Medicine & Life Sciences
Mexican Americans
100%
Type 2 Diabetes Mellitus
49%
Genome
46%
Genes
45%
Phenotype
44%
Exome
38%
Genome-Wide Association Study
38%
Chromosomes
34%
Diabetic Nephropathies
30%
Pedigree
29%
Genetic Variation
27%
African Americans
26%
Population
23%
Human Genetics
23%
Single Nucleotide Polymorphism
23%
Obesity
21%
Brain
18%
Chromosomes, Human, Pair 7
18%
National Heart, Lung, and Blood Institute (U.S.)
17%
Whole Genome Sequencing
17%
Chromosomes, Human, Pair 6
17%
Depression
17%
Genetic Loci
17%
Genotype
17%
Quantitative Trait Loci
16%
Chromosome Mapping
16%
Molecular Epidemiology
16%
North American Indians
15%
Albuminuria
15%
Human Chromosomes
14%
Endophenotypes
14%
Carotid Intimal Medial Thickness 1
14%
Insulin
14%
Metabolic Syndrome
13%
Meta-Analysis
12%
Fasting
12%
Population Genetics
12%
Proteins
11%
Nuclear Family
11%
Genetic Association Studies
10%
Lod Score
10%
Alleles
10%
Population Biological Variation
10%
Progranulins
10%
High-Throughput Nucleotide Sequencing
10%
Medical Genetics
9%
CCR5 Receptors
9%
Rare Diseases
9%
Major Depressive Disorder
9%
Acanthosis Nigricans
9%
Chromosomes, Human, Pair 11
9%
Insulin Resistance
9%
Age of Onset
9%
Catalogs
9%
Blood Pressure
9%
Gallbladder Diseases
9%
Hexosaminidases
8%
Precision Medicine
8%
Open Reading Frames
8%
Chromosomes, Human, Pair 1
8%
United States Department of Veterans Affairs
8%
Databases
7%
JC Virus
7%
5' Untranslated Regions
7%
Proinsulin
7%
Nucleotides
7%
Datasets
7%
Child
7%
Sleep Apnea Syndromes
7%
Tunica Intima
7%
Hippocampus
7%
Cannabis
6%
Haplotypes
6%
Genomics
6%
Protein Domains
6%
Amygdala
6%
Glucose
6%
Carotid Arteries
6%
Carboxypeptidases A
6%
Protein Isoforms
6%
Crohn Disease
6%
Birth Weight
6%
Sample Size
6%
Names
6%
Social Class
6%
Psychological Power
6%
Cysteine
6%
Primates
6%
Common Carotid Artery
6%
White Matter
6%
Introns
5%
Triglycerides
5%
Fats
5%
Renal Insufficiency
5%
Psychology Recognition
5%
India
5%
Smoking
5%
Schizophrenia
5%
Disease Progression
5%
Cognition
5%