50%
Mutation
49%
Mitochondrial DNA
46%
Phenotype
44%
National Heart, Lung, and Blood Institute (U.S.)
43%
Venous Thromboembolism
38%
Precision Medicine
36%
Whole Genome Sequencing
35%
Pituitary ACTH Hypersecretion
32%
Atherosclerosis
31%
Population
30%
Whole Exome Sequencing
28%
Alleles
25%
African Americans
24%
C-Reactive Protein
20%
Age of Onset
19%
Genomics
19%
Hispanic Americans
19%
Epidemiology
19%
Leukocytes
17%
Factor VII
17%
Random Allocation
17%
Fibrinogen
17%
Blood Cells
16%
Hematopoiesis
16%
Disease Susceptibility
16%
Gene Frequency
15%
Pediatrics
15%
Abdominal Aortic Aneurysm
15%
Telomere
15%
factor VIII, von Willebrand factor drug combination
14%
Osteosarcoma
14%
Chromosomes
13%
Inborn Genetic Diseases
13%
Alzheimer Disease
13%
Erythrocytes
13%
Datasets
13%
Child
12%
Hemostatics
12%
Mendelian Randomization Analysis
12%
Endothelial Protein C Receptor
12%
Genotype
11%
Odds Ratio
11%
Germ Cell and Embryonal Neoplasms
11%